MoS2/WS2 Heterojunction for Photoelectrochemical Water Oxidation

• Published in: ACS catalysis 2017-08, Vol.7 (8), p.4990-4998
• Main Authors: Pesci, Federico M, Sokolikova, Maria S, Grotta, Chiara, Sherrell, Peter C, Reale, Francesco, Sharda, Kanudha, Ni, Na, Palczynski, Pawel, Mattevi, Cecilia
• Format: Article
• Language: English
• ISSN: 2155-5435; 2155-5435
• DOI: 10.1021/acscatal.7b01517

The solar-assisted oxidation of water is an essential half reaction for achieving a complete cycle of water splitting. The search of efficient photoanodes that can absorb light in the visible range is of paramount importance to enable cost-effective solar energy-conversion systems. Here, we demonstrate that atomically thin layers of MoS2 and WS2 can oxidize water to O2 under incident light. Thin films of solution-processed MoS2 and WS2 nanosheets display n-type positive photocurrent densities of 0.45 mA cm–2 and O2 evolution under simulated solar irradiation. WS2 is significantly more efficient than MoS2; however, bulk heterojunctions (B-HJs) of MoS2 and WS2 nanosheets results in a 10-fold increase in incident-photon-to-current-efficiency, compared to the individual constituents. This proves that charge carrier lifetime is tailorable in atomically thin crystals by creating heterojunctions of different compositions and architectures. Our results suggest that the MoS2 and WS2 nanosheets and their B-HJ blend are interesting photocatalytic systems for water oxidation, which can be coupled with different reduction processes for solar-fuel production.