{"title":"先进锂电池用纳米纤维素增强纳米纤维复合聚芳醚酮聚合物电解质。","authors":"Yangyang Yu, Xiaohui Guo, Yuhan Liu, Chengzhe Liu, Baijun Liu, Qiao Wang, Zhaoyan Sun, Yongfeng Men, Yunji Xie, Zihao Xing, Wei Hu","doi":"10.1016/j.ijbiomac.2025.139560","DOIUrl":null,"url":null,"abstract":"<p><p>Solid polymer batteries (SPEs) are highly desirable for energy storage because of the urgent need for higher energy density and safer lithium ion batteries (LIBs). In this work, the single-ion lithium salt PAEK<sub>50</sub>-LiCPSI was synthesized by grafting 3-chloropropanesulfonyl trifluoromethanesulimide lithium (LiCPSI) onto poly(aryl ether ketone)<sub>50</sub> (PAEK<sub>50</sub>). Nanocellulose (NCC), PAEK<sub>50</sub>-LiCPSI, and poly(vinylidene fluoride) (PVDF-HFP) were compounded to obtain NCC reinforced high-performance nanofiber composite polymer electrolytes (NCC/PAEK/PVDF) through electrospinning, which presented tensile strength of 15.35 MPa, ionic conductivity of 1.13 × 10<sup>-4</sup> S cm<sup>-1</sup>, and Li<sup>+</sup> transfer number as high as 0.80 at 25 °C. The assembled LIBs with NCC/PAEK/PVDF illustrated an initial discharge specific capacity of 155.2 mAh g<sup>-1</sup> at 0.2C, and the capacity retention rate was close to 93 % after cycling 700 cycles at 25 °C. Furthermore, its initial specific discharge capacity at -20 °C was 103.4 mAh g<sup>-1</sup>, and can cycle over 300 cycles. The NCC with sulfonic acid group reinforced the mechanical performance, promoted the dissociation of Li<sup>+</sup>, and synergized with PAEK<sub>50</sub>-LiCPSI and PVDF-HFP to form a 3D nanofiber ionic bridge network through hydrogen bond, which promoted the more stable and faster Li<sup>+</sup> transportation. This work suggested that the NCC/PAEK/PVDF can be a good choice of solid polymer electrolytes (SPE) for the next generation of LIBs, even working at low-temperatures.</p>","PeriodicalId":333,"journal":{"name":"International Journal of Biological Macromolecules","volume":" ","pages":"139560"},"PeriodicalIF":8.5000,"publicationDate":"2025-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Nanocellulose-reinforced nanofiber composite poly(aryl ether ketone) polymer electrolyte for advanced lithium batteries.\",\"authors\":\"Yangyang Yu, Xiaohui Guo, Yuhan Liu, Chengzhe Liu, Baijun Liu, Qiao Wang, Zhaoyan Sun, Yongfeng Men, Yunji Xie, Zihao Xing, Wei Hu\",\"doi\":\"10.1016/j.ijbiomac.2025.139560\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Solid polymer batteries (SPEs) are highly desirable for energy storage because of the urgent need for higher energy density and safer lithium ion batteries (LIBs). In this work, the single-ion lithium salt PAEK<sub>50</sub>-LiCPSI was synthesized by grafting 3-chloropropanesulfonyl trifluoromethanesulimide lithium (LiCPSI) onto poly(aryl ether ketone)<sub>50</sub> (PAEK<sub>50</sub>). Nanocellulose (NCC), PAEK<sub>50</sub>-LiCPSI, and poly(vinylidene fluoride) (PVDF-HFP) were compounded to obtain NCC reinforced high-performance nanofiber composite polymer electrolytes (NCC/PAEK/PVDF) through electrospinning, which presented tensile strength of 15.35 MPa, ionic conductivity of 1.13 × 10<sup>-4</sup> S cm<sup>-1</sup>, and Li<sup>+</sup> transfer number as high as 0.80 at 25 °C. The assembled LIBs with NCC/PAEK/PVDF illustrated an initial discharge specific capacity of 155.2 mAh g<sup>-1</sup> at 0.2C, and the capacity retention rate was close to 93 % after cycling 700 cycles at 25 °C. Furthermore, its initial specific discharge capacity at -20 °C was 103.4 mAh g<sup>-1</sup>, and can cycle over 300 cycles. The NCC with sulfonic acid group reinforced the mechanical performance, promoted the dissociation of Li<sup>+</sup>, and synergized with PAEK<sub>50</sub>-LiCPSI and PVDF-HFP to form a 3D nanofiber ionic bridge network through hydrogen bond, which promoted the more stable and faster Li<sup>+</sup> transportation. This work suggested that the NCC/PAEK/PVDF can be a good choice of solid polymer electrolytes (SPE) for the next generation of LIBs, even working at low-temperatures.</p>\",\"PeriodicalId\":333,\"journal\":{\"name\":\"International Journal of Biological Macromolecules\",\"volume\":\" \",\"pages\":\"139560\"},\"PeriodicalIF\":8.5000,\"publicationDate\":\"2025-03-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"International Journal of Biological Macromolecules\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://doi.org/10.1016/j.ijbiomac.2025.139560\",\"RegionNum\":1,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2025/1/6 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q1\",\"JCRName\":\"BIOCHEMISTRY & MOLECULAR BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"International Journal of Biological Macromolecules","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1016/j.ijbiomac.2025.139560","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/1/6 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 0
摘要
由于迫切需要更高的能量密度和更安全的锂离子电池,固体聚合物电池(spe)是非常理想的储能材料。本研究将3-氯丙磺酸基三氟甲烷磺酰锂(LiCPSI)接枝到聚芳醚酮50 (PAEK50)上,合成了单离子锂盐PAEK50-LiCPSI。将纳米纤维素(NCC)、PAEK50-LiCPSI和聚偏氟乙烯(PVDF- hfp)经静电纺丝复配得到NCC增强高性能纳米纤维复合聚合物电解质(NCC/PAEK/PVDF),其抗拉强度为15.35 MPa,离子电导率为1.13 × 10-4 S cm-1, 25 ℃时Li+转移数高达0.80。NCC/PAEK/PVDF组装的LIBs在0.2C下的初始放电比容量为155.2 mAh g-1,在25 °C下循环700 次后,容量保持率接近93 %。此外,在-20 °C时,其初始比放电容量为103.4 mAh g-1,可循环超过300次 次。带有磺酸基的NCC增强了力学性能,促进了Li+的解离,并与PAEK50-LiCPSI和PVDF-HFP通过氢键协同形成三维纳米纤维离子桥网络,促进了Li+更稳定、更快的运输。这项工作表明,NCC/PAEK/PVDF可以作为下一代lib的固体聚合物电解质(SPE)的良好选择,即使在低温下也可以工作。
Solid polymer batteries (SPEs) are highly desirable for energy storage because of the urgent need for higher energy density and safer lithium ion batteries (LIBs). In this work, the single-ion lithium salt PAEK50-LiCPSI was synthesized by grafting 3-chloropropanesulfonyl trifluoromethanesulimide lithium (LiCPSI) onto poly(aryl ether ketone)50 (PAEK50). Nanocellulose (NCC), PAEK50-LiCPSI, and poly(vinylidene fluoride) (PVDF-HFP) were compounded to obtain NCC reinforced high-performance nanofiber composite polymer electrolytes (NCC/PAEK/PVDF) through electrospinning, which presented tensile strength of 15.35 MPa, ionic conductivity of 1.13 × 10-4 S cm-1, and Li+ transfer number as high as 0.80 at 25 °C. The assembled LIBs with NCC/PAEK/PVDF illustrated an initial discharge specific capacity of 155.2 mAh g-1 at 0.2C, and the capacity retention rate was close to 93 % after cycling 700 cycles at 25 °C. Furthermore, its initial specific discharge capacity at -20 °C was 103.4 mAh g-1, and can cycle over 300 cycles. The NCC with sulfonic acid group reinforced the mechanical performance, promoted the dissociation of Li+, and synergized with PAEK50-LiCPSI and PVDF-HFP to form a 3D nanofiber ionic bridge network through hydrogen bond, which promoted the more stable and faster Li+ transportation. This work suggested that the NCC/PAEK/PVDF can be a good choice of solid polymer electrolytes (SPE) for the next generation of LIBs, even working at low-temperatures.
期刊介绍:
The International Journal of Biological Macromolecules is a well-established international journal dedicated to research on the chemical and biological aspects of natural macromolecules. Focusing on proteins, macromolecular carbohydrates, glycoproteins, proteoglycans, lignins, biological poly-acids, and nucleic acids, the journal presents the latest findings in molecular structure, properties, biological activities, interactions, modifications, and functional properties. Papers must offer new and novel insights, encompassing related model systems, structural conformational studies, theoretical developments, and analytical techniques. Each paper is required to primarily focus on at least one named biological macromolecule, reflected in the title, abstract, and text.