电催化剂
三元运算
纳米棒
复合数
硫化物
材料科学
金属
硫化氢
化学工程
氢
无机化学
纳米技术
电化学
化学
冶金
电极
物理化学
复合材料
有机化学
硫黄
计算机科学
工程类
程序设计语言
作者
Dong Duan,Sen Ren,Yan Huang,Zikang Tang,Yan Wang,Xin Chen,Xingbo Ge
出处
期刊:Langmuir
[American Chemical Society]
日期:2025-04-22
卷期号:41 (17): 10884-10892
标识
DOI:10.1021/acs.langmuir.5c00087
摘要
In this study, a self-supported material with a unique ternary metal sulfide nanorod array structure was fabricated in situ on copper foam via a facile one-step electrodeposition approach ((NiCo-Cu)Sx/CF). The electrochemically driven rapid generation of abundant S2- ions from thiourea accelerates their combination with Ni2+ and Co2+, resulting in a catalytically enriched surface on the nanorod array. The high-density nanorod arrays provide maximally accessible active sites, thereby enhancing the hydrogen evolution reaction (HER). The in situ grown self-supported structure effectively eliminates the need for binders (common in conventional catalysts), avoids additional interfacial resistance, and ensures long-term stability during electrocatalytic operation. The synergistic interactions among the metal components (Ni, Co, and Cu) optimize the local electronic environment, creating favorable conditions for catalytic hydrogen evolution. The experimental results demonstrate that the ternary metal sulfide nanocomposite (denoted as (NiCo-Cu)Sx/CF) exhibits superior hydrogen evolution reaction performance compared to its binary counterparts. Remarkably, the catalyst required only 42 and 161 mV overpotential to deliver 10 mA·cm-2 and 100 mA·cm-2 current densities in 1 M KOH, respectively, with 100 h operational stability. This work provides a viable strategy for developing self-supported ternary non-noble metal catalysts for energy conversion applications.
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