J. Mater. Sci. Technol. ›› 2022, Vol. 124: 209-216.DOI: 10.1016/j.jmst.2021.12.071

• Research Article • Previous Articles     Next Articles

Photodeposition of CoOx and MoS2 on CdS as dual cocatalysts for photocatalytic H2 production

Tingmin Dia, Quanrong Denga, Geming Wanga, Shenggao Wanga,*(), Linxi Wangb,*(), Yuhua Mac,*()   

  1. aHubei Key Laboratory of Plasma Chemistry and Advanced Materials, School of Materials Science and Engineering, Wuhan Institute of Technology, Wuhan 430205, China
    bLaboratory of Solar Fuel, Faculty of Materials Science and Chemistry, China University of Geosciences, Wuhan 430074, China
    cCollege of Chemistry and Chemical Engineering, Xinjiang Normal University, Urumqi 830054, China
  • Received:2021-10-19 Revised:2021-12-17 Accepted:2021-12-23 Published:2022-10-10 Online:2022-03-21
  • Contact: Shenggao Wang,Linxi Wang,Yuhua Ma
  • About author:15199141253@163.com (Y. Ma).
    linxiwang91@126.com (L. Wang),
    E-mail addresses: wyysg@163.com (S. Wang),

Abstract:

Photocatalytic H2 production from water splitting has a promising prospect for alleviating energy and environmental issues. However, the fast recombination of photogenerated charge carriers limits the photocatalytic efficiency and its practical application. Cocatalyst engineering is an effective strategy to spatially separate photogenerated charge carriers. In this work, noble-metal-free MoS2 and CoOx cocatalysts are loaded on CdS nanorods by a two-step photodeposition method. The MoS2 functions as the reduction cocatalyst to trap electrons and CoOx as the oxidation cocatalyst to trap holes. Transmission electron microscopy (TEM), inductively coupled plasma (ICP), X-ray photoelectron spectroscopy (XPS) and Mott-Schottky results demonstrate the effectiveness of photodeposition for loading MoS2 and CoOx dual cocatalysts on CdS and their impact on the photochemical properties. The optimized CdS-MoS2-CoOx composite exhibits a high photocatalytic H2-production rate of 7.4 mmol g-1 h-1 and an apparent quantum efficiency (QE) of 7.6% at 420 nm. Further analysis on time-resolved photoluminescence (TRPL) indicates that the introduction of dual cocatalysts greatly prolongs the lifetime of photogenerated charge carriers and deceases the charge recombination rates, consequently leading to superior photocatalytic H2-production performance. This work provides a facile and effective strategy for the construction of highly efficient dual-cocatalyst-modified CdS photocatalyst for high-performance photocatalytic H2 production.

Key words: Photocatalytic H2 production, CdS, Dual cocatalysts, MoS2, CoOx, Photodeposition