塔菲尔方程
过电位
电催化剂
电化学
材料科学
循环伏安法
分解水
密度泛函理论
MXenes公司
化学工程
异质结
氢
纳米技术
电极
化学
催化作用
物理化学
光电子学
光催化
计算化学
有机化学
工程类
生物化学
作者
Jizhou Jiang,Fangyi Li,Saishuai Bai,Yongjing Wang,Kun Xiang,Haitao Wang,Jing Zou,Jyh‐Ping Hsu
出处
期刊:Nano Research
[Springer Science+Business Media]
日期:2022-11-19
卷期号:16 (4): 4656-4663
被引量:96
标识
DOI:10.1007/s12274-022-5112-x
摘要
Renewable energy powered electrocatalytic water splitting is a promising strategy for hydrogen generation, and the design and development of high-efficiency and earth-abundant electrocatalysts for hydrogen evolution reaction (HER) are highly desirable. Herein, MoS 2 nanoflowers decorated two-dimensional carbonitride-based MXene Ti 3 CN(OH) x hybrids have been constructed by etching and post-hydrothermal methods. The electrochemical performance of the as-obtained Ti 3 CN(OH) x @MoS 2 hybrids having a quasi core—shell structure is fascinating: An overpotential of 120 mV and a Tafel slope of 64 mV·dec −1 can be delivered at a current density of 10 mA·cm −2 . And after 3,000 cyclic voltammetry cycles, it can be seen that there is no apparent attenuation. Both the experimental results and density functional theory (DFT) calculations indicate that the synergetic effects between Ti 3 CN(OH) x and MoS 2 are responsible for the robust electrochemical HER performance. The electrons of −OH group in Ti 3 CN(OH) x are transferred to MoS 2 , making the adsorption energy of the composite for H almost vanish. The metallic Ti 3 CN(OH) x is also beneficial to the fast charge transfer kinetics. The construction of MXene-based hybrids with optimal electronic structure and unique morphology tailored to the applications can be further used in other promising energy storage and conversion devices.
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