TY - JOUR
T1 - Theoretical Study on the Construction of Efficient Electron Transport Materials with A-DA′D-A Structures toward Efficient Perovskite Solar Cells
AU - Guo, Qian
AU - Li, Quan Song
N1 - Publisher Copyright:
© 2024 American Chemical Society
PY - 2024/5/27
Y1 - 2024/5/27
N2 - Electron transport materials (ETMs) in perovskite solar cells (PSCs) are essential for enhancing photoelectric conversion efficiency, increasing stability, and reducing hysteresis effects. In this work, a series of novel A-DA′D-A type ETMs with an electron-deficient naphthalene diimide (NDI) core as acceptor A′, thiophene rings of different lengths as donors (D), and end groups (A) with different electron-withdrawing ability were designed. The effects of π-conjugation lengths and electronic properties with end-capped engineering, electron transfer mobility, interfacial interaction, and antihumidity have been comprehensively examined using density functional theory (DFT), time-dependent DFT (TD-DFT), and ab initio molecular dynamics (AIMD). The enhanced electron transport and interfacial characteristics along with appropriate energy levels are present in the designed ETMs. Moreover, compared to the parent molecule NDI, the electron mobility of the new ETMs is significantly higher by up to 3 orders of magnitude. In addition, AIMD simulations show that the newly designed molecule NDI-6Th-H has a strong interaction with the perovskite surface, resulting in stronger moisture resistance than NDI. Along with improving knowledge of the structure-property relationship of ETMs, this work offers a set of prospective ETMs for high-performance PSCs.
AB - Electron transport materials (ETMs) in perovskite solar cells (PSCs) are essential for enhancing photoelectric conversion efficiency, increasing stability, and reducing hysteresis effects. In this work, a series of novel A-DA′D-A type ETMs with an electron-deficient naphthalene diimide (NDI) core as acceptor A′, thiophene rings of different lengths as donors (D), and end groups (A) with different electron-withdrawing ability were designed. The effects of π-conjugation lengths and electronic properties with end-capped engineering, electron transfer mobility, interfacial interaction, and antihumidity have been comprehensively examined using density functional theory (DFT), time-dependent DFT (TD-DFT), and ab initio molecular dynamics (AIMD). The enhanced electron transport and interfacial characteristics along with appropriate energy levels are present in the designed ETMs. Moreover, compared to the parent molecule NDI, the electron mobility of the new ETMs is significantly higher by up to 3 orders of magnitude. In addition, AIMD simulations show that the newly designed molecule NDI-6Th-H has a strong interaction with the perovskite surface, resulting in stronger moisture resistance than NDI. Along with improving knowledge of the structure-property relationship of ETMs, this work offers a set of prospective ETMs for high-performance PSCs.
KW - antihumidity
KW - density functional theory
KW - electron transport material
KW - interfacial properties
KW - naphthalene diimide derivatives
KW - perovskite solar cells
UR - http://www.scopus.com/inward/record.url?scp=85193612391&partnerID=8YFLogxK
U2 - 10.1021/acssuschemeng.4c01587
DO - 10.1021/acssuschemeng.4c01587
M3 - Article
AN - SCOPUS:85193612391
SN - 2168-0485
VL - 12
SP - 8225
EP - 8235
JO - ACS Sustainable Chemistry and Engineering
JF - ACS Sustainable Chemistry and Engineering
IS - 21
ER -