In-situ fabrication of bimetallic FeCo2O4-FeCo2S4 heterostructure for high-efficient alkaline freshwater/seawater electrolysis

材料科学 分解水 化学工程 电解 氧化物 碱性水电解 双功能 电解质 阳极 海水 无机化学 化学 电极 催化作用 冶金 光催化 海洋学 物理化学 工程类 地质学 生物化学
作者
Junming Zhang,Yingjian Fang,Yao Chen,Xiaojie Zhang,He Xiao,Man Zhao,Chaoyue Zhao,Xiongfeng Ma,Tianjun Hu,Ergui Luo,Jianfeng Jia,Haishun Wu
出处
期刊:Journal of Colloid and Interface Science [Elsevier BV]
卷期号:653 (Pt A): 821-832 被引量:30
标识
DOI:10.1016/j.jcis.2023.09.126
摘要

Rational construction of bifunctional electrocatalysts with long-term stability and high electrocatalytic activity is of great importance, but it is challenging to obtain highly efficient non-precious metal-based catalysts for overall seawater electrolysis. Herein, a nickel foam (NF) self-supporting CoFe-layered double hydroxide (CoFe-LDH/NF) was directly converted into FeCo2O4-FeCo2S4 heterostructure via hydrothermal method in 50 mM Na2S solution, instead of FeCo2O4@FeCo2S4 core-shell structure. The FeCo2O4-FeCo2S4 heterojunction shows nanosheets structure with rough surface (the thickness of ∼ 198.9 nm), which provides rich oxide/sulfide interfaces, high electrochemical active area, a large number of active sites, as well as fast charge and mass transfer. In 1.0 M KOH solution, 1.0 M KOH + 0.5 M NaCl, and alkaline natural seawater, the FeCo2O4-FeCo2S4 heterojunction exhibits eminently electrocatalytic performance, with overpotentials of η-100 = 225 mV, η-100 = 233 mV, and η-100 = 238 mV for OER, as well as η-100 = 271 mV, η-100 = 273 mV, and η-100 = 277 mV for HER, respectively. Furthermore, self-supporting FeCo2O4-FeCo2S4 electrode (FeCo2O4-FeCo2S4/NF) as the cathode and anode of an electrolyzer exhibits a lower cell voltage of E-100 = 1.75 V in alkaline seawater than those of FeCo2S4/NF (1.77 V), CoFe-LDH/NF (1.87 V), and FeCo2O4/NF (1.91 V). Specifically, FeCo2O4-FeCo2S4 electrolyzer can stably produce hydrogen for over 48 h in alkaline freshwater/seawater electrolyte. These outstanding electrocatalytic performances and corrosion resistance to salty-water can be attributed to the surface reconstruction behavior of the FeCo2O4-FeCo2S4/NF catalyst during OER, which leads to the in-situ formation of metal oxyhydroxides. In particular, the FeCo2O4-FeCo2S4 heterojunction is also very competitive among most state-of-the-art non-noble metal-based catalysts, whether in KOH or alkaline salty-water electrolytes.
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