{"title":"“基因编辑”设计升级具有超高Li+电导率的共晶聚合物电解质。","authors":"Zhenghao Li, Hongyao Wang, Yun Zheng, Yanfei Zhu, Bingsen Qin, Zongtao Lu, Wei Yan, Jiujun Zhang","doi":"10.1002/anie.202508857","DOIUrl":null,"url":null,"abstract":"<p><p>Deep eutectic polymer electrolytes (DEPEs) have emerged as highly promising next-generation electrolytes, offering unparalleled electrochemical performance and safety. Their excellence stems from a synergistic blend of the robust mechanical stability of solid polymer electrolytes and the exceptional interfacial wettability and superior thermal resilience of deep eutectic electrolytes. However, conventional DEPEs frequently exhibit suboptimal Li<sup>+</sup> conductivity due to strong coordination between Li<sup>+</sup> and oxygen-containing polymer moieties. Inspired by the concept of 'gene-editing' in biology, we propose a novel deep eutectic polymer electrolyte (GEPE) with precisely tailored molecular architectures This approach exploits the steric hindrance and electron-withdrawing inductive effects from isophorone diisocyanate-derived segments to reduce Li<sup>+</sup>-polymer interactions, thereby enabling an extraordinary ionic conductivity of 3.00 mS cm⁻¹ at 25 °C and a Li<sup>+</sup> transference number of 0.61. Remarkably, GEPE exhibits extraordinary cycling stability in Li||Li symmetric cells for over 3000 h, demonstrating dendrite-free Li metal deposition during prolonged cycling. Moreover, the assembled lithium metal batteries demonstrate exceptional electrochemical performance when incorporating diverse cathodes, including LiNi<sub>0.5</sub>Co<sub>0.2</sub>Mn<sub>0.3</sub>O<sub>2</sub>, LiNi<sub>0.8</sub>Co<sub>0.1</sub>Mn<sub>0.1</sub>O<sub>2</sub>, and LiFePO<sub>4</sub>. Notably, the Li|GEPE|LiFePO<sub>4</sub> cells achieve an impressive nearly 100% Coulombic efficiency and remarkable long-term stability over 10 000 cycles at 5C.</p>","PeriodicalId":520556,"journal":{"name":"Angewandte Chemie (International ed. in English)","volume":" ","pages":"e202508857"},"PeriodicalIF":0.0000,"publicationDate":"2025-06-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"\\\"Gene-Editing\\\" Design Upgrades Eutectic-Polymer Electrolytes with Ultra-High Li<sup>+</sup> Conductivity.\",\"authors\":\"Zhenghao Li, Hongyao Wang, Yun Zheng, Yanfei Zhu, Bingsen Qin, Zongtao Lu, Wei Yan, Jiujun Zhang\",\"doi\":\"10.1002/anie.202508857\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Deep eutectic polymer electrolytes (DEPEs) have emerged as highly promising next-generation electrolytes, offering unparalleled electrochemical performance and safety. Their excellence stems from a synergistic blend of the robust mechanical stability of solid polymer electrolytes and the exceptional interfacial wettability and superior thermal resilience of deep eutectic electrolytes. However, conventional DEPEs frequently exhibit suboptimal Li<sup>+</sup> conductivity due to strong coordination between Li<sup>+</sup> and oxygen-containing polymer moieties. Inspired by the concept of 'gene-editing' in biology, we propose a novel deep eutectic polymer electrolyte (GEPE) with precisely tailored molecular architectures This approach exploits the steric hindrance and electron-withdrawing inductive effects from isophorone diisocyanate-derived segments to reduce Li<sup>+</sup>-polymer interactions, thereby enabling an extraordinary ionic conductivity of 3.00 mS cm⁻¹ at 25 °C and a Li<sup>+</sup> transference number of 0.61. Remarkably, GEPE exhibits extraordinary cycling stability in Li||Li symmetric cells for over 3000 h, demonstrating dendrite-free Li metal deposition during prolonged cycling. Moreover, the assembled lithium metal batteries demonstrate exceptional electrochemical performance when incorporating diverse cathodes, including LiNi<sub>0.5</sub>Co<sub>0.2</sub>Mn<sub>0.3</sub>O<sub>2</sub>, LiNi<sub>0.8</sub>Co<sub>0.1</sub>Mn<sub>0.1</sub>O<sub>2</sub>, and LiFePO<sub>4</sub>. Notably, the Li|GEPE|LiFePO<sub>4</sub> cells achieve an impressive nearly 100% Coulombic efficiency and remarkable long-term stability over 10 000 cycles at 5C.</p>\",\"PeriodicalId\":520556,\"journal\":{\"name\":\"Angewandte Chemie (International ed. in English)\",\"volume\":\" \",\"pages\":\"e202508857\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2025-06-09\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Angewandte Chemie (International ed. in English)\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1002/anie.202508857\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Angewandte Chemie (International ed. in English)","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1002/anie.202508857","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
摘要
深共晶聚合物电解质(Deep共晶polymer electrolyte, DEPEs)具有无可比拟的电化学性能和安全性,是极具发展前景的新一代电解质。它们的卓越源于固体聚合物电解质强大的机械稳定性和深层共晶电解质优异的界面润湿性和优异的热弹性的协同混合。然而,由于Li+和含氧聚合物之间的强配位,传统的DEPEs经常表现出不理想的Li+导电性。受生物学中“基因编辑”概念的启发,我们提出了一种具有精确定制分子结构的新型深共晶聚合物电解质(GEPE)。该方法利用异草酮二异氰酸酯衍生片段的空间位阻和电子抽离感应效应来减少Li+与聚合物的相互作用,从而在25°C下实现了3.00 mS cm-1的非凡离子电导率和0.61的Li+转移数。值得注意的是,GEPE在Li||Li对称电池中表现出超过3000小时的循环稳定性,在长时间循环中表现出无枝晶的锂金属沉积。此外,当加入不同的阴极,包括LiNi0.5Co0.2Mn0.3O2, LiNi0.8Co0.1Mn0.1O2和LiFePO4时,组装的锂金属电池表现出优异的电化学性能。值得注意的是,Li|GEPE|LiFePO4电池实现了令人印象深刻的近100%的库仑效率和在5C下超过10000次循环的显着长期稳定性。
"Gene-Editing" Design Upgrades Eutectic-Polymer Electrolytes with Ultra-High Li+ Conductivity.
Deep eutectic polymer electrolytes (DEPEs) have emerged as highly promising next-generation electrolytes, offering unparalleled electrochemical performance and safety. Their excellence stems from a synergistic blend of the robust mechanical stability of solid polymer electrolytes and the exceptional interfacial wettability and superior thermal resilience of deep eutectic electrolytes. However, conventional DEPEs frequently exhibit suboptimal Li+ conductivity due to strong coordination between Li+ and oxygen-containing polymer moieties. Inspired by the concept of 'gene-editing' in biology, we propose a novel deep eutectic polymer electrolyte (GEPE) with precisely tailored molecular architectures This approach exploits the steric hindrance and electron-withdrawing inductive effects from isophorone diisocyanate-derived segments to reduce Li+-polymer interactions, thereby enabling an extraordinary ionic conductivity of 3.00 mS cm⁻¹ at 25 °C and a Li+ transference number of 0.61. Remarkably, GEPE exhibits extraordinary cycling stability in Li||Li symmetric cells for over 3000 h, demonstrating dendrite-free Li metal deposition during prolonged cycling. Moreover, the assembled lithium metal batteries demonstrate exceptional electrochemical performance when incorporating diverse cathodes, including LiNi0.5Co0.2Mn0.3O2, LiNi0.8Co0.1Mn0.1O2, and LiFePO4. Notably, the Li|GEPE|LiFePO4 cells achieve an impressive nearly 100% Coulombic efficiency and remarkable long-term stability over 10 000 cycles at 5C.