Layered 2D transition metal (W, Mo, and Pt) chalcogenides for hydrogen evolution reaction

Research output: Chapter in Book/Report/Conference proceedingChapter

1 Citation (Scopus)

Abstract

Hydrogen production from water via electrolysis is widely investigated these days with several electrocatalysts in order to make it economically viable. From precious noble metals to highly abundant Fe, each element has its own energy of interaction with the intermediates involved in total water electrosplitting and behaves according to the environment in which it is put to. Of all the materials that have been reported till now, the unique layered 2D transition metal chalcogenides (2D TMDs) have attracted humongous attention because of their excellent electrocatalytic activity toward the cathodic half-cell reaction of water electrolysis, the hydrogen evolution reaction. Particularly, the sulfides and selenides of W, Mo, and Pt are often reported with several structural and electronic inflections for ameliorating the HER activity in all pH. In this chapter, the evolution of this class of materials, their properties, synthetic strategies, and methods of evaluation are discussed with specific examples. In addition, the key intellectual advancements made in this area are highlighted discretely as found appropriate.

Original languageEnglish
Title of host publicationSulfide and Selenide Based Materials for Emerging Applications
Subtitle of host publicationSustainable Energy Harvesting and Storage Technology
PublisherElsevier
Pages495-525
Number of pages31
ISBN (Electronic)9780323998604
ISBN (Print)9780323998826
DOIs
Publication statusPublished - 2022 Jan 1

Keywords

  • 2D metal chalcogenide
  • Electrocatalysis
  • H generation
  • Hydrogen evolution reaction
  • Water splitting

ASJC Scopus subject areas

  • Engineering(all)
  • Materials Science(all)

Fingerprint

Dive into the research topics of 'Layered 2D transition metal (W, Mo, and Pt) chalcogenides for hydrogen evolution reaction'. Together they form a unique fingerprint.

Cite this