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Reversed Active Sites Boost the Intrinsic Activity of Graphene‐like Cobalt Selenide for Hydrogen Evolution
Author(s) -
Shen Shijie,
Lin Zhiping,
Song Kai,
Wang Zongpeng,
Huang Liangai,
Yan Linghui,
Meng Fanqi,
Zhang Qinghua,
Gu Lin,
Zhong Wenwu
Publication year - 2021
Publication title -
angewandte chemie international edition
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.831
H-Index - 550
eISSN - 1521-3773
pISSN - 1433-7851
DOI - 10.1002/anie.202102961
Subject(s) - overpotential , tafel equation , graphene , gibbs free energy , hydrogen production , selenide , cobalt , inorganic chemistry , adsorption , hydrogen , chemistry , active site , materials science , electrochemistry , catalysis , nanotechnology , thermodynamics , electrode , selenium , organic chemistry , physics
Abstract Optimizing the hydrogen adsorption Gibbs free energy (Δ G H ) of active sites is essential to improve the overpotential of the electrocatalytic hydrogen evolution reaction (HER). We doped graphene‐like Co 0.85 Se with sulfur and found that the active sites are reversed (from cationic Co sites to anionic S sites), which contributed to an enhancement in electrocatalytic HER performance. The optimal S‐doped Co 0.85 Se composite has an overpotential of 108 mV (at 10 mA cm −2 ) and a Tafel slope of 59 mV dec −1 , which exceeds other reported Co 0.85 Se‐based electrocatalysts. The doped S sites have much higher activity than the Co sites, with a hydrogen adsorption Gibbs free energy (Δ G H ) close to zero (0.067 eV), which reduces the reaction barrier for hydrogen production. This work provides inspiration for optimizing the intrinsic HER activity of other related transition metal chalcogenides.