Solid-phase hot-pressing of POMs-ZIFs precursor and derived phosphide for overall water splitting

磷化物 分解水 电催化剂 析氧 材料科学 阳极 化学工程 电化学 氧化物 阴极 纳米技术 电极 化学 催化作用 冶金 金属 物理化学 工程类 光催化 生物化学
作者
Yujia Tang,Hong‐Jing Zhu,Long‐Zhang Dong,A‐Man Zhang,Shun‐Li Li,Jiang Liu,Ya‐Qian Lan
出处
期刊:Applied Catalysis B-environmental [Elsevier BV]
卷期号:245: 528-535 被引量:148
标识
DOI:10.1016/j.apcatb.2019.01.007
摘要

Rational design of electrocatalyst with high performance for both hydrogen and oxygen evolution reaction is attracting considerable attention in recent years. However, most electrocatalysts are powders and require to deposit on conductive substrates with binders, leading to complicated steps and hindering the improvement of long-term stability. This work exhibits a solid-phase hot-pressing method to prepare polyoxometalates based zeolitic imidazolate frameworks (POMs-ZIFs) precursor on carbon cloth (CC) rapidly and mildly. After phosphidation treatment, nitrogen-doped graphitic carbon layers coated phosphide on CC (CoP/[email protected]/CC) is synthesized. CoP/[email protected]/CC has excellent electrocatalytic performance for water splitting due to the synergistic effect of CoP, MoP and as-formed oxide/hydroxide layers. It shows the low overpotentials of 94 mV for HER and 270 mV for OER at the current density of 10 mA cm−2 in alkaline medium, which is superior to most of the reported phosphide-based electrocatalysts. Notably, the ultra-high current density of 1000 mA cm−2 can be reached at the overpotentials of only 475 mV for HER and 657 mV for OER. As both cathode and anode for overall water splitting, CoP/[email protected] can achieve the current density of 50 mA cm−2 at the cell voltage of 1.71 V. The solid-phase hot-pressing method ensures the tight and uniform growth of the fast nucleating and stable materials on substrate and applies for more electrochemical reactions.
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