Controllable synthesis of large-scale SnSe2 nanosheet arrays and Te/SnSe2 vertical mixed-dimensional heterostructures for hydrogen evolution reaction

H Huafeng Wang Y Yulong Hao (School of Physics and Optoelectronics and Hunan Key Laboratory for Micro-Nano Energy Materials and Devices, Xiangtan University 1 , Xiangtan 411105,) T Ting Shu (University of Rochester, Rochester, New York, United States) X Xuemei Lu J Jie Zhou A Aolin Peng (School of Physics and Optoelectronics and Hunan Institute of Advanced Sensing and Information Technology, Xiangtan University 1 , Xiangtan 411105,) J Jin Li G Guolin Hao (School of Physics and Optoelectronics and Hunan Key Laboratory for Micro-Nano Energy Materials and Devices, Xiangtan University 1 , Xiangtan 411105,)

Abstract

As a characteristic two-dimensional (2D) layered material, SnSe2 exhibits promising applications in optoelectronic devices and energy catalysis due to its distinct physical and chemical properties. However, the controllable synthesis of large-scale SnSe2 nanostructures remains a significant challenge. In this study, we present an innovative growth strategy utilizing an FTO substrate as an in situ Sn source, enabling controlled synthesis of large-area (4 cm × 4 cm) SnSe2 nanosheet arrays. One-dimensional (1D) Te/two-dimensional (2D) SnSe2 vertical mixed-dimensional heterostructures were further fabricated. The Te/SnSe2 vertical heterostructures demonstrate significantly enhanced hydrogen evolution reaction performance compared to individual Te and SnSe2 nanostructures, achieving an overpotential of 0.73 V at 10 mA/cm2 and a Tafel slope of 110.05 mV/dec in a 1 M KOH electrolyte. The first-principles calculation results reveal that interfacial charge redistribution at the heterojunction substantially lowers the water dissociation energy barrier while optimizing hydrogen adsorption free energy. This growth strategy establishes a viable pathway for fabricating large-area 1D/2D vertical heterojunctions, and the combined experimental and theoretical findings advance our fundamental understanding of their hydrogen evolution reaction mechanisms.

Article Details

Volume / Issue Vol. 127, Issue 11
Published September 15, 2025
ISSN 0003-6951
Publisher American Institute of Physics

Journal Info

Applied Physics Letters

American Institute of Physics

ISSN: 0003-6951 Physical Sciences

Authors (8)

H

Huafeng Wang

Y

Yulong Hao

School of Physics and Optoelectronics and Hunan Key Laboratory for Micro-Nano Energy Materials and Devices, Xiangtan University 1 , Xiangtan 411105,

T

Ting Shu

University of Rochester, Rochester, New York, United States

X

Xuemei Lu

J

Jie Zhou

A

Aolin Peng

School of Physics and Optoelectronics and Hunan Institute of Advanced Sensing and Information Technology, Xiangtan University 1 , Xiangtan 411105,

J

Jin Li

G

Guolin Hao

School of Physics and Optoelectronics and Hunan Key Laboratory for Micro-Nano Energy Materials and Devices, Xiangtan University 1 , Xiangtan 411105,