1972
DOI: 10.1016/0013-4686(72)90010-2
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Investigation into the use of quinone compounds-for battery cathodes

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Cited by 169 publications
(108 citation statements)
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“…[32][33][34][35] Although crystalline quinone derivatives have the potential to be Phase separation of polymers and crystals K Sato et al incorporated in the high-density state and to inhibit dissolution during the redox reaction, crystalline quinone derivatives showed lower utilization rates, such as 58% at 2.2 A g −1 , 6.4% at 0.5 A g −1 and 27% at 2.0 A g −1 , in earlier works (Supplementary Table S3 in the Supplementary Information). 25,31,40 In the present work, the utilization rate of a crystalline quinone derivative in the segregated composite was 54% at 5.0 A g −1 , which is comparable to quinone molecules adsorbed on carbon (Supplementary Table S1 in the Supplementary Information). The high utilization rate is ascribed to the smooth redox reaction originating from the segregated composite structure with the PPy nanoparticles (Supplementary Figure S8 in the Supplementary Information).…”
Section: Resultssupporting
confidence: 59%
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“…[32][33][34][35] Although crystalline quinone derivatives have the potential to be Phase separation of polymers and crystals K Sato et al incorporated in the high-density state and to inhibit dissolution during the redox reaction, crystalline quinone derivatives showed lower utilization rates, such as 58% at 2.2 A g −1 , 6.4% at 0.5 A g −1 and 27% at 2.0 A g −1 , in earlier works (Supplementary Table S3 in the Supplementary Information). 25,31,40 In the present work, the utilization rate of a crystalline quinone derivative in the segregated composite was 54% at 5.0 A g −1 , which is comparable to quinone molecules adsorbed on carbon (Supplementary Table S1 in the Supplementary Information). The high utilization rate is ascribed to the smooth redox reaction originating from the segregated composite structure with the PPy nanoparticles (Supplementary Figure S8 in the Supplementary Information).…”
Section: Resultssupporting
confidence: 59%
“…Quinone derivatives have high theoretical specific capacity based on the two-electron redox reaction. 25,26 For example, the theoretical capacity of DCNQ is calculated to be 237 mAh g −1 . 26 The island-like DCNQ nanocrystals in the conductive PPy sea domain have potentials for a smooth redox reaction.…”
Section: Resultsmentioning
confidence: 99%
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“…90 There has been interest in using quinones in batteries for a long time. [91][92][93] Recently, poly(vinylanthraquinone) polymer immersed in 30 wt % NaOH or KOH solutions was found to exhibit a capacity of 123 mWh/ g and stability for over 500 cycles as a rechargeable air battery (Figure 16(a)). 94 The redox current increased dramatically going from neutral to basic pH, and this was explained by better electrolyte permeation in basic pH due to the swelling of polymer chains from charge repulsion between negative Q 2−…”
mentioning
confidence: 99%
“…The stability enhancement by acidic electrolytes seemed to be generally applicable. A tetrachloro-p-benzoquinone electrode lost < 5% capacity after 50 cycles in a 3 M H2SO4 electrolyte, [40] which contrasted drastically with the > 70% capacity loss within 20 cycles in a carbo- Figure 7 Improving the cyclability organic electrodes by the use of acidic electrolytes. (a) Cyclability of PTO in 4.4 M H2SO4.…”
Section: Aqueous Electrolytesmentioning
confidence: 99%