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Efficient hole-transporting materials (HTMs) are important for improving the stability and performance of all-small-molecules organic solar cells (ASM-OSCs) and perovskite solar cells (PSCs). However, low photovoltaic efficiencies, due to challenges in the designing of small molecular electron donors (SMEDs) with ideal energy levels, light absorption, and optoelectronic properties, hinder their widespread usage. This study presents an end-capped molecular engineering strategy to develop highly efficient HTMs for PSCs and donor materials for OSCs. The approach involves integrating acceptor-anchor groups via a thiophene spacer into the anthanthrone (ANT) core with triphenylamine side groups, leading to a series of six newly designed HTMs (AZU1-AZU6). Quantum simulations employing density functional theory (DFT) and time-dependent density functional theory (TD-DFT) methods were conducted to analyze their electronic and photophysical properties. The designed HTMs exhibit an impressive intrinsic charge transfer of 90% and small exciton binding energy (0.11-0.44 eV), facilitating efficient charge separation. The HOMO energy levels of the designed HTMs (- 4.96 to - 5.01 eV) show significant stabilization compared to the reference molecule (- 4.82 eV), promoting better energy level alignment with the perovskite absorber and PCBM polymer. Optical analysis reveals a broad and transparent absorption profile across the visible spectrum (573-737 nm in solvent), minimizing thermalization losses and optimizing light harvesting. The designed HTMs also exhibit smaller hole reorganization energies (0.1427-0.1513 eV) and higher transfer integrals (0.2251-0.2484), suggesting superior hole mobility. Moreover, their higher solvation-free energy values (-22.54 to -32 kJ/mol) indicate enhanced solubility and surface-wetting properties. Notably, the designed HTMs achieve higher open-circuit voltage (V) values (1.57-1.62 V) compared to the reference (1.42 V), underscoring their potential for improved photovoltaic performance. Overall, this study highlights the promising role of ANT-based HTMs in advancing PSC and OSC technology through enhanced charge dynamics and optimized energy levels.
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http://dx.doi.org/10.1007/s10895-025-04309-8 | DOI Listing |
Phys Chem Chem Phys
September 2025
College of Science, Northeast Forestry University, Harbin 150040, Heilongjiang, China.
Hole transport materials (HTMs) are instrumental in determining the performance and stability of perovskite solar cells (PSCs). Consequently, it is essential to develop suitable HTMs that can effectively facilitate hole extraction and transport within PSCs. In this study, we conducted theoretical investigations utilizing quantum chemistry methods on the promising HTM molecule YZT1, which features a diacetylene-based Zn porphyrin as its core moiety and dibutyl aniline as the donor moiety on either side.
View Article and Find Full Text PDFChem Asian J
August 2025
Department of Chemistry, Chung Yuan Christian University, Zhongli, Taoyuan, 320, Taiwan.
The development of efficient and stable hole-transporting materials (HTMs) is critical for advancing perovskite solar cell (PSC) technology. This study presents two novel HTMs, LK-1 and LK-2, based on fused dithienoheterocycle derivatives, namely, dithieno[3,2-f:2',3'-h]quinoxaline (DTQu) and dithieno[3,2-a:2',3'-c]phenazine (DTPh), designed for PSCs. These donor-acceptor-donor (D-A-D) structured HTMs exhibit planar, rigid cores that enhance π-π stacking, improving hole mobility and stability.
View Article and Find Full Text PDFACS Appl Mater Interfaces
August 2025
Ministry of Education and Tianjin Key Laboratory for Photoelectric Materials and Devices, National Demonstration Center for Experimental Function Materials Education, School of Materials Science and Engineering, Tianjin University of Technology, Tianjin 300384, China.
As an essential component in blue perovskite light-emitting diodes (PeLEDs), functionally tailored hole transport materials (HTMs) play a decisive role in reducing the hole injection barrier, mitigating interfacial defects, and thus enhancing device performance. Herein, we report two solution-processable D-π-A hemicyanine dyes, which exhibit asymmetric/symmetric configurations and contain electron-withdrawing groups and Lewis base donors. As multifunctional HTMs, two dyes not only present high hole mobilities with improved energy level alignment in PeLEDs, but also enable the perovskite defects passivation and phases manipulation.
View Article and Find Full Text PDFSmall
July 2025
Institute for Energy Research, School of Energy and Power Engineering, Jiangsu University, Zhenjiang, 212013, China.
High-performance, dopant-free hole transport materials (HTMs) play a crucial role in stabilized perovskite solar cells (PSCs). Skillfully using noncovalent bonding strategies to construct dopant-free HTM is both attractive and challenging. In this work, two dopant-free HTMs with multisite passivation are designed and synthesized.
View Article and Find Full Text PDFPhys Chem Chem Phys
July 2025
School of Natural and Environmental Sciences, Newcastle University, Bedson Building, NE1 7RU, Newcastle upon Tyne, UK.
We report a rapid and controllable solid-state formation process of copper coordination complex hole-transport materials (HTMs) in dye-sensitized solar cells (DSCs), reducing processing times from over 48 h to 20 min. By thermally-induced phase transition of Cu(tmby)-based liquid electrolytes from 50 °C to 110 °C, we demonstrated that a 70 °C post-treatment for 20 min is ideal for creating an amorphous HTM with minimal crystallization. Time-dependent Raman spectra confirmed near-complete solvent removal within 20 min, while scanning electron microscopy highlighted a compact, defect-minimized HTM morphology when 4--butylpyridine was employed -methylbenzimidazole.
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