TY - JOUR
T1 - Healing High-Loading Sulfur Electrodes with Unprecedented Long Cycling Life
T2 - Spatial Heterogeneity Control
AU - Peng, Hong Jie
AU - Huang, Jia Qi
AU - Liu, Xin Yan
AU - Cheng, Xin Bing
AU - Xu, Wen Tao
AU - Zhao, Chen Zi
AU - Wei, Fei
AU - Zhang, Qiang
N1 - Publisher Copyright:
© 2017 American Chemical Society.
PY - 2017/6/28
Y1 - 2017/6/28
N2 - Self-healing capability helps biological systems to maintain their survivability and extend their lifespan. Similarly, self-healing is also beneficial to next-generation secondary batteries because high-capacity electrode materials, especially the cathodes such as oxygen or sulfur, suffer from shortened cycle lives resulting from irreversible and unstable phase transfer. Herein, by mimicking a biological self-healing process, fibrinolysis, we introduced an extrinsic healing agent, polysulfide, to enable the stable operation of sulfur microparticle (SMiP) cathodes. An optimized capacity (∼3.7 mAh cm-2) with almost no decay after 2000 cycles at a high sulfur loading of 5.6 mg(S) cm-2 was attained. The inert SMiP is activated by the solubilization effect of polysulfides whereas the unstable phase transfer is mediated by mitigated spatial heterogeneity of polysulfides, which induces uniform nucleation and growth of solid compounds. The comprehensive understanding of the healing process, as well as of the spatial heterogeneity, could further guide the design of novel healing agents (e.g., lithium iodine) toward high-performance rechargeable batteries.
AB - Self-healing capability helps biological systems to maintain their survivability and extend their lifespan. Similarly, self-healing is also beneficial to next-generation secondary batteries because high-capacity electrode materials, especially the cathodes such as oxygen or sulfur, suffer from shortened cycle lives resulting from irreversible and unstable phase transfer. Herein, by mimicking a biological self-healing process, fibrinolysis, we introduced an extrinsic healing agent, polysulfide, to enable the stable operation of sulfur microparticle (SMiP) cathodes. An optimized capacity (∼3.7 mAh cm-2) with almost no decay after 2000 cycles at a high sulfur loading of 5.6 mg(S) cm-2 was attained. The inert SMiP is activated by the solubilization effect of polysulfides whereas the unstable phase transfer is mediated by mitigated spatial heterogeneity of polysulfides, which induces uniform nucleation and growth of solid compounds. The comprehensive understanding of the healing process, as well as of the spatial heterogeneity, could further guide the design of novel healing agents (e.g., lithium iodine) toward high-performance rechargeable batteries.
UR - http://www.scopus.com/inward/record.url?scp=85021687127&partnerID=8YFLogxK
U2 - 10.1021/jacs.6b12358
DO - 10.1021/jacs.6b12358
M3 - Article
C2 - 28301151
AN - SCOPUS:85021687127
SN - 0002-7863
VL - 139
SP - 8458
EP - 8466
JO - Journal of the American Chemical Society
JF - Journal of the American Chemical Society
IS - 25
ER -