The Mo as electron trapper and donor to modulate the electron of CoP2 in phosphating process

电子转移 电子 电催化剂 电化学 化学 价电子 兴奋剂 电子传输链 纳米技术 材料科学 电极 光电子学 物理 光化学 物理化学 生物化学 量子力学
作者
Peilin Wu,Lin Gao,Liuyan Dong,Zihan Lin,Lili Cui
出处
期刊:International Journal of Hydrogen Energy [Elsevier]
卷期号:48 (39): 14543-14553 被引量:5
标识
DOI:10.1016/j.ijhydene.2022.12.309
摘要

To prepare bifunctional electrocatalyst towards HER and OER is extremely important for promoting the development of electrochemical water splitting technology. Herein, the element doping method is employed to tune the electron environment of cobalt phosphide (CoP). The Mo-doped CoP supported on carbon cloth (CC) is constructed by solvothermal and annealing method. The effect of Mo on the electron modulation of CoP during different phosphating time was studied carefully. It is noted that the Mo play an important role in tuning the electron state of Co and P elements which can trap the electron and was reduced to low valence, then transfer the electron to Co and P. With increasing the phosphating time, the electron transfer phenomenon between Mo and CoP is obvious. Benefiting from the electron engineering of Mo, Co and P as well as thin and wrinkle sheets structure, the optimal electrocatalyst only requires 39 mV and 251 mV to deliver 10 mA cm−2 for HER and OER, respectively. Also, as for the whole water splitting performance, it delivers 10 mA cm−2 at cell voltage of 1.56 V. Importantly, Faraday efficiency of the optimal catalyst achieves 99.9% for HER due to the tuned electron state of Co and P, high ECSA and low Rct.
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