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Asymmetric Electron Acceptors for High-Efficiency and Low-Energy-Loss Organic Photovoltaics

Li, Shuixing (författare)
Zhejiang Univ, Peoples R China
Zhan, Lingling (författare)
Zhejiang Univ, Peoples R China
Jin, Yingzhi (författare)
Linköpings universitet,Biomolekylär och Organisk Elektronik,Tekniska fakulteten
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Zhou, Guanqing (författare)
Shanghai Jiao Tong Univ, Peoples R China
Lau, Tsz-Ki (författare)
Chinese Univ Hong Kong, Peoples R China
Qin, Ran (författare)
Zhejiang Univ, Peoples R China
Shi, Minmin (författare)
Zhejiang Univ, Peoples R China
Li, Chang-Zhi (författare)
Zhejiang Univ, Peoples R China
Zhu, Haiming (författare)
Zhejiang Univ, Peoples R China
Lu, Xinhui (författare)
Chinese Univ Hong Kong, Peoples R China
Zhang, Fengling (författare)
Linköpings universitet,Biomolekylär och Organisk Elektronik,Tekniska fakulteten
Chen, Hongzheng (författare)
Zhejiang Univ, Peoples R China
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 (creator_code:org_t)
2020-05-11
2020
Engelska.
Ingår i: Advanced Materials. - : WILEY-V C H VERLAG GMBH. - 0935-9648 .- 1521-4095. ; 32
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • Low energy loss and efficient charge separation under small driving forces are the prerequisites for realizing high power conversion efficiency (PCE) in organic photovoltaics (OPVs). Here, a new molecular design of nonfullerene acceptors (NFAs) is proposed to address above two issues simultaneously by introducing asymmetric terminals. Two NFAs, BTP-S1 and BTP-S2, are constructed by introducing halogenated indandione (A(1)) and 3-dicyanomethylene-1-indanone (A(2)) as two different conjugated terminals on the central fused core (D), wherein they share the same backbone as well-known NFA Y6, but at different terminals. Such asymmetric NFAs with A(1)-D-A(2) structure exhibit superior photovoltaic properties when blended with polymer donor PM6. Energy loss analysis reveals that asymmetric molecule BTP-S2 with six chlorine atoms attached at the terminals enables the corresponding devices to give an outstanding electroluminescence quantum efficiency of 2.3 x 10(-2)%, one order of magnitude higher than devices based on symmetric Y6 (4.4 x 10(-3)%), thus significantly lowering the nonradiative loss and energy loss of the corresponding devices. Besides, asymmetric BTP-S1 and BTP-S2 with multiple halogen atoms at the terminals exhibit fast hole transfer to the donor PM6. As a result, OPVs based on the PM6:BTP-S2 blend realize a PCE of 16.37%, higher than that (15.79%) of PM6:Y6-based OPVs. A further optimization of the ternary blend (PM6:Y6:BTP-S2) results in a best PCE of 17.43%, which is among the highest efficiencies for single-junction OPVs. This work provides an effective approach to simultaneously lower the energy loss and promote the charge separation of OPVs by molecular design strategy.

Ämnesord

NATURVETENSKAP  -- Kemi -- Teoretisk kemi (hsv//swe)
NATURAL SCIENCES  -- Chemical Sciences -- Theoretical Chemistry (hsv//eng)

Nyckelord

asymmetric acceptors; charge separation; molecular design strategies; nonfullerene acceptors; organic photovoltaics

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