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Donor-acceptor polymers containing thiazole-fused benzothiadiazole acceptor units for organic solar cells.
Nakamura, Tomoya; Ishikura, Yasuhisa; Arakawa, Noriko; Hori, Megumi; Satou, Motoi; Endo, Masaru; Masui, Hisashi; Fuse, Shinichiro; Takahashi, Takashi; Murata, Yasujiro; Murdey, Richard; Wakamiya, Atsushi.
Afiliación
  • Nakamura T; Institute for Chemical Research, Kyoto University Gokasho Uji Kyoto 611-0011 Japan wakamiya@scl.kyoto-u.ac.jp.
  • Ishikura Y; Institute for Chemical Research, Kyoto University Gokasho Uji Kyoto 611-0011 Japan wakamiya@scl.kyoto-u.ac.jp.
  • Arakawa N; Institute for Chemical Research, Kyoto University Gokasho Uji Kyoto 611-0011 Japan wakamiya@scl.kyoto-u.ac.jp.
  • Hori M; Institute for Chemical Research, Kyoto University Gokasho Uji Kyoto 611-0011 Japan wakamiya@scl.kyoto-u.ac.jp.
  • Satou M; Institute for Chemical Research, Kyoto University Gokasho Uji Kyoto 611-0011 Japan wakamiya@scl.kyoto-u.ac.jp.
  • Endo M; Institute for Chemical Research, Kyoto University Gokasho Uji Kyoto 611-0011 Japan wakamiya@scl.kyoto-u.ac.jp.
  • Masui H; Department of Pharmaceutical Sciences, Yokohama University of Pharmacy 601, Matano-cho, Totsuka-ku Yokohama 245-0066 Japan.
  • Fuse S; Laboratory for Chemistry and Life Science, Institute of Innovative Research, Tokyo Institute of Technology 4259 Nagatsuta-cho, Midori-ku Yokohama Kanagawa 226-8503 Japan.
  • Takahashi T; Department of Pharmaceutical Sciences, Yokohama University of Pharmacy 601, Matano-cho, Totsuka-ku Yokohama 245-0066 Japan.
  • Murata Y; Institute for Chemical Research, Kyoto University Gokasho Uji Kyoto 611-0011 Japan wakamiya@scl.kyoto-u.ac.jp.
  • Murdey R; Institute for Chemical Research, Kyoto University Gokasho Uji Kyoto 611-0011 Japan wakamiya@scl.kyoto-u.ac.jp.
  • Wakamiya A; Institute for Chemical Research, Kyoto University Gokasho Uji Kyoto 611-0011 Japan wakamiya@scl.kyoto-u.ac.jp.
RSC Adv ; 9(13): 7107-7114, 2019 Mar 01.
Article en En | MEDLINE | ID: mdl-35519982
ABSTRACT
Two p-type semiconducting donor-acceptor polymers were designed and synthesized for use in organic solar cells. The polymers combine a benzodithiophene (BDT) donor and a thiazole-fused benzothiadiazole (TzBT) acceptor. Two TzBT acceptor units are compared, one with an alkylthio group (P1) and the other with a more strongly electron-withdrawing alkylsulfonyl group (P2) at the fused thiazole ring. The strongly electron-accepting nature of the TzBT unit lowers the lowest unoccupied molecular orbital (LUMO) energy of P1 and P2 relative to that of the BT analog (PBDT-BT), without altering the energy of the highest occupied molecular orbital (HOMO). Despite the smaller optical band gaps, bulk heterojunction organic solar cells fabricated using these polymers in a PC71BM blend showed high open-circuit voltages. The power conversion efficiency (PCE) of the P1-based device reached 6.13%. Though efficiency of the P2-based device was lower, photoelectric conversion extended into the near-IR region up to 950 nm.

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: RSC Adv Año: 2019 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: RSC Adv Año: 2019 Tipo del documento: Article