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Chemical Bonding and Physical Trapping of Sulfur in Mesoporous Magnéli Ti 4 O 7 Microspheres for High‐Performance Li–S Battery
Author(s) -
Wei Hao,
Rodriguez Erwin F.,
Best Adam S.,
Hollenkamp Anthony F.,
Chen Dehong,
Caruso Rachel A.
Publication year - 2017
Publication title -
advanced energy materials
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 10.08
H-Index - 220
eISSN - 1614-6840
pISSN - 1614-6832
DOI - 10.1002/aenm.201601616
Subject(s) - mesoporous material , materials science , sulfur , cathode , lithium (medication) , chemical engineering , electrochemistry , chemical bond , chemical state , nanotechnology , electrode , catalysis , chemistry , x ray photoelectron spectroscopy , metallurgy , organic chemistry , engineering , endocrinology , medicine
Various host materials have been investigated to address the intrinsic drawbacks of lithium sulfur batteries, such as the low electronic conductivity of sulfur and inevitable decay in capacity during cycling. Besides the widely investigated carbonaceous materials, metal oxides have drawn much attention because they form strong chemical bonds with the soluble lithium polysulfides. Here, mesoporous Magnéli Ti 4 O 7 microspheres are prepared via an in situ carbothermal reduction that exhibit interconnected mesopores (20.4 nm), large pore volume (0.39 cm 3 g −1 ), and high surface area (197.2 m 2 g −1 ). When the sulfur cathode is embedded in a matrix of mesoporous Magnéli Ti 4 O 7 microspheres, it exhibits a superior reversible capacity of 1317.6 mA h g −1 at moderate current (C/10) and a low decay in capacity of 12% after 400 cycles at C/5. Strong chemical bonding of the lithium polysulfides to Ti 4 O 7 , as well as effective physical trapping in the mesopores and voids in the matrix are considered responsible for the improved electrochemical performance. A mechanism of the physical and chemical interactions between mesoporous Magnéli Ti 4 O 7 microspheres and sulfur is proposed based on systematic investigations.