Highly Stable Polymer Solar Cells Based on Poly(dithienobenzodithiophene-co-thienothiophene)

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• 作者：Nara Shin ; Hui-Jun Yun ; Youngwoon Yoon ; Hae Jung Son ; Sang-Yong Ju ; Soon-Ki Kwon ; BongSoo Kim ; Yun-Hi Kim
• 刊名：Macromolecules
• 出版年：2015
• 出版时间：June 23, 2015
• 年：2015
• 卷：48
• 期：12
• 页码：3890-3899
• 全文大小：609K
• ISSN：1520-5835

文摘

It is important to develop new donor (D)鈥揳cceptor (A) type low band gap polymers for highly stable polymer solar cells (PSCs). Here, we describe the synthesis and photovoltaic properties of two D鈥揂 type low band gap polymers. The polymers consist of dithienobenzodithiophene (DTBDT) moieties with expanded conjugation side groups as donors and 2-ethyl-1-(thieno[3,4-b]thiophen-2-yl)hexan-1-one (TTEH) or 6-octyl-5H-thieno[3鈥?4鈥?4,5]thieno[2,3-c]pyrrole-5,7(6H)-dione (DTPD) as acceptors to give pDTBDT-TTEH and pDTBDT-DTPD polymers, respectively. The pDTBDT-TTEH is quite flat, resulting in a highly crystalline film. In contrast, the pDTBDT-DTPD is highly twisted to yield an amorphous film. Photovoltaic devices based on pDTBDT-TTEH and pDTBDT-DTPD exhibited power conversion efficiencies (PCEs) of 6.74% and 4.44%, respectively. The PCE difference results mainly from morphological differences between the two polymer:PC₇₁BM blend films; the pDTBDT-TTEH polymer formed a nanoscopically networked domains in the blend state, while the pDTBDT-DTPD polymer film contained aggregated domains with large phase separation between the polymer and PC₇₁BM molecules. Importantly, we observed that pDTBDT-TTEH-based devices showed excellent stability鈥攊n air, retaining 95% of the initial PCE after storage for over 1000 h without encapsulation. The high stability of the pDTBDT-TTEH-based device was originated mainly by the crystalline nature of the pDTBDT-TTEH:PC₇₁BM film. This work suggests that designing highly conjugated planar backboned polymers is crucial to improve not only the photovoltaic performance but also the stability of PSCs.