A two-dimensional halogenated thiophene side-chain strategy for balancing V oc and J sc and improving efficiency of non-fullerene small molecule acceptor-based organic solar cells

A two-dimensional (2D) halogenated thiophene side chain strategy was proposed and two new 2D halogenated electron-rich fused central core units, FBDT and ClBDT , based on linear benzo[1,2- b :4,5- b ′]di(cyclopenta[2,1- b :3,4- b ′]dithiophene) with fluorinated and chlorinated thiophene side chains...

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Veröffentlicht in:Journal of materials chemistry. A, Materials for energy and sustainability Materials for energy and sustainability, 2019-09, Vol.7 (35), p.20274-20284
Hauptverfasser: Yuan, Gui-Zhou, Fan, Haijun, Wan, Shi-Sheng, Jiang, Zhao, Liu, Yan-Qiang, Liu, Kai-Kai, Bai, Hai-Rui, Zhu, Xiaozhang, Wang, Jin-Liang
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container_issue 35
container_start_page 20274
container_title Journal of materials chemistry. A, Materials for energy and sustainability
container_volume 7
creator Yuan, Gui-Zhou
Fan, Haijun
Wan, Shi-Sheng
Jiang, Zhao
Liu, Yan-Qiang
Liu, Kai-Kai
Bai, Hai-Rui
Zhu, Xiaozhang
Wang, Jin-Liang
description A two-dimensional (2D) halogenated thiophene side chain strategy was proposed and two new 2D halogenated electron-rich fused central core units, FBDT and ClBDT , based on linear benzo[1,2- b :4,5- b ′]di(cyclopenta[2,1- b :3,4- b ′]dithiophene) with fluorinated and chlorinated thiophene side chains have been developed for the first time, respectively. Then, a family of multihalogenated A–D–A structured non-fullerene small molecule acceptors (NF-SMAs), namely HBDT-4Cl , FBDT-4Cl and ClBDT-4Cl , based on the same dichlorinated 1,1-dicyanomethylene-3-indanone (IC) as the terminal group and three different electron-rich central donor cores (a simple thiophene side chain functionalized central donor core HBDT , its fluorinated analogue FBDT , and its chlorinated analogue ClBDT ), respectively, were synthesized for high performance organic solar cells. Compared to nonhalogenated analogues, HBDT-4Cl , FBDT-4Cl and ClBDT-4Cl exhibit slightly wider bandgaps and enhanced molar absorption coefficients, slightly down-shifted energy levels, and obviously improved crystallinity in neat thin films. After blending with the polymer donor PBDB-T-2F , the as-cast FBDT-4Cl / PBDB-T-2F blend films show the highest and most balanced hole/electron mobilities, the highest charge dissociation and collection efficiency, and the most proper phase separation feature among these blend films. Thus, the as-cast FBDT-4Cl / PBDB-T-2F based device exhibits the best power conversion efficiency (PCE) of 12.36%, which is higher than that of ClBDT-4Cl (11.65%) and HBDT-4Cl (10.35%) based devices owing to the higher J sc and FF. The PCE of 12.36% is the highest value for fluorinated central core functionalized NF-SMA-based binary organic solar cells. Our results revealed that introduction of halogenated thiophene side chains, especially fluorinated thiophene side chains, in an electron-rich fused central core is an effective strategy to achieve high-performance two-dimensional aromatic side-chain functionalized NF-SMAs.
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Then, a family of multihalogenated A–D–A structured non-fullerene small molecule acceptors (NF-SMAs), namely HBDT-4Cl , FBDT-4Cl and ClBDT-4Cl , based on the same dichlorinated 1,1-dicyanomethylene-3-indanone (IC) as the terminal group and three different electron-rich central donor cores (a simple thiophene side chain functionalized central donor core HBDT , its fluorinated analogue FBDT , and its chlorinated analogue ClBDT ), respectively, were synthesized for high performance organic solar cells. Compared to nonhalogenated analogues, HBDT-4Cl , FBDT-4Cl and ClBDT-4Cl exhibit slightly wider bandgaps and enhanced molar absorption coefficients, slightly down-shifted energy levels, and obviously improved crystallinity in neat thin films. After blending with the polymer donor PBDB-T-2F , the as-cast FBDT-4Cl / PBDB-T-2F blend films show the highest and most balanced hole/electron mobilities, the highest charge dissociation and collection efficiency, and the most proper phase separation feature among these blend films. Thus, the as-cast FBDT-4Cl / PBDB-T-2F based device exhibits the best power conversion efficiency (PCE) of 12.36%, which is higher than that of ClBDT-4Cl (11.65%) and HBDT-4Cl (10.35%) based devices owing to the higher J sc and FF. The PCE of 12.36% is the highest value for fluorinated central core functionalized NF-SMA-based binary organic solar cells. 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A, Materials for energy and sustainability</title><description>A two-dimensional (2D) halogenated thiophene side chain strategy was proposed and two new 2D halogenated electron-rich fused central core units, FBDT and ClBDT , based on linear benzo[1,2- b :4,5- b ′]di(cyclopenta[2,1- b :3,4- b ′]dithiophene) with fluorinated and chlorinated thiophene side chains have been developed for the first time, respectively. Then, a family of multihalogenated A–D–A structured non-fullerene small molecule acceptors (NF-SMAs), namely HBDT-4Cl , FBDT-4Cl and ClBDT-4Cl , based on the same dichlorinated 1,1-dicyanomethylene-3-indanone (IC) as the terminal group and three different electron-rich central donor cores (a simple thiophene side chain functionalized central donor core HBDT , its fluorinated analogue FBDT , and its chlorinated analogue ClBDT ), respectively, were synthesized for high performance organic solar cells. Compared to nonhalogenated analogues, HBDT-4Cl , FBDT-4Cl and ClBDT-4Cl exhibit slightly wider bandgaps and enhanced molar absorption coefficients, slightly down-shifted energy levels, and obviously improved crystallinity in neat thin films. After blending with the polymer donor PBDB-T-2F , the as-cast FBDT-4Cl / PBDB-T-2F blend films show the highest and most balanced hole/electron mobilities, the highest charge dissociation and collection efficiency, and the most proper phase separation feature among these blend films. Thus, the as-cast FBDT-4Cl / PBDB-T-2F based device exhibits the best power conversion efficiency (PCE) of 12.36%, which is higher than that of ClBDT-4Cl (11.65%) and HBDT-4Cl (10.35%) based devices owing to the higher J sc and FF. The PCE of 12.36% is the highest value for fluorinated central core functionalized NF-SMA-based binary organic solar cells. 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A, Materials for energy and sustainability</jtitle><date>2019-09-10</date><risdate>2019</risdate><volume>7</volume><issue>35</issue><spage>20274</spage><epage>20284</epage><pages>20274-20284</pages><issn>2050-7488</issn><eissn>2050-7496</eissn><abstract>A two-dimensional (2D) halogenated thiophene side chain strategy was proposed and two new 2D halogenated electron-rich fused central core units, FBDT and ClBDT , based on linear benzo[1,2- b :4,5- b ′]di(cyclopenta[2,1- b :3,4- b ′]dithiophene) with fluorinated and chlorinated thiophene side chains have been developed for the first time, respectively. Then, a family of multihalogenated A–D–A structured non-fullerene small molecule acceptors (NF-SMAs), namely HBDT-4Cl , FBDT-4Cl and ClBDT-4Cl , based on the same dichlorinated 1,1-dicyanomethylene-3-indanone (IC) as the terminal group and three different electron-rich central donor cores (a simple thiophene side chain functionalized central donor core HBDT , its fluorinated analogue FBDT , and its chlorinated analogue ClBDT ), respectively, were synthesized for high performance organic solar cells. Compared to nonhalogenated analogues, HBDT-4Cl , FBDT-4Cl and ClBDT-4Cl exhibit slightly wider bandgaps and enhanced molar absorption coefficients, slightly down-shifted energy levels, and obviously improved crystallinity in neat thin films. After blending with the polymer donor PBDB-T-2F , the as-cast FBDT-4Cl / PBDB-T-2F blend films show the highest and most balanced hole/electron mobilities, the highest charge dissociation and collection efficiency, and the most proper phase separation feature among these blend films. Thus, the as-cast FBDT-4Cl / PBDB-T-2F based device exhibits the best power conversion efficiency (PCE) of 12.36%, which is higher than that of ClBDT-4Cl (11.65%) and HBDT-4Cl (10.35%) based devices owing to the higher J sc and FF. The PCE of 12.36% is the highest value for fluorinated central core functionalized NF-SMA-based binary organic solar cells. Our results revealed that introduction of halogenated thiophene side chains, especially fluorinated thiophene side chains, in an electron-rich fused central core is an effective strategy to achieve high-performance two-dimensional aromatic side-chain functionalized NF-SMAs.</abstract><doi>10.1039/C9TA06311K</doi><tpages>11</tpages><orcidid>https://orcid.org/0000-0002-6812-0856</orcidid><orcidid>https://orcid.org/0000-0001-5726-3336</orcidid><orcidid>https://orcid.org/0000-0002-6231-4799</orcidid></addata></record>
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title A two-dimensional halogenated thiophene side-chain strategy for balancing V oc and J sc and improving efficiency of non-fullerene small molecule acceptor-based organic solar cells
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