研究论文

分级多孔N, P共掺杂rGO改性隔膜增强锂硫电池的循环稳定性

  • 陈锋 ,
  • 程晓琴 ,
  • 赵振新 ,
  • 王晓敏
展开
  • a 太原理工大学 材料科学与工程学院 太原 030024
    b 太原理工大学 新能源材料与器件山西省重点实验室 太原 030024

收稿日期: 2021-03-27

  网络出版日期: 2021-05-25

基金资助

国家自然科学基金(U1710256); 国家自然科学基金(U1810115); 国家自然科学基金(52072256); 山西省重点研发项目(201803D121038); 山西省科技重大专项(20181102018); 山西省科技重大专项(2181102019); 山西省科技重大专项(20191102004); 山西省科技重大专项(20201101016)

Hierarchical Porous N, P co-doped rGO Modified Separator to Enhance the Cycling Stability of Lithium-sulfur Batteries

  • Feng Chen ,
  • Xiaoqin Cheng ,
  • Zhenxin Zhao ,
  • Xiaomin Wang
Expand
  • a College of Materials Science and Engineering, Taiyuan University of Technology, Taiyuan 030024, China
    b Shanxi Key Laboratory of New Energy Materials and Devices, Taiyuan University of Technology, Taiyuan 030024, China

Received date: 2021-03-27

  Online published: 2021-05-25

Supported by

National Natural Science Foundation of China(U1710256); National Natural Science Foundation of China(U1810115); National Natural Science Foundation of China(52072256); Key Research and Development (R&D) Projects of Shanxi Province(201803D121038); Shanxi Science and Technology Major Project(20181102018); Shanxi Science and Technology Major Project(2181102019); Shanxi Science and Technology Major Project(20191102004); Shanxi Science and Technology Major Project(20201101016)

摘要

多硫化物(LiPSs)的穿梭效应和低硫利用率会导致电池容量的快速衰减, 这严重阻碍了锂硫电池的商业化进程. 为了抑制LiPSs的穿梭效应和提高硫的利用率, 本工作采用一步高温还原法合成了具有分级多孔结构的N, P共掺杂还原氧化石墨烯(NPG), 并将其用于锂硫电池的隔膜改性. 高导电性NPG具有丰富的分级多孔结构, 提供了大量的LiPSs锚定位点和丰富的离子/电子传输通道, 实现了可溶性中间体的快速转化, 高效抑制了LiPSs的穿梭效应. 归因于以上优点, NPG改性聚丙烯隔膜(NPG/PP)能够有效抑制LiPSs的穿梭并提高硫的利用率. 结果表明, NPG/PP改性隔膜的电池展现出优异的循环性能(在1 C的电流密度下, 循环500圈以后容量仍保持在612.5 mAh•g-1, 每圈的衰减仅为0.052%)和出色的倍率性能(在2 C的电流密度下容量仍保持在617.9 mAh•g-1). 这种构建分级多孔N, P共掺杂rGO改性隔膜的思路为锂硫电池的研究提供了新的方向.

本文引用格式

陈锋 , 程晓琴 , 赵振新 , 王晓敏 . 分级多孔N, P共掺杂rGO改性隔膜增强锂硫电池的循环稳定性[J]. 化学学报, 2021 , 79(7) : 941 -947 . DOI: 10.6023/A21030117

Abstract

Lithium-sulfur batteries with high energy density (2600 Wh•kg-1) and theoretical capacity (1675 mAh•g-1) have attracted much attention. Furthermore, as a cathode active material, sulfur has prominent advantages such as rich in natural resources, low cost and environmental friendliness. Attributed to the above merits, lithium-sulfur batteries deemed to be one of the most promising energy storage devices. However, poor utilization of sulfur and the shuttle effect of lithium polysulfides (LiPSs) causes dramatic capacity degradation, which severely restricts the commercial application of lithium-sulfur batteries. These problems are mainly attributed to the insulating nature of sulfur and its final discharge products (Li2S2/Li2S), which reduces the sulfur utilization, as well as the poor adsorption capability and slow reaction kinetics, which give rise to the shuttle effect of soluble LiPSs. To solve the above problems, carbon materials are regarded as the most suitable cathode materials for lithium-sulfur batteries, because its superior electrical conductivity and rich porous structure can effectively improve the sulfur utilization and mitigate the shuttle effect of LiPSs. However, the shuttling of LiPSs is difficult to suppressed completely due to the weak adsorption interaction between nonpolar carbon materials and polar LiPSs. Based on this, heteroatom doping is beneficial to enrich the chemical adsorption sites of LiPSs in carbon materials, enhancing the interaction between carbon materials and LiPSs. Thus, the shuttle effect of LiPSs is efficiently suppressed and the cycle stability of lithium-sulfur batteries is improved. Hence, N, P co-doped reduced graphene oxide (NPG) with hierarchical porous structure was prepared by one-step high-temperature reduction method and used for the polypropylene (PP) separator modification of lithium-sulfur batteries. The highly conductive NPG with abundant hierarchical porous structure provides a large number of anchor sites for LiPSs and sufficient ion/electron transport channels, facilitating the conversion of the soluble intermediates and efficiently suppressing the shuttle effect of LiPSs. In consequence, the NPG/PP modified separator can effectively inhibit the shuttle of LiPSs and improve the sulfur utilization. The results show that the cells with NPG/PP modified separator exhibit excellent cycling performance (the degradation per cycle is only 0.052% and the capacity remains at 612.5 mAh•g-1 after 500 cycles at 1 C) and excellent rate performance (high specific capacity of 617.9 mAh•g-1 at 2 C). This idea of constructing hierarchical porous N, P co-doped rGO modified separators provides a new strategy for the study of lithium-sulfur battery.

参考文献

[1]
(a) Zhao, Z.; Pathak, R.; Wang, X.; Yang, Z.; Li, H.; Qiao, Q. Electrochim. Acta 2020, 364, 137117.
[1]
(b) Huang, S.; Lim, Y. V.; Zhang, X.; Wang, Y.; Zheng, Y.; Kong, D.; Ding, M.; Yang, S. A.; Yang, H. Y. Nano Energy 2018, 51, 340.
[2]
(a) Li, J.; Zhou, J.; Wang, T.; Chen, X.; Zhang, Y.; Wan, Q.; Zhu, J. Nanoscale 2020, 12, 8991.
[2]
(b) Song, C.-L.; Li, G.-H.; Yang, Y.; Hong, X.-J.; Huang, S.; Zheng, Q.-F.; Si, L.-P.; Zhang, M.; Cai, Y.-P. Chem. Eng. J. 2020, 381, 122701.
[3]
(a) Cha, E.; Patel, M. D.; Park, J.; Hwang, J.; Prasad, V.; Cho, K.; Choi, W. Nat. Nanotechnol. 2018, 13, 337.
[3]
(b) Guo, W.; Han, Q.; Jiao, J.; Wu, W.; Zhu, X.; Chen, Z.; Zhao, Y. Angew. Chem. Int. Ed. 2021, 60, 2.
[4]
Shin, H.; Baek, M.; Gupta, A.; Char, K.; Manthiram, A.; Choi, J. W. Adv. Energy Mater. 2020, 10, 2001456.
[5]
(a) Guang, Z.; Huang, Y.; Chen, C.; Liu, X.; Xu, Z.; Dou, W. Chem. Eng. J. 2020, 383, 123163.
[5]
(b) Lin, J.; Zhang, K.; Zhu, Z.; Zhang, R.; Li, N.; Zhao, C. ACS Appl. Mater. Interfaces 2020, 12, 2497.
[5]
(c) Pan, H.; Tan, Z.; Zhou, H.; Jiang, L.; Huang, Z.; Feng, Q.; Zhou, Q.; Ma, S.; Kuang, Y. J. Energ. Chem. 2019, 39, 101.
[5]
(d) Rana, M.; Li, M.; He, Q.; Luo, B.; Wang, L.; Gentle, I.; Knibbe, R. J. Energ. Chem. 2020, 44, 51.
[6]
Fu, A.; Wang, C.; Pei, F.; Cui, J.; Fang, X.; Zheng, N. Small 2019, 15, e1804786.
[7]
Chung, S. H.; Manthiram, A. J. Phys. Chem. Lett. 2014, 5, 1978.
[8]
(a) Qiu, Y.; Li, W.; Zhao, W.; Li, G.; Hou, Y.; Liu, M.; Zhou, L.; Ye, F.; Li, H.; Wei, Z.; Yang, S.; Duan, W.; Ye, Y.; Guo, J.; Zhang, Y. Nano Lett. 2014, 14, 4821.
[8]
(b) Wang, X.; Li, Y.; Du, L.; Gao, F.; Wu, Q.; Yang, L.; Chen, Q.; Wang, X.; Hu, Z. Acta Chim. Sinica 2018, 76, 627. (in Chinese)
[8]
(王啸, 李有彬, 杜玲玉, 高福杰, 吴强, 杨立军, 陈强, 王喜章, 胡征, 化学学报, 2018, 76, 627.)
[9]
(a) Paraknowitsch, J. P.; Thomas, A. Energy Environ. Sci. 2013, 6, 2839.
[9]
(b) Talapaneni, S. N.; Hwang, T. H.; Je, S. H.; Buyukcakir, O.; Choi, J. W.; Coskun, A. Angew. Chem. Int. Ed. 2016, 55, 3106.
[9]
(c) Chen, K.; Sun, Z.; Fang, R.; Li, F.; Cheng, H. Acta Phys.-Chim. Sin. 2018, 34, 377. (in Chinese)
[9]
(陈克, 孙振华, 方若翩, 李峰, 成会明, 物理化学学报, 2018, 34, 377.)
[9]
(d) Li, B.-Q.; Peng, H.-J.; Chen, X.; Zhang, S.-Y.; Xie, J.; Zhao, C.-X.; Zhang, Q. CCS Chem. 2019, 1, 128.
[10]
Li, W.; Ma, Q.; Zheng, Z.; Zhang, Y. Acta Chim. Sinica 2017, 75, 225.. (in Chinese)
[10]
(李宛飞, 马倩, 郑召召, 张跃钢, 化学学报, 2017, 75, 225.)
[11]
Zhang, K.; Zhang, F.; Pan, H.; Yu, J.; Wang, L.; Wang, D.; Wang, L.; Hu, G.; Zhang, J.; Qian, Y. Electrochim. Acta 2020, 354, 136648.
[12]
Shan, J.; Liu, Y.; Su, Y.; Liu, P.; Zhuang, X.; Wu, D.; Zhang, F.; Feng, X. J. Mater. Chem. A 2016, 4, 314.
[13]
Zhu, J.; Li, K.; Xiao, M.; Liu, C.; Wu, Z.; Ge, J.; Xing, W. J. Mater. Chem. A 2016, 4, 7422.
[14]
(a) Liu, Y.; Yuan, L.; Yang, M.; Zheng, Y.; Li, L.; Gao, L.; Nerngchamnong, N.; Nai, C. T.; Sangeeth, C. S.; Feng, Y. P.; Nijhuis, C. A.; Loh, K. P. Nat. Commun. 2014, 5, 5461.
[14]
(b) Chen, K.; Zhang, S.; Li, A.; Tang, X.; Li, L.; Guo, L. ACS Nano 2018, 12, 4269.
[15]
Yang, Z.; Gao, Y.; Zhao, Z.; Wang, Y.; Wu, Y.; Wang, X. J. Power Sources 2020, 474, 228500.
[16]
Li, J.; Yun, X.; Hu, Z.; Xi, L.; Li, N.; Tang, H.; Lu, P.; Zhu, Y. J. Mater. Chem. A 2019, 7, 26311.
[17]
(a) Zhang, J.; Qu, L.; Shi, G.; Liu, J.; Chen, J.; Dai, L. Angew. Chem. Int. Ed. 2016, 55, 2230.
[17]
(b) Wu, X.; Li, S.; Wang, B.; Liu, J.; Yu, M. Renewable Energy 2020, 158, 509.
[17]
(c) Chabu, J. M.; Zeng, K.; Jin, G.; Zhang, M.; Li, Y.; Liu, Y.-N. Mater. Chem. Phys. 2019, 229, 226.
[18]
(a) Song, Z.-C.; Lu, X.-L. Hu, Q.; Ren, J.; Zhang, W.-Q.; Zheng, Q.-J.; Lin, D.-M. J. Power Sources 2019, 421, 23.
[18]
(b) Xiang, M.; Yang, L.; Zheng, Y.; Huang, J.; Jing, P.; Wu, H.; Zhang, Y.; Liu, H. J. Mater. Chem. A 2017, 5, 18020.
[19]
Zegeye, T. A.; Tsai, M.-C.; Cheng, J.-H.; Lin, M.-H.; Chen, H.-M.; Rick, J.; Su, W.-N.; Kuo, C. -F. J.; Hwang, B.-J. J. Power Sources 2017, 353, 298.
[20]
Ren, J.; Xia, L.; Zhou, Y.; Zheng, Q.; Liao, J.; Lin, D. Carbon 2018, 140, 30.
[21]
Maiti, U. N.; Lee, W. J.; Lee, J. M.; Oh, Y.; Kim, J. Y.; Kim, J. E.; Shim, J.; Han, T. H.; Kim, S. O. Adv. Mater. 2014, 26, 40.
[22]
Cai, J.; Wu, C.; Zhu, Y.; Zhang, K.; Shen, P. K. J. Power Sources 2017, 341, 165.
[23]
Wu, C.; Kopold, P.; van Aken, P. A.; Maier, J.; Yu, Y. Adv. Mater. 2017, 29, 1604015.
[24]
Li, M.; Zhou, X.; Ma, X.; Chen, L.; Zhang, D.; Xu, S.; Duan, D.; Chen, C.; Yuan, Q.; Liu, S. Chem. Eng. J. 2021, 409, 128164.
[25]
Gao, Y.; Yang, Z.; Wang, Y.; Wang, X. Electrochim. Acta 2021, 368, 137646.
[26]
Zhou, S.; Yang, S.; Ding, X.; Lai, Y.; Nie, H.; Zhang, Y.; Chan, D.; Duan, H.; Huang, S.; Yang, Z. ACS Nano 2020, 14, 7538.
文章导航

/