Nanocomposite All-Solid-State Polymer Electrolyte for High-Performance Lithium Batteries

被引:10
作者
Wang, Shi [1 ]
Xu, Hao [1 ]
Wang, Ailian [1 ]
Liu, Xu [1 ]
Chen, Jie [1 ]
Wang, Zhinan [1 ]
Feng, Di [2 ]
Zeng, Qinghui [1 ]
Zhang, Liaoyun [1 ]
机构
[1] Univ Chinese Acad Sci, Sch Chem Sci, Beijing 100049, Peoples R China
[2] Beijing Agr Univ, Beijing, Peoples R China
基金
中国国家自然科学基金;
关键词
hybrid all-solid-state electrolyte; click chemistry; chemically modified nano-silica; linear copolymer; lithium-ion batteries; ION BATTERIES; NANOPARTICLES; CONDUCTIVITY; ENHANCEMENT; CHALLENGES; SEPARATOR; SHAPE;
D O I
10.1002/ente.201800362
中图分类号
TE [石油、天然气工业]; TK [能源与动力工程];
学科分类号
0807 ; 0820 ;
摘要
An inorganic-polymeric hybrid all-solid-state electrolyte (SSE) composed of chemically modified nano-silica, linear poly(trifluoroethyl methacrylate)-co-poly(poly(ethylene glycol) methyl ether methacrylate copolymer (PTFEMA-co-PPEGMA or LCP) and lithium salt is prepared and used in lithium-ion batteries (LIBs) for the first time. Nano-silica is transformed to SiO2-SH via esterification reaction. Then, SiO2-PEGMA is synthesized through click chemistry of SiO2-SH and PEGMA. The compatibility of the nano-SiO2 and the LCP can be effectively improved due to the excellent dispersibility of the chemically modified nano-SiO2 in the polymer matrix. As a result, the hybrid SSE has good thermal stability, excellent film-forming ability. Furthermore, the hybrid SSE shows superior comprehensive electrochemical properties, which makes the corresponding LiFePO4/Li cells have good cycling performance (the discharge capacity reaches 144 mAh g(-1) at 0.3 C) and rate capability (90 mAh g(-1) is reached at 1 C). Thus, the hybrid electrolyte can be a powerful SSE for high-safety and high-performance LIBs.
引用
收藏
页码:122 / 130
页数:9
相关论文
共 36 条
  • [1] [Anonymous], 2016, Adv. Energy Mater., DOI DOI 10.1002/AENM.201600467
  • [2] Bouchet R, 2013, NAT MATER, V12, P452, DOI [10.1038/nmat3602, 10.1038/NMAT3602]
  • [3] The enhancement of lithium ion dissociation in polyelectrolyte gels on the addition of ceramic nano-fillers
    Byrne, N
    Efthimiadis, J
    MacFarlane, DR
    Forsyth, M
    [J]. JOURNAL OF MATERIALS CHEMISTRY, 2004, 14 (01) : 127 - 133
  • [4] Biomimetic ant-nest ionogel electrolyte boosts the performance of dendrite-free lithium batteries
    Chen, Nan
    Dai, Yujuan
    Xing, Yi
    Wang, Lili
    Guo, Cui
    Chen, Renjie
    Guo, Shaojun
    Wu, Feng
    [J]. ENERGY & ENVIRONMENTAL SCIENCE, 2017, 10 (07) : 1660 - 1667
  • [5] The pursuit of solid-state electrolytes for lithium batteries: from comprehensive insight to emerging horizons
    Chen, Renjie
    Qu, Wenjie
    Guo, Xing
    Li, Li
    Wu, Feng
    [J]. MATERIALS HORIZONS, 2016, 3 (06) : 487 - 516
  • [6] Dendrite-Free Lithium Deposition Induced by Uniformly Distributed Lithium Ions for Efficient Lithium Metal Batteries
    Cheng, Xin-Bing
    Hou, Ting-Zheng
    Zhang, Rui
    Peng, Hong-Jie
    Zhao, Chen-Zi
    Huang, Jia-Qi
    Zhang, Qiang
    [J]. ADVANCED MATERIALS, 2016, 28 (15) : 2888 - 2895
  • [7] Ionic conductivity, mechanical strength and Li-ion battery performance of mono-functional and bi-functional ("Janus") "soggy sand" electrolytes
    Das, Shyamal K.
    Mandal, Soumit S.
    Bhattacharyya, Aninda J.
    [J]. ENERGY & ENVIRONMENTAL SCIENCE, 2011, 4 (04) : 1391 - 1399
  • [8] Trends in polymer electrolytes for secondary lithium batteries
    Dias, FB
    Plomp, L
    Veldhuis, JBJ
    [J]. JOURNAL OF POWER SOURCES, 2000, 88 (02) : 169 - 191
  • [9] Influence of Fe2O3 Nanofiller Shape on the Conductivity and Thermal Properties of Solid Polymer Electrolytes: Nanorods versus Nanospheres
    Do, Nhu Suong T.
    Schaetzl, Dean M.
    Dey, Barnali
    Seabaugh, Alan C.
    Fullerton-Shirey, Susan K.
    [J]. JOURNAL OF PHYSICAL CHEMISTRY C, 2012, 116 (40) : 21216 - 21223
  • [10] Structure and Mobility of PEO/LiClO4 Solid Polymer Electrolytes Filled with Al2O3 Nanoparticles
    Fullerton-Shirey, Susan K.
    Maranas, Janna K.
    [J]. JOURNAL OF PHYSICAL CHEMISTRY C, 2010, 114 (20) : 9196 - 9206