材料科学
催化作用
电解质
化学工程
制氢
氢
金属
无机化学
电极
化学
冶金
有机化学
物理化学
工程类
作者
Deliang Zhang,Miaomiao Xing,Xiaoming Mou,Caixia Song,Debao Wang
标识
DOI:10.1016/j.apsusc.2022.155283
摘要
Metal nitrides are considered promising catalysts for the hydrogen evolution reaction integrated with electrooxidation reaction of biomass due to their metal-like properties. However, the synthesis of metal nitrides involves multi-step reactions and requires continuous reactions under a large amount of NH3 atmosphere. Herein, we exploit deep eutectic solvent (DES) to induce in-situ synthesize N-doped carbon (NC) composite Co4N ultrathin nanosheets self-supporting electrode on carbon cloth (Co4N/NC@CC) without additional input NH3 atmosphere. XAFS spectra showed that the strong interaction between Co4N and NC accelerated the electron transport at the interface, and the ultrathin nanostructure of Co4N/NC is beneficial to increasing the catalytic active sites, thereby effectively improving the catalytic performance of Co4N/NC@CC. During the HER process, Co4N/NC@CC only needs 62, 98, and 60 mV overpotentials to reach a current density of 10 mA/cm2 in alkaline, neutral, and acidic electrolytes. When Co4N/NC@CC is used to produce 2,5-furandicarboxylic acid (FDCA) and hydrogen fuel synchronously in alkaline electrolytes, only a low voltage of 1.38 V is required at 10 mA/cm2, and the conversion rate of 5-hydroxymethylfurfural (HMF) is close to 100 % and the selectivity of FDCA is 98.6 %.
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