Faculty of Physics and CENIDE, Universität Duisburg-Essen, 47057 Duisburg, Germany.
Nanoscale. 2018 Dec 13;10(48):22908-22916. doi: 10.1039/c8nr04696d.
Two-dimensional molybdenum-disulfide (MoS2) catalysts can achieve high catalytic activity for the hydrogen evolution reaction upon appropriate modification of their surface. The intrinsic inertness of the compound's basal planes can be overcome by either increasing the number of catalytically active edge sites or by enhancing the activity of the basal planes via a controlled creation of sulfur vacancies. Here, we report a novel method of activating the MoS2 surface using swift heavy ion irradiation. The creation of nanometer-scale structures by an ion beam, in combination with the partial sulfur depletion of the basal planes, leads to a large increase of the number of low-coordinated Mo atoms, which can form bonds with adsorbing species. This results in a decreased onset potential for hydrogen evolution, as well as in a significant enhancement of the electrochemical current density by over 160% as compared to an identical but non-irradiated MoS2 surface.
二维二硫化钼 (MoS2) 催化剂通过适当修饰其表面,可以实现高效的析氢催化活性。通过增加催化活性边缘位点的数量,或者通过控制硫空位的形成来增强基面的活性,可以克服化合物基面的固有惰性。在此,我们报告了一种使用重离子辐照来激活 MoS2 表面的新方法。离子束形成的纳米级结构,再加上基面的部分硫缺失,导致低配位 Mo 原子数量大量增加,这些 Mo 原子可以与吸附物种形成键。这导致析氢的起始电位降低,与未经辐照的相同 MoS2 表面相比,电化学电流密度显著提高了 160%以上。