[go: up one dir, main page]

 
 
Sign in to use this feature.

Years

Between: -

Subjects

remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline

Journals

remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline

Article Types

Countries / Regions

remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline

Search Results (1,539)

Search Parameters:
Keywords = CEOS

Order results
Result details
Results per page
Select all
Export citation of selected articles as:
20 pages, 4634 KiB  
Article
Comparative Assessment of First-Row 3d Transition Metals (Ti-Zn) Supported on CeO2 Nanorods for CO2 Hydrogenation
by Maria Lykaki, Sofia Stefa, Georgios Varvoutis, Vassilios D. Binas, George E. Marnellos and Michalis Konsolakis
Catalysts 2024, 14(9), 611; https://doi.org/10.3390/catal14090611 - 11 Sep 2024
Viewed by 187
Abstract
Herein, motivated by the excellent redox properties of rod-shaped ceria (CeO2-NR), a series of TM/CeO2 catalysts, employing the first-row 3d transition metals (Ti, V, Cr, Mn, Fe, Co, Ni, Cu, and Zn) as active metal phases, were comparatively assessed under [...] Read more.
Herein, motivated by the excellent redox properties of rod-shaped ceria (CeO2-NR), a series of TM/CeO2 catalysts, employing the first-row 3d transition metals (Ti, V, Cr, Mn, Fe, Co, Ni, Cu, and Zn) as active metal phases, were comparatively assessed under identical synthesis and reaction conditions to decipher the role of active metal in the CO2 hydrogenation process. Notably, a volcano-type dependence of CO2 hydrogenation activity/selectivity was disclosed as a function of metal entity revealing a maximum for the Ni-based sample. Ni/CeO2 is extremely active and fully selective to methane (YCH4 = 90.8% at 350 °C), followed by Co/CeO2 (YCH4 = 45.2%), whereas the rest of the metals present an inferior performance. No straightforward relationship was disclosed between the CO2 hydrogenation performance and the textural, structural, and redox properties, whereas, on the other hand, a volcano-shaped trend was established with the relative concentration of oxygen vacancies and partially reduced Ce3+ species. The observed trend is also perfectly aligned with the previously reported volcano-type dependence of atomic hydrogen adsorption energy and CO2 activation as a function of 3d-orbital electron number, revealing the key role of intrinsic electronic features of each metal in conjunction to metal–support interactions. Full article
Show Figures

Graphical abstract

Graphical abstract
Full article ">Figure 1
<p>XRD patterns of CeO<sub>2</sub>-NR and TM/CeO<sub>2</sub> samples.</p>
Full article ">Figure 2
<p>SEM images of the samples: (<b>a</b>) Ti/CeO<sub>2</sub>, (<b>b</b>) V/CeO<sub>2</sub>, (<b>c</b>) Cr/CeO<sub>2</sub>, (<b>d</b>) Mn/CeO<sub>2</sub>, (<b>e</b>) Fe/CeO<sub>2</sub>, (<b>f</b>) Co/CeO<sub>2</sub>, (<b>g</b>) Ni/CeO<sub>2</sub>, (<b>h</b>) Cu/CeO<sub>2</sub> and (<b>i</b>) Zn/CeO<sub>2</sub>.</p>
Full article ">Figure 3
<p>TEM images of the samples: (<b>a</b>) CeO<sub>2</sub>-NR, (<b>b</b>) Ti/CeO<sub>2</sub>, (<b>c</b>) V/CeO<sub>2</sub>, (<b>d</b>) Cr/CeO<sub>2</sub>, (<b>e</b>) Mn/CeO<sub>2</sub>, (<b>f</b>) Fe/CeO<sub>2</sub>, (<b>g</b>) Co/CeO<sub>2</sub>, (<b>h</b>) Ni/CeO<sub>2</sub>, (<b>i</b>) Cu/CeO<sub>2</sub> and (<b>j</b>) Zn/CeO<sub>2</sub>.</p>
Full article ">Figure 4
<p>H<sub>2</sub>-TPR profiles of CeO<sub>2</sub>-NR and representative TM/CeO<sub>2</sub> samples.</p>
Full article ">Figure 5
<p>XPS spectra of (<b>a</b>) Ce 3d and (<b>b</b>) O 1s of the reduced CeO<sub>2</sub>-NR and optimum catalysts (Fe, Co, Ni, Cu).</p>
Full article ">Figure 6
<p>XPS spectra of (<b>a</b>) Cu 2p, (<b>b</b>) Co 2p, (<b>c</b>) Fe 2p, and (<b>d</b>) Ni 2p of the reduced optimum catalysts (Fe, Co, Ni, Cu).</p>
Full article ">Figure 6 Cont.
<p>XPS spectra of (<b>a</b>) Cu 2p, (<b>b</b>) Co 2p, (<b>c</b>) Fe 2p, and (<b>d</b>) Ni 2p of the reduced optimum catalysts (Fe, Co, Ni, Cu).</p>
Full article ">Figure 7
<p>Comparative assessment of (<b>a</b>) CO<sub>2</sub> conversion and (<b>b</b>) selectivity to CO for the first-row 3d transition metals supported on CeO<sub>2</sub> nanorods. Reaction conditions: WHSV = 30 L·g<sup>−1</sup>·h<sup>−1</sup>, H<sub>2</sub>:CO<sub>2</sub> = 4, P = 1 bar.</p>
Full article ">Figure 8
<p>Metal entity-dependence of CO<sub>2</sub> conversion (solid line) and CH<sub>4</sub> selectivity (dashed line) at 350 °C for the first-row 3d transition metals supported on CeO<sub>2</sub> nanorods.</p>
Full article ">Figure 9
<p>(<b>a</b>) Atomic H adsorption energy on P-2,5-DCP-CTF-M-CO2 ((2-pyridyl)-s-triazine is the simplified unit model of the covalent triazine frameworks (CTF), the unit model and its metal complex is P-2,5-DCP-CTF-M (M = Sc, Ti, V, Cr, Mn, Fe, Co, Ni, Cu, Zn)), (<b>b</b>) barrier energy, and (<b>c</b>) change in CO<sub>2</sub> charge from IS to TS (C) in the formate pathway as a function of 3d-orbital electron number. Initial state (IS) of CO<sub>2</sub> hydrogenation corresponding to the co-adsorption configuration of CO<sub>2</sub> and H atom on the active metal site; transition states (TS); Sc, Ti, and V atoms with less than four 3d-orbital electrons were divided in the left region (orange). The metal atoms, including Mn, Fe, Co, Ni, and Cu, having more than four 3d-orbital electrons were divided in the right region (blue). Reproduced with permission from [<a href="#B58-catalysts-14-00611" class="html-bibr">58</a>].</p>
Full article ">Figure 10
<p>Relationship among the CO<sub>2</sub> conversion rate and CH<sub>4</sub> selectivity at 350 °C with the relative oxygen vacancy and Ce<sup>3+</sup> concentrations for the optimum reduced catalysts (Fe, Co, Ni, Cu).</p>
Full article ">
13 pages, 3575 KiB  
Article
The Effect of Hatch Spacing on the Electrochemistry and Discharge Performance of a CeO2/Al6061 Anode for an Al-Air Battery via Selective Laser Melting
by Yinbiao Li and Weipeng Duan
Crystals 2024, 14(9), 797; https://doi.org/10.3390/cryst14090797 - 9 Sep 2024
Viewed by 249
Abstract
To improve the electrochemical activity and discharge performance of an aluminum-air (Al-air) battery, a commercial 6061 alloy (Al6061) was selected as the anode, and CeO2 was also added inside the anode to enhance its performance. The CeO2/Al6061 composite was prepared [...] Read more.
To improve the electrochemical activity and discharge performance of an aluminum-air (Al-air) battery, a commercial 6061 alloy (Al6061) was selected as the anode, and CeO2 was also added inside the anode to enhance its performance. The CeO2/Al6061 composite was prepared using selective laser melting (SLM) technology. The influence of hatch spacing on the forming quality, corrosion resistance, and discharge performance of the anode was studied in detail. The results showed that with an increase in hatch spacing, the density, corrosion resistance, and discharge performance of the anode first increased and then decreased. When the hatch spacing is 0.13 mm, the anode has the best forming quality. At this point, the density reaches 98.39%, and the self-corrosion rate (SCR) decreases to 2.596 × 10−4 g·cm−2·min−1. Meanwhile, the anode exhibits its highest electrochemical activity and discharge voltage, which is up to −1.570 V. The change in anode performance is related to the defects generated during the SLM forming process. For samples with fewer defects, the anode can dissolve uniformly, while for samples with more defects, the electrode solution is prone to penetrate the defects, causing uneven corrosion and reducing electrochemical and discharge activity. Full article
(This article belongs to the Section Materials for Energy Applications)
Show Figures

Figure 1

Figure 1
<p>Morphology diagram of powder: (<b>a</b>) Al6061 (×500); and (<b>b</b>) CeO<sub>2</sub>/Al6061 (×3.0 k).</p>
Full article ">Figure 2
<p>Surface morphology and density in samples of different hatch spacing.</p>
Full article ">Figure 3
<p>Self-corrosion in samples of different hatch spacing.</p>
Full article ">Figure 4
<p>OCV of samples at different hatch spacing.</p>
Full article ">Figure 5
<p>Polarization curves in samples of different hatch spacing.</p>
Full article ">Figure 6
<p>EIS of samples under different hatch spacing.</p>
Full article ">Figure 7
<p>Equivalent circuit of aluminum anode with different hatch spacing.</p>
Full article ">Figure 8
<p>Discharge parameters of samples of different hatch spacing: (<b>a</b>) real-time discharge voltage; (<b>b</b>) discharge voltage and anode utilization rate.</p>
Full article ">Figure 9
<p>Surface morphology after discharge of anode of different hatch spacing.</p>
Full article ">
17 pages, 447 KiB  
Article
Is the Nexus between Gender Diversity and Firm Financial Distress Moderated by CEO Duality?
by Muhammad Tahir Khan, Waqar Ahmad, Sajjad Nawaz Khan, Valentin Marian Antohi, Costinela Fortea and Monica Laura Zlati
Economies 2024, 12(9), 240; https://doi.org/10.3390/economies12090240 - 9 Sep 2024
Viewed by 311
Abstract
This study examines the impact of gender diversity in the positions of board commissioners, executive directors, and audit committee members on the financial performance of firms experiencing financial trouble. It also evaluates whether the presence of a CEO with multiple responsibilities moderates this [...] Read more.
This study examines the impact of gender diversity in the positions of board commissioners, executive directors, and audit committee members on the financial performance of firms experiencing financial trouble. It also evaluates whether the presence of a CEO with multiple responsibilities moderates this relationship. The analysis encompassed 224 publicly traded companies from the non-financial sector, spanning the years 2012 to 2021. The study employed the dynamic panel model system GMM to address issues of endogeneity, simultaneity, and heterogeneity in the data. The findings indicate that the presence of women on supervisory boards and in senior positions has a substantial impact. Companies with a higher number of female board members have reduced financial hardship among Malaysian listed enterprises. Female directors exhibit a greater level of caution and risk aversion while participating in management choices, which is a significant conclusion. Research indicates that the majority of financial variables are inherently endogenous, so dynamic models are better suited for analyzing the interaction between these variables. This study also presents the notable correlation between gender diversity on boards of management, CEO duality, and financial difficulty. Full article
Show Figures

Figure 1

Figure 1
<p>Conceptual framework of the study.</p>
Full article ">
14 pages, 5235 KiB  
Article
Highly Active Cerium Oxide Supported Solution Combustion Cu/Mn Catalysts for CO-PrOx in a Hydrogen-Rich Stream
by Sbusiso Motha, Abdul S. Mahomed, Sooboo Singh and Holger B. Friedrich
Catalysts 2024, 14(9), 603; https://doi.org/10.3390/catal14090603 - 7 Sep 2024
Viewed by 332
Abstract
Mono- and di-substituted cerium oxide catalysts, viz. Ce0.95Cu0.05O2-δ, Ce0.90Cu0.10O2-δ, Ce0.90 Cu0.05Mn0.05O2-δ, Ce0.85Cu0.10Mn0.05O2-δ, and Ce0.80Cu0.10 [...] Read more.
Mono- and di-substituted cerium oxide catalysts, viz. Ce0.95Cu0.05O2-δ, Ce0.90Cu0.10O2-δ, Ce0.90 Cu0.05Mn0.05O2-δ, Ce0.85Cu0.10Mn0.05O2-δ, and Ce0.80Cu0.10Mn0.10O2-δ, were synthesized via a one-step urea-assisted solution combustion method. The elemental composition and textural and structural properties of the catalysts were determined by various physical, electronic, and chemical characterization techniques. Hydrogen temperature-programmed reduction showed that co-doping of copper and manganese ions into the CeO2-δ lattice improved the reducibility of copper. Powder XRD, XPS, HR-TEM, and Raman spectroscopy showed that the catalysts were a singled-phased, solid-solution metal oxide with a cerium oxide cubic fluorite (cerianite) structure, and evidence of oxygen vacancies was observed. Catalytic results in the preferential oxidation of CO in a hydrogen-rich stream showed that complete CO conversion occurred between 150 and 180 °C. Furthermore, at 150 °C, Ce0.90Cu0.05Mn0.05O2-δ, Ce0.90 Cu0.10O2-δ, and Ce0.85Cu0.10Mn0.05O2-δ catalysts were the most active, achieving complete CO conversion and CO2 selectivity of 81, 79, and 71%, respectively. The catalysts performed moderately in the presence of CO2 and water, with the Ce0.90Cu0.05Mn0.05O2-δ catalyst giving a CO conversion of 80% in CO2, which decreased to about 60% when water was added. Full article
(This article belongs to the Special Issue Catalytic CO Oxidation and Preferential CO Oxidation (PROX) II)
Show Figures

Figure 1

Figure 1
<p>(<b>A</b>) Powder X-ray diffractograms and (<b>B</b>) Raman spectra of the catalysts.</p>
Full article ">Figure 2
<p>TEM images of the catalysts.</p>
Full article ">Figure 3
<p>HR-TEM images with lattice fringes and corresponding electron diffraction patterns of the catalysts.</p>
Full article ">Figure 4
<p>De-convoluted Cu (2<span class="html-italic">p</span>) core-level spectra of the catalysts.</p>
Full article ">Figure 5
<p>De-convoluted Mn (2<span class="html-italic">p</span>) core-level spectra of the catalysts.</p>
Full article ">Figure 6
<p>De-convoluted Ce (3d) core-level spectra of the catalysts.</p>
Full article ">Figure 7
<p>CO conversion (<b>A</b>), selectivity towards CO<sub>2</sub> (<b>B</b>), and O<sub>2</sub> conversion (<b>C</b>) as a function of temperature for CO-PrOx over Ce<sub>0.95</sub>Cu<sub>0.05</sub>O<sub>2-δ</sub> (<span style="color:#002060">▲</span>), Ce<sub>0.90</sub>Cu<sub>0.10</sub>O<sub>2-δ</sub> (<span style="color:#ED7D31">■</span>), Ce<sub>0.90</sub>Cu<sub>0.05</sub>Mn<sub>0.05</sub>O<sub>2-δ</sub> (<span style="color:red">●</span>), Ce<sub>0.85</sub>Cu<sub>0.10</sub>Mn<sub>0.05</sub>O<sub>2-δ</sub> (<span style="color:green">✕</span>), and Ce<sub>0.80</sub>Cu<sub>0.10</sub>Mn<sub>0.10</sub>O<sub>2-δ</sub> (<span style="color:blue">◆</span>) (Feed composition: 1 vol. % CO, 1 vol. % O<sub>2</sub>, 50 vol. % H<sub>2</sub> and balance, N<sub>2</sub>; GHSV = 60,000 h<sup>−1</sup>).</p>
Full article ">Figure 8
<p>CO conversion (<span style="color:blue">▲</span>), selectivity towards CO<sub>2</sub> (<span style="color:red">▲</span>), and O<sub>2</sub> conversion (<span style="color:green">▲</span>) as a function of time for CO-PrOx over the Ce<sub>0.90</sub>Cu<sub>0.05</sub>Mn<sub>0.05</sub>O<sub>2-δ</sub> catalyst (Feed composition: 1 vol. % CO, 1 vol. % O<sub>2</sub>, 50 vol.% H<sub>2</sub>, 0–15 vol.% CO<sub>2</sub> and balance, N<sub>2</sub>; GHSV = 60,000 h<sup>−1</sup>, Temperature = 150 °C).</p>
Full article ">Figure 9
<p>CO conversion (<span style="color:blue">◆</span>), selectivity towards CO<sub>2</sub> (<span style="color:red">◆</span>), and O<sub>2</sub> conversion (<span style="color:green">◆</span>) as a function of time for CO-PrOx over the Ce<sub>0.90</sub>Cu<sub>0.05</sub>Mn<sub>0.05</sub>O<sub>2-δ</sub> catalyst (Feed composition: 1 vol.% CO, 1 vol.% O<sub>2</sub>, 50 vol.% H<sub>2</sub>, 15 vol.% CO<sub>2</sub>, 7 vol.% H<sub>2</sub>O and balance, N<sub>2</sub>; GHSV = 60,000 h<sup>−1</sup>, Temperature = 150 °C).</p>
Full article ">
13 pages, 7474 KiB  
Article
Construction of ZnCdS Quantum-Dot-Modified CeO2 (0D–2D) Heterojunction for Enhancing Photocatalytic CO2 Reduction and Mechanism Insight
by Junzhi Yan, Yuming Sun, Junxi Cai, Ming Cai, Bo Hu, Yan Yan, Yue Zhang and Xu Tang
Catalysts 2024, 14(9), 599; https://doi.org/10.3390/catal14090599 - 6 Sep 2024
Viewed by 429
Abstract
It is important to improve the separation ability of photogenerated electrons and the adsorption capacity of carbon dioxide (CO2) for efficient photoreduction of CO2. Here, we synthesized ZnCdS quantum dots (ZCS-QDs) and cerium dioxide nanosheets (CeO2) using [...] Read more.
It is important to improve the separation ability of photogenerated electrons and the adsorption capacity of carbon dioxide (CO2) for efficient photoreduction of CO2. Here, we synthesized ZnCdS quantum dots (ZCS-QDs) and cerium dioxide nanosheets (CeO2) using the solvothermal method and calcination method. We combined CeO2 and ZCS-QDs to effectively enhance the charge separation efficiency, and the lifetime of photogenerated electrons was increased 4.5 times. The CO evolution rate of the optimized composite (ZCS-QDs/CeO2) was up to 495.8 μmol g−1 h−1, and it had 100% product selectivity. In addition, the stability remained high after five cycles. The CO2 adsorption capacity of the catalyst surface was observed by in situ FTIR. The test results showed that improving CO2 capture ability and promoting photogenic electron separation had positive effects on enhancing photoreduction of CO2. This study provides a reference for constructing a zero-dimensional–two-dimensional (0D–2D) heterojunction and explores potential CO2 reduction reaction mechanisms. Full article
(This article belongs to the Special Issue Mineral-Based Composite Catalytic Materials)
Show Figures

Graphical abstract

Graphical abstract
Full article ">Figure 1
<p>(<b>a</b>) XRD patterns of CeO<sub>2</sub>, ZCS-QDs, and x ZCS-QDs/CeO<sub>2</sub> (x = 5, 8, 10, 12, and 15%), (<b>b</b>–<b>d</b>) TEM image of CeO<sub>2</sub> and ZCS-QDs, (<b>e</b>) TEM image of 12% ZCS-QDs/CeO<sub>2</sub>, (<b>f</b>) HRTEM image of 12% ZCS-QDs/CeO<sub>2</sub>, (<b>g</b>) EDS elemental mapping images of 12% ZCS-QDs/CeO<sub>2</sub>.</p>
Full article ">Figure 2
<p>XPS spectra of (<b>a</b>) survey spectra, (<b>b</b>) Ce 3d, (<b>c</b>) O 1s, (<b>d</b>) S 2p of 12% ZCS-QDs/CeO<sub>2</sub>, (<b>e</b>) Cd 3d of 12% ZCS-QDs/CeO<sub>2</sub>, and (<b>f</b>) Zn 2p of 12% ZCS-QDs/CeO<sub>2</sub>.</p>
Full article ">Figure 3
<p>(<b>a</b>) UV–Vis DRS, (<b>b</b>) plots of (<span class="html-italic">αhv</span>)<sup>1/2</sup> versus (<span class="html-italic">hv</span>), (<b>c</b>,<b>d</b>) VB-XPS spectra of CeO<sub>2</sub> and ZCS-QDs, and (<b>e</b>) bandgap structure diagram of CeO<sub>2</sub> and ZCS-QDs.</p>
Full article ">Figure 4
<p>(<b>a</b>) TR-PL decay spectra of CeO<sub>2</sub>, ZCS-QDs, and 12% ZCS-QDs/CeO<sub>2</sub>; (<b>b</b>) TPR and (<b>c</b>) EIS of CeO<sub>2</sub>, ZCS-QDs, and 12% ZCS-QDs/CeO<sub>2</sub>.</p>
Full article ">Figure 5
<p>(<b>a</b>) Photocatalytic activity of CeO<sub>2</sub>, ZCS-QDs, and x ZCS-QDs/CeO<sub>2</sub>; (<b>b</b>) photocatalytic performance of 12% ZCS-QDs/CeO<sub>2</sub> under CO<sub>2</sub> and N<sub>2</sub>; (<b>c</b>) cycling test of 12% ZCS-QDs/CeO<sub>2</sub>.</p>
Full article ">Figure 6
<p>DRIFTS spectra of CO<sub>2</sub> adsorption of (<b>a</b>) ZCS-QDs, (<b>b</b>) CeO<sub>2</sub>, and (<b>c</b>) 12% ZCS-QDs/CeO<sub>2</sub>.</p>
Full article ">Figure 7
<p>DRIFTS spectra of (<b>a</b>) CeO<sub>2</sub>, (<b>b</b>) ZCS-QDs, and (<b>c</b>) 12% ZCS-QDs/CeO<sub>2</sub>.</p>
Full article ">Figure 8
<p>Photocatalytic CO<sub>2</sub> reduction mechanism of 0D–2D ZCS-QDs/CeO<sub>2</sub>.</p>
Full article ">Scheme 1
<p>Synthesis diagram of ZCS-QDs/CeO<sub>2</sub>.</p>
Full article ">
12 pages, 3303 KiB  
Article
The Synergistic Effect of CeO2 and Micron-Cu Enhances the Hydrogenation of CO2 to CO
by Bowen Lu, Huiying Sang, Liang Liu, Zhijian Yu, Yaqin Guo and Yongqing Xu
Processes 2024, 12(9), 1912; https://doi.org/10.3390/pr12091912 - 6 Sep 2024
Viewed by 378
Abstract
The catalytic applications of micron Cu powder are limited due to its large particle size and small specific surface area. Modifying micro-Cu powder to achieve a high catalytic performance is a challenge in the application of micron copper. In this work, micro-Cu was [...] Read more.
The catalytic applications of micron Cu powder are limited due to its large particle size and small specific surface area. Modifying micro-Cu powder to achieve a high catalytic performance is a challenge in the application of micron copper. In this work, micro-Cu was used to synthesize a CeO2–Cu catalyst, and the phase composition and surface pore structure were analyzed using XRD, BET, etc. The CO2 hydrogenation performance of the CeO2–Cu catalyst was analyzed in comparison with CeO2 and Cu, and we found that the CeO2–Cu catalyst exhibited a synergistic effect between Cu and cerium, resulting in a much higher hydrogenation performance at 500 °C than CeO2 or Cu alone. H2-TPR and TEM characterization revealed that the CeO2–Cu catalyst formed interfacial interactions with a relatively large Ce–Cu interface, where cerium oxide could promote the reduction of CuO and lower the reduction temperature. Additionally, cerium oxide formed a confinement structure for Cu, and the CeO2–Cu catalyst exhibited a higher oxygen vacancy concentration, thereby promoting the CO2 hydrogenation performance. Cu–CeO2 interaction provides valuable insights into the catalytic application of micron Cu powder. Full article
Show Figures

Figure 1

Figure 1
<p>XRD patterns for CeO<sub>2</sub>–Cu, CeO<sub>2</sub>, and micro-Cu.</p>
Full article ">Figure 2
<p>(<b>a</b>). N<sub>2</sub> adsorption–desorption isotherms and (<b>b</b>) pore diameter distributions of CeO<sub>2</sub>–Cu, CeO<sub>2</sub>, and Cu catalysts.</p>
Full article ">Figure 3
<p>Hydrogenation performance of CeO<sub>2</sub>–Cu, CeO<sub>2</sub>, and Cu: (<b>a</b>) CO<sub>2</sub> conversion activity, (<b>b</b>) CO selectivity (100 mL/min).</p>
Full article ">Figure 4
<p>TEM images of CeO<sub>2</sub>–Cu, Cu, and CeO<sub>2</sub>: (<b>a</b>) TEM image of Cu powder, (<b>b</b>) HRTEM of CeO<sub>2</sub>, (<b>c</b>) TEM image of CeO<sub>2</sub>–Cu powder, (<b>d</b>) HRTEM of CeO<sub>2</sub>–Cu, (<b>e</b>) HADDF of CeO<sub>2</sub>–Cu, and line distribution of Ce and Cu.</p>
Full article ">Figure 5
<p>H<sub>2</sub>-TPR of CeO<sub>2</sub>–Cu, Cu, and CeO<sub>2</sub> catalysts.</p>
Full article ">Figure 6
<p>Raman spectrum of CeO<sub>2</sub>–Cu, Cu, and CeO<sub>2</sub> catalysts.</p>
Full article ">Figure 7
<p>CO<sub>2</sub> conversion of the CeO<sub>2</sub>–Cu catalyst at 700 °C and a flow speed of 100 mL/min.</p>
Full article ">Figure 8
<p>TEM image (<b>a</b>) and HRTEM image (<b>b</b>) of CeO<sub>2</sub>–Cu after RWGS reaction.</p>
Full article ">
21 pages, 860 KiB  
Article
CTO Characteristics and ESG Performance of Corporation: Evidence from Korea
by Taejin Lim, Donggi Kim and Keuntae Cho
Sustainability 2024, 16(17), 7703; https://doi.org/10.3390/su16177703 - 5 Sep 2024
Viewed by 613
Abstract
While there has been a steady stream of research on chief technology officers (CTOs), studies specifically examining the expanding role of CTOs, particularly in the areas of environmental, social, and governance (ESG), remain scarce. Despite extensive research on boards of directors (BODs), chief [...] Read more.
While there has been a steady stream of research on chief technology officers (CTOs), studies specifically examining the expanding role of CTOs, particularly in the areas of environmental, social, and governance (ESG), remain scarce. Despite extensive research on boards of directors (BODs), chief executive officers (CEOs), and corporate social responsibility (CSR) committees, there is a significant lack of research on the role of CTOs in integrating ESG considerations into technology development and operations. To fill this gap, this study investigated the impact of CTO characteristics (personal, positional, and career-related) on corporate ESG performance. Based on previous studies, we created a conceptual model and proposed 12 hypotheses. A sample of 218 publicly traded corporations in Korea was selected, and a structural equation model was used to test the fit of the research model and hypotheses. The results indicate that the positional characteristics of the CTO positively affect a corporation’s ESG performance, whereas the career-related characteristics of the CTO negatively affect it. However, personal characteristics did not exhibit significant effects. Therefore, this study underscores the need for corporations to empower technology leaders, such as the CTO, and enable them to play an important role in strategic decision-making. By doing so, organizations can enhance their social responsibility, improve environmental sustainability, and maintain competitiveness. Full article
(This article belongs to the Section Sustainable Management)
Show Figures

Figure 1

Figure 1
<p>Research model.</p>
Full article ">Figure 2
<p>Research model and results. * <span class="html-italic">p</span> &lt; 0.05, ** <span class="html-italic">p</span> &lt; 0.01, *** <span class="html-italic">p</span> &lt; 0.001.</p>
Full article ">
17 pages, 4184 KiB  
Article
Enhanced Photocatalytic Degradation of Herbicide 2,4-Dichlorophenoxyacetic Acid Using Sulfated CeO2
by Carlos Rodríguez, Claudia Castañeda, Edwin Sosa, José J. Martínez, Sonia Mancipe, Hugo Rojas, Francisco Tzompantzi and Ricardo Gómez
Catalysts 2024, 14(9), 594; https://doi.org/10.3390/catal14090594 - 4 Sep 2024
Viewed by 424
Abstract
The present study presents the results obtained from evaluating the photocatalytic behavior of a series of sulfated CeO2 materials in the photocatalytic degradation of the herbicide 2,4-dichlorophenoxyacetic acid. The CeO2 photocatalytic support was prepared using the precipitation synthesis method. Subsequently, the [...] Read more.
The present study presents the results obtained from evaluating the photocatalytic behavior of a series of sulfated CeO2 materials in the photocatalytic degradation of the herbicide 2,4-dichlorophenoxyacetic acid. The CeO2 photocatalytic support was prepared using the precipitation synthesis method. Subsequently, the support was wetly impregnated with different contents of sulfate ions (0.5, 1.0, and 2.0 wt.%). The materials were characterized using X-ray diffraction, nitrogen physisorption, infrared spectroscopy, diffuse reflectance UV–Vis spectrophotometry, and thermal analysis. The characterization results showed that the sulfation of the material promoted an increase in the surface area and a decrease in the average size of the crystallites. Likewise, it was possible to demonstrate the surface sulfation of the support through bidentate coordination of the sulfate groups to the semiconductor metal. Concerning photoactivity, the convenience of the surface modification of CeO2 was confirmed because the sulfate groups acted as capturers of the electrons generated during the photocatalytic process, reducing the frequency of recombination of the charge carriers and allowing the availability of the gaps to favor the degradation reaction of the contaminant. Finally, it was evident that a percentage of 1.0 wt.% of the sulfate anion is the optimal content to improve the photocatalytic properties of CeO2. Full article
(This article belongs to the Special Issue Catalytic Energy Conversion and Catalytic Environmental Purification)
Show Figures

Figure 1

Figure 1
<p>X-ray diffraction results of the materials studied.</p>
Full article ">Figure 2
<p>N<sub>2</sub> adsorption–desorption isotherms of the materials studied.</p>
Full article ">Figure 3
<p>ATR-FTIR spectra of the materials studied.</p>
Full article ">Figure 4
<p>(<b>a</b>) UV–Vis spectra and (<b>b</b>) Tauc plot of the materials studied.</p>
Full article ">Figure 5
<p>TGA-MS results of (<b>a</b>) uncalcined CeO<sub>2</sub> support and (<b>b</b>) 1.0SO<sub>4</sub><sup>2−</sup>/CeO<sub>2</sub> photocatalyst.</p>
Full article ">Figure 6
<p>Photoluminescence spectra of the materials studied.</p>
Full article ">Figure 7
<p>(<b>a</b>) UV spectra of the 2,4-D photodegradation using 1.0SO<sub>4</sub><sup>2−</sup>/CeO<sub>2</sub> photocatalyst, and (<b>b</b>) variation of the relative concentration of 2,4-D as a function of reaction time using materials studied.</p>
Full article ">Figure 8
<p>(<b>a</b>) UV spectra of the 2,4-D adsorption using 1.0SO<sub>4</sub><sup>2−</sup>/CeO<sub>2</sub> photocatalyst. (<b>b</b>) Comparison between the adsorption reaction and the photocatalytic degradation of the 2,4-D herbicide.</p>
Full article ">Figure 9
<p>Representation of the photocatalytic process in the degradation of 2,4-D using the 1.0SO<sub>4</sub><sup>2−</sup>/CeO<sub>2</sub> material.</p>
Full article ">Figure 10
<p>(<b>a</b>) Surface plots and (<b>b</b>) contour plots representing the effect of 2,4-D concentration and photocatalyst mass on the degradation percentage.</p>
Full article ">Figure 11
<p>Reuse of the 1.0SO<sub>4</sub><sup>2−</sup>/CeO<sub>2</sub> photocatalyst in the photocatalytic degradation of 2,4-dichlorophenoxyacetic acid (2,4-D).</p>
Full article ">Figure 12
<p>ATR-FTIR spectra of the 1.0SO<sub>4</sub><sup>2−</sup>/CeO<sub>2</sub> material reused in the cycle experiments and the material used in the adsorption test.</p>
Full article ">
18 pages, 2336 KiB  
Article
Performance and Board Diversity: A Practical AI Perspective
by Lee-Wen Yang, Thi Thanh Binh Nguyen and Wei-Ju Young
Big Data Cogn. Comput. 2024, 8(9), 106; https://doi.org/10.3390/bdcc8090106 - 4 Sep 2024
Viewed by 307
Abstract
The face of corporate governance is changing as new technologies in the scope of artificial intelligence and data analytics are used to make better future-oriented decisions on performance management. This study attempts to provide empirical results to analyze when the impact of diversity [...] Read more.
The face of corporate governance is changing as new technologies in the scope of artificial intelligence and data analytics are used to make better future-oriented decisions on performance management. This study attempts to provide empirical results to analyze when the impact of diversity on the board of directors is most evident through the multi-breaks model and artificial neural networks. The input data for the simulation includes 853 electronic companies listed on the Taiwan Stock Exchange from 2000 to 2021. The empirical results show that the higher the percentage of female board members, the more influential the company’s performance is, which is only evident when the company is in good business condition. By integrating ANNs with multi-breakpoint regression, this study introduces a novel approach to management research, providing a detailed perspective on how board diversity impacts firm performance across different conditions. The ANN results show that using the number of business board members for predicting Return on Assets yields the highest accuracy, with female board members following closely in predictive effectiveness. The presence of women on the board contributes positively to ROA, particularly when the company is experiencing favorable business conditions and high profitability. Our analysis also reveals that a higher percentage of male board members improves company performance, but this benefit is observed only in highly favorable and unfavorable business conditions. Conversely, a higher percentage of business members tends to affect performance during periods of high profitability negatively. The power of the board of directors and significant shareholders is positively correlated with performance, whereas CEO power positively impacts performance only when it is not extremely low. Independent board members generally do not have a significant effect on profits. Additionally, the company’s asset value positively influences performance primarily when the return on assets is high, and increased financial leverage is associated with reduced profitability. Full article
(This article belongs to the Special Issue Machine Learning Applications and Big Data Challenges)
Show Figures

Figure 1

Figure 1
<p>The critical stages involved in the ANN model process.</p>
Full article ">Figure 2
<p>ROA and board structure.</p>
Full article ">Figure 3
<p>ROA and women on the board.</p>
Full article ">Figure 4
<p>ROA and men/businesses on the board.</p>
Full article ">Figure 5
<p>Processing unit. where <math display="inline"><semantics> <mrow> <msub> <mrow> <mi>x</mi> </mrow> <mrow> <mi>i</mi> </mrow> </msub> </mrow> </semantics></math> are the inputs; <math display="inline"><semantics> <mrow> <msub> <mrow> <mi>w</mi> </mrow> <mrow> <mi>j</mi> <mi>i</mi> </mrow> </msub> </mrow> </semantics></math> are the weights corresponding to the inputs; <math display="inline"><semantics> <mrow> <msub> <mrow> <mi>θ</mi> </mrow> <mrow> <mi>j</mi> </mrow> </msub> </mrow> </semantics></math> is the deviation (bias); <math display="inline"><semantics> <mrow> <msub> <mrow> <mi>a</mi> </mrow> <mrow> <mi>j</mi> </mrow> </msub> <mo> </mo> </mrow> </semantics></math> is the network input (net-input); <math display="inline"><semantics> <mrow> <msub> <mrow> <mi>z</mi> </mrow> <mrow> <mi>j</mi> </mrow> </msub> </mrow> </semantics></math> is the output of the neuron; <math display="inline"><semantics> <mrow> <mi mathvariant="normal">f</mi> <mo>(</mo> <msub> <mrow> <mi>a</mi> </mrow> <mrow> <mi>j</mi> </mrow> </msub> <mo>)</mo> </mrow> </semantics></math> is the transfer function (activation function).</p>
Full article ">Figure 6
<p>The ANNs are fitted for the three WBD, MBD, and BBD models.</p>
Full article ">Figure 7
<p>The accuracy of the ANNs of WBD, MBD, and BBD.</p>
Full article ">Figure 7 Cont.
<p>The accuracy of the ANNs of WBD, MBD, and BBD.</p>
Full article ">
15 pages, 8974 KiB  
Article
Multi-Objective Optimization for the Forming Quality of a CeO2/Al6061 Alloy as an Aluminum–Air Battery Anode Manufactured via Selective Laser Melting
by Guangpan Peng, Chenhao Niu, Yuankun Geng, Weipeng Duan and Shu Cao
Crystals 2024, 14(9), 784; https://doi.org/10.3390/cryst14090784 - 3 Sep 2024
Viewed by 343
Abstract
To improve the discharge performance of aluminum–air batteries, CeO2/Al6061 composites were prepared as an anode using selective laser melting (SLM). Response surface methodology (RSM) was employed, and the test results were linearly fitted. A prediction model for the forming quality of [...] Read more.
To improve the discharge performance of aluminum–air batteries, CeO2/Al6061 composites were prepared as an anode using selective laser melting (SLM). Response surface methodology (RSM) was employed, and the test results were linearly fitted. A prediction model for the forming quality of the composite anode was established, and the reliability of the model and the interaction between process parameters were explored based on variance analysis and significance testing. On this basis, with corrosion potential, self-corrosion rate, and discharge voltage as optimization objectives, the optimal solution set of the SLM forming CeO2/Al6061 anode process parameter was solved through a genetic algorithm, and experimental verification was conducted. The results indicate that the optimal process range for the forming quality and various properties of composite materials is laser power of 265~285 W, scanning speed of 985~1025 mm/s, and scanning spacing of 0.116~0.140 mm. The optimized process parameters were selected for reliability testing, and the errors were all within 3.0%, verifying the accuracy and reliability of the model. Full article
(This article belongs to the Section Materials for Energy Applications)
Show Figures

Figure 1

Figure 1
<p>Morphology of the powder: (<b>a</b>) Al6061; (<b>b</b>) CeO<sub>2</sub>; (<b>c</b>) 1.0 wt.% CeO<sub>2</sub>/Al6061.</p>
Full article ">Figure 2
<p>Performance regression prediction model residual normal distribution diagram: (<b>a</b>) corrosion potential; (<b>b</b>) self-corrosion rate; (<b>c</b>) discharge voltage.</p>
Full article ">Figure 3
<p>Interaction diagram of the influence of the process parameters on corrosion potential: (<b>a</b>) laser power and scanning speed; (<b>b</b>) laser power and scan spacing; (<b>c</b>) scanning speed and scan spacing.</p>
Full article ">Figure 3 Cont.
<p>Interaction diagram of the influence of the process parameters on corrosion potential: (<b>a</b>) laser power and scanning speed; (<b>b</b>) laser power and scan spacing; (<b>c</b>) scanning speed and scan spacing.</p>
Full article ">Figure 4
<p>Interaction diagram of the influence of the process parameters on the self-corrosion rate: (<b>a</b>) laser power and scanning speed; (<b>b</b>) laser power and scan spacing; (<b>c</b>) scanning speed and scan spacing.</p>
Full article ">Figure 5
<p>Interaction diagram of the influence of the process parameters on the discharge voltage: (<b>a</b>) laser power and scanning speed; (<b>b</b>) laser power and scan spacing; (<b>c</b>) scanning speed and scan spacing.</p>
Full article ">
21 pages, 6889 KiB  
Review
Advanced-Functional-Material-Modified Electrodes for the Monitoring of Nitrobenzene: Progress in Nitrobenzene Electrochemical Sensing
by Khursheed Ahmad and Tae Hwan Oh
Processes 2024, 12(9), 1884; https://doi.org/10.3390/pr12091884 - 2 Sep 2024
Viewed by 602
Abstract
Nitrobenzene (NB) is one of the nitro-aromatic compounds that is extensively used in various chemical industries. Despite its potential applications, NB is considered to be a toxic compound that has significant hazardous effects on human health and the environment. Thus, it can be [...] Read more.
Nitrobenzene (NB) is one of the nitro-aromatic compounds that is extensively used in various chemical industries. Despite its potential applications, NB is considered to be a toxic compound that has significant hazardous effects on human health and the environment. Thus, it can be said that the NB level should be monitored to avoid its negative impacts on human health. In this vein, the electrochemical method has emerged as one of the most efficient sensing techniques for the determination of NB. The sensing performance of the electrochemical techniques depends on the electro-catalytic properties and conductivity of the electrode materials. In the past few years, various electrode materials, such as conductive metal ions, semiconducting metal oxides, metal–organic frameworks, and two-dimensional (2D) materials, have been used as the electrode material for the construction of the NB sensor. Thus, it is worth summarizing previous studies on the design and synthesis of electrode materials for the construction of the NB sensor. In this mini-review article, we summarize the previous reports on the synthesis of various advanced electrode materials, such as platinum (Pt) nanoparticles (NPs), silver (Ag) NPs, carbon dots (CDs), graphene, graphitic carbon nitride (g-C3N4), zinc stannate (ZnSnO3), cerium oxide (CeO2), zinc oxide (ZnO), and so on. Furthermore, the impacts of different electrode materials are systematically discussed for the sensing of NB. The advantages of, limitations of, and future perspectives on the construction of NB sensors are discussed. The aim of the present mini-review article is to enhance the knowledge and overall literature, working towards the construction of NB sensors. Full article
Show Figures

Figure 1

Figure 1
<p>(<b>a</b>) Schematic picture for the synthesis of ZnSnO<sub>3</sub>/g-C<sub>3</sub>N<sub>4</sub> composite. (<b>b</b>) XRD pattern of the ZnSnO<sub>3</sub>, g-C<sub>3</sub>N<sub>4</sub>, and ZnSnO<sub>3</sub>/g-C<sub>3</sub>N<sub>4</sub> composite. (<b>c</b>) Selectivity test (DPV curves) of the NB sensor in presence of various interfering substances. (<b>d</b>) Selectivity results for NB sensing. Reprinted with permission [<a href="#B30-processes-12-01884" class="html-bibr">30</a>].</p>
Full article ">Figure 2
<p>(<b>a</b>) Schematic representation of the synthesis of GO/MgO composite, fabrication of GO/MgO/GC electrode and its working for NB sensing. (<b>b</b>) CV graphs of the different electrodes for NB sensing. (<b>c</b>) Current value versus pH graph for the sensing of NB using GO/MgO/GC electrode. (<b>d</b>) DPV graphs of the GO/MgO/GC electrode in presence of various concentrations of NB. Reprinted with permission [<a href="#B31-processes-12-01884" class="html-bibr">31</a>].</p>
Full article ">Figure 3
<p>(<b>a</b>) Schematic diagram presents the synthetic procedure for MnO<sub>2</sub> NRs. (<b>b</b>) CV of the MnO<sub>2</sub> NRs/GCE In presence of NB at different scan rates. (<b>c</b>) Calibration plot between current response and square root of scan rate. (<b>d</b>) DPV curves of the MnO<sub>2</sub> NRs/GCE in presence of different concentrations of NB. (<b>e</b>) Calibration plot between current response and concentration of NB. Reprinted with permission [<a href="#B32-processes-12-01884" class="html-bibr">32</a>].</p>
Full article ">Figure 4
<p>(<b>a</b>) Schematic picture for the preparation of NHSP<sub>s-x</sub>. (<b>b</b>) DPV graphs of the NHCPs-750–GC electrode in different concentration of NB. (<b>c</b>) Selectivity nature of NHCPs-750–GC electrode for NB sensing. Reprinted with permission [<a href="#B38-processes-12-01884" class="html-bibr">38</a>].</p>
Full article ">Figure 5
<p>(<b>a</b>) CV curve of the (a) GRGO/Ni-TPP/GCE in the absence of NB. CV of (b) bare GCE, (c) GRGO/GCE, (d) NiTPP/GCE, (e) GO/NiTPP/GCE and (f) GRGO/Ni-TPP/GCE in the presence of NB. (<b>b</b>) CV responses of the GRGO/Ni-TPP/GCE electrode in the presence of NB under different pH conditions. (<b>c</b>) DPV curves of the GRGO/Ni-TPP/GCE in the presence of different concentration of NB. (<b>d</b>) Corresponding calibration curve between current response and concentration of NB. Reprinted with permission [<a href="#B41-processes-12-01884" class="html-bibr">41</a>].</p>
Full article ">Figure 6
<p>(<b>a</b>) CV patterns of the alumina/GCE for the presence of 50 µM NB at different pHs. (<b>b</b>) DPV curves of the alumina/GCE in the presence of different concentrations of NB. (<b>c</b>) Selectivity of alumina/GCE for NB sensing. Reprinted with permission [<a href="#B48-processes-12-01884" class="html-bibr">48</a>].</p>
Full article ">Figure 7
<p>(<b>a</b>) Nyquist curves and (<b>b</b>) CV graphs of bare GCE, MoS<sub>2</sub> NSAs/GCE, and MoS<sub>2</sub> NSAs/rGO/GCE in [Fe(CN)<sub>6</sub>]<sup>3−/4−</sup> redox probe (0.1 M KCl). (<b>c</b>) CV curves of MoS<sub>2</sub> NSAs/rGO/GCE at different scan rates in the redox system and (<b>d</b>) corresponding calibration plot between peak current response and square root of scan rate. (<b>e</b>) CV curves and (<b>f</b>) cathodic current response of different volume of MoS<sub>2</sub> NSAs/rGO/GCE in the presence of 200 µM NB in 0.05 M PBS. (<b>g</b>) CV curves and (<b>h</b>) cathodic current response of bare GCE, MoS<sub>2</sub> NSAs/GCE, and MoS<sub>2</sub> NSAs/rGO/GCE in the presence of 200 µM NB. (<b>i</b>) DPV curves of the MoS<sub>2</sub>/NSA/rGO/GCE in different concentrations of NB. (<b>j</b>) Calibration curve between current responses and concentration of NB. (<b>k</b>) DPV curves and (<b>l</b>) corresponding relative peak of the MoS<sub>2</sub>/NSA/rGO/GCE for selectivity test towards the sensing of NB in the presence of interfering substances. Reprinted with permission [<a href="#B51-processes-12-01884" class="html-bibr">51</a>].</p>
Full article ">Figure 8
<p>(<b>a</b>) Schematic representation for the preparation of ZIF67@PS-derived Co-NC. (<b>b</b>) CV curves and (<b>c</b>) corresponding current values of the Co-NC-800-GCE (different mass loadings) in the presence of NB. (<b>d</b>) DPV curves of Co-NC-800-GCE in different concentrations of NB and (<b>e</b>) corresponding calibration plot between peak current and concentration of NB. Reprinted with permission [<a href="#B56-processes-12-01884" class="html-bibr">56</a>].</p>
Full article ">Figure 9
<p>(<b>a</b>) Schematic representation for the synthesis of CuS-BCN and surface modification of GC electrode for the sensing of NB. (<b>b</b>) CV curves of the GCE, BCN/GCE, and CuS/BCN/GCE in the presence of NB. (<b>c</b>) SWV curves of the CuS/BCN/GCE at different concentrations of NB and (<b>d</b>) corresponding calibration plot between peak current and concentration of NB. Reprinted with permission [<a href="#B58-processes-12-01884" class="html-bibr">58</a>].</p>
Full article ">Figure 10
<p>(<b>a</b>) Schematic representation for the working mechanism of Ni/Fe(SDS)-LDH-modified GC electrode towards the determination of NB. (<b>b</b>) CV curves of the different electrodes in absence and presence of NB. (<b>c</b>) DPV curves of the different electrodes in the presence of NB. Reprinted with permission [<a href="#B59-processes-12-01884" class="html-bibr">59</a>].</p>
Full article ">
22 pages, 2307 KiB  
Article
A Fuzzy-Set Qualitative Comparative Analysis for Understanding the Interactive Effects of Good Governance Practices and CEO Profiles on ESG Performance
by Nieves Remo-Diez, Cristina Mendaña-Cuervo and Mar Arenas-Parra
Mathematics 2024, 12(17), 2726; https://doi.org/10.3390/math12172726 - 31 Aug 2024
Viewed by 467
Abstract
The impact of corporate governance mechanisms has been examined directly and independently, considering that such characteristics compete to explain environmental, social, and governance (ESG) performance. However, the nexus may be more complex than that suggested by most scholars, and more research is needed. [...] Read more.
The impact of corporate governance mechanisms has been examined directly and independently, considering that such characteristics compete to explain environmental, social, and governance (ESG) performance. However, the nexus may be more complex than that suggested by most scholars, and more research is needed. This study applied a fuzzy-set qualitative comparative analysis to a sample of Spanish-listed companies in 2018–2020 to explore how good governance practices interact with CEO profiles to promote corporate sustainability practices. Our analysis discovered the importance of establishing sustainability committees and identified five pathways shaping governance practice bundles. Specifically, listed companies with a high code of good governance (GGC) compliance and a sustainability committee improve high ESG performance globally and for each ESG dimension. Furthermore, the effect is more relevant than the effect of the CEO profile, requiring either CEO duality (pathway 1) or extended CEO tenure (pathway 2). Concurrently, findings indicate three CEO profile configurations for GGC-neutral firms, providing companies with more flexibility in CEO selection. Two suggest that younger CEOs with longer tenure tend to be more motivated to engage in the G and S pillars (pathways 3 and 5). The third indicates that CEOs of older age and early tenure improve the E pillar (pathway 4). Full article
Show Figures

Figure 1

Figure 1
<p>Conceptual model. The interactive effects of the GGC, CSR Committee, and CEO profiles on ESG performance. Abbreviations: GGC, Good Governance Code; BS, board size; BI, board independence; BM, board meeting; BG, board gender diversity; BT, board tenure; CSR Committee, corporate social responsibility committee; CEOA, CEO age; CEOD, CEO duality; CEOT, CEO tenure.</p>
Full article ">Figure 2
<p>Steps of fsQCA methodology.</p>
Full article ">Figure 3
<p>An S-shaped membership function.</p>
Full article ">Figure 4
<p>An S-shaped membership function with log-<span class="html-italic">odds</span> approximation.</p>
Full article ">Figure A1
<p>Contrarian case analysis 2018–2020. Note. The main effects are represented in <b><span class="html-italic">bold</span></b>; the contrarian cases are in <span class="html-italic">italics</span>.</p>
Full article ">
15 pages, 3542 KiB  
Article
Effect of (Ba1/3Nb2/3)4+ Substitution on Microstructure, Bonding Properties and Microwave Dielectric Properties of Ce2Zr3(MoO4)9 Ceramics
by Huamin Gao, Xiangyu Xu, Xinwei Liu, Xiaoyu Zhang, Mingling Li, Jialun Du and Haitao Wu
Ceramics 2024, 7(3), 1172-1186; https://doi.org/10.3390/ceramics7030077 - 29 Aug 2024
Viewed by 284
Abstract
In this study, Ce2[Zr1−x(Ba1/3Nb2/3)x]3(MoO4)9 (0.02 ≤ x ≤ 0.1, CZ1−xNx) ceramics were sintered at 600 °C and 700 °C using the traditional [...] Read more.
In this study, Ce2[Zr1−x(Ba1/3Nb2/3)x]3(MoO4)9 (0.02 ≤ x ≤ 0.1, CZ1−xNx) ceramics were sintered at 600 °C and 700 °C using the traditional solid-state method. An analysis conducted through XRD and Rietveld refinement confirmed that all the CZ1−xNx ceramics displayed a single phase with a trigonal structure (space group R-3c). The observed increases in cell volume with increasing x values indicate the successful substitution of (Ba1/3Nb2/3)4+. The high densification of the synthesized phase was validated by the density and SEM results. Additionally, the P-V-L theory demonstrates a strong correlation between the Ce-O bond and εr, as well as τf, and between the Mo-O bond and Q×f. Notably, the CZ0.98N0.02 ceramics demonstrated superior performance at 675 °C, exhibiting εr = 10.41, Q×f = 53,296 GHz, and τf = −23.45 ppm/°C. Finally, leveraging CZ0.98N0.02 ceramics as substrate materials enabled the design of a patch antenna suitable for the 5G communication band, demonstrating its significant potential in this field. Full article
(This article belongs to the Special Issue Advances in Electronic Ceramics)
Show Figures

Figure 1

Figure 1
<p>XRD patterns of CZ<sub>1−<span class="html-italic">x</span></sub>N<span class="html-italic"><sub>x</sub></span> ceramics sintered at the optimal temperature with different <span class="html-italic">x</span> values.</p>
Full article ">Figure 2
<p>Rietveld refinement of CZ<sub>1−<span class="html-italic">x</span></sub>N<span class="html-italic"><sub>x</sub></span> ceramics at the optimal sintering temperature with different <span class="html-italic">x</span> values.</p>
Full article ">Figure 3
<p>Lattice parameter changes (<b>a</b>) <span class="html-italic">a</span> and <span class="html-italic">b</span>, (<b>b</b>) <span class="html-italic">c</span>, and (<b>c</b>) <span class="html-italic">V<sub>m</sub></span> of CZ<sub>1−<span class="html-italic">x</span></sub>N<span class="html-italic"><sub>x</sub></span> ceramics as a function of <span class="html-italic">x</span> values.</p>
Full article ">Figure 4
<p>Crystal structure diagram of CZ<sub>1−<span class="html-italic">x</span></sub>N<span class="html-italic"><sub>x</sub></span> ceramics.</p>
Full article ">Figure 5
<p>(<b>a</b>) Diameter shrinkage, (<b>b</b>) apparent density (the relative density at the optimal sintering temperature as a function of <span class="html-italic">x</span> values are shown in the inset) of CZ<sub>1−<span class="html-italic">x</span></sub>N<span class="html-italic"><sub>x</sub></span> ceramics at 600 to 700 °C.</p>
Full article ">Figure 6
<p>Microstructure of CZ<sub>1−<span class="html-italic">x</span></sub>N<span class="html-italic"><sub>x</sub></span> ceramics at optimal sintering temperature with different <span class="html-italic">x</span> values.</p>
Full article ">Figure 7
<p>CZ<sub>1−<span class="html-italic">x</span></sub>N<span class="html-italic"><sub>x</sub></span> ceramics (<b>a</b>) <span class="html-italic">ε<sub>r</sub></span> at a sintering temperature of 600 ℃ to 700 ℃, (<b>b</b>) <span class="html-italic">ε<sub>r</sub></span>, (<b>c</b>) <span class="html-italic">ε<sub>corr.</sub></span>, (<b>d</b>) <span class="html-italic">α<sub>theo.</sub></span>, and (<b>e</b>) <span class="html-italic">f<sub>iave.</sub></span><sub>(Ce-O)</sub> at the optimal sintering temperature as a function of <span class="html-italic">x</span> values.</p>
Full article ">Figure 8
<p>CZ<sub>1−<span class="html-italic">x</span></sub>N<span class="html-italic"><sub>x</sub></span> ceramics (<b>a</b>) <span class="html-italic">Q</span>×<span class="html-italic">f</span> at a sintering temperature of 600 ℃ to 700 ℃, (<b>b</b>) <span class="html-italic">Q</span>×<span class="html-italic">f</span>, and (<b>c</b>) <span class="html-italic">U<sub>ave.</sub></span><sub>(Mo-O)</sub> at the optimal sintering temperature as a function of <span class="html-italic">x</span> values.</p>
Full article ">Figure 9
<p>CZ<sub>1−<span class="html-italic">x</span></sub>N<span class="html-italic"><sub>x</sub></span> ceramics (<b>a</b>) <span class="html-italic">τ<sub>f</sub></span>, (<b>b</b>) <span class="html-italic">α<sub>ave.</sub></span><sub>(Ce-O)</sub>, and (<b>c</b>) <span class="html-italic">E<sub>ave.</sub></span><sub>(Mo-O)</sub> at the optimal sintering temperature as a function of <span class="html-italic">x</span> values.</p>
Full article ">Figure 10
<p>(<b>a</b>) The design model and dimensions, (<b>b</b>) simulated S11 parameters, (<b>c</b>) 3D radiation pattern, (<b>d</b>) E-plane, and (<b>e</b>) H-plane of the antenna.</p>
Full article ">
12 pages, 2681 KiB  
Article
Interpretable Structural Evaluation of Metal-Oxide Nanostructures in Scanning Transmission Electron Microscopy (STEM) Images via Persistent Homology
by Ryuto Eguchi, Yu Wen, Hideki Abe and Ayako Hashimoto
Nanomaterials 2024, 14(17), 1413; https://doi.org/10.3390/nano14171413 - 29 Aug 2024
Viewed by 370
Abstract
Persistent homology is a powerful tool for quantifying various structures, but it is equally crucial to maintain its interpretability. In this study, we extracted interpretable geometric features from the persistent diagrams (PDs) of scanning transmission electron microscopy (STEM) images of self-assembled Pt-CeO2 [...] Read more.
Persistent homology is a powerful tool for quantifying various structures, but it is equally crucial to maintain its interpretability. In this study, we extracted interpretable geometric features from the persistent diagrams (PDs) of scanning transmission electron microscopy (STEM) images of self-assembled Pt-CeO2 nanostructures synthesized under different annealing conditions. We focused on PD quadrants and extracted five interpretable features from the zeroth and first PDs of nanostructures ranging from maze-like to striped patterns. A combination of hierarchical clustering and inverse analysis of PDs reconstructed by principal component analysis through vectorization of the PDs highlighted the importance of the number of arc-like structures of the CeO2 phase in the first PDs, particularly those that were smaller than a characteristic size. This descriptor enabled us to quantify the degree of disorder, namely the density of bends, in nanostructures formed under different conditions. By using this descriptor along with the width of the CeO2 phase, we classified 12 Pt-CeO2 nanostructures in an interpretable way. Full article
Show Figures

Figure 1

Figure 1
<p>Conceptual diagram for extraction of interpretable structural features from STEM images by using PH and classification of nanostructures by using the determined effective features.</p>
Full article ">Figure 2
<p>Binarized high-angle annular dark-field scanning transmission electron microscopy (HAADF-STEM) images of Pt-CeO<sub>2</sub> nanostructures synthesized at (<b>a</b>) 500 °C, (<b>b</b>) 600 °C, and (<b>c</b>) 700 °C with a CO:O<sub>2</sub> gas ratio of 2:1. Scale bars represent 100 nm. (<b>d</b>), (<b>e</b>), and (<b>f</b>) Zeroth and (<b>g</b>), (<b>h</b>), and (<b>i</b>) first persistent diagrams (PDs) of CeO<sub>2</sub> phases in the nanostructures corresponding to (<b>a</b>), (<b>b</b>), and (<b>c</b>), respectively. The color bars indicate the number of <span class="html-italic">b</span>-<span class="html-italic">d</span> pairs.</p>
Full article ">Figure 3
<p>Sum of the frequency distributions of the number of <span class="html-italic">b</span>-<span class="html-italic">d</span> pairs from the seven images as a function of <span class="html-italic">b</span> determined from zeroth PDs of nanostructures synthesized at (<b>a</b>) 500 °C, (<b>b</b>) 600 °C, and (<b>c</b>) 700 °C with a CO:O<sub>2</sub> gas ratio of 2:1. The blue solid lines indicate the Gaussian fitting at the center of each binary region. (<b>d</b>) Dependence of the number of <span class="html-italic">b</span>-<span class="html-italic">d</span> pairs with positive <span class="html-italic">d</span> values derived from the zeroth PDs of the nanostructures on synthesis temperature.</p>
Full article ">Figure 4
<p>(<b>a</b>) Hierarchical clustering of Pt-CeO<sub>2</sub> nanostructures with cosine dissimilarity calculated from zeroth vectorized PDs. The branch points are numbered as 1, 2, … in descending order of cosine dissimilarity. The dashed line is the threshold for clustering and is the maximum deviation calculated from the mean of cosine dissimilarity for the same set of synthesis conditions. The 12 nanostructures were finally clustered into six groups (G1–G6). (<b>b</b>) Binarized STEM images of Pt-CeO<sub>2</sub> nanostructures surrounded by the colors corresponding to those of the six groups (G1–G6) in (<b>a</b>).</p>
Full article ">Figure 5
<p>Zeroth (<b>a</b>) and first (<b>c</b>) reconstructed PDs of Pt-CeO<sub>2</sub> nanostructures obtained from PC1 of PCA. The color bars indicate the PC1 coefficients. PC1 values from all 84 vectorized (<b>b</b>) zeroth and (<b>d</b>) first PDs categorized into six groups through hierarchical clustering. Inset images show the inverse analysis results obtained from the (<b>a</b>) zeroth and (<b>c</b>) first reconstructed PDs for the nanostructures synthesized at 700 °C with a CO:O<sub>2</sub> gas ratio of 1:1 (left) and at 700 °C with a CO:O<sub>2</sub> gas ratio of 2:1 (right). The blue and red regions in the image in (<b>b</b>) correspond to the nanostructures from the <span class="html-italic">b</span>-<span class="html-italic">d</span> pairs with −4 nm <math display="inline"><semantics> <mrow> <mo>≤</mo> </mrow> </semantics></math> <span class="html-italic">b</span>, <span class="html-italic">d &lt;</span> 0 and <span class="html-italic">b</span> <math display="inline"><semantics> <mrow> <mo>&lt;</mo> </mrow> </semantics></math> −4 nm, <span class="html-italic">d</span> &lt; 0 in the zeroth PDs, respectively, and those in (<b>d</b>) correspond to the structures from the <span class="html-italic">b</span>-<span class="html-italic">d</span> pairs with 0 <math display="inline"><semantics> <mrow> <mo>&lt;</mo> </mrow> </semantics></math> <span class="html-italic">b</span>, <span class="html-italic">d</span> <math display="inline"><semantics> <mrow> <mo>≤</mo> </mrow> </semantics></math> 4 nm and 0 <math display="inline"><semantics> <mrow> <mo>&lt;</mo> </mrow> </semantics></math> <span class="html-italic">b</span>, 4 nm <math display="inline"><semantics> <mrow> <mo>≤</mo> </mrow> </semantics></math> <span class="html-italic">d</span> in the first PDs, respectively.</p>
Full article ">Figure 6
<p>Scatter plot of the number of small arcs with the characteristic size and the width of the CeO<sub>2</sub> phase for 12 Pt-CeO<sub>2</sub> nanostructures fabricated at different annealing temperatures and gas ratios. The colors show that there are three well-classified groups that were fabricated at different temperatures but with the same gas ratio. Inset images are corresponding binarized STEM images for each group.</p>
Full article ">
23 pages, 363 KiB  
Article
The Influence of Women on Boards on the Relationship between Executive and Employee Remuneration
by María L. Gallén and Carlos Peraita
Int. J. Financial Stud. 2024, 12(3), 84; https://doi.org/10.3390/ijfs12030084 - 23 Aug 2024
Viewed by 365
Abstract
The growing presence of women at the top of companies has sparked interest in examining their role in the remuneration gap between senior managers and employees. This article analyses the traditional Chief Executive Officer (CEO)-to-employee pay ratio but includes a new relation, the [...] Read more.
The growing presence of women at the top of companies has sparked interest in examining their role in the remuneration gap between senior managers and employees. This article analyses the traditional Chief Executive Officer (CEO)-to-employee pay ratio but includes a new relation, the senior-management-to-employee pay ratio, and extends the research by including six positions for women in company management: on the board of directors, executive directors, CEOs, proprietary directors, independent directors, and senior managers. The study is based on a sample of 77 listed companies in Spain from 2015 to 2022 and the panel data models have been estimated using the Generalised Method of Moments (GMM). The main findings indicate that the proportion of women in different categories of board and senior management positions has a positive effect on the CEO-to-employee pay ratio, especially in companies with higher market capitalisation. In contrast, the proportion of women in senior management positions has a negative effect on the CEO-to-employee pay ratio in all the samples analysed. Government agencies should prioritise the participation of women in non-board senior management positions in order to at least reduce the pay gap between senior managers and employees. Full article
Back to TopTop