Radical polymers as interfacial layers in inverted hybrid perovskite solar cells

被引:41
|
作者
Zheng, Luyao [1 ]
Mukherjee, Sanjoy [2 ]
Wang, Kai [1 ]
Hay, Martha E. [2 ]
Boudouris, Bryan W. [2 ,3 ]
Gong, Xiong [1 ]
机构
[1] Univ Akron, Coll Polymer Sci & Polymer Engn, Dept Polymer Engn, Akron, OH 44325 USA
[2] Purdue Univ, Charles D Davidson Sch Chem Engn, W Lafayette, IN 47907 USA
[3] Purdue Univ, Dept Chem, W Lafayette, IN 47907 USA
基金
美国国家科学基金会;
关键词
CHARGE-TRANSPORT; EFFICIENT; RECOMBINATION; HYSTERESIS;
D O I
10.1039/c7ta07732g
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
We report high performance hybrid perovskite solar cells (PSCs) through the introduction of a radical polymer-based copolymer that contains a second moiety capable of undergoing crosslinking through simple exposure to ultraviolet (UV) light, poly(2,2,6,6-tetramethylpiperidinyloxy-4-yl methacrylate)-co-(4-benzoylphenyl methacrylate) (PTMA-BP). The PTMA-BP thin film engineered the surface of a poly(3,4-ethylenedioxythiophene): polystyrene sulfonate (PEDOT:PSS) hole extraction layer (HEL). Systematic investigations indicate that PTMA-BP can induce better band alignment between PEDOT: PSS and perovskite hybrids, reduce interfacial charge carrier recombination, and improve the crystallization of perovskite hybrids that are cast on the top of the HEL. As a result, the stable PSCs incorporated with PTMA-BP exhibit a 15% power conversion efficiency, which is more than a 15% enhancement compared to cells that lacked the PTMA-BP interfacial modifying layer.
引用
收藏
页码:23831 / 23839
页数:9
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