| Literature DB >> 36271080 |
Kaian Sun1, Xueyan Wu2, Zewen Zhuang1,3, Leyu Liu1, Jinjie Fang4, Lingyou Zeng5, Junguo Ma1, Shoujie Liu1, Jiazhan Li1, Ruoyun Dai1, Xin Tan1, Ke Yu1, Di Liu1, Weng-Chon Cheong1, Aijian Huang6, Yunqi Liu5, Yuan Pan5, Hai Xiao1, Chen Chen7.
Abstract
Hydrogen evolution reaction (HER) in neutral media is of great practical importance for sustainable hydrogen production, but generally suffers from low activities, the cause of which has been a puzzle yet to be solved. Herein, by investigating the synergy between Ru single atoms (RuNC) and RuSex cluster compounds (RuSex) for HER using ab initio molecular dynamics, operando X-ray absorption spectroscopy, and operando surface-enhanced infrared absorption spectroscopy, we establish that the interfacial water governs neutral HER. The rigid interfacial water layer in neutral media would inhibit the transport of H2O*/OH* at the electrode/electrolyte interface of RuNC, but the RuSex can promote H2O*/OH* transport to increase the number of available H2O* on RuNC by disordering the interfacial water network. With the synergy of RuSex and RuNC, the resulting neutral HER performance in terms of mass-specific activity is 6.7 times higher than that of 20 wt.% Pt/C at overpotential of 100 mV.Entities:
Year: 2022 PMID: 36271080 DOI: 10.1038/s41467-022-33984-5
Source DB: PubMed Journal: Nat Commun ISSN: 2041-1723 Impact factor: 17.694