材料科学
铂金
钼
贵金属
氮化物
电化学
氢
化学工程
多孔性
电极
无机化学
多孔介质
分解水
纳米技术
金属
催化作用
复合材料
冶金
化学
光催化
物理化学
生物化学
有机化学
图层(电子)
工程类
作者
Shaobo Xi,Cong Luo,Kui Xie
标识
DOI:10.1002/adma.202502583
摘要
Abstract Platinum is widely used in the important components in most electrochemical energy conversion systems while as a noble metal it faces the inevitable challenge of limited reserves. Herein, porous single–crystalline (PSC) molybdenum nitride (MoN) monoliths are reported at the centimeter scale that surpass platinum for all–pH hydrogen evolution. Free–standing PSC MoN electrode with the pore size of ≈6 nm and porosity of ≈72% present both noble–metal–like electronic structure and unsaturated Mo─N coordination structures at surface, contributing to remarkably high intrinsic electrocatalytic activity. The unprecedented overpotentials of as low as 13 and 11 mV are presented at the geometrical current density of 10 mA cm −2 for hydrogen evolution in H 2 SO 4 (pH 0) and KOH (pH 14) media, respectively, which is dramatically superior to commercial Pt electrodes. As a result of the structural stability, the outstanding long–term durability for all pH hydrogen evolution is demonstrated without visible degradation in a continuous operation for 300 h.
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