Tuning the coordination number of Fe single atoms for the efficient reduction of CO2-Reference-Cited by-同舟云学术

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Tuning the coordination number of Fe single atoms for the efficient reduction of CO2

Published:2020 Issue:21 Volume:22 Page:7529-7536
ISSN:1463-9262
Container-title:Green Chemistry
language:en
Short-container-title:Green Chem.

Author:

Chen Huihuang¹²³⁴⁵^ORCID,Guo Xu¹²³⁴⁵,Kong Xiangdong¹²³⁴⁵,Xing Yulin¹²³⁴⁵,Liu Yan¹²³⁴⁵,Yu Bolong¹²³⁴⁵,Li Qun-Xiang¹²³⁴⁵^ORCID,Geng Zhigang¹²³⁴⁵,Si Rui⁶⁷⁸⁹¹⁰^ORCID,Zeng Jie¹²³⁴⁵^ORCID

Affiliation:

1. Hefei National Laboratory for Physical Sciences at the Microscale

2. CAS Key Laboratory of Strongly-Coupled Quantum Matter Physics

3. Key Laboratory of Surface and Interface Chemistry and Energy Catalysis of Anhui Higher Education Institutes

4. Department of Chemical Physics

5. University of Science and Technology of China

6. Shanghai Synchrotron Radiation Facility

7. Shanghai Institute of Applied Physics

8. Chinese Academy of Sciences

9. Shanghai 201204

10. P. R. China

Abstract

The coordination number of Fe single-atom catalysts (Fe–N₅/Fe–N₆) significantly affects the electrocatalytic performance during CO₂-to-CO conversion.

Funder

National Science Fund for Distinguished Young Scholars

China Postdoctoral Science Foundation

National Natural Science Foundation of China

National Key Research and Development Program of China

Chinese Academy of Sciences

Fundamental Research Funds for the Central Universities

Publisher

Royal Society of Chemistry (RSC)

Subject

Pollution,Environmental Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2020/GC/D0GC02689A

Reference46 articles.

1. Carbon capture and conversion using metal–organic frameworks and MOF-based materials

2. Air as the renewable carbon source of the future: an overview of CO2 capture from the atmosphere

3. Recent Advances in Electrochemical CO2 -to-CO Conversion on Heterogeneous Catalysts

4. A review of catalysts for the electroreduction of carbon dioxide to produce low-carbon fuels

5. Catalysts and Reaction Pathways for the Electrochemical Reduction of Carbon Dioxide

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