Issue 17, 2025

Controlled oxidation of V2O5/VO2 hollow nanospheres as photocathodes for photo-rechargeable zinc ion batteries with an ultrahigh capacity enhancement

Abstract

Photo-charging batteries are emerging as a new battery technology for large-scale energy storage systems. However, their specific capacity, cycling stability, and light efficiency have reached a bottleneck due to low light-absorption capability, sluggish separation and migration of photoinduced charge carriers, and severe photocorrosion. Herein, hollow nanospheres composed of divanadium pentaoxide/vanadium dioxide (V2O5/VO2) are constructed to broaden light harvesting and improve the redox activity of photo-rechargeable zinc ion batteries (ZIBs). Due to an in situ chemical reaction, V2O5 and VO2 are intimately connected to form a V2O5/VO2 heterojunction, thus facilitating the separation and migration of photoinduced charge carriers. As a result, this V2O5/VO2 heterojunction demonstrated a maximum surface photovoltage (SPV) of 25.73 mV, resulting in an ultrahigh specific capacity of 785.6 mA h g−1 at 200 mA g−1 through a light-discharging process. This delivers a high light enhancement of 77.8% with a power conversion efficiency (PCE) of 4.3%. In addition, ZIBs show promising stability under light irradiation, where a high retention of 53.1% can be achieved even at high current density of 1000 mA g−1 after 4000 cycles. This work has pushed forward ZIB technology into a green and sustainable path that can utilize solar energy to promote electrochemical energy storage.

Graphical abstract: Controlled oxidation of V2O5/VO2 hollow nanospheres as photocathodes for photo-rechargeable zinc ion batteries with an ultrahigh capacity enhancement

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Article information

Article type
Paper
Submitted
19 Jan 2025
Accepted
17 Mar 2025
First published
18 Mar 2025

J. Mater. Chem. A, 2025,13, 12216-12225

Controlled oxidation of V2O5/VO2 hollow nanospheres as photocathodes for photo-rechargeable zinc ion batteries with an ultrahigh capacity enhancement

H. Yang, S. Wu, A. M. Badalge, X. Li, Q. Wang, Y. L. Zhong and T. Zhu, J. Mater. Chem. A, 2025, 13, 12216 DOI: 10.1039/D5TA00517E

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