Fused Benzotriazole A-Unit Constructs a D-π-A Polymer Donor for Efficient Organic Photovoltaics.

Herein, we originally developed a fused ring building block as an acceptor unit, namely, 2,6,10-trihydro-carbazole[3,4-c:5,6-c]bis[1,2,5]-triazole (CTA), through fusing two benzotriazoles (BTA) with a pyrrole ring. A p-type polymer PE93 containing the CTA unit exhibits relatively high molecular energy levels and excellent luminescent properties. The PE93:BTA76-based solar cell obtained a device efficiency of 12.16%, with a VOC of 0.94 V and a low nonradiative recombination loss of 0.18 eV. The results suggest that the CTA unit is an efficient acceptor unit to achieve excellent photovoltaic performance.

Recent Advances in Organic Photovoltaic Materials Based on Thiazole-Containing Heterocycles.

Organic solar cells (OSCs) have achieved great progress, driven by the rapid development of wide bandgap electron donors and narrow bandgap non-fullerene acceptors (NFAs). Among a large number of electron-accepting (A) building blocks, thiazole (Tz) and its derived fused heterocycles have been widely used to construct photovoltaic materials, especially conjugated polymers. Benefiting from the electron deficiency, rigidity, high planarity, and enhanced intra/intermolecular interactions of Tz-containing heterocycles, some related photovoltaic materials exhibit proper energy levels, optimized molecular aggregation, and active layer morphology, leading to excellent photovoltaic performance. This review focuses on the progress of Tz-based photovoltaic materials in the field of OSCs. First, the Tz-based donor and acceptor photovoltaic materials are reviewed. Then, the materials based on promising Tz-containing heterocycles, mainly including thiazolo[5,4-d]thiazole (TzTz), benzo[1,2-d:4,5-d']bis(thiazole) (BBTz), and benzo[d]thiazole (BTz) are summarized and discussed. In addition, the new emerging Tz-fused structures and their application in OSCs are introduced. Finally, perspectives and outlooks for the further development of Tz-containing heterocycle-based photovoltaic materials are proposed.

Carboxylate-Containing Wide-Bandgap Polymers for High-Voltage Non-Fullerene Organic Solar Cells.

As one of the polymer modification strategies, carboxylate functionalization has proved effective in downshifting the energy levels and enhancing polymer crystallinity and aggregation. However, high-performance carboxylate-containing polymers are still limited for organic solar cells (OSCs), especially with open-circuit voltage (VOC) above 1.0 V. Herein, we utilize two carboxylate-functionalized wide-band gap (WBG) donor polymers (TTC-F and TTC-Cl) to pair with two WBG electron acceptors (BTA5 and F-BTA5) for high-voltage OSCs. Due to the deeper molecular energy levels, chlorinated polymer TTC-Cl shows higher VOC than fluorinated polymer TTC-F. Furthermore, because of the stronger aggregation in the film, the TTC-Cl-based devices attain suppressed energetic disorders and trap-assisted recombination, decreasing voltage loss and JSC loss. Finally, the TTC-Cl: F-BTA5 blend achieves a higher VOC of 1.17 V and an excellent PCE of 10.98%, one of the best results for high-voltage carboxylate-containing polymers. In addition, the TTC-Cl: BTA5 combination demonstrates the highest VOC of 1.25 V with an ultralow nonradiative energy loss of 0.17 eV. Our results indicate that the carboxylate-containing polymer donors have significant application potential for high-voltage OSCs due to reduced energy loss and improved charge transport and dissociation. Furthermore, the matched absorption spectra with the indoor light sources and low voltage loss promote these material combinations to construct high-performance indoor photovoltaics.