In this work, a series of A-D-A'-D-A-type electron acceptors based on alkylated indacenodithiophene (C8IDT), dicyanated thiophene-flanked 2,1,3-benzothiadiazole (CNDTBT), and 2-(3-oxo-2,3-dihydro-1-inden-1-ylidene)malononitrile (INCN) or 2-(5,6-difluoro-3-oxo-2,3-dihydro-1-inden-1-ylidene) malononitrile (FINCN) are synthesized in order to investigate the effect of substituents on their photovoltaic properties. The corresponding CNDTBT-C8IDT-INCN and CNDTBT-C8IDT-FINCN acceptors vary in their optical, electrochemical, morphological, and charge transport properties. The fluorinated-INCN-based acceptor (CNDTBT-C8IDT-FINCN) exhibits lower energy levels, improved absorptivity, narrower π-π spacing, and prominent fibrillar structures when it is blended with poly[(2,6-(4,8-bis(5-(2-ethylhexyl)thiophen-2-yl)-benzo[1,2-:4,5-']dithiophene))--5,5-(1',3'-di-2-thienyl-5',7'-bis(2-ethylhexyl)benzo [1',2'-:4',5'-']dithiophene-4,8-dione)] (PBDB-T). CNDTBT-C8IDT-FINCN exhibits a high power conversion efficiency (PCE) of 12.33% due to its high and well-balanced charge carrier mobility and distinct face-on orientation. Furthermore, large-area organic solar cells (OSCs) (active area: 55.45 cm) with CNDTBT-C8IDT-FINCN exhibit a high PCE of 9.21%. This result demonstrates that CNDTBT-C8IDT-FINCN is a suitable and promising electron acceptor for large-area OSCs.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1021/acsami.0c13277 | DOI Listing |
ACS Appl Mater Interfaces
January 2025
The Affiliated Cancer Hospital of Xiangya School of Medicine, Central South University/Hunan Cancer Hospital, Changsha 410013, Hunan, People's Republic of China.
In modern computing, the Von Neumann architecture faces challenges such as the memory bottleneck, hindering efficient processing of large datasets and concurrent programs. Neuromorphic computing, inspired by the brain's architecture, emerges as a promising alternative, offering unparalleled computational power while consuming less energy. Artificial synaptic devices play a crucial role in this paradigm shift.
View Article and Find Full Text PDFAcc Chem Res
January 2025
Laboratory for Chemistry and Life Science (CLS), Institute of Integrated Research, Institute of Science Tokyo, 4259 Nagatsuta, Midori-ku, Yokohama 226-8501, Japan.
ConspectusThe design of properties and functions of molecular assemblies requires not only a proper choice of building blocks but also control over their packing arrangements. A highly versatile unit in this context is a particular type of triptycene with substituents at the 1,8,13-positions, called tripodal triptycene, which offers predictable molecular packing and multiple functionalization sites, both at the opposite 4,5,16- or 10 (bridgehead)-positions. These triptycene building blocks are capable of two-dimensional (2D) nested hexagonal packing, leading to the formation of 2D sheets, which undergo one-dimensional (1D) stacking into well-defined "2D+1D" structures.
View Article and Find Full Text PDFACS Nano
December 2024
Key Laboratory of Mesoscopic Chemistry of MOE, School of Chemistry and Chemical Engineering, Nanjing University, Nanjing, Jiangsu, 210023, China.
As the keystones of molecular electronics, high-quality nanodielectric layers are challenging to assemble due to the strictest criteria for their reliability and uniformity over a large area. Here, we report a strained poly(4-vinylphenol) monolayer, ready to be stacked to form defect-free wafer-scale nanodielectrics. The thickness of the nanodielectrics can be precisely adjusted in integral multiples of the 1.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
December 2024
State Key Laboratory and Institute of Elemento-Organic Chemistry, Frontiers Science Center for New Organic Matter, The Centre of Nanoscale Science and Technology and Key Laboratory of Functional Polymer Materials, Renewable Energy Conversion and Storage Center (RECAST), College of Chemistry, Nankai University, Tianjin, 300071, China.
Organic photovoltaic materials that can be processed via non-halogenated solvents are crucial for the large-area manufacturing of organic solar cells (OSCs). However, the limited available of electron acceptors with adequate solubility and favorable molecular packing presents a challenge in achieving efficient non-halogenated solvent-processed OSCs. Herein, inspired by the three-dimensional dimeric acceptor CH8-4, we employed a molecular isomerization strategy to synthesize its isomers, CH8-4A and CH8-4B, by tuning the position of fluorine (F) atom in the central unit.
View Article and Find Full Text PDFAdv Mater
December 2024
Institute for Chemical and Bioengineering, ETH Zürich, Zürich, 8093, Switzerland.
In the last decade, momentous progress in lead halide perovskite (LHP) light-emitting diodes (LEDs) is witnessed as their external quantum efficiency (η) has increased from 0.1 to more than 30%. Indeed, perovskite LEDs (PeLEDs), which can in principle reach 100% internal quantum efficiency as they are not limited by the spin-statistics, are reaching their full potential and approaching the theoretical limit in terms of device efficiency.
View Article and Find Full Text PDFEnter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!