Chia Xinyi, Ambrosi Adriano, Sedmidubský David, Sofer Zdeněk, Pumera Martin
Division of Chemistry and Biological Chemistry, School of Physical and Mathematical Sciences, Nanyang Technological University, Singapore 637371 (Singapore).
Chemistry. 2014 Dec 22;20(52):17426-32. doi: 10.1002/chem.201404832. Epub 2014 Oct 24.
MoS2 has become particularly popular for its catalytic properties towards the hydrogen evolution reaction (HER). It has been shown that the metallic 1T phase of MoS2 , obtained by chemical exfoliation after lithium intercalation, possesses enhanced catalytic activity over the semiconducting 2H phase due to the improved conductivity properties which facilitate charge-transfer kinetics. Here we demonstrate a simple electrochemical method to precisely tune the electron-transfer kinetics as well as the catalytic properties of both exfoliated and bulk MoS2 -based films. A controlled reductive or oxidative electrochemical treatment can alter the surface properties of the film with consequently improved or hampered electrochemical and catalytic properties compared to the untreated film. Density functional theory calculations were used to explain the electrochemical activation of MoS2 . The electrochemical tuning of electrocatalytic properties of MoS2 opens the doors to scalable and facile tailoring of MoS2 -based electrochemical devices.
二硫化钼(MoS₂)因其对析氢反应(HER)的催化性能而变得格外受欢迎。研究表明,通过锂嵌入后化学剥离获得的MoS₂金属1T相,由于其改善的导电性能促进了电荷转移动力学,因而比半导体2H相具有更高的催化活性。在此,我们展示了一种简单的电化学方法,可精确调节剥落的和块状MoS₂基薄膜的电子转移动力学以及催化性能。与未处理的薄膜相比,可控的还原或氧化电化学处理可以改变薄膜的表面性质,从而改善或阻碍其电化学和催化性能。密度泛函理论计算用于解释MoS₂的电化学活化。MoS₂电催化性能的电化学调谐为基于MoS₂的电化学器件的可扩展和简便定制打开了大门。