摘要
Electrides,in which anionic electrons are trapped in structural cavities,have garnered significant attention for exceptionalfunctionalities based on their low work function.In low-dimensional electrides,a strong quantum confinement of anionicelectrons leads to many interesting phenomena,but a severe chemical instability due to their open structures is one of the majordisadvantages for practical applications.Here we report that one-dimensional(1D)dititanium sulfide electride exhibits an ex-traordinary stability originating from the surface self-passivation and consequent durability in bifunctional electrocatalytic activity.Theoretical calculations identify the uniqueness of the 1D[Ti_(2)S]^(2+)·2e^(−)electride,where multiple cavities form two distinct channelstructures of anionic electrons.Combined surface structure analysis and in-situ work function measurement indicate that thenatural formation of amorphous titanium oxide surface layer in air is responsible for the remarkable inertness in water and pH-varied solutions.This makes the[Ti_(2)S]^(2+)·2e^(−)electride an ideal support for a heterogenous metal-electride hybrid catalyst,demonstrating the enhanced efficiency and superior durability in both the hydrogen evolution and oxygen reduction reactionscompared to commercial Pt/C catalysts.This study will stimulate further exploratory research for developing a chemically stableelectride in reactive conditions,evoking a strategy for a practical electrocatalyst for industrial energy conversions.
基金
supported by the National Research Foundation of Korea(NRF)grant funded by the Korean government(MSIT)(2022M3H4A1A01010832 and RS-2024-00449682)
the Basic Science Research Program through the NRF funded by the Ministry of Education(2021R1A6A1A03039696)
Computer time allocation has been provided by the US DOE INCITE program(DE-AC02-06CH11357)
National ScienceFoundation ACCESS program(NSF-2138296)。
