| Literature DB >> 32449199 |
Yishang Wu1, Jinyan Cai1, Yufang Xie1, Shuwen Niu1, Yipeng Zang1, Shaoyang Wu1, Yun Liu1, Zheng Lu1, Yanyan Fang1, Yong Guan2, Xusheng Zheng2, Junfa Zhu2, Xiaojing Liu1, Gongming Wang1, Yitai Qian1.
Abstract
The capability of manipulating the interfacial electronic coupling is the key to achieving on-demand functionalities of catalysts. Herein, it is demonstrated that the electronic coupling of Fe2 N can be effectively regulated for hydrogen evolution reaction (HER) catalysis by vacancy-mediated orbital steering. Ex situ refined structural analysis reveals that the electronic and coordination states of Fe2 N can be well manipulated by nitrogen vacancies, which impressively exhibit strong correlation with the catalytic activities. Theoretical studies further indicate that the nitrogen vacancy can uniquely steer the orbital orientation of the active sites to tailor the electronic coupling and thus benefit the surface adsorption capability. This work sheds light on the understanding of the catalytic mechanism in real systems and could contribute to revolutionizing the current catalyst design for HER and beyond.Entities:
Keywords: Fe2N; electrocatalysts; hydrogen evolution reaction; nitrogen vacancies; orbital tuning
Year: 2020 PMID: 32449199 DOI: 10.1002/adma.201904346
Source DB: PubMed Journal: Adv Mater ISSN: 0935-9648 Impact factor: 30.849