碳化
催化作用
纳米颗粒
材料科学
电解质
电催化剂
电极
解吸
可逆氢电极
氢
吸附
化学工程
密度泛函理论
纳米技术
电化学
化学
物理化学
计算化学
有机化学
参比电极
工程类
作者
Jangwon Bang,In Kyu Moon,Youngkwang Kim,Jungwoo Oh
标识
DOI:10.1002/sstr.202200283
摘要
Mo 2 C is a promising non‐precious hydrogen evolution reaction (HER) electrocatalyst. However, regulating the strong hydrogen adsorption characteristics of Mo 2 C and finding suitable support electrodes are essential processes before Mo 2 C can replace Pt to realize a sustainable hydrogen economy. Herein, the facile synthesis of heterostructured Mo 2 N–Mo 2 C nanoparticles on N‐doped carbonized wood (Mo 2 N–Mo 2 C/N‐CW) as a self‐supported electrode through carbonization and NH 3 plasma treatment is demonstrated. The synergistic effects of heterostructured Mo 2 N–Mo 2 C and N‐CW with aligned microchannels provide enhanced catalytic activity, fast charge transfer kinetics, additional active site exposure, and rapid transport of the electrolyte and H 2 bubbles, which improves the HER performance. Consequently, the Mo 2 N–Mo 2 C/N‐CW electrode exhibits superior HER performance with low overpotentials of only 79 and 311 mV to reach 10 and 500 mA cm −2 in an acidic solution, respectively. It also exhibits long‐term stability for 20 h in the high‐current‐density region (110 mA cm −2 ). The density functional theory (DFT) calculations at various sites reveal that the heterointerface of Mo 2 N and Mo 2 C promoted the catalytic activity by optimizing the adsorption/desorption of hydrogen.
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