4.8 Article

Development of Spiro[cyclopenta[1,2-b:5,4-b′]dithiophene-4,9′-fluorene]-Based A-π-D-π-A Small Molecules with Different Acceptor Units for Efficient Organic Solar Cells

期刊

ACS APPLIED MATERIALS & INTERFACES
卷 9, 期 5, 页码 4614-4625

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acsami.6b14114

关键词

spiro[cyclopenta[1,2-b:5,4-b ']dithiophene-4,9 '-fluorene]; A-pi-D-pi-A small molecule; organic solar cells; photovoltaic properties; acceptor unit

资金

  1. National Natural Science Foundation of China [21574111]
  2. Natural Science Foundation of Hunan Province, China [2015JJ3019]
  3. Key Research Foundation of Education Bureau of Hunan Province, China [14A147]
  4. Program for Innovative Research Cultivation Team in University of Ministry of Education of China [1337304]

向作者/读者索取更多资源

Three acceptor-pi-donor-pi-acceptor (A-pi-D-pi-A) small molecules (STFYT, STFRDN, and STFRCN) with Spiro [cydopenta[1,2-b:5,4-b']dithiophene-4,9'-fluorene] (STF) as the central donor unit, terthiophene as the pi-conjugated bridge, indenedione, 3-ethylrhodanine, or 2-(1,1-dicyanomethylene)rhodanine as the acceptor unit are designed, synthesized, and characterized as electron donor materials in solution-processing organic solar cells (OSCs). The effects of the spiro STF-based central core and different acceptors on the molecular configuration, absorption properties, electronic energy levels, carrier transport properties, the morphology of active layers, and photovoltaic properties are investigated in detail. The three molecules exhibit desirable physicochemical features: wide absorption bands (300-850 nm) and high molar absorption coefficients (4.82 X 10(4) to 7.56 X 10(4) M-1 cm(-1)) and relatively low HOMO levels (-5.15 to-5.38 eV). Density functional theory calculations reveal that the spiro STF central core benefits to reduce the steric hindrance effect between the central donor block and terthiophene bridge and suppress excessive intermolecular aggregations. The optimized OSCs based on these molecules deliver power conversion efficiencies (PCEs) of 6.68%, 3.30%, and 4.33% for STFYT, STFRDN, and STFRCN, respectively. The higher PCE of STFYT-based OSCs should be ascribed to its better absorption ability, higher and balanced hole and electron mobilities, and superior active layer morphology as compared to the other two compounds. So far, this is the first example of developing the A-pi-D-pi-A type small molecules with a spiro central donor core for high-performance OSC applications. Meanwhile, these results demonstrate that using spiro central block to construct A-pi-D-pi-A molecule is an alternative and effective strategy for achieving high-performance small molecule donor materials.

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