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Accelerated Hydrogen Evolution Reaction in CoS2 by Transition-Metal Doping
ACS Energy Letters ( IF 19.3 ) Pub Date : 2018-03-05 00:00:00 , DOI: 10.1021/acsenergylett.8b00066
Jingyan Zhang 1 , Yuchan Liu 1 , Changqi Sun 1 , Pinxian Xi 1 , Shanglong Peng 1 , Daqiang Gao 1 , Desheng Xue 1
Affiliation  

Cobalt pyrite (CoS2) is one of the promising candidate catalysts for electrocatalytic hydrogen evolution because of its efficient catalytic activity sites and inherent metallicity. Herein, we report the greatly improved electrocatalytic activity of CoS2 resulting from Mn doping. First, we give the theoretical prediction that Mn is the most excellent dopant to activate the electrocatalytic activity of CoS2 with the smallest Gibbs free energy (|ΔGH*|) while remaining metallic. Second, to provide experimental evidence, Mn-doped CoS2 nanowires are prepared by a hydrothermal and postsulfuration method. The optimized sample shows a low overpotential of 43 mV at 10 mA/cm2, a Tafel slope of only 34 mV/dec, and long-time stability for the hydrogen evolution reaction. This work reveals a new way to stimulate the electrocatalytic activity of other pristine candidate catalysts.

中文翻译:

过渡金属掺杂在CoS 2中加速氢析出反应

黄铁酸钴(CoS 2)由于其有效的催化活性位点和固有的金属性,是用于电催化制氢的有希望的候选催化剂之一。在此,我们报道了由于Mn掺杂而大大提高了CoS 2的电催化活性。首先,我们给出理论上的预测,即锰是激活CoS 2电催化活性最优异的掺杂剂,具有最小的吉布斯自由能(| ΔG H * |),同时保持金属态。其次,为了提供实验证据,通过水热和后硫化法制备了Mn掺杂的CoS 2纳米线。优化的样品在10 mA / cm 2时显示出43 mV的低过电势,Tafel斜率仅为34 mV / dec,并且对于析氢反应具有长期稳定性。这项工作揭示了一种刺激其他原始候选催化剂电催化活性的新方法。
更新日期:2018-03-05
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