Enhancing Photoinduced Charge Separation through Donor Moiety in Donor–Acceptor Organic Semiconductors

Three systems were designed, synthesized, and characterized to understand decay processes of photoinduced charge separation in organic semiconductors that are imperative for efficient solar energy conversion. A styrene-based indoline derivative (YD) was used as donor moiety (D), a triazine derivative (TRC) as the first acceptor (A₁), and 9,10-anthraquinone (AEAQ) as a second acceptor (A₂) in constructing two systems, YD-TRC and YD-TRC-AEAQ. The lifetime of the photoinduced charge-separated states in YD-TRC, a D–A₁ system, was found to be 215 ns and that in YD-TRC-AEAQ, a D–A₁–A₂ system, to be 1.14 μs, a 5-fold increase with respect to that of the YD-TRC. These results show that YD is a more effective donor in YD-TRC and YD-TRC-AEAQ systems at forming long-lived charge-separated states compared to a previously reported atriphenylamine derivative (MTPA) that generated charge-separated states with a lifetime of 80 ns in MTPA-TRC and 650 ns in MTPA-TRC-AEAQ. The third system was constructed using a metal-free porphyrin derivative (MHTPP) to form a MHTPP-TRC-AEAQ structure, a D–L (linker)–A system with a charge separation lifetime less than 10 ns. Therefore, the D–A₁–A₂ architecture is the best at generating long-lived charge-separated states and thus is a promising design strategy for organic photovoltaics materials

Enhancing Photoinduced Charge Separation through Donor Moiety in Donor–Acceptor Organic Semiconductors

Three systems were designed, synthesized, and characterized to understand decay processes of photoinduced charge separation in organic semiconductors that are imperative for efficient solar energy conversion. A styrene-based indoline derivative (YD) was used as donor moiety (D), a triazine derivative (TRC) as the first acceptor (A₁), and 9,10-anthraquinone (AEAQ) as a second acceptor (A₂) in constructing two systems, YD-TRC and YD-TRC-AEAQ. The lifetime of the photoinduced charge-separated states in YD-TRC, a D–A₁ system, was found to be 215 ns and that in YD-TRC-AEAQ, a D–A₁–A₂ system, to be 1.14 μs, a 5-fold increase with respect to that of the YD-TRC. These results show that YD is a more effective donor in YD-TRC and YD-TRC-AEAQ systems at forming long-lived charge-separated states compared to a previously reported atriphenylamine derivative (MTPA) that generated charge-separated states with a lifetime of 80 ns in MTPA-TRC and 650 ns in MTPA-TRC-AEAQ. The third system was constructed using a metal-free porphyrin derivative (MHTPP) to form a MHTPP-TRC-AEAQ structure, a D–L (linker)–A system with a charge separation lifetime less than 10 ns. Therefore, the D–A₁–A₂ architecture is the best at generating long-lived charge-separated states and thus is a promising design strategy for organic photovoltaics materials