Nanosecond Laser Synthesis of MXene‐Derived TiO <sub>2</sub> /High‐Entropy Alloys for Photo‐Assisted Zinc–Air Batteries

S Shuyu Cui (Department of Materials Science and Engineering and SUSTech Energy Institute for Carbon Neutrality Southern University of Science and Technology Shenzhen 518055 China) X Xiongwei Zhong Z Zhitong Li P Peide Zhu (Department of Materials Science and Engineering) J Junjie Hu (Key Laboratory of Biomacromolecules, Institute of Biophysics, Chinese Academy of Sciences) X Xiaolong Zhou (Department of Cellular and Genetic Medicine, School of Basic Medical Sciences, Fudan University) P Pinit Kidkhunthod (Synchrotron Light Research Institute (Public Organization), 111 University Avenue, Muang, Nakhon Ratchasima 30000, Thailand) X Xingzhu Wang (School of Physics and Optoelectronics) B Bingbao Mei B Baomin Xu (Department of Materials Science and Engineering)

Abstract

Abstract Photo‐assisted zinc–air batteries have garnered significant attention for applying solar energy to decrease the charge voltage and improve energy efficiency. However, the uniform and rapid synthesis of highly active, stable, and low‐cost photoelectrocatalysts for zinc–air batteries remains a significant challenge. Herein, a pulsed laser method is reported for the rapid preparation of MXene‐derived TiO 2 /high‐entropy alloy heterojunctions (M‐TiO 2 /HEAs) as photoelectrocatalysts. Benefiting from the exceptional photo‐thermal conversion capability of MXene, the local temperature reaches up to 2800 K under laser irradiation, along with ultra‐fast heating and cooling rates (≈10 6  K s −1 ), enabling the successful synthesis of M‐TiO 2 /HEAs. Zinc–air batteries incorporating M‐TiO 2 /HEAs exhibit a low charge voltage of 1.87 V at 10 mA cm −2 under light irradiation. In addition, it exhibits exceptional cycle stability, maintaining stable cycling for 1000 h at a current density of 10 mA cm −2 . Experiments and theoretical calculations reveal that M‐TiO 2 /HEAs heterojunctions exhibit strong electronic interactions. These interactions effectively promote the separation of photogenerated charge carriers and the conversion of electrochemical intermediates, thereby enhancing oxygen evolution reaction activity under light irradiation. This work offers valuable insights into the rapid fabrication of photoelectrocatalysts, providing new perspectives for developing light‐enhanced energy storage systems.

Article Details

Volume / Issue Vol. 37, Issue 35
Published September 01, 2025
ISSN 0935-9648
Publisher Unknown Publisher

Journal Info

Advanced Materials

Unknown Publisher

ISSN: 0935-9648 Physical Sciences

Authors (10)

S

Shuyu Cui

Department of Materials Science and Engineering and SUSTech Energy Institute for Carbon Neutrality Southern University of Science and Technology Shenzhen 518055 China

X

Xiongwei Zhong

Z

Zhitong Li

P

Peide Zhu

Department of Materials Science and Engineering

J

Junjie Hu

Key Laboratory of Biomacromolecules, Institute of Biophysics, Chinese Academy of Sciences

X

Xiaolong Zhou

Department of Cellular and Genetic Medicine, School of Basic Medical Sciences, Fudan University

P

Pinit Kidkhunthod

Synchrotron Light Research Institute (Public Organization), 111 University Avenue, Muang, Nakhon Ratchasima 30000, Thailand

X

Xingzhu Wang

School of Physics and Optoelectronics

B

Bingbao Mei

B

Baomin Xu

Department of Materials Science and Engineering