Water- and acid-stable self-passivated dihafnium sulfide electride and its persistent electrocatalytic reaction

Electrides have emerged as promising materials with exotic properties, such as extraordinary electron-donating ability. However, the inevitable instability of electrides, which is caused by inherent excess electrons, has hampered their widespread applications. We report that a self-passivated dihafnium sulfide electride ([Hf(2)S](2+)∙2e(−)) by double amorphous layers exhibits a strong oxidation resistance in water and acid solutions, enabling a persistent electrocatalytic hydrogen evolution reaction. The naturally formed amorphous Hf(2)S layer on the cleaved [Hf(2)S](2+)∙2e(−) surface reacts with oxygen to form an outermost amorphous HfO(2) layer with ~10-nm thickness, passivating the [Hf(2)S](2+)∙2e(−) electride. The excess electrons in the [Hf(2)S](2+)∙2e(−) electride are transferred through the thin HfO(2) passivation layer to water molecules under applied electric fields, demonstrating the first electrocatalytic reaction with excellent long-term sustainability and no degradation in performance. This self-passivation mechanism in reactive conditions can advance the development of stable electrides for energy-efficient applications.