Atomically Dispersed CoN3C1‐TeN1C3 Diatomic Sites Anchored in N‐Doped Carbon as Efficient Bifunctional Catalyst for Synergistic Electrocatalytic Hydrogen Evolution and Oxygen Reduction (Small 29/2022)
Source abstract
Abstract
Bifunctional Catalysts In article number 2201974, Yunqi Liu, Xuan Yang, Xiang Feng, Yuan Pan, and co-workers propose an encapsulation-adsorption-pyrolysis strategy for constructing Co-Te diatomic sites with special CoN3C1-TeN1C3 coordination structure anchored in N-doped carbon, as efficient bifunctional catalysts for synergistic electrocatalytic hydrogen evolution and oxygen reduction. This work provides numerous opportunities for the rational design and artificial synthesis of diatomic sites catalysts for energy conversion.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Electrocatalysts for Energy Conversion · Fuel Cells and Related Materials · Machine Learning in Materials Science
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Affiliations
State Key Laboratory of Heavy Oil Processing China University of Petroleum (East China) Qingdao 266580 China
Department of Chemistry Tsinghua University Beijing 100084 China
School of Chemistry and Chemical Engineering Shaanxi Normal University Xi'an 710119 China
School of Chemistry and Chemical Engineering Huazhong University of Science and Technology Wuhan 430074 China
References
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