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揭示用于析氢反应的硫化钼基电催化剂活性位点的最新进展。

Recent advances in unveiling active sites in molybdenum sulfide-based electrocatalysts for the hydrogen evolution reaction.

作者信息

Seo Bora, Joo Sang Hoon

机构信息

Department of Chemistry, Ulsan National Institute of Science and Technology (UNIST), 50 UNIST-gil, Ulsan, 44919 Republic of Korea.

School of Energy and Chemical Engineering, Ulsan National Institute of Science and Technology (UNIST), 50 UNIST-gil, Ulsan, 44919 Republic of Korea.

出版信息

Nano Converg. 2017;4(1):19. doi: 10.1186/s40580-017-0112-3. Epub 2017 Jul 25.

Abstract

Hydrogen has received significant attention as a promising future energy carrier due to its high energy density and environmentally friendly nature. In particular, the electrocatalytic generation of hydrogen fuel is highly desirable to replace current fossil fuel-dependent hydrogen production methods. However, to achieve widespread implementation of electrocatalytic hydrogen production technology, the development of highly active and durable electrocatalysts based on Earth-abundant elements is of prime importance. In this context, nanostructured molybdenum sulfides (MoS ) have received a great deal of attention as promising alternatives to precious metal-based catalysts. In this focus review, we summarize recent efforts towards identification of the active sites in MoS -based electrocatalysts for the hydrogen evolution reaction (HER). We also discuss recent synthetic strategies for the engineering of catalyst structures to achieve high active site densities. Finally, we suggest ongoing and future research challenges in the design of advanced MoS -based HER electrocatalysts.

摘要

由于氢具有高能量密度和环境友好的特性,作为一种有前景的未来能源载体,它已受到广泛关注。特别是,通过电催化生成氢燃料非常有助于取代当前依赖化石燃料的制氢方法。然而,为了实现电催化制氢技术的广泛应用,开发基于储量丰富元素的高活性和耐用的电催化剂至关重要。在此背景下,纳米结构的硫化钼(MoS )作为贵金属基催化剂的有前途的替代品受到了广泛关注。在这篇重点综述中,我们总结了近期在确定基于MoS 的电催化剂中用于析氢反应(HER)的活性位点方面所做的努力。我们还讨论了用于构建催化剂结构以实现高活性位点密度的近期合成策略。最后,我们提出了在设计先进的基于MoS 的HER电催化剂方面当前和未来的研究挑战。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e037/6141982/52629f77feb8/40580_2017_112_Fig1_HTML.jpg

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