Qicheng Zhang, Jing Zhang, Xinyang Yue, Xiaoya He, Min Wang, Lei Xu, Wei Gao, Mingming Fang*, Juntao Ren* and Zheng Liang*,
{"title":"通过缺陷碳基质优化LiNO3转化,作为高耐用和快速充电锂金属电池的催化集流器","authors":"Qicheng Zhang, Jing Zhang, Xinyang Yue, Xiaoya He, Min Wang, Lei Xu, Wei Gao, Mingming Fang*, Juntao Ren* and Zheng Liang*, ","doi":"10.1021/acs.nanolett.4c0505810.1021/acs.nanolett.4c05058","DOIUrl":null,"url":null,"abstract":"<p >Lithium nitrate (LiNO<sub>3</sub>) stands as an effective electrolyte additive, mitigating the degradation of Li metal anodes by forming a Li<sub>3</sub>N-rich solid electrolyte interphase (SEI). However, its conversion kinetics are impeded by energy-consuming eight-electron transfer reactions. Herein, an isoreticular metal–organic framework-8-derived carbon is incorporated into the carbon cloth (RMCC) as a catalytic current collector to regulate the LiNO<sub>3</sub> conversion kinetics and boost Li<sub>3</sub>N generation inside the SEI. Our findings reveal that reducing LiNO to Li<sub>3</sub>N during LiNO<sub>3</sub> transformation occurs more favorably on the RMCC than on conventional substrates. The robust electrostatic attraction between LiNO and vacancy defects in the RMCC renders the chemical bonds of intermediate LiNO susceptible to cracking. Consequently, the RMCC-derived SEI exhibits effective Li dendrite restriction; the symmetric Li and LiFePO<sub>4</sub> full cells with prelithiated RMCC anodes demonstrate improved cycling stability without short-circuiting, outperforming their counterparts.</p>","PeriodicalId":53,"journal":{"name":"Nano Letters","volume":"25 4","pages":"1389–1396 1389–1396"},"PeriodicalIF":9.1000,"publicationDate":"2025-01-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Optimizing LiNO3 Conversion through a Defective Carbon Matrix as Catalytic Current Collectors for Highly Durable and Fast-Charging Li Metal Batteries\",\"authors\":\"Qicheng Zhang, Jing Zhang, Xinyang Yue, Xiaoya He, Min Wang, Lei Xu, Wei Gao, Mingming Fang*, Juntao Ren* and Zheng Liang*, \",\"doi\":\"10.1021/acs.nanolett.4c0505810.1021/acs.nanolett.4c05058\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >Lithium nitrate (LiNO<sub>3</sub>) stands as an effective electrolyte additive, mitigating the degradation of Li metal anodes by forming a Li<sub>3</sub>N-rich solid electrolyte interphase (SEI). However, its conversion kinetics are impeded by energy-consuming eight-electron transfer reactions. Herein, an isoreticular metal–organic framework-8-derived carbon is incorporated into the carbon cloth (RMCC) as a catalytic current collector to regulate the LiNO<sub>3</sub> conversion kinetics and boost Li<sub>3</sub>N generation inside the SEI. Our findings reveal that reducing LiNO to Li<sub>3</sub>N during LiNO<sub>3</sub> transformation occurs more favorably on the RMCC than on conventional substrates. The robust electrostatic attraction between LiNO and vacancy defects in the RMCC renders the chemical bonds of intermediate LiNO susceptible to cracking. Consequently, the RMCC-derived SEI exhibits effective Li dendrite restriction; the symmetric Li and LiFePO<sub>4</sub> full cells with prelithiated RMCC anodes demonstrate improved cycling stability without short-circuiting, outperforming their counterparts.</p>\",\"PeriodicalId\":53,\"journal\":{\"name\":\"Nano Letters\",\"volume\":\"25 4\",\"pages\":\"1389–1396 1389–1396\"},\"PeriodicalIF\":9.1000,\"publicationDate\":\"2025-01-21\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Nano Letters\",\"FirstCategoryId\":\"88\",\"ListUrlMain\":\"https://pubs.acs.org/doi/10.1021/acs.nanolett.4c05058\",\"RegionNum\":1,\"RegionCategory\":\"材料科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Nano Letters","FirstCategoryId":"88","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acs.nanolett.4c05058","RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
Optimizing LiNO3 Conversion through a Defective Carbon Matrix as Catalytic Current Collectors for Highly Durable and Fast-Charging Li Metal Batteries
Lithium nitrate (LiNO3) stands as an effective electrolyte additive, mitigating the degradation of Li metal anodes by forming a Li3N-rich solid electrolyte interphase (SEI). However, its conversion kinetics are impeded by energy-consuming eight-electron transfer reactions. Herein, an isoreticular metal–organic framework-8-derived carbon is incorporated into the carbon cloth (RMCC) as a catalytic current collector to regulate the LiNO3 conversion kinetics and boost Li3N generation inside the SEI. Our findings reveal that reducing LiNO to Li3N during LiNO3 transformation occurs more favorably on the RMCC than on conventional substrates. The robust electrostatic attraction between LiNO and vacancy defects in the RMCC renders the chemical bonds of intermediate LiNO susceptible to cracking. Consequently, the RMCC-derived SEI exhibits effective Li dendrite restriction; the symmetric Li and LiFePO4 full cells with prelithiated RMCC anodes demonstrate improved cycling stability without short-circuiting, outperforming their counterparts.
期刊介绍:
Nano Letters serves as a dynamic platform for promptly disseminating original results in fundamental, applied, and emerging research across all facets of nanoscience and nanotechnology. A pivotal criterion for inclusion within Nano Letters is the convergence of at least two different areas or disciplines, ensuring a rich interdisciplinary scope. The journal is dedicated to fostering exploration in diverse areas, including:
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