水溶液
溶解
石墨烯
溶剂化
阴极
动力学
电解质
氧化物
化学工程
电池(电)
分子
化学
蒽醌
材料科学
无机化学
纳米技术
电极
物理化学
有机化学
量子力学
物理
工程类
功率(物理)
作者
Jin Yang,Rong Tang,Yuanhong Kang,Qian Zhang,Guanhong Chen,Zeheng Lv,Zhipeng Wen,Cheng Chao Li,Yang Yang,Jinbao Zhao
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2024-08-27
卷期号:: 4598-4606
标识
DOI:10.1021/acsenergylett.4c01692
摘要
Aqueous zinc-organic batteries, featuring safe aqueous electrolytes and cost-effective materials, demonstrate broad application prospects. However, small-molecule organic cathodes encounter critical challenges, including poor electronic conductivity and severe dissolution issues. Herein, a small-molecule quinone guest (sodium anthraquinone-2-sulfonaterationate, SAS) is incorporated with a conductive host (reduced graphene oxide, rGO) through noncovalent bonding to obtain a free-standing SAS@rGO electrode. Theoretical calculations and experimental characterizations indicate host–guest interactions prevent the dissolution of active material and facilitate electron transport. Furthermore, various in/ex situ characterizations reveal that SAS@rGO remains stable during cycling, maintaining a high capacity retention of 90.4% after 300 cycles even at 0.5 C. Moreover, 1,4-butyrolactone is adopted as cosolvent to break the hydrogen bonding network, ensuring rapid ion transport kinetics at low temperatures. Combining the principles of host–guest and solvation chemistry synergistically, the Zn//SAS@rGO battery achieves exceptional cycling stability for over 3000 cycles at 1 A g–1 and −40 °C.
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