非阻塞I/O
电解
电催化剂
材料科学
电极
镍
阳极
化学工程
电化学
冶金
催化作用
化学
电解质
物理化学
生物化学
工程类
作者
Jinlong Zheng,Wei Zhou,Tong Liu,Shijie Liu,Chengbo Wang,Lin Guo
出处
期刊:Nanoscale
[The Royal Society of Chemistry]
日期:2017-01-01
卷期号:9 (13): 4409-4418
被引量:130
摘要
Homologous NiO, Ni3S2, and Ni2P nanoarrays were obtained by thermolysis, sulfuration, and phosphorization of the Ni(SO4)0.3OH1.4 belt-like precursors. The three types of porous nickel compound films grown on nickel foam with a thickness of ∼8 μm have been used as anodes and cathodes in a two-electrode setup for overall water splitting. The electrode pairing of NixMy//NixMy (M = O, S, and P) for electrocatalysis in order of superiority is as follows: NiO//Ni2P > Ni3S2//Ni2P > Ni2P//Ni2P > Ni3S2//Ni3S2 > NiO//Ni3S2 > NiO//NiO. The other two sets of NixMy with different thicknesses of ∼5 and ∼11 μm also follow the abovementioned order. The well matched electrode pair of NiOOER//Ni2PHER only needs 1.65 V, whereas NiO//NiO pair needs 1.84 V to afford the current of 10 mA cm-2 in 1 mol L-1 of aqueous KOH solution. In particular, the current density retention of the NiO//Ni2P reached 92% after 120 hours of electrolysis at 1.70 V (NiO//NiO only maintains 72% after 30-hour electrolysis). The novelty of this study focuses on fabricating a well matched electrode pair to substantially enhance its electrochemical performance and durability, which would provide a new insight into developing non-noble, highly efficient, and stable electrode pairs.
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