4.8 Article

Ultrafine nano 1T-MoS2 monolayers with NiOx as dual co-catalysts over TiO2 photoharvester for efficient photocatalytic hydrogen evolution

Journal

APPLIED CATALYSIS B-ENVIRONMENTAL
Volume 279, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.apcatb.2020.119387

Keywords

Molybdenum disulfide; Hydrogen evolution reaction; Dual co-catalysts; Photocatalytic

Funding

  1. Basic Science Center Program for Ordered Energy Conversion of the National Natural Science Foundation of China [51888103]
  2. Fundamental Research Funds for the Central Universities [NE2019103]
  3. World Premier International Research Center Initiative (WPI Initiative) on Materials Nano-architectonics (MANA)
  4. Photoexcitonix Project in Hokkaido University

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Molybdenum disulfide (MoS2) of 1 T phase was found to potentially replace N as efficient co-catalyst for the hydrogen evolution reaction (HER). Herein, an ultrafine nano 1 T-MoS2 monolayer of around 10 nm was successfully synthesized and showed a high electrocatalytic HER activity with low overpotential of 78 mV at 10 mA cm(-2). When the 1 T-MoS2 is loaded onto P25 TiO2, its ultrafine size dramatically promotes the superior interface bonding with TiO2 and a high photocatalytic HER activity of 300.3 mu mol h(-1) is obtained. Furthermore, a strategy by introducing NiOx co-catalyst into the 1 T-MoS 2 /P25 to fabricate a dual co-catalyst composite 1 T-MoS2/P25/NiOx significantly improves the photocatalytic HER activity to 1629.1 mu mol h(-4) which is very close to Pt/P25 of 2196.8 mu mol h(-1). The close interface-bonding between the nanosized 1 T-MoS2 monolayer and P25 along with the assistance of NiOx results in the superior photocatalytic HER activity by the enhanced separation and transfer of the photogenerated electrons and holes.

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