纳米团簇
材料科学
过电位
离解(化学)
分解水
电解水
氢
催化作用
化学工程
阴极
无机化学
光化学
活化能
纳米柱
次磷酸
无定形固体
碱性水电解
水的自电离
动力学
纳米技术
物理化学
硝基苯
制氢
协调数
作者
Xue Bai,Biao Feng,Jiyao Huang,Jingyi Tian,Y Jiang,Y P Yu,Xizhang Wang,Lijun Yang,H Huang,Zheng Hu,Qiang Wu
摘要
ABSTRACT Alkaline hydrogen evolution (HER) performance of Ru catalysts is limited by the high activation energy barriers of water dissociation and the poisoning of active sites by OH * intermediates. Herein, the Mo x C nanoclusters with distinct crystalline phases (MoC and Mo 2 C) are supported on hierarchical N‐doped carbon nanocages (hNCNC). Long‐range disordered Ru nanoclusters are induced to grow on the MoC nanoclusters due to the presence of Mo vacancies, while crystalline Ru nanoclusters grow on both Mo 2 C nanoclusters and hNCNC due to fewer defects. The Ru‐MoC/hNCNC achieves an ultralow overpotential (@10 mA cm −2 ) of 20 mV, a high turnover frequency of 21.8 H 2 s −1 and robust durability in 1 M KOH, much superior to the counterpart of Ru‐Mo 2 C/hNCNC. The anion‐exchange membrane water electrolysis device with Ru‐MoC/hNCNC cathode delivers an industrial‐scale current of 1 A cm −2 at ≈1.65 V in 1.0 M KOH. The theoretical calculation, together with in situ Raman spectra, reveals that the Ru‐MoC heterointerfaces promote the water dissociation kinetics on Mo sites, leading to the detached formation of OH * on MoC and H * on Ru. This spatial decoupling of OH * and H * can mitigate the OH * poisoning of Ru and promote subsequent H 2 formation, thereby demonstrating excellent alkaline HER performance.
科研通智能强力驱动
Strongly Powered by AbleSci AI