p–d hybridization in CoFe LDH nanoflowers for efficient oxygen evolution electrocatalysis-Reference-Cited by-同舟云学术

p–d hybridization in CoFe LDH nanoflowers for efficient oxygen evolution electrocatalysis

Published:2022 Issue:20 Volume:9 Page:5296-5304
ISSN:2052-1553
Container-title:Inorganic Chemistry Frontiers
language:en
Short-container-title:Inorg. Chem. Front.

Author:

Hu Liuyong¹,Tian Liliang²³,Ding Xiang⁴,Wang Xia¹,Wang Xiaosi⁴,Qin Ying⁴,Gu Wenling⁴,Shi Le²^ORCID,Zhu Chengzhou⁴^ORCID

Affiliation:

1. Hubei Key Laboratory of Plasma Chemistry and Advanced Materials, Hubei Engineering Technology Research Center of Optoelectronic and New Energy Materials, Wuhan Institute of Technology, Wuhan 430205, P. R. China

2. State key Laboratory of Electrical Insulation and Power Equipment, Center of Nanomaterials for Renewable Energy, School of Electrical Engineering, Xi'an Jiaotong University, Xi'an 710049, P. R. China

3. Fujian Shuikou Power Generation Group Corp, Fuzhou 350004, P.R. China

4. College of Chemistry, Central China Normal University, Wuhan, 430079, P. R. China

Abstract

Organic ligands can induce p–d orbital hybridization at the interface of CoFe LDH, resulting in a downshift of the d-band center of CoFe LDH and the optimization of the binding strength of intermediates during the OER.

Funder

Fundamental Research Funds for the Central Universities

National Natural Science Foundation of China

Natural Science Foundation of Hubei Province

Publisher

Royal Society of Chemistry (RSC)

Subject

Inorganic Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2022/QI/D2QI01688E

Reference63 articles.

1. Recent advancements in Pt and Pt-free catalysts for oxygen reduction reaction