Realizing the 4e–/2e– Pathway Transition of O2 Reduction on Co–N4–C Catalysts by Regulating the Chemical Structures beyond the Second Coordination Shells-Reference-Cited by-同舟云学术

Realizing the 4e^–/2e^– Pathway Transition of O₂ Reduction on Co–N₄–C Catalysts by Regulating the Chemical Structures beyond the Second Coordination Shells

Published:2024-04-04 Issue:8 Volume:14 Page:5961-5971
ISSN:2155-5435
Container-title:ACS Catalysis
language:en
Short-container-title:ACS Catal.

Author:

Wang Wang¹,Hu Youcheng¹,Li Peng¹,Liu Yucheng²,Chen Shengli¹^ORCID

Affiliation:

1. Hubei Electrochemical Power Sources Key Laboratory, College of Chemistry and Molecular Sciences, Wuhan University, Wuhan 430072, China

2. Core Facility of Wuhan University, Wuhan University, Wuhan 430072, China

Funder

China Postdoctoral Science Foundation

National Natural Science Foundation of China

Publisher

American Chemical Society (ACS)

Link

https://pubs.acs.org/doi/pdf/10.1021/acscatal.4c00781

Reference51 articles.

1. Modifying the Electrocatalytic Selectivity of Oxidation Reactions with Ionic Liquids

2. Tackling the Activity and Selectivity Challenges of Electrocatalysts toward the Nitrogen Reduction Reaction via Atomically Dispersed Biatom Catalysts

3. Ultrastable nickel single-atom catalysts with high activity and selectivity for electrocatalytic CO2 methanation

4. Rational Design of Atomic Site Catalysts for Electrocatalytic Nitrogen Reduction Reaction: One Step Closer to Optimum Activity and Selectivity

5. Hydrogen bonding steers the product selectivity of electrocatalytic CO reduction

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