电催化剂
过电位
分解水
双功能
材料科学
双金属片
石墨烯
析氧
碳化物
MXenes公司
过渡金属
催化作用
化学工程
肖特基势垒
纳米技术
无机化学
化学
电极
金属
光催化
电化学
光电子学
物理化学
复合材料
冶金
有机化学
工程类
二极管
作者
Gokul Raj,Debanjan Das,Bidushi Sarkar,Shauvik Biswas,Karuna Kar Nanda
标识
DOI:10.1016/j.susmat.2022.e00451
摘要
Transition metal carbides (TMCs) have gained considerable attention as a non-precious multifunctional, highly active, stable electrocatalyst for efficient hydrogen evolution reaction (HER) due to its platinum like d-band electronic structure. The efforts to untie the gordian knot of developing a first-rate bifunctional electrocatalyst for efficient water splitting reaction via electronically modulated bimetallic carbides using a dual transition metal strategy have been reported here. Herein we in-situ fabricated a composite architecture consisting of N-doped CNT/ graphene hybrid anchoring Co/MoC, Co/WC and Co/VC Via an integrated pyrolysis technique to have a beneficial synergistic co-operation between each component and dual Mott-Schottky junctions resulting in a bifunctional HER and OER (oxygen evolution reaction) active catalyst exhibiting exemplary activity in both acidic and basic media. Co/[email protected] exhibits the best activity with a lower overpotential of 279 and 260 mV towards OER and 92 and 143 mV towards HER to achieve a current density of 10 mA/cm2 in basic and acidic media, respectively. Along with this, it presents excellent water splitting performance in basic media, showing a relatively low cell voltage of about 1.686 V for driving a current of 10 mA/cm2 with decent stability. It is anticipated that the tandem electron transfer between the Co, MoC moieties and nitrogen doping-induced defects in graphene/ CNT hybrid-based conductive network support might be a reason for the superiority over other recently reported Mo based carbide materials.
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