光电阴极
上部结构
材料科学
储能
碳纤维
钒
带隙
光电子学
纳米技术
冶金
复合材料
复合数
地质学
电子
功率(物理)
物理
海洋学
量子力学
作者
Yingying Zhao,Tianqi He,Jinhang Li,Chunling Zhu,Yujie Tan,Kai Zhu,Shulei Chou,Yujin Chen
出处
期刊:Angewandte Chemie
[Wiley]
日期:2024-06-26
卷期号:63 (38): e202408218-e202408218
被引量:30
标识
DOI:10.1002/anie.202408218
摘要
Photorechargeable zinc ion batteries (PZIBs), which can directly harvest and store solar energy, are promising technologies for the development of a renewable energy society. However, the incompatibility requirement between narrow band gap and wide coverage has raised severe challenges for high-efficiency dual-functional photocathodes. Herein, half-metallic vanadium (III) oxide (V2O3) was first reported as a dual-functional photocathode for PZIBs. Theoretical and experimental results revealed its unique photoelectrical and zinc ion storage properties for capturing and storing solar energy. To this end, a synergistic protective etching strategy was developed to construct carbon superstructure-supported V2O3 nanospheres (V2O3@CSs). The half-metallic characteristics of V2O3, combined with the three-dimensional superstructure assembled by ultrathin carbon nanosheets, established rapid charge transfer networks and robust framework for efficient and stable solar-energy storage. Consequently, the V2O3@CSs photocathode delivered record zinc ion storage properties, including a photo-assisted discharge capacities of 463 mA ⋅ h ⋅ g-1 at 2.0 A ⋅ g-1 and long-term cycling stability over 3000 cycles. Notably, the PZIBs assembled using V2O3@CSs photocathodes could be photorecharged without an external circuit, exhibiting a high photo conversion efficiency (0.354 %) and photorecharge voltage (1.0 V). This study offered a promising direction for the direct capture and storage of solar energy.
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