5 years ago

2H → 1T Phase Change in Direct Synthesis of WS2 Nanosheets via Solution-Based Electrochemical Exfoliation and Their Catalytic Properties

2H → 1T Phase Change in Direct Synthesis of WS2 Nanosheets via Solution-Based Electrochemical Exfoliation and Their Catalytic Properties
Jan Luxa, Xinyi Chia, Carmen C. Mayorga-Martinez, Martin Pumera, Zdeněk Sofer, Shi Xuan Leong
Metallic 1T-WS2 has various interesting properties such as increased density of catalytically active sites on both the basal planes and edges as well as metallic conductivity which allows it to be used in applications such as biosensing and energy devices. Hence, it is highly beneficial to develop a simple, efficient, and low-cost synthesis method of 1T-WS2 nanosheets from commercially available bulk 2H-WS2. In this study, we reported WS2 nanosheets synthesized directly from bulk WS2 via solution-based electrochemical exfoliation with bipolar electrodes and investigated their electrocatalytic performances toward hydrogen evolution and oxygen reduction reactions. We successfully synthesized WS2 nanosheets of regular hexagonal symmetry with a 2H → 1T phase transition. This represents a novel method of producing 1T-WS2 nanosheets from bulk 2H-WS2 without compromising on its electrocatalytic properties.

Publisher URL: http://dx.doi.org/10.1021/acsami.7b06898

DOI: 10.1021/acsami.7b06898

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.