Angular-Shaped 4,10-Dialkylanthradiselenophene and Its Donor鈥揂cceptor Conjugated Polymers: Synthesis, Physical, Transistor, and Photovoltaic Properties

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• 作者：Yu-Ying Lai ; Huan-Hsuan Chang ; Yun-Yu Lai ; Wei-Wei Liang ; Che-En Tsai ; Yen-Ju Cheng
• 刊名：Macromolecules
• 出版年：2015
• 出版时间：October 13, 2015
• 年：2015
• 卷：48
• 期：19
• 页码：6994-7006
• 全文大小：982K
• ISSN：1520-5835

文摘

An angular-shaped and isomerically pure 4,10-di(2-octyl)dodecylanthradiselenophene (aADS) was successfully developed. The expedient synthesis to form the framework of aADS with two lateral side chains regioselectively at its 4,10-positions is via a base-induced propargyl鈥揳llenyl isomerization/6蟺-electrocyclization/aromatization protocol. This pentacyclic distannylated aADS unit was then copolymerized with dithienyldiketopyrrolopyrrole (DPP) and dithienyl-5,6-difluoro-2,1,3-benzothiadiazole (DTFBT) acceptors with different alkyl side chains to afford four donor鈥揳cceptor copolymers: PaADSDPP, PaADSDTFBT-C₄, PaADSDTFBT-C₈, and PaADSDTFBT-C₈C₁₂. UV鈥搗is spectroscopy and cyclic voltammetry revealed that PaADSDPP has the narrowest energy band gap, and PaADSDTFBT-C₈C₁₂ has larger band gap than PaADSDTFBT-C₄ and PaADSDTFBT-C₈. Two layer ONIOM (our own n-layered integrated molecular orbital and molecular mechanics) calculations were implemented to investigate the disparity in optical, electrochemical, and device properties between these polymers. Both experimental and theoretical data suggest that the aliphatic side chains play a significant role in determining the physical, transistor, and photovoltaic properties of the polymers. PaADSDTFBT-C₄ and PaADSDTFBT-C₈ exhibited organic-field-effect-transistor hole mobilities of 2.7 脳 10^鈥? and 1.0 脳 10^鈥? cm² V^鈥? s^鈥?, greatly outperforming that of PaADSDTFBT-C₈C₁₂ with a mobility of 5.4 脳 10^鈥? cm² V^鈥? s^鈥?. Polymer solar cells were fabricated on the basis of ITO/PEDOT:PSS/polymer:PC₇₁BM/Ca/Al configuration. The efficiency decreased as the increase of bulkiness of the aliphatic side chains installed on DTFBT units (4.4% for PaADSDTFBT-C₄, 3.5% for PaADSDTFBT-C₈, 0.3% for PaADSDTFBT-C₈C₁₂). Atomic force microscopy images reveal that the degree of aggregation for the polymer:fullerene blends is influenced significantly by the bulkiness of aliphatic side chain installed on DTFBT. Noticeable aggregation was found for the PaADSDTFBT-C₈C₁₂:PC₇₁BM blend. These results are in good agreement with the computational results elucidating that the intermolecular interactions between the polymers and PC₇₁BM are sterically hindered by the bulky 2-octyldodecyl groups. This work not only presents a promising selenophene-based aADS building block but also provides insights into the side-chain engineering for donor鈥揳cceptor conjugated copolymers.