Thermocleavage of Partial Side Chains in Polythiophenes Offers Appreciable Photovoltaic Efficiency and Significant Morphological Stability

被引:17
|
作者
Son, Sung Yun [1 ]
Samson, Stephanie [2 ]
Siddika, Salma [3 ,4 ]
O'Connor, Brendan T. [4 ,5 ]
You, Wei [1 ]
机构
[1] Univ N Carolina, Dept Chem, Chapel Hill, NC 27599 USA
[2] Univ N Carolina, Dept Appl Phys Sci, Chapel Hill, NC 27599 USA
[3] North Carolina State Univ, Dept Mat Sci & Engn, Raleigh, NC 27695 USA
[4] North Carolina State Univ, Organ & Carbon Elect Labs ORaCEL, Raleigh, NC 27695 USA
[5] North Carolina State Univ, Dept Mech & Aerosp Engn, Raleigh, NC 27695 USA
关键词
POLYMER SOLAR-CELLS; PERFORMANCE; DEGRADATION; TEMPERATURE; SOLUBILITY; COPOLYMERS; INTERFACE; MECHANISM; IMPACT; INDIGO;
D O I
10.1021/acs.chemmater.1c01305
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The intrinsic degradation of conjugated polymer (CP) based solar cells (PSCs) due to morphological change by heat is an outstanding challenge. Increasing the glass transition temperature (T-g) of the materials used in PSCs can largely mitigate the thermal instability, yet most CPs used in high-efficiency PSCs only show low T-g values, mainly due to the long and bulky side chains needed for solution processing of such polymers. Thermally removing cleavable side chains is an effective approach to regain the high T-g of CPs after the film formation, thereby achieving higher stability; however, previous results using polythiophenes only achieved moderate efficiency (0.8% with PC61BM) after a high temperature (300 degrees C) treatment to remove all side chains. To better understand and utilize thermocleavable side chains (TCSs), we explore a series of regioregular polythiophenes having TCSs and hexyl side chains by varying the ratio of different side chains, from 0 mol % TCSs to 100 mol % TCSs at an increment of 20 mol %. Through a systematic investigation, we find that the polymers with more TCSs than hexyl side chains exhibit sufficient stability under a rather harsh condition (100 degrees C, in air and under continuous ambient light). While a complete removal of alkyl chains might offer a higher stability, the device efficiency was very low (similar to 0.14%); by contrast, the polymer having similar to 70 mol % of TCSs achieved the highest efficiency (similar to 1.5%) after alkyl chain cleavage at 200 degrees C and significant morphological stability. Under our stability test (150 degrees C, 24 h and ambient light), these specific polymer:PC61BM based solar cells were able to retain 90% of the original efficiency. These key findings, together with mechanistic understanding of the thermocleavage process, provide valuable insight into the impact of TCS and present a new design rationale to achieve PSCs with both high efficiency and improved stability.
引用
收藏
页码:4745 / 4756
页数:12
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