2008
DOI: 10.1016/j.jpowsour.2008.07.079
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Poly[3,4-(ethylenedithio)thiophene]: High specific capacity cathode active material for lithium rechargeable batteries

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Cited by 50 publications
(29 citation statements)
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“…159e163 The most representative element of this family of OEMs is undoubtedly PTMA ( Table 6.2, entry II), which has a theoretical capacity of 111 mAh/g. 170 As previously explained in paragraph 2 of this chapter, the sulfur element is intrinsically interesting due to its multielectron redox chemistry but the production of soluble Ps as the discharge/charge proceed constitutes a brake in developing efficient Li-S batteries. However, the low electronic conductivity of such redox-active polymers implies the use of high loadings of conductive additive limiting the specific capacity of a practical composite PTMA-based electrode to w55 mAh/g.…”
Section: Most Representative Organic Electrode Materialsmentioning
confidence: 94%
“…159e163 The most representative element of this family of OEMs is undoubtedly PTMA ( Table 6.2, entry II), which has a theoretical capacity of 111 mAh/g. 170 As previously explained in paragraph 2 of this chapter, the sulfur element is intrinsically interesting due to its multielectron redox chemistry but the production of soluble Ps as the discharge/charge proceed constitutes a brake in developing efficient Li-S batteries. However, the low electronic conductivity of such redox-active polymers implies the use of high loadings of conductive additive limiting the specific capacity of a practical composite PTMA-based electrode to w55 mAh/g.…”
Section: Most Representative Organic Electrode Materialsmentioning
confidence: 94%
“…The C theo (374 mAh g − 1 ) and discharge potential ( ∼ 2.2 V vs Li/Li + ) of thioether 48 was just comparable to that of disulfi des, but the cycling stability is remarkably improved. [ 86 ] Considering that the thiophene core in 51 also undergoes reversible p-doping, Zhan et al supposed that oxidation and reduction occur at the thiophene and S + sites, S S n REVIEW respectively, followed by intramolecular electron transfer to each other. To eliminate the nonplanarity between the thiolane ring and the polyphenyl main chain for better electron transfer, thioether 49 was synthesized.…”
Section: P-type Organosulfur Polymersmentioning
confidence: 99%
“…For example, EDTT has a lower oxidation potential compared to EDOT, and there is a better electronic interaction between polymer chains through intermolecular S … S attractions in PEDTT than PEDOT 15, 35, 39, 40. Nowadays, PEDTT and its derivatives have found possible applications as the electron donor materials in photovoltaic devices,35, 37, 38, 41–44 and as the cathode active materials for rechargeable lithium batteries with better cathode capacity than PEDOT 45. More recently, electrosynthesized PEDTT materials were introduced into organic electronic display field and sensors owing to their electrochromic and electrochemical catalytic properties 21, 46–48.…”
Section: Introductionmentioning
confidence: 99%