The deployment of robust catalysts for electrochemical reactions is a critical topic for energy conversion techniques. Te-based nanomaterials have attracted increasing attention for their application in electrochemical reactions due to their positive influence on the electrocatalytic performance induced by their distinctive electronic and physicochemical properties. Herein, we have summarized the recent progress on Te-based nanocatalysts for electrocatalytic reactions by primarily focusing on the positive influence of Te on electrocatalysts. Firstly, Te-based nanomaterials can serve as an ideal template for the construction of well-defined nanostructures. Secondly, Te doping can significantly modify the electronic structure of the host catalyst, thereby, leading to the optimization of binding strength with intermediates. Furthermore, the Te etching strategy can also create a high density of surface defects, thereby leading to substantial improvement in the electrocatalytic performance. Additionally, many representative Te-based nanocatalysts for electrocatalytic reactions are also summarized and systematically discussed. Finally, a conclusive and perspective discussion is also provided to provide guidance for the future development of more efficient electrocatalysts.
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http://dx.doi.org/10.1039/d2dt03253h | DOI Listing |
J Am Chem Soc
January 2025
Department of Chemistry and Guangdong Provincial Key Laboratory of Catalysis, Southern University of Science and Technology, Shenzhen 518055, Guangdong, China.
Single-atom catalysts (SACs) have attracted widespread attention due to their potential to replace platinum-based catalysts in achieving efficient oxygen reduction reaction (ORR), yet the rational optimization of SACs remains challenging due to their elusive reaction mechanisms. Herein, by employing ab initio molecular dynamics simulations and a thermodynamic integration method, we have constructed the potential-dependent free energetics of ORR on a single iron atom catalyst dispersed on nitrogen-doped graphene (Fe-N/C) and further integrated these parameters into a microkinetic model. We demonstrate that the rate-determining step (RDS) of the ORR on SACs is potential-dependent rather than invariant within the operative potential range.
View Article and Find Full Text PDFSmall
January 2025
Department of Chemistry, Indian Institute of Technology Delhi, Hauz Khas, New Delhi, Delhi, 110016, India.
Crystalline γ-FeO(OH) dominantly possessing ─OH terminals (𝛾-FeO(OH)), polycrystalline γ-FeO(OH) containing multiple ─O, ─OH, and Fe terminals (𝛾-FeO(OH)), and α-FeO majorly containing ─O surface terminals are used as electrocatalysts to study the effect of surface terminals on electrocatalytic nitrate reduction reaction (eNORR) selectivity and stabilization of reaction intermediates. Brunauer-Emmett-Teller analysis and electrochemically determined surface area suggest a high active surface area of 117.79 m g (ECSA: 0.
View Article and Find Full Text PDFDalton Trans
January 2025
Faculty of Metallurgical and Energy Engineering, Kunming University of Science and Technology, Kunming, China.
During the oxygen evolution reaction (OER), metal-organic framework (MOF) catalysts undergo structural reorganization, a phenomenon that is still not fully comprehended. Additionally, designing MOFs that undergo structural reconstruction to produce highly active OER catalysts continues to pose significant challenges. Herein, a bimetallic MOF (CoNi-MOF) with carboxylate oxygen and pyridine nitrogen coordination has been synthesized and its reconstruction behavior has been analyzed.
View Article and Find Full Text PDFResearch (Wash D C)
January 2024
School of Materials Science and Engineering, Zhejiang Sci-Tech University, Hangzhou 310018, China.
The electrocatalytic carbon dioxide reduction reaction (CORR) at industrial-level current densities provides a sustainable approach to converting CO into value-added fuels and feedstocks using renewable electricity. However, the CORR conducted typically in alkaline and neutral electrolytes encounters some challenges due to the inevitable reaction between CO and OH ions, which undermines CO utilization and leads to poor operational stability. Acidic media present a viable alternative by reducing (bi)carbonate production, thereby enhancing the carbon efficiency and stability in CORR.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
January 2025
Nanjing University of Aeronautics and Astronautics, College of Materials Science and Technology, No. 169 Sheng Tai West Road, Jiangning District, Nanjing, Jiangsu, China, 211106, Nanjing, CHINA.
Transition metal-based catalysts with high efficiency and stability for overall water splitting (OWS) offer significant potential for reducing green hydrogen production costs. Utilizing sputtering deposition technology, we propose a deposition-diffusion strategy to fabricate heterojunction coatings composed of ultrafine FeCoNi-C-N transition metal interstitial solid solution (TMISS) nanocrystals and amorphous nitrided carbon (NC) on the pre-deposited NC micro column arrays. The diffusion of C and N atoms results in the formation of uniformly distributed TMISS nanocrystals, with an average diameter of ~1.
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