A 2,1,3-Benzooxadiazole Moiety in a D-A-D-type Hole-Transporting Material for Boosting the Photovoltage in Perovskite Solar Cells

被引:43
作者
Wu, Guohua [1 ]
Zhang, Yaohong [2 ]
Kaneko, Ryuji [1 ,3 ]
Kojima, Yoshiyuki [1 ]
Shen, Qing [2 ]
Islam, Ashraful [3 ]
Sugawa, Kosuke [1 ]
Otsuki, Joe [1 ]
机构
[1] Nihon Univ, Coll Sci & Technol, Chiyoda Ku, 1-18-14 Kanda Surugadai, Tokyo 1018308, Japan
[2] Univ Electrocommun, Fac Informat & Engn, Dept Engn Sci, Chofu, Tokyo 1828585, Japan
[3] NIMS, Photovolta Mat Grp, Sengen 1-2-1, Tsukuba, Ibaraki 3050047, Japan
基金
日本科学技术振兴机构;
关键词
HIGH-PERFORMANCE; FACILE SYNTHESIS; EFFICIENT; IMPEDANCE; RECOMBINATION; DERIVATIVES; SEMICONDUCTORS; HYSTERESIS; POLYMERS; ORIGIN;
D O I
10.1021/acs.jpcc.7b04614
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
A donor acceptor donor molecule with a 2,1,3-benzooxadiazole moiety, named BTPA-3, was successfully synthesized and employed as a hole transporting material (HTM) for, Cs-0.05(MA(0.17)FA(0.83))(0.95)Pb(I0.83Br0.17)(3)- and CH3NH3PbBr3-based perovskite solar cells (PSCs). The best CH3NH3PbBr3-based PSC with BTPA-3 exhibited a superior efficiency (5.91%) compared to the cell with spiro-OMeTAD (5.61%), even an 80 mV higher open-circuit voltage (V-oc) being recorded in the reverse scan (average V-oc: 1.41 V for BTPA-3 and 1.33 V for spiro-OMeTAD). The higher V-oc is attributed to larger recombination resistance and the resulting longer photovoltage lifetimes in the cells with BTPA-3. In the meantime, for the Cs-0.05(MA(0.17)FA(0.83))(0.95)Pb(I0.83Br0.17)(3)-based PSC, BTPA-3 exhibited a much lower conversion efficiency (9.81%) compared with the cell with spiro-OMeTAD (13.2%) due to a small driving force for the hole injection. The morphologies and conductivities of the hole-transport layers were also investigated, and the results are discussed in relation to the performances of the PSCs, Finally, PSCs with BTP4-3 as an HTM based on both perovskite lead halide materials exhibited good long-term stabilities.
引用
收藏
页码:17617 / 17624
页数:8
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