TY - JOUR
T1 - Revealing Intrinsic Free Charge Generation
T2 - Promoting the Construction of Over 19% Efficient Planar p-n Heterojunction Organic Solar Cells
AU - Wang, Junjie
AU - Li, Yonghai
AU - Bi, Fuzhen
AU - Yang, Chunpeng
AU - Vasilopoulou, Maria
AU - Chu, Junhao
AU - Bao, Xichang
N1 - Publisher Copyright:
© 2025 Wiley-VCH GmbH.
PY - 2025/2/3
Y1 - 2025/2/3
N2 - Due to high binding energy and extremely short diffusion distance of Frenkel excitons in common organic semiconductors at early stage, mechanism of interface charge transfer-mediated free carrier generation has dominated the development of bulk heterojunction (BHJ) organic solar cells (OSCs). However, considering the advancements in materials and device performance, it is necessary to reexamine the photoelectric conversion in current-stage efficient OSCs. Here, we propose that the conjugated materials with specific three-dimensional donor-acceptor conjugated packing potentially exhibit distinctive charge photogeneration mechanism, which spontaneously split Wannier-Mott excitons to free carriers in pure phases. Subsequently, the pure planar p-n heterojunction (PHJ) OSCs based on green orthogonal solvents were prepared and exhibited comparable even greater performance to that of BHJ OSCs. More interestingly, by introducing PVDF-TrFE as intrinsic region to regulate built-in electric field of the device, the planar p-i-n PHJ OSCs achieved much higher efficiency (>18%) and stability. Moreover, a prominent efficiency of over 19% has been obtained via ternary optimization, which is the new efficiency record for PHJ OSCs up to date. This study points towards the distinguishing intrinsic free charge generation mechanism, opens up a new avenue for OSCs to collectively realize high-efficiency, long-term duration, and simplified device engineering for future commercialization.
AB - Due to high binding energy and extremely short diffusion distance of Frenkel excitons in common organic semiconductors at early stage, mechanism of interface charge transfer-mediated free carrier generation has dominated the development of bulk heterojunction (BHJ) organic solar cells (OSCs). However, considering the advancements in materials and device performance, it is necessary to reexamine the photoelectric conversion in current-stage efficient OSCs. Here, we propose that the conjugated materials with specific three-dimensional donor-acceptor conjugated packing potentially exhibit distinctive charge photogeneration mechanism, which spontaneously split Wannier-Mott excitons to free carriers in pure phases. Subsequently, the pure planar p-n heterojunction (PHJ) OSCs based on green orthogonal solvents were prepared and exhibited comparable even greater performance to that of BHJ OSCs. More interestingly, by introducing PVDF-TrFE as intrinsic region to regulate built-in electric field of the device, the planar p-i-n PHJ OSCs achieved much higher efficiency (>18%) and stability. Moreover, a prominent efficiency of over 19% has been obtained via ternary optimization, which is the new efficiency record for PHJ OSCs up to date. This study points towards the distinguishing intrinsic free charge generation mechanism, opens up a new avenue for OSCs to collectively realize high-efficiency, long-term duration, and simplified device engineering for future commercialization.
KW - excellent stability
KW - intrinsic free charge
KW - planar p-n heterojunction organic solar cells
KW - regulated built-in field
KW - specific three-dimensional stacking
UR - https://www.scopus.com/pages/publications/85214994170
U2 - 10.1002/anie.202417143
DO - 10.1002/anie.202417143
M3 - 文章
C2 - 39776226
AN - SCOPUS:85214994170
SN - 1433-7851
VL - 64
JO - Angewandte Chemie - International Edition
JF - Angewandte Chemie - International Edition
IS - 6
M1 - e202417143
ER -