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用于高度可逆锌基多碘化物氧化还原液流电池的淀粉介导胶体化学

Starch-mediated colloidal chemistry for highly reversible zinc-based polyiodide redox flow batteries.

作者信息

Wei Zhiquan, Huang Zhaodong, Liang Guojin, Wang Yiqiao, Wang Shixun, Yang Yihan, Hu Tao, Zhi Chunyi

机构信息

Department of Materials Science and Engineering, City University of Hong Kong, Hong Kong, China.

Hong Kong Center for Cerebro-Cardiovascular Health Engineering (COCHE), Hong Kong, China.

出版信息

Nat Commun. 2024 May 7;15(1):3841. doi: 10.1038/s41467-024-48263-8.

Abstract

Aqueous Zn-I flow batteries utilizing low-cost porous membranes are promising candidates for high-power-density large-scale energy storage. However, capacity loss and low Coulombic efficiency resulting from polyiodide cross-over hinder the grid-level battery performance. Here, we develop colloidal chemistry for iodine-starch catholytes, endowing enlarged-sized active materials by strong chemisorption-induced colloidal aggregation. The size-sieving effect effectively suppresses polyiodide cross-over, enabling the utilization of porous membranes with high ionic conductivity. The developed flow battery achieves a high-power density of 42 mW cm at 37.5 mA cm with a Coulombic efficiency of over 98% and prolonged cycling for 200 cycles at 32.4 Ah L (50% state of charge), even at 50 °C. Furthermore, the scaled-up flow battery module integrating with photovoltaic packs demonstrates practical renewable energy storage capabilities. Cost analysis reveals a 14.3 times reduction in the installed cost due to the applicability of cheap porous membranes, indicating its potential competitiveness for grid energy storage.

摘要

使用低成本多孔膜的水系锌碘液流电池是高功率密度大规模储能的有前景的候选者。然而,多碘化物穿越导致的容量损失和低库仑效率阻碍了电网级电池性能。在此,我们开发了用于碘淀粉阴极电解液的胶体化学,通过强化学吸附诱导的胶体聚集赋予更大尺寸的活性材料。尺寸筛分效应有效抑制了多碘化物穿越,使得能够使用具有高离子电导率的多孔膜。所开发的液流电池在37.5 mA cm时实现了42 mW cm的高功率密度,库仑效率超过98%,并且即使在50°C下,在32.4 Ah L(50%充电状态)下也能延长循环200次。此外,与光伏组件集成的放大液流电池模块展示了实际的可再生能源存储能力。成本分析表明,由于廉价多孔膜的适用性,安装成本降低了14.3倍,表明其在电网储能方面具有潜在的竞争力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/994b/11076626/677dfb60db2c/41467_2024_48263_Fig1_HTML.jpg

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