4.8 Article

Modulation of morphology and electronic structure on MoS2-based electrocatalysts for water splitting

期刊

NANO RESEARCH
卷 15, 期 8, 页码 6862-6887

出版社

TSINGHUA UNIV PRESS
DOI: 10.1007/s12274-022-4297-3

关键词

MoS2; morphology; electronic structure; electrocatalysis; water splitting

资金

  1. National Natural Science Foundation of China [21902157]
  2. Starting fund for scientific research of high-level talents, Anhui Agricultural University [rc382108]
  3. Open Fund of The State Key Laboratory of Catalysis in DICP, CAS [N-21-12]
  4. Open Fund of The State Key Laboratory of Molecular Reaction Dynamics in DICP, CAS [SKLMRD-K202223]

向作者/读者索取更多资源

This review discusses the important fabrication approaches of MoS2 ultrathin nanosheet to improve its intrinsic catalytic activity. Several modification strategies involve either morphology modulation or electron structural modulation to enhance charge transfer kinetics. The key challenges and future directions of developing high-performance MoS2-based electrocatalysts for overall water splitting are also discussed.
Electrocatalytic water splitting into hydrogen is one of the most favorable approaches to produce renewable energy. MoS2 has received great research attention for both hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) due to its unique structure and ability to be chemically modified, enabling its electrocatalytic activity to be further enhanced or made comparable to that of Pt-based materials. In this review, we discuss the important fabrication approaches of MoS2 ultrathin nanosheet (MoS2 NS) to improve the intrinsic catalytic activity of bulk MoS2. Moreover, several modification strategies involve either morphology modulation or electron structural modulation to improve the charge transfer kinetics, including doping, vacancy, and heterojunction construction or single-atom anchor. Our perspectives on the key challenges and future directions of developing high-performance MoS2-based electrocatalysts for overall water splitting are also discussed.

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