塔菲尔方程
材料科学
电催化剂
纳米管
电子
基质(水族馆)
亚稳态
相(物质)
化学物理
纳米技术
化学工程
碳纳米管
电极
电化学
化学
物理
物理化学
工程类
地质学
有机化学
海洋学
量子力学
作者
Ting Zhang,Tingxuan Yang,Guoxing Qu,Saifang Huang,Peng Cao,Wei Gao
标识
DOI:10.1016/j.jechem.2021.10.031
摘要
1T phase MoS2 (1T-MoS2) is a promising substitute of platinum electrocatalyst for hydrogen evolution reaction (HER) due to its high intrinsic activity but suffering from thermodynamical instability. Although great efforts have been made to synthesize 1T-MoS2 and enhance its stability, it remains a big challenge to realize the phase control and stabilization of 1T-MoS2. Herein, based on crystal field theory analysis, we propose a new solution by designing an electrocatalyst of 1T-MoS2 nanosheets anchoring on black TiO2−x nanotube arrays in-situ grown on Ti plate (1T-MoS2/TiO2−x@Ti). The black TiO2−x substrate is expected to play as electron donors to increase the charge in Mo 4d orbits of 1T-MoS2 and thus weaken the asymmetric occupation of electrons in the Mo 4d orbits. Experimental results demonstrate that black TiO2−x nanotubes shift electrons to MoS2 and induce MoS2 to generate more 1T phase due to stabilizing the 1T-MoS2 nanosheets compared with a Ti substrate. Thus 1T-MoS2/TiO2−x@Ti shows much improved HER performance with a small Tafel slope of 42 mV dec−1 and excellent catalytic stability with negligible degradation for 24 h. Theoretical calculations confirm that the black TiO2−x substrate can effectively stabilize metastable 1T-MoS2 due to electrons transferring from black TiO2−x to Mo 4d orbits. This work sheds light on the instability of 1T-MoS2 and provides an essential method to stabilize and efficiently utilize 1T-MoS2 for HER.
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