College of Chemistry and Molecular Engineering, Zhengzhou University , Zhengzhou 450001, People's Republic of China.
ACS Appl Mater Interfaces. 2016 Oct 12;8(40):26794-26800. doi: 10.1021/acsami.6b08740. Epub 2016 Sep 29.
A simple hydrothermal method is developed for synthesizing crystalline MoS@TiO nanohybrids with metal-organic framework (MOF) as precursor. At an optimal ratio of 14.6 wt % MoS, the resultant material exhibits prominent catalytic activity for hydrogen evolution reaction (HER) with a high hydrogen production rate of 10 046 μmol h g under visible light illumination with fluorescein as photosensitizer. Furthermore, the synthesized catalyst also possesses an attractive electrocatalytic activity with an onset overpotential of -300 mV (vs RHE) and a Tafel slope of ∼81 mV dec. The enhanced catalyst performances are mainly attributed to the in situ formed active sites, featuring a uniform dispersion and strong connection of MoS and TiO, which can facilitate electron transfer. In addition, the MoS@TiO nanohybrids are highly stable and completely recyclable over HER.
一种简单的水热法被开发用于合成具有金属有机骨架(MOF)为前体的结晶 MoS@TiO 纳米杂化物。在最佳的 14.6wt% MoS 比例下,所得材料在可见光照下以荧光素为敏化剂时表现出突出的析氢反应(HER)催化活性,具有高达 10046μmol h g 的高氢气生成速率。此外,所合成的催化剂还具有吸引人的电催化活性,具有 -300 mV(相对于 RHE)的起始过电势和 ∼81 mV dec 的塔菲尔斜率。增强的催化剂性能主要归因于原位形成的活性位点,具有 MoS 和 TiO 的均匀分散和强连接,这有利于电子转移。此外,MoS@TiO 纳米杂化物在 HER 中具有高稳定性和完全可回收性。