Статья

Potassium‐Based Dual‐Ion Batteries Operating at −60 °C Enabled By Co‐Intercalation Anode Chemistry

Lan‐Fang QueEngineering Research Center of Environment‐Friendly Functional Materials Ministry of Education Institute of Materials Physical Chemistry Huaqiao University Xiamen 361021 ChinaJihuai WuEngineering Research Center of Environment‐Friendly Functional Materials Ministry of Education Institute of Materials Physical Chemistry Huaqiao University Xiamen 361021 ChinaZhang LanEngineering Research Center of Environment‐Friendly Functional Materials Ministry of Education Institute of Materials Physical Chemistry Huaqiao University Xiamen 361021 ChinaYiming XieEngineering Research Center of Environment‐Friendly Functional Materials Ministry of Education Institute of Materials Physical Chemistry Huaqiao University Xiamen 361021 ChinaFu‐Da YuEngineering Research Center of Environment‐Friendly Functional Materials Ministry of Education Institute of Materials Physical Chemistry Huaqiao University Xiamen 361021 ChinaZhen‐Bo WangCollege of Materials Science and Engineering Shenzhen University Shenzhen Guangdong 518071 ChinaJiashen MengSchool of Materials Science and Engineering Wuhan University of Technology Wuhan 430070 ChinaXingcai ZhangSchool of Engineering and Applied Sciences Harvard University Cambridge MA 02138 USA

2023en

ABI

Аннотация

Abstract Battery performance at subzero is restricted by sluggish interfacial kinetics. To resolve this issue, potassium‐based dual‐ion batteries (K‐DIBs) based on the polytriphenylamine (PTPAn) cathode with anion storage chemistry and the hydrogen titanate (HTO) anode with K + /solvent co‐intercalation mechanism are constructed. Both the PTPAn cathode and the HTO anode do not undergo the desolvation process, which can effectively accelerate the interfacial kinetics at subzero. As revealed by theoretical calculations and experimental analysis, the strong K + /solvent binding energy in the dilute electrolyte, the charge shielding effect of the crystal water, and the uniform SEI layer with high content of the flexible organic species synergically promote HTO to undergo K + /solvent co‐intercalation behavior. The special co‐intercalation mechanism and anion storage chemistry enable HTO||PTPAn K‐DIBs with superior rate performance and cycle durability, maintaining a capacity retention of 94.1% after 6000 cycles at −40 °C and 91% after 1000 cycles at −60 °C. These results provide a step forward for achieving high‐performance energy storage devices at low temperatures.

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Идентификаторы

DOI: 10.1002/adma.202307592

Цитирования и источники

Цитирований: 3Использованных источников: 0

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