Your browser doesn't support javascript.
loading
Bispentafluorophenyl-Containing Additive: Enhancing Efficiency and Morphological Stability of Polymer Solar Cells via Hand-Grabbing-Like Supramolecular Pentafluorophenyl-Fullerene Interactions.
Hung, Kai-En; Tsai, Che-En; Chang, Shao-Ling; Lai, Yu-Ying; Jeng, U-Ser; Cao, Fong-Yi; Hsu, Chain-Shu; Su, Chun-Jen; Cheng, Yen-Ju.
Afiliação
  • Hung KE; National Chiao Tung University , Department of Applied Chemistry, University Road, Hsinchu 30010, Taiwan.
  • Tsai CE; National Chiao Tung University , Department of Applied Chemistry, University Road, Hsinchu 30010, Taiwan.
  • Chang SL; National Chiao Tung University , Department of Applied Chemistry, University Road, Hsinchu 30010, Taiwan.
  • Lai YY; Institute of Polymer Science and Engineering, National Taiwan University , No.1, Sec.4, Roosevelt Rd, Taipei 10617, Taiwan.
  • Jeng US; National Synchrotron Radiation Research Center , 101 Hsin-Ann Road, Hsinchu Science Park, Hsinchu 30076, Taiwan.
  • Cao FY; National Tsing Hua University , Department of Chemical Engineering, 101, Section 2, Kuang-Fu Road, Hsinchu 30013, Taiwan.
  • Hsu CS; National Chiao Tung University , Department of Applied Chemistry, University Road, Hsinchu 30010, Taiwan.
  • Su CJ; National Chiao Tung University , Department of Applied Chemistry, University Road, Hsinchu 30010, Taiwan.
  • Cheng YJ; National Synchrotron Radiation Research Center , 101 Hsin-Ann Road, Hsinchu Science Park, Hsinchu 30076, Taiwan.
ACS Appl Mater Interfaces ; 9(50): 43861-43870, 2017 Dec 20.
Article em En | MEDLINE | ID: mdl-29165989
ABSTRACT
A new class of additive materials bis(pentafluorophenyl) diesters (BFEs) where the two pentafluorophenyl (C6F5) moieties are attached at the both ends of a linear aliphatic chain with tunable tether lengths (BF5, BF7, and BF13) were designed and synthesized. In the presence of BF7 to restrict the migration of fullerene by hand-grabbing-like supramolecular interactions induced between the C6F5 groups and the surface of fullerene, the P3HTPC61BMBF7 device showed stable device characteristics after thermal heating at 150 °C for 25 h. The morphologies of the active layers were systematically investigated by optical microscopy, grazing-incidence small-angle X-ray scattering (GISAXS), and atomic force microscopy. The tether length between the two C6F5 groups plays a pivotal role in controlling the intermolecular attractions. BF13 with a long and flexible tether might form a BF13-fullerene sandwich complex that fails to prevent fullerene's movement and aggregation, while BF5 with too short tether length decreases the possibility of interactions between the C6F5 groups and the fullerenes. BF7 with the optimal tether length has the best ability to stabilize the morphology. In sharp contrast, the nonfluorinated BP7 analogue without C6F5-C60 physical interactions does not have the capability of morphological stabilization, unambiguously revealing the necessity of the C6F5 group. Most importantly, the function of BF7 can be also applied to the high-performance PffBT4BT-2ODPC71BM system, which exhibited an original PCE of 8.80%. After thermal heating at 85 °C for 200 h, the efficiency of the PffBT4BT-2ODPC71BMBF7 device only decreased slightly to 7.73%, maintaining 88% of its original efficiency. To the best of our knowledge, this is the first time that the thermal-driven morphological evolution of the high-performance PffBT4BT-2OD polymer has been investigated, and its morphological stability in the inverted device can be successfully preserved by the incorporation of BF7. This research also demonstrates that BF7 is not only effective with PC61BM but also to PC71BM.
Palavras-chave

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: ACS Appl Mater Interfaces Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: ACS Appl Mater Interfaces Ano de publicação: 2017 Tipo de documento: Article