TY - JOUR
T1 - Miscibility driven morphology modulation in ternary solar cells
AU - Yu, Ting
AU - Tintori, Francesco
AU - Zhang, Yuchen
AU - He, Wanting
AU - Cieplechowicz, Edward
AU - Bobba, Raja Sekhar
AU - Kaswekar, Poojan Indrajeet
AU - Jafari, Maziar
AU - Che, Yuxuan
AU - Wang, Yong
AU - Siaj, Mohamed
AU - Izquierdo, Ricardo
AU - Perepichka, Dmytro F.
AU - Qiao, Quinn
AU - Welch, Gregory C.
AU - Ma, Dongling
N1 - Publisher Copyright:
© 2023 The Royal Society of Chemistry
PY - 2023/2/8
Y1 - 2023/2/8
N2 - Organic solar cells (OSCs) are viable power sources for photovoltaic applications. In this work, a non-fullerene acceptor, PDI-EH, was designed to form a nearly orthogonal structure to suppress its aggregation, and integrated into ternary OSCs. In addition to enhanced photon absorption and matched charge cascade, a PDI-EH acceptor modulated the morphology, which is crucial to affect device efficiency. Detailed analysis revealed that PDI-EH can fine-tune the miscibility of the host donor and acceptor (D/A) materials to form an optimally intermixed phase with short-range molecular order. Photo-induced force microscopy (PiFM) for selective PiFM imaging of D/A materials provided strong evidence that D/A materials formed well-mixed films after PDI-EH incorporation. Additionally, nanoscale spatial mapping of charge carrier dynamics was realized for the first time in a ternary film using a novel transient photo-response atomic force microscopy (TP-AFM) technique. The resulting TP-AFM data revealed a reduced charge transport time, increased charge recombination lifetime and extended charge diffusion length. These improvements brought about by PDI-EH benefit the photovoltaic performance of ternary OSCs under both 1-sun and indoor illuminations. Our work offers insights into morphology modulation and the resulting local charge carrier dynamic, thereby facilitating the development of OSCs in practical applications.
AB - Organic solar cells (OSCs) are viable power sources for photovoltaic applications. In this work, a non-fullerene acceptor, PDI-EH, was designed to form a nearly orthogonal structure to suppress its aggregation, and integrated into ternary OSCs. In addition to enhanced photon absorption and matched charge cascade, a PDI-EH acceptor modulated the morphology, which is crucial to affect device efficiency. Detailed analysis revealed that PDI-EH can fine-tune the miscibility of the host donor and acceptor (D/A) materials to form an optimally intermixed phase with short-range molecular order. Photo-induced force microscopy (PiFM) for selective PiFM imaging of D/A materials provided strong evidence that D/A materials formed well-mixed films after PDI-EH incorporation. Additionally, nanoscale spatial mapping of charge carrier dynamics was realized for the first time in a ternary film using a novel transient photo-response atomic force microscopy (TP-AFM) technique. The resulting TP-AFM data revealed a reduced charge transport time, increased charge recombination lifetime and extended charge diffusion length. These improvements brought about by PDI-EH benefit the photovoltaic performance of ternary OSCs under both 1-sun and indoor illuminations. Our work offers insights into morphology modulation and the resulting local charge carrier dynamic, thereby facilitating the development of OSCs in practical applications.
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U2 - 10.1039/d2ta09928d
DO - 10.1039/d2ta09928d
M3 - Article
AN - SCOPUS:85148496808
SN - 2050-7488
VL - 11
SP - 5037
EP - 5047
JO - Journal of Materials Chemistry A
JF - Journal of Materials Chemistry A
IS - 10
ER -