有机太阳能电池
材料科学
富勒烯
接受者
光电流
电子供体
电子受体
吸收(声学)
超快激光光谱学
带隙
光电子学
聚合物太阳能电池
激子
光化学
能量转换效率
光谱学
聚合物
化学
物理
有机化学
催化作用
复合材料
量子力学
凝聚态物理
作者
Yuze Lin,Fuwen Zhao,Shyamal K. K. Prasad,Jing-De Chen,Wanzhu Cai,Jin Zhai,Kai Chen,Yang Chang Wu,Wei Ma,Feng Gao,Yan-Qing Li,Liping Wang,Wei You,Justin M. Hodgkiss,Xiaowei Zhan
标识
DOI:10.1002/adma.201706363
摘要
Relative to electron donors for bulk heterojunction organic solar cells (OSCs), electron acceptors that absorb strongly in the visible and even near-infrared region are less well developed, which hinders the further development of OSCs. Fullerenes as traditional electron acceptors have relatively weak visible absorption and limited electronic tunability, which constrains the optical and electronic properties required of the donor. Here, high-performance fullerene-free OSCs based on a combination of a medium-bandgap polymer donor (FTAZ) and a narrow-bandgap nonfullerene acceptor (IDIC), which exhibit complementary absorption, matched energy levels, and blend with pure phases on the exciton diffusion length scale, are reported. The single-junction OSCs based on the FTAZ:IDIC blend exhibit power conversion efficiencies up to 12.5% with a certified value of 12.14%. Transient absorption spectroscopy reveals that exciting either the donor or the acceptor component efficiently generates mobile charges, which do not suffer from recombination to triplet states. Balancing photocurrent generation between the donor and nonfullerene acceptor removes undesirable constraints on the donor imposed by fullerene derivatives, opening a new avenue toward even higher efficiency for OSCs.
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