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 RuSe cluster compounds (RuSe) 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 HO*/OH* at the electrode/electrolyte interface of RuNC, but the RuSe can promote HO*/OH* transport to increase the number of available HO* on RuNC by disordering the interfacial water network. With the synergy of RuSe 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.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9587018 | PMC |
http://dx.doi.org/10.1038/s41467-022-33984-5 | DOI Listing |
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