TY - JOUR
T1 - Electrical Conductivity-Relay between Organic Charge-Transfer and Radical Salts toward Conductive Additive-Free Rechargeable Battery
AU - Fujihara, Yui
AU - Fujihara, Yui
AU - Kobayashi, Hiroaki
AU - Takaishi, Shinya
AU - Tomai, Takaaki
AU - Yamashita, Masahiro
AU - Yamashita, Masahiro
AU - Yamashita, Masahiro
AU - Honma, Itaru
N1 - Funding Information:
We thank Hideyuki Magara for his support with SEM-EDX measurements. This work was supported in part by the “Dynamic Alliance for Open Innovation Bridging Human, Environment and Materials” from the Ministry of Education, Culture, Sports, Science and Technology of Japan (MEXT) and JSPS KAKENHI Grant number JP19K15668. M.Y. is grateful for the support by the 111 project (B18030) from China.
Publisher Copyright:
Copyright © 2020 American Chemical Society.
PY - 2020/6/10
Y1 - 2020/6/10
N2 - In recent years, organic electrode materials have been strongly considered for use in sustainable batteries. However, most organic electrode materials have low electrical conductivity and require a lot of conductive additives, which decrease the effective capacity based on the entire electrode weight/volume. In this study, we propose a novel electrical conductivity-relay system that imparts electrical conductivity to organic small molecular electrodes without any conductive additive throughout the charge/discharge cycles. It consists of the combination of the charge-transfer phenomenon in a pristine state and the formation of organic radical salts in redox states. Herein, we demonstrate this electrical conductivity-relay system using a simply mixed molecular crystal couple of tetrathiafulvalene (TTF) and tetracyanoquinodimethane (TCNQ) as a cathode without any conductive additive and aqueous sodium bromide as an electrolyte. During charge/discharge, the electrical conductivity of the cathode is supported by charge-transfer at the TTF/TCNQ interface and (TTF)Brn (0.7 ≤ n ≤ 0.8) and NaTCNQ radical salts, and the cathode exhibits a specific capacity of 112 mAh g-1 and a retention rate of 80.7% at the 30th cycle. Furthermore, the molecular crystal couple electrode of TTF and TCNQ shows better charge/discharge performance than the pure charge-transfer complex electrode, indicating that this system expands candidates for organic electrode materials to various pairs and mixing ratios of small molecules that do not form charge-transfer complexes.
AB - In recent years, organic electrode materials have been strongly considered for use in sustainable batteries. However, most organic electrode materials have low electrical conductivity and require a lot of conductive additives, which decrease the effective capacity based on the entire electrode weight/volume. In this study, we propose a novel electrical conductivity-relay system that imparts electrical conductivity to organic small molecular electrodes without any conductive additive throughout the charge/discharge cycles. It consists of the combination of the charge-transfer phenomenon in a pristine state and the formation of organic radical salts in redox states. Herein, we demonstrate this electrical conductivity-relay system using a simply mixed molecular crystal couple of tetrathiafulvalene (TTF) and tetracyanoquinodimethane (TCNQ) as a cathode without any conductive additive and aqueous sodium bromide as an electrolyte. During charge/discharge, the electrical conductivity of the cathode is supported by charge-transfer at the TTF/TCNQ interface and (TTF)Brn (0.7 ≤ n ≤ 0.8) and NaTCNQ radical salts, and the cathode exhibits a specific capacity of 112 mAh g-1 and a retention rate of 80.7% at the 30th cycle. Furthermore, the molecular crystal couple electrode of TTF and TCNQ shows better charge/discharge performance than the pure charge-transfer complex electrode, indicating that this system expands candidates for organic electrode materials to various pairs and mixing ratios of small molecules that do not form charge-transfer complexes.
KW - charge-transfer
KW - conductive additive-free cathode
KW - organic battery
KW - radical salt
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U2 - 10.1021/acsami.0c03642
DO - 10.1021/acsami.0c03642
M3 - Article
C2 - 32412238
AN - SCOPUS:85086345947
SN - 1944-8244
VL - 12
SP - 25748
EP - 25755
JO - ACS applied materials & interfaces
JF - ACS applied materials & interfaces
IS - 23
ER -