TY - JOUR
T1 - Modulating the Mixing Gibbs Free Energy to Enhance Solid–Liquid Phase Separation for High-Performance Organic Solar Cells
AU - He, Xinjun
AU - Chan, Christopher C.S.
AU - Zou, Xinhui
AU - Zhang, Sen
AU - Fong, Patrick Wai Keung
AU - Kim, Jinwook
AU - Li, Gang
AU - Hu, Xiaotian
AU - Ma, Wei
AU - Wong, Kam Sing
AU - Choy, Wallace C.H.
N1 - Funding Information:
This research was supported by the seed funds (Grant Nos. 202011159254 and 202111159113), from the University Grant Council of the University of Hong Kong, the General Research Fund (Grant Nos. 17201819, 17211220, and 17200021), Collaborative Research Fund (Grant Nos. C7035‐20G and C5037‐18G) and Innovation and Technology Fund (MRP/040/21X) from Hong Kong Special Administrative Region, China. K.S.W. would like to acknoweldge the support from Grant C6023‐19G. GIWAXS data were acquired at beamlines 7.3.3 at the Advanced Light Source, which was supported by the Director, Office of Science, Office of Basic Energy Sciences, of the U.S. Department of Energy under Contract No. DE‐AC02‐05CH11231. The authors thank Chenhui Zhu at beamline 7.3.3 for assistance with data acquisition.
Publisher Copyright:
© 2023 Wiley-VCH GmbH.
PY - 2023/3/17
Y1 - 2023/3/17
N2 - Organic solar cells (OSC) feature a hierarchical structure with the electron donor/acceptor layer sandwiched by anode and cathode, which raises the importance of controlling the molecular crystal orientation, domain size, and vertical distribution to facilitate the charge collection at electrodes. However, the similar conjugated backbone of donor/acceptor material and fast film-formation kinetics have led to spinodal-decomposition-orientated phase separation that result in the film presenting an intimately mixed morphology and random molecular orientation. To solve the issue, the mixing Gibbs free energy-triggered solid–liquid phase separation during the film formation process is enhanced by solidifying one component and solvating the other based on a liquid additive. Following the liquid evaporation process, a favorable vertical distribution is obtained. Meanwhile, the prolonged solvation process enlarges the domain size and assists the molecules to diffuse and orient properly, enabling better exciton/charge dynamics during the power conversion processes. As a result, the fabricated devices exhibit a fill factor over 80% and an efficiency of 18.72%, which is one of the top efficiencies for binary OSCs. Insights and a methodology is provided here to manipulate the organic donor/acceptor phase separation in terms of mixing Gibbs free energy.
AB - Organic solar cells (OSC) feature a hierarchical structure with the electron donor/acceptor layer sandwiched by anode and cathode, which raises the importance of controlling the molecular crystal orientation, domain size, and vertical distribution to facilitate the charge collection at electrodes. However, the similar conjugated backbone of donor/acceptor material and fast film-formation kinetics have led to spinodal-decomposition-orientated phase separation that result in the film presenting an intimately mixed morphology and random molecular orientation. To solve the issue, the mixing Gibbs free energy-triggered solid–liquid phase separation during the film formation process is enhanced by solidifying one component and solvating the other based on a liquid additive. Following the liquid evaporation process, a favorable vertical distribution is obtained. Meanwhile, the prolonged solvation process enlarges the domain size and assists the molecules to diffuse and orient properly, enabling better exciton/charge dynamics during the power conversion processes. As a result, the fabricated devices exhibit a fill factor over 80% and an efficiency of 18.72%, which is one of the top efficiencies for binary OSCs. Insights and a methodology is provided here to manipulate the organic donor/acceptor phase separation in terms of mixing Gibbs free energy.
KW - liquid additives
KW - mixing Gibbs free energy
KW - morphology control
KW - organic solar cells
KW - solid–liquid phase separation
UR - http://www.scopus.com/inward/record.url?scp=85148002571&partnerID=8YFLogxK
U2 - 10.1002/aenm.202203697
DO - 10.1002/aenm.202203697
M3 - Journal article
AN - SCOPUS:85148002571
SN - 1614-6832
VL - 13
SP - 1
EP - 10
JO - Advanced Energy Materials
JF - Advanced Energy Materials
IS - 11
M1 - 2203697
ER -