The ultraviolet (UV) radiation in the solar spectrum causes most of the decay under sunlight for solar cells based on organic photovoltaics (OPV). One‐year outdoor lifetime still remains challenging for OPV. The lifetime of 2000 h under continuous laboratory light corresponds to a 1 year outdoor lifetime. Herein, the stability of the OPVs is studied under continuous irradiation by a UV light emitting diode of 365 nm with a long tracking time. The intensity of 50 W m−2 is the same as the sunlight UV. The compositions of the active layer and cathode interfacial layer are sensitive to UV irradiation. In general, ternary devices have better UV stability than binary devices. In particular, a good stability is achieved for the ternary device based on the high‐performance blend with poly[(2,6‐(4,8‐bis(5‐(2‐ethylhexyl‐3‐fluoro)thiophen‐2‐yl)‐benzo[1,2‐b:4,5‐b']dithiophene))‐alt‐(5,5‐(1',3'‐di‐2‐thienyl‐5',7'‐bis(2‐ethylhexyl)benzo[1',2'‐c:4',5'‐c']dithiophene‐4,8‐dione)] (PM6) as the donor. The acceptor is 2,2'‐((2Z,2'Z)‐((12,13‐bis(2‐ethylhexyl)‐3,9‐diundecyl‐12,13‐dihydro‐[1,2,5]thiadiazolo[3,4‐e]thieno[2",3":4',5']thieno[2',3':4,5]pyrrolo[3,2‐g]thieno[2',3':4,5]thieno[3,2‐b]indole‐2,10‐diyl)bis(methanylylidene))bis(5,6‐difluoro‐3‐oxo‐2,3‐dihydro‐1H‐indene‐2,1‐diylidene))dimalononitrile (Y6). The fullerene derivative [6,6]‐phenyl C71‐butyric acid methyl ester (PC71BM) is added as the second acceptor, whereas a polymer poly[(2,6‐(4,8‐bis(5‐(2‐ethylhexyl)thiophen‐2‐yl)benzo[1,2‐b:4,5‐b']dithiophene))‐co‐(1,3‐di(5‐thiophene‐2‐yl)‐5,7‐bis(2‐ethylhexyl)benzo[1,2‐c:4,5‐c']dithiophene‐4,8‐dione)] (PBDB‐T) is added as the second donor. For the PM6:Y6 ternary device, the UV half lifetime is 1750 h, which is close to the 2000 h target set by the outdoor of a 1 year lifetime.
The ultraviolet (UV) part in the sunlight is known to cause most damage to organic photovoltaics (OPV). UV filters therefore can improve stability. The lifetime of the UV‐filtered OPV is determined by visible light. Herein, visible sunlight is divided into several bands and modeled by light‐emitting diodes to study the stability of ternary OPV. Poly[(2,6‐(4,8‐bis(5‐(2‐ethylhexyl‐3‐fluoro)thiophen‐2‐yl)‐benzo[1,2‐b:4,5‐b′]dithiophene))‐alt‐(5,5‐(1′,3′‐di‐2‐thienyl‐5′,7′‐bis(2‐ethylhexyl)benzo[1′,2′‐c:4′,5′‐c′]dithiophene‐4,8‐dione)] (PM6) is used as the donor. 2,2′‐((2Z,2′Z)‐((12,13‐bis(2‐ethylhexyl)‐3,9‐diundecyl‐12,13‐dihydro‐[1,2,5]thiadiazolo[3,4‐e]thieno[2",3″:4′,5′]thieno[2′,3′:4,5]pyrrolo[3,2‐g]thieno[2′,3′:4,5]thieno[3,2‐b]indole‐2,10‐diyl)bis(methanylylidene))bis(5,6‐difluoro‐3‐oxo‐2,3‐dihydro‐1H‐indene‐2,1‐diylidene))dimalononitrile (Y6) is used as the acceptor. Another polymer is added as the second donor to improve the stability. As expected, the deep and light blue bands dominate the decay under visible light. After about 1200 h of blue irradiation, the devices enter a relatively stable state up to 3000 h of tracking, in sharp contrast to the continuous decay under UV. No chemical reaction is observed under blue light. Years of outdoor lifetime for nonfullerene OPV are projected with the UV filter.
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