Nikam Revannath Dnyandeo, Lu Ang-Yu, Sonawane Poonam Ashok, Kumar U Rajesh, Yadav Kanchan, Li Lain-Jong, Chen Yit-Tsong
Department of Chemistry, National Taiwan University , Taipei 106, Taiwan.
Institute of Atomic and Molecular Sciences, Academia Sinica , Taipei 106, Taiwan.
ACS Appl Mater Interfaces. 2015 Oct 21;7(41):23328-35. doi: 10.1021/acsami.5b07960. Epub 2015 Oct 8.
Molybdenum disulfide (MoS2) is a promising catalyst for hydrogen evolution reaction (HER) because of its unique nature to supply active sites in the reaction. However, the low density of active sites and their poor electrical conductivity have limited the performance of MoS2 in HER. In this work, we synthesized MoS2 nanosheets on three-dimensional (3D) conductive MoO2 via a two-step chemical vapor deposition (CVD) reaction. The 3D MoO2 structure can create structural disorders in MoS2 nanosheets (referred to as 3D MoS2/MoO2), which are responsible for providing the superior HER activity by exposing tremendous active sites of terminal disulfur of S2(-2) (in MoS2) as well as the backbone conductive oxide layer (of MoO2) to facilitate an interfacial charge transport for the proton reduction. In addition, the MoS2 nanosheets could protect the inner MoO2 core from the acidic electrolyte in the HER. The high activity of the as-synthesized 3D MoS2/MoO2 hybrid material in HER is attributed to the small onset overpotential of 142 mV, a largest cathodic current density of 85 mA cm(-2), a low Tafel slope of 35.6 mV dec(-1), and robust electrochemical durability.
二硫化钼(MoS2)因其在反应中提供活性位点的独特性质,是一种很有前景的析氢反应(HER)催化剂。然而,活性位点的低密度及其较差的导电性限制了MoS2在析氢反应中的性能。在这项工作中,我们通过两步化学气相沉积(CVD)反应在三维(3D)导电的MoO2上合成了MoS2纳米片。3D MoO2结构可以在MoS2纳米片中产生结构无序(称为3D MoS2/MoO2),这通过暴露S2(-2)(在MoS2中)末端二硫的大量活性位点以及(MoO2的)主链导电氧化物层来促进质子还原的界面电荷传输,从而提供优异的析氢反应活性。此外,MoS2纳米片可以保护内部的MoO2核免受析氢反应中酸性电解质的侵蚀。所合成的3D MoS2/MoO2杂化材料在析氢反应中的高活性归因于142 mV的小起始过电位、85 mA cm(-2)的最大阴极电流密度、35.6 mV dec(-1)的低塔菲尔斜率以及强大的电化学耐久性。