Binglin Zhang , Yu Jiang , Shiyao Deng , Xuemin Yan
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引用次数: 0
Abstract
VOPO4, as one of the most potential cathodes for AZIBs, suffered from the heavy decomposition and dissolution in aqueous electrolytes during cycling, thus sabotaging the merits of its cyclability and high working potential. Free water in internal Helmholtz layer seems to be one of the main causes to this problem. Thereby, this paper intends to regulate the structure of internal Helmholtz layer by introducing small organic molecule on VOPO4 (VPS), which might restrain the erosion of free water and change the storage mode of Zn2+. Specifically, hydrophobic groups from the small organic molecule effectively hinder the approach of H2O, while zincophilic groups from the small organic molecule enhance diffusion kinetics of Zn2+. Benefitting from this strategy, VPS exhibits a high discharge capacity of 145 mAh g−1 at 0.2 A g−1 and advanced cycling durability for over 1000 cycles at 1 A g−1. This study provides new insights into the modification direction for improving the development of VOPO4.
voo4作为AZIBs最有潜力的阴极之一,在循环过程中受到水溶液的严重分解和溶解,从而破坏了其可循环性和高工作电位的优点。内部亥姆霍兹层中的游离水似乎是造成这一问题的主要原因之一。因此,本文拟通过在VOPO4 (VPS)上引入有机小分子来调节内部亥姆霍兹层的结构,从而抑制自由水的侵蚀,改变Zn2+的储存方式。具体来说,来自有机小分子的疏水性基团有效地阻碍了H2O的接近,而来自有机小分子的亲锌基团则增强了Zn2+的扩散动力学。得益于这种策略,VPS在0.2 a g−1时具有145 mAh g−1的高放电容量,并且在1 a g−1时具有超过1000次循环的高级循环耐久性。本研究为改进VOPO4的发展提供了新的修饰方向。
期刊介绍:
Journal of energy storage focusses on all aspects of energy storage, in particular systems integration, electric grid integration, modelling and analysis, novel energy storage technologies, sizing and management strategies, business models for operation of storage systems and energy storage developments worldwide.