5 years ago

In Situ Electrochemical Activation of Atomic Layer Deposition Coated MoS2 Basal Planes for Efficient Hydrogen Evolution Reaction

In Situ Electrochemical Activation of Atomic Layer Deposition Coated MoS2 Basal Planes for Efficient Hydrogen Evolution Reaction
Hyung Ju Kim, Tae-Wan Kim, Noejung Park, Thomas F. Kuech, Ho-Jeong Chae, David H. K. Jackson, Youngmin Kim, Hyunju Chang, Soon-Yong Jeong, Daewon Lee, Hyun Woo Kim, Min Choi
Molybdenum disulfide (MoS2), which is composed of active edge sites and a catalytically inert basal plane, is a promising catalyst to replace the state-of-the-art Pt for electrochemically catalyzing hydrogen evolution reaction (HER). Because the basal plane consists of the majority of the MoS2 bulk materials, activation of basal plane sites is an important challenge to further enhance HER performance. Here, an in situ electrochemical activation process of the MoS2 basal planes by using the atomic layer deposition (ALD) technique to improve the HER performance of commercial bulk MoS2 is first demonstrated. The ALD technique is used to form islands of titanium dioxide (TiO2) on the surface of the MoS2 basal plane. The coated TiO2 on the MoS2 surface (ALD(TiO2)-MoS2) is then leached out using an in situ electrochemical activation method, producing highly localized surface distortions on the MoS2 basal plane. The MoS2 catalysts with activated basal plane surfaces (ALD(Act.)-MoS2) have dramatically enhanced HER kinetics, resulting from more favorable hydrogen-binding. The catalytically inert basal plane of MoS2 is activated for the hydrogen evolution reaction (HER) by combining the atomic layer deposition (ALD) technique and an in situ electrochemical activation process. The basal plane activated MoS2 (ALD(Act.)-MoS2) catalysts significantly improve the HER performance, resulting from more favorable hydrogen-binding.

Publisher URL: http://onlinelibrary.wiley.com/resolve/doi

DOI: 10.1002/adfm.201701825

You might also like
Discover & Discuss Important Research

Keeping up-to-date with research can feel impossible, with papers being published faster than you'll ever be able to read them. That's where Researcher comes in: we're simplifying discovery and making important discussions happen. With over 19,000 sources, including peer-reviewed journals, preprints, blogs, universities, podcasts and Live events across 10 research areas, you'll never miss what's important to you. It's like social media, but better. Oh, and we should mention - it's free.

  • Download from Google Play
  • Download from App Store
  • Download from AppInChina

Researcher displays publicly available abstracts and doesn’t host any full article content. If the content is open access, we will direct clicks from the abstracts to the publisher website and display the PDF copy on our platform. Clicks to view the full text will be directed to the publisher website, where only users with subscriptions or access through their institution are able to view the full article.