Prediction of High Photoconversion Efficiency and Photocatalytic Water Splitting in Vertically Stacked TMD Heterojunctions MX₂/WS₂ and MX₂/MoSe₂ (M = Cr, Mo, W; X= S, Se, Te)

Abstract

Based on two-dimensional (2D) transition metal dichalcogenides (TMDs) exhibiting strong light-matter interactions and spin-valley locking properties, we construct two types of MX2/WS2 and MX2/MoSe2 (M=Cr, Mo, W, and X=S, Se, Te) heterojunctions to investigate their electronic and optical properties based on first-principles calculations. The calculated results indicate that eight heterojunctions are semiconductors with staggered gaps, which are beneficial for prolonging the lifetime of excitons and promoting the efficient separation of photogenerated electrons and holes. The absorption coefficients of these heterojunctions reach the order of 105 cm-1 in the visible range, especially the MX2/MoSe2 heterojunctions. Among the considered heterojunctions, MoS2/WS2, MoSe2/WS2, WSe2/WS2, and WSe2/MoSe2 heterojunctions exhibit suitable band gaps and high carrier mobility, indicating promising potential for photocatalysis. Meanwhile, a promising water splitting photocatalyst WSe2/MoSe2 is predicted successfully by analyzing the corresponding photocatalytic water splitting properties. More importantly, the photoconversion efficiency (PCE) of the MoTe2/MoSe2 heterojunction is as high as 25.84%, which has a larger value compared to the PCE of the OsNCl/FeNCl heterojunction (23.45%) reported recently. These findings provide theoretical evidence and identify excellent candidate materials for the advancement of optoelectronics and photocatalysis.

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Article information

Article type
Paper
Submitted
01 Dec 2024
Accepted
20 Feb 2025
First published
22 Feb 2025

J. Mater. Chem. A, 2025, Accepted Manuscript

Prediction of High Photoconversion Efficiency and Photocatalytic Water Splitting in Vertically Stacked TMD Heterojunctions MX₂/WS₂ and MX₂/MoSe₂ (M = Cr, Mo, W; X= S, Se, Te)

J. Ma, X. Kuang, J. Pang, X. Wanying, A. Mao and J. Yang, J. Mater. Chem. A, 2025, Accepted Manuscript , DOI: 10.1039/D4TA08513B

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