过电位
分解水
塔菲尔方程
堆积
电催化剂
材料科学
钴
纳米颗粒
析氧
纳米技术
无机化学
化学
电极
催化作用
电化学
物理化学
有机化学
光催化
生物化学
作者
Yousen Wu,Ying Wang,Guozhe Sui,Dongxuan Guo,Dawei Chu,Guang Xu,Jinlong Li,Yue Li,Dong‐Feng Chai
标识
DOI:10.1016/j.jcis.2024.07.025
摘要
Nowadays, the inherent re-stacking nature and weak d-p hybridization orbital interactions within MXene remains significant challenges in the field of electrocatalytic water splitting, leading to unsatisfactory electrocatalytic activity and cycling stability. Herein, this work aims to address these challenges and improve electrocatalytic performance by utilizing cobalt nanoparticles intercalation coupled with enhanced π-donation effect. Specifically, cobalt nanoparticles are integrated into V2C MXene nanosheets to mitigate the re-stacking issue. Meanwhile, a notable charge redistribution from cobalt to vanadium elevates orbital levels, reduces π*-antibonding orbital occupancy and alleviates Jahn-Teller distortion. Doping with tellurium induces localized electric field rearrangement resulting from the changes in electron cloud density. As a result, Co-V2C MXene-Te acquires desirable activity for hydrogen evolution reaction and oxygen evolution reaction with the overpotential of 80.8 mV and 287.7 mV, respectively, at the current density of −10 mA cm−2 and 10 mA cm−2. The overall water splitting device achieves an impressive low cell voltage requirement of 1.51 V to obtain 10 mA cm−2. Overall, this work could offer a promising solution when facing the re-stacking issue and weak d-p hybridization orbital interactions of MXene, furnishing a high-performance electrocatalyst with favorable electrocatalytic activity and cycling stability.
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