Xiaolin Ma, Ke Han, Hong-Xing Li, Lulu Song, Yuan Lin, Liangxu Lin, Yang Liu, Yi Zhao, Zhen Yang, Wei Huang
{"title":"逐步实现 MXene 和 MOF 转化辅助超薄双碳保护 V2O3 纳米片,实现超快持久的锌离子存储","authors":"Xiaolin Ma, Ke Han, Hong-Xing Li, Lulu Song, Yuan Lin, Liangxu Lin, Yang Liu, Yi Zhao, Zhen Yang, Wei Huang","doi":"10.1039/d4ee04387a","DOIUrl":null,"url":null,"abstract":"Vanadium oxides with high theoretical capacity are attractive cathodes for aqueous zinc-ion batteries (AZIBs), while their practical usage is still obstructed by the vanadium dissolution, structure deterioration, and sluggish reaction kinetics during cycles. Herein, ultrathin dual-carbon protected V<small><sub>2</sub></small>O<small><sub>3</sub></small> nanosheets are developed to tackle these issues through stepwise MXene and MOF conversion. As-designed C@V<small><sub>2</sub></small>O<small><sub>3</sub></small>@C nanosheets exhibit structure merits of large surface area, porous structure, small size, high V<small><sub>2</sub></small>O<small><sub>3</sub></small> content, and ultrathin inner/outer dual-carbon matrix. For Zn-ion storage, these structure superiorities enable C@V<small><sub>2</sub></small>O<small><sub>3</sub></small>@C cathode good capacity retention of ~100% at 1 A/g and excellent cycling performance over 3000 cycles. Remarkably, it manifests an exceptional rate capability of 402 mA h/g at 50 A/g, outperforming most reported cathode materials for AZIBs. Combined in/ex-situ experiments and theoretical calculation further illuminate the reaction mechanism of V<small><sub>2</sub></small>O<small><sub>3</sub></small> with initial activation process and subsequent reversible H<small><sup>+</sup></small>/Zn<small><sup>2+</sup></small> co-insertion/extraction reactions, along with the effect of carbon matrix on the superior performance by suppressing the V-dissolution, enhancing the structural stability, improving the pseudocapacitive behavior, and boosting the electron/ion transportation ability of vanadium oxide cathode. As a proof of concept, as-assembled flexible ZIBs with excellent battery performance can be integrated into a self-powered sensor system for human motion monitoring, highlighting the potential application of C@V<small><sub>2</sub></small>O<small><sub>3</sub></small>@C cathode for wearable electronics.","PeriodicalId":72,"journal":{"name":"Energy & Environmental Science","volume":"12 1","pages":""},"PeriodicalIF":32.4000,"publicationDate":"2024-11-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Stepwise MXene and MOF Conversion Assisted Ultrathin Dual-Carbon Protected V2O3 Nanosheets for Ultrafast and Durable Zn-Ion Storage\",\"authors\":\"Xiaolin Ma, Ke Han, Hong-Xing Li, Lulu Song, Yuan Lin, Liangxu Lin, Yang Liu, Yi Zhao, Zhen Yang, Wei Huang\",\"doi\":\"10.1039/d4ee04387a\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Vanadium oxides with high theoretical capacity are attractive cathodes for aqueous zinc-ion batteries (AZIBs), while their practical usage is still obstructed by the vanadium dissolution, structure deterioration, and sluggish reaction kinetics during cycles. Herein, ultrathin dual-carbon protected V<small><sub>2</sub></small>O<small><sub>3</sub></small> nanosheets are developed to tackle these issues through stepwise MXene and MOF conversion. As-designed C@V<small><sub>2</sub></small>O<small><sub>3</sub></small>@C nanosheets exhibit structure merits of large surface area, porous structure, small size, high V<small><sub>2</sub></small>O<small><sub>3</sub></small> content, and ultrathin inner/outer dual-carbon matrix. For Zn-ion storage, these structure superiorities enable C@V<small><sub>2</sub></small>O<small><sub>3</sub></small>@C cathode good capacity retention of ~100% at 1 A/g and excellent cycling performance over 3000 cycles. Remarkably, it manifests an exceptional rate capability of 402 mA h/g at 50 A/g, outperforming most reported cathode materials for AZIBs. Combined in/ex-situ experiments and theoretical calculation further illuminate the reaction mechanism of V<small><sub>2</sub></small>O<small><sub>3</sub></small> with initial activation process and subsequent reversible H<small><sup>+</sup></small>/Zn<small><sup>2+</sup></small> co-insertion/extraction reactions, along with the effect of carbon matrix on the superior performance by suppressing the V-dissolution, enhancing the structural stability, improving the pseudocapacitive behavior, and boosting the electron/ion transportation ability of vanadium oxide cathode. 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Stepwise MXene and MOF Conversion Assisted Ultrathin Dual-Carbon Protected V2O3 Nanosheets for Ultrafast and Durable Zn-Ion Storage
Vanadium oxides with high theoretical capacity are attractive cathodes for aqueous zinc-ion batteries (AZIBs), while their practical usage is still obstructed by the vanadium dissolution, structure deterioration, and sluggish reaction kinetics during cycles. Herein, ultrathin dual-carbon protected V2O3 nanosheets are developed to tackle these issues through stepwise MXene and MOF conversion. As-designed C@V2O3@C nanosheets exhibit structure merits of large surface area, porous structure, small size, high V2O3 content, and ultrathin inner/outer dual-carbon matrix. For Zn-ion storage, these structure superiorities enable C@V2O3@C cathode good capacity retention of ~100% at 1 A/g and excellent cycling performance over 3000 cycles. Remarkably, it manifests an exceptional rate capability of 402 mA h/g at 50 A/g, outperforming most reported cathode materials for AZIBs. Combined in/ex-situ experiments and theoretical calculation further illuminate the reaction mechanism of V2O3 with initial activation process and subsequent reversible H+/Zn2+ co-insertion/extraction reactions, along with the effect of carbon matrix on the superior performance by suppressing the V-dissolution, enhancing the structural stability, improving the pseudocapacitive behavior, and boosting the electron/ion transportation ability of vanadium oxide cathode. As a proof of concept, as-assembled flexible ZIBs with excellent battery performance can be integrated into a self-powered sensor system for human motion monitoring, highlighting the potential application of C@V2O3@C cathode for wearable electronics.
期刊介绍:
Energy & Environmental Science, a peer-reviewed scientific journal, publishes original research and review articles covering interdisciplinary topics in the (bio)chemical and (bio)physical sciences, as well as chemical engineering disciplines. Published monthly by the Royal Society of Chemistry (RSC), a not-for-profit publisher, Energy & Environmental Science is recognized as a leading journal. It boasts an impressive impact factor of 8.500 as of 2009, ranking 8th among 140 journals in the category "Chemistry, Multidisciplinary," second among 71 journals in "Energy & Fuels," second among 128 journals in "Engineering, Chemical," and first among 181 scientific journals in "Environmental Sciences."
Energy & Environmental Science publishes various types of articles, including Research Papers (original scientific work), Review Articles, Perspectives, and Minireviews (feature review-type articles of broad interest), Communications (original scientific work of an urgent nature), Opinions (personal, often speculative viewpoints or hypotheses on current topics), and Analysis Articles (in-depth examination of energy-related issues).