海水
电解
纳米颗粒
碳纤维
碳纳米颗粒
化学工程
兴奋剂
材料科学
化学
核化学
环境化学
纳米技术
海洋学
电极
物理化学
电解质
光电子学
地质学
复合材料
复合数
工程类
作者
Dawei Wang,Xuehong Wang,Huiqian Qiu,Yixuan Tao,Jie Yin,Juan Li,Wenpin Wang,Zhongcheng Li
出处
期刊:Fuel
[Elsevier]
日期:2024-05-24
卷期号:371: 131995-131995
被引量:1
标识
DOI:10.1016/j.fuel.2024.131995
摘要
Electric-driven water dissociation is considered to be a sustainable approach for the generation of H2. Ni nanoparticles show poor freshwater/seawater electrolysis activity owing to the severe aggregation of Ni, which blocks the active sites to catalyze water splitting. Here, we present Ni nanoparticles/N-doped carbon sheets by the thermal treatment of Ni-based triazole-benzoic acid complexes. The electronic state and coordination environment of Ni are modulated by the formation of the confined space with the N-doped carbon layer. Ni/N-doped carbon sheets promote acidic/alkaline hydrogen evolution activity with 143/81 mV@10 mA/cm2. Upon being used as the catalysts for water oxidation reaction, it expedited alkaline oxygen evolution 218/312 mV@10/50 mA/cm2 for Ni/N-doped carbon, which is even superior to commercial RuO2 with 309/364 mV. Tests for alkaline freshwater/seawater splitting find that Ni/N-doped carbon sheets possess remarkable activity with 1.56/1.62 V@10 mA/cm2 as well as outstanding stability. Our work offers an efficient strategy to rationally regulate the coordination structure of metal nanoparticles for promoting water electrolysis activity.
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