材料科学
电极
部分
有机自由基电池
溶解
纳米技术
四氰基对醌二甲烷
电导率
氧化物
溶解度
化学工程
电化学
有机化学
化学
物理化学
分子
工程类
冶金
作者
Sechan Lee,Jin Hong,Sung‐Kyun Jung,Kyojin Ku,Giyun Kwon,Won Mo Seong,Hyungsub Kim,Gabin Yoon,Inyeong Kang,Kootak Hong,Ho Won Jang,Kisuk Kang
标识
DOI:10.1016/j.ensm.2019.05.001
摘要
Organic redox compounds are potential substitutes for transition-metal-oxide electrode materials in rechargeable batteries because of their low cost, minimal environmental footprint, and chemical diversity. However, their inherently low electrical conductivity and high solubility in organic solvents are serious impediments to achieving performance comparable to that of currently used inorganic-based electrode materials. Herein, we report organic charge-transfer complexes as a novel class of electrode materials with intrinsically high electrical conductivity and low solubility that can potentially overcome the chronic drawbacks associated with organic electrodes. The formation of the charge-transfer complexes, phenazine–7,7,8,8-tetracyanoquinodimethane and dibenzo-1,4-dioxin–7,7,8,8-tetracyanoquinodimethane, via a room-temperature process leads to enhancement in the electrical conductivity and reduction in the dissolution resulting in the high power and cycle performances that far outperform those of each single-moiety counterpart. This finding demonstrates the general applicability of the charge-transfer complex to simultaneously improve the electrical conductivity and mitigate the shortcomings of existing single-moiety-based organic electrode materials, and opens up an uncharted pathway toward the development of high-performance organic electrode materials via the exploration of various combinations of donor–acceptor monomers with different stoichiometry.
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