Phase-controlled synthesis of starch-derived Mo 2 C - MoC/C heterostructure catalyst for electrocatalytic hydrogen evolution reaction

被引:5
|
作者
Zou, Xiang [1 ]
Tang, Haitong [1 ]
Li, Junzhi [1 ]
Gao, Guichen [1 ]
Geng, Zhibing [1 ]
Li, Liping [1 ]
Li, Guangshe [1 ]
机构
[1] Jilin Univ, Coll Chem, State Key Lab Inorgan Synth & Preparat Chem, Changchun 130012, Peoples R China
基金
中国国家自然科学基金;
关键词
Controlled and eco-friendly synthesis; Mo 2 C-MoC heterostructure; Hydrogen evolution reaction; Operando EIS; Distribution of times (DRT); MOLYBDENUM CARBIDE; HYDROTHERMAL CARBONIZATION; RELAXATION-TIMES; IMPEDANCE; EFFICIENT; BIOMASS; SPECTROSCOPY; MECHANISM; GRAPHITE; DISORDER;
D O I
10.1016/j.ijhydene.2024.07.023
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The electronic structure of molybdenum carbide closely resembles that of Pt, making it a promising candidate material for replacing noble metal catalysts. However, the primary challenge is the controlled and eco-friendly synthesis of molybdenum carbide. Herein, we developed a sustainable and controlled method for synthesizing a heterostructure catalyst for the electrocatalytic hydrogen evolution reaction (HER) using starch as the raw material. Through a hydrothermal redox reaction and subsequent temperature-programmed treatment under an inert atmosphere, the hexagonal Mo 2 C-cubic MoC heterostructure nanoparticles were dispersed on a carbon matrix. Our investigation into the synthesis process extensively covered the growth of MoO 2 nanocrystals and hydrochar during the hydrothermal redox reaction, as well as the phase evolution during the subsequent temperature-programmed treatment. Electrochemical assessments demonstrated the catalyst's remarkable efficiency for the hydrogen evolution reaction across both acidic and alkaline media, achieving a current density of 10 mA/cm 2 with an overpotential of 139.4 mV in 1 M KOH solution and 160.7 mV in 0.5 M H 2 SO 4 solution. Combining a series of electrochemical characterizations and applying the distribution of relaxation times (DRT) analysis to operando electrochemical impedance spectroscopy (EIS) data, the superior kinetic performance of the Mo 2 C-MoC/C was demonstrated, outperforming that of single-phase molybdenum carbide. Furthermore, the catalyst has demonstrated remarkable stability even at high current densities in both acidic and alkaline electrolytes, underscoring its potential as a cathode catalyst in both alkaline water electrolyzers and proton exchange membrane (PEM) electrolyzers.
引用
收藏
页码:525 / 536
页数:12
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