{"title":"用于锂硫电池的生物衍生高极性分层多孔电极","authors":"Jinsheng He, Fumiao Liu, Xiaoxin Dou, Yuqing Cai, Yajuan Zhou, Qian Wu, Zehuan Chen, Langyu Lin, Keda Lin, Zhen Peng and Yuanzheng Luo*, ","doi":"10.1021/acs.energyfuels.5c0072910.1021/acs.energyfuels.5c00729","DOIUrl":null,"url":null,"abstract":"<p >Lithium–sulfur (Li–S) batteries hold great promise as future energy storage solutions owing to their low cost and environmental friendliness. Nature provides biomass materials that can serve as carriers for sulfur, featuring micropores, mesopores, and hierarchical pore structures. In this study, we utilized corncob-originated activated porous carbon (CPC), abundant agricultural wastes (AWs), as the sulfur host to prepare MXene (Ti<sub>3</sub>C<sub>2</sub>T<sub><i>x</i></sub>) enhanced hierarchical bioderived porous electrode. The synthesis and function of CPC for Li–S batteries are presented, and the electrochemical effects of structural diversity, porosity and surface heteroatom doping of the Mxene in Li–S batteries are discussed. Brunauer–Emmett–Teller (BET) analysis revealed that CPC exhibited a specific surface area (SSA) of 1015.59 m<sup>2</sup> g<sup>–1</sup> and a total pore volume of 0.44 cm<sup>3</sup> g<sup>–1</sup>, significantly higher than those of P-CPC (35.30 m<sup>2</sup> g<sup>–1</sup> and 0.022 cm<sup>3</sup> g<sup>–1</sup>). Furthermore, the CPC/MXene@S composite electrode demonstrated an impressive initial discharge capacity of 1358 mAh g<sup>–1</sup> at 0.1C and retained a reversible capacity of 695 mAh g<sup>–1</sup> after 500 cycles at 0.2C, with a capacity decay rate of only 0.05% per cycle. Additionally, it showed excellent rate performance, delivering a capacity of 776 mAh g<sup>–1</sup> even at a high current density of 2C. The superior electrochemical performance of this composite electrode can be attributed to MXene’s effective adsorption of polysulfides. This study provides a new methodology for utilizing waste biomass as a carrier for sulfur electrodes. In addition, the economic benefits, new trends and challenges are also proposed for further design excellent AWs for Li–S batteries.</p>","PeriodicalId":35,"journal":{"name":"Energy & Fuels","volume":"39 16","pages":"7901–7913 7901–7913"},"PeriodicalIF":5.3000,"publicationDate":"2025-04-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Bioderived Hierarchically Porous Electrode with High Polarity for Lithium–Sulfur Batterties\",\"authors\":\"Jinsheng He, Fumiao Liu, Xiaoxin Dou, Yuqing Cai, Yajuan Zhou, Qian Wu, Zehuan Chen, Langyu Lin, Keda Lin, Zhen Peng and Yuanzheng Luo*, \",\"doi\":\"10.1021/acs.energyfuels.5c0072910.1021/acs.energyfuels.5c00729\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >Lithium–sulfur (Li–S) batteries hold great promise as future energy storage solutions owing to their low cost and environmental friendliness. Nature provides biomass materials that can serve as carriers for sulfur, featuring micropores, mesopores, and hierarchical pore structures. In this study, we utilized corncob-originated activated porous carbon (CPC), abundant agricultural wastes (AWs), as the sulfur host to prepare MXene (Ti<sub>3</sub>C<sub>2</sub>T<sub><i>x</i></sub>) enhanced hierarchical bioderived porous electrode. The synthesis and function of CPC for Li–S batteries are presented, and the electrochemical effects of structural diversity, porosity and surface heteroatom doping of the Mxene in Li–S batteries are discussed. Brunauer–Emmett–Teller (BET) analysis revealed that CPC exhibited a specific surface area (SSA) of 1015.59 m<sup>2</sup> g<sup>–1</sup> and a total pore volume of 0.44 cm<sup>3</sup> g<sup>–1</sup>, significantly higher than those of P-CPC (35.30 m<sup>2</sup> g<sup>–1</sup> and 0.022 cm<sup>3</sup> g<sup>–1</sup>). Furthermore, the CPC/MXene@S composite electrode demonstrated an impressive initial discharge capacity of 1358 mAh g<sup>–1</sup> at 0.1C and retained a reversible capacity of 695 mAh g<sup>–1</sup> after 500 cycles at 0.2C, with a capacity decay rate of only 0.05% per cycle. Additionally, it showed excellent rate performance, delivering a capacity of 776 mAh g<sup>–1</sup> even at a high current density of 2C. The superior electrochemical performance of this composite electrode can be attributed to MXene’s effective adsorption of polysulfides. This study provides a new methodology for utilizing waste biomass as a carrier for sulfur electrodes. In addition, the economic benefits, new trends and challenges are also proposed for further design excellent AWs for Li–S batteries.</p>\",\"PeriodicalId\":35,\"journal\":{\"name\":\"Energy & Fuels\",\"volume\":\"39 16\",\"pages\":\"7901–7913 7901–7913\"},\"PeriodicalIF\":5.3000,\"publicationDate\":\"2025-04-09\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Energy & Fuels\",\"FirstCategoryId\":\"5\",\"ListUrlMain\":\"https://pubs.acs.org/doi/10.1021/acs.energyfuels.5c00729\",\"RegionNum\":3,\"RegionCategory\":\"工程技术\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"ENERGY & FUELS\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Energy & Fuels","FirstCategoryId":"5","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acs.energyfuels.5c00729","RegionNum":3,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"ENERGY & FUELS","Score":null,"Total":0}
引用次数: 0
摘要
锂硫(li -硫)电池由于其低成本和环境友好性,在未来的能源存储解决方案中具有很大的前景。自然界提供了可以作为硫载体的生物质材料,具有微孔、中孔和分层孔结构。本研究以玉米芯源活性炭(CPC)和丰富的农业废弃物(AWs)为硫载体,制备了MXene (Ti3C2Tx)增强层次化生物衍生多孔电极。介绍了锂硫电池用CPC的合成及其功能,讨论了结构多样性、孔隙率和表面杂原子掺杂对锂硫电池电化学性能的影响。brunauer - emmet - teller (BET)分析显示,CPC的比表面积(SSA)为1015.59 m2 g-1,总孔容为0.44 cm3 g-1,显著高于P-CPC的35.30 m2 g-1和0.022 cm3 g-1。此外,CPC/MXene@S复合电极在0.1C下的初始放电容量为1358 mAh g-1,在0.2C下循环500次后仍保持695 mAh g-1的可逆容量,每循环的容量衰减率仅为0.05%。此外,它还表现出出色的倍率性能,即使在2C的高电流密度下也能提供776 mAh g-1的容量。该复合电极优异的电化学性能可归因于MXene对多硫化物的有效吸附。本研究为利用废生物质作为硫电极载体提供了一种新的方法。此外,还提出了经济效益、新趋势和挑战,为进一步设计出优质的Li-S电池AWs提供了可能。
Bioderived Hierarchically Porous Electrode with High Polarity for Lithium–Sulfur Batterties
Lithium–sulfur (Li–S) batteries hold great promise as future energy storage solutions owing to their low cost and environmental friendliness. Nature provides biomass materials that can serve as carriers for sulfur, featuring micropores, mesopores, and hierarchical pore structures. In this study, we utilized corncob-originated activated porous carbon (CPC), abundant agricultural wastes (AWs), as the sulfur host to prepare MXene (Ti3C2Tx) enhanced hierarchical bioderived porous electrode. The synthesis and function of CPC for Li–S batteries are presented, and the electrochemical effects of structural diversity, porosity and surface heteroatom doping of the Mxene in Li–S batteries are discussed. Brunauer–Emmett–Teller (BET) analysis revealed that CPC exhibited a specific surface area (SSA) of 1015.59 m2 g–1 and a total pore volume of 0.44 cm3 g–1, significantly higher than those of P-CPC (35.30 m2 g–1 and 0.022 cm3 g–1). Furthermore, the CPC/MXene@S composite electrode demonstrated an impressive initial discharge capacity of 1358 mAh g–1 at 0.1C and retained a reversible capacity of 695 mAh g–1 after 500 cycles at 0.2C, with a capacity decay rate of only 0.05% per cycle. Additionally, it showed excellent rate performance, delivering a capacity of 776 mAh g–1 even at a high current density of 2C. The superior electrochemical performance of this composite electrode can be attributed to MXene’s effective adsorption of polysulfides. This study provides a new methodology for utilizing waste biomass as a carrier for sulfur electrodes. In addition, the economic benefits, new trends and challenges are also proposed for further design excellent AWs for Li–S batteries.
期刊介绍:
Energy & Fuels publishes reports of research in the technical area defined by the intersection of the disciplines of chemistry and chemical engineering and the application domain of non-nuclear energy and fuels. This includes research directed at the formation of, exploration for, and production of fossil fuels and biomass; the properties and structure or molecular composition of both raw fuels and refined products; the chemistry involved in the processing and utilization of fuels; fuel cells and their applications; and the analytical and instrumental techniques used in investigations of the foregoing areas.