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形态和表面化学工程实现高电流密度下通用 pH 值的析氢催化剂。

Morphology and surface chemistry engineering toward pH-universal catalysts for hydrogen evolution at high current density.

机构信息

Shenzhen Geim Graphene Center (SGC), Tsinghua-Berkeley Shenzhen Institute (TBSI), Tsinghua University, Shenzhen, 518055, PR China.

Shenyang National Laboratory for Materials Science, Institute of Metal Research, Chinese Academy of Sciences, Shenyang, 110016, PR China.

出版信息

Nat Commun. 2019 Jan 17;10(1):269. doi: 10.1038/s41467-018-07792-9.

Abstract

Large-scale implementation of electrochemical hydrogen production requires several fundamental issues to be solved, including understanding the mechanism and developing inexpensive electrocatalysts that work well at high current densities. Here we address these challenges by exploring the roles of morphology and surface chemistry, and develop inexpensive and efficient electrocatalysts for hydrogen evolution. Three model electrocatalysts are flat platinum foil, molybdenum disulfide microspheres, and molybdenum disulfide microspheres modified by molybdenum carbide nanoparticles. The last catalyst is highly active for hydrogen evolution independent of pH, with low overpotentials of 227 mV in acidic medium and 220 mV in alkaline medium at a high current density of 1000 mA cm, because of enhanced transfer of mass (reactants and hydrogen bubbles) and fast reaction kinetics due to surface oxygen groups formed on molybdenum carbide during hydrogen evolution. Our work may guide rational design of electrocatalysts that work well at high current densities.

摘要

大规模电化学制氢需要解决几个基本问题,包括了解机制和开发在高电流密度下工作良好的廉价电催化剂。在这里,我们通过探索形态和表面化学的作用来应对这些挑战,并开发出廉价高效的析氢电催化剂。三种模型电催化剂为:平坦的铂箔、二硫化钼微球和碳化钼纳米颗粒修饰的二硫化钼微球。最后一种催化剂在 pH 值无关的情况下对析氢具有高活性,在高电流密度为 1000 mA cm 时,在酸性介质中的过电位低至 227 mV,在碱性介质中的过电位低至 220 mV,这是因为碳化钼在析氢过程中形成的表面氧基团增强了质量(反应物和氢气气泡)的传递和快速反应动力学。我们的工作可能会指导在高电流密度下工作良好的电催化剂的合理设计。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9051/6336864/560403dc39e0/41467_2018_7792_Fig1_HTML.jpg

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