Zhang Tengfei, Xu Dan, Liu Ping, Liu Huan, Chen Long, Gu Tiantian, Yu Feng, Liu Yanyan, Wang Gang
School of Chemistry and Chemical Engineering/State Key Laboratory Incubation Base for Green Processing of Chemical Engineering, Shihezi University, Shihezi 832003, China.
Dalton Trans. 2023 Dec 12;52(48):18287-18294. doi: 10.1039/d3dt03088a.
The construction of bifunctional catalysts for the oxygen evolution reaction (OER) and urea oxidation reaction (UOR) is important for accelerating the development of the hydrogen economy. Herein, a novel three-dimensional core-shell heterostructure (Ni-Mo-S@NiFeLDH/NF) was prepared by vertically growing NiFe layered double hydroxide (NiFe LDH) nanosheets on nickel foam (NF)-supported arrays of Ni-Mo-S (NiS, NiS, MoS) nanorods a hydrothermal-sulfide-hydrothermal process. Benefiting from the unique core-shell structure with numerous exposed active sites, the optimized Ni-Mo-S@NiFe LDH/NF shows excellent OER/UOR activity, with an overpotential of only 274 mV for OER to reach 100 mA cm and 1.318 V for UOR to reach 10 mA cm. Moreover, the assembled Ni-Mo-S@NiFe LDH||Pt/C urea electrolytic system requires only 1.348 V to achieve 10 mA cm, as much as 159 mV lower than pure water electrolysis. This work provides an idea for researching NiFe LDH-based OER/UOR bifunctional catalysts.
用于析氧反应(OER)和尿素氧化反应(UOR)的双功能催化剂的构建对于加速氢经济的发展至关重要。在此,通过水热-硫化-水热过程在泡沫镍(NF)负载的Ni-Mo-S(NiS、NiS、MoS)纳米棒阵列上垂直生长NiFe层状双氢氧化物(NiFe LDH)纳米片,制备了一种新型的三维核壳异质结构(Ni-Mo-S@NiFeLDH/NF)。得益于具有大量暴露活性位点的独特核壳结构,优化后的Ni-Mo-S@NiFe LDH/NF表现出优异的OER/UOR活性,OER达到100 mA cm-2时的过电位仅为274 mV,UOR达到10 mA cm-2时的过电位为1.318 V。此外,组装的Ni-Mo-S@NiFe LDH||Pt/C尿素电解系统仅需1.348 V即可达到10 mA cm-2,比纯水分解低159 mV。这项工作为研究基于NiFe LDH的OER/UOR双功能催化剂提供了思路。