Benefiting from the synergistic development of material design, device engineering, and the mechanistic understanding of device physics, the certified power conversion efficiencies (PCEs) of single-junction non-fullerene organic solar cells (OSCs) have already reached a very high value of exceeding 19%. However, in addition to PCEs, the poor stability is now a challenging obstacle for commercial applications of organic photovoltaics (OPVs). Herein, recent progress made in exploring operational mechanisms, anomalous photoelectric behaviors, and improving long-term stability in non-fullerene OSCs are highlighted from a novel and previously largely undiscussed perspective of engineering exciton and charge carrier pathways. Considering the intrinsic connection among multiple temporal-scale photocarrier dynamics, multi-length scale morphologies, and photovoltaic performance in OPVs, this review delineates and establishes a comprehensive and in-depth property-function relationship for evaluating the actual device stability. Moreover, this review has also provided some valuable photophysical insights into employing the advanced characterization techniques such as transient absorption spectroscopy and time-resolved fluorescence imagings. Finally, some of the remaining major challenges related to this topic are proposed toward the further advances of enhancing long-term operational stability in non-fullerene OSCs.

Download full-text PDF

Source
http://dx.doi.org/10.1002/smtd.202300397DOI Listing

Publication Analysis

Top Keywords

engineering exciton
8
exciton charge
8
charge carrier
8
stability non-fullerene
8
non-fullerene oscs
8
stability
5
organic photovoltaic
4
photovoltaic stability
4
stability understanding
4
understanding role
4

Similar Publications

Ultrathin, Friendly Environmental, and Flexible CsPb(Cl/Br)-Silica Composite Film for Blue-Light-Emitting Diodes.

Langmuir

December 2024

Key Laboratory of Photonic Materials and Devices Physics for Oceanic Applications, Ministry of Industry and Information Technology of China, College of Physics and Optoelectronic Engineering, Harbin Engineering University, Harbin 150001, China.

Due to intrinsic defects in blue-light-emitting perovskite materials, the charge carriers are prone to being trapped by the trap states. Therefore, the preparation of efficient blue-light-emitting perovskite materials remains a significant challenge. Herein, CsPb(Cl/Br) nanocrystal (NCs)@SiO structures were fabricated through hydrolyzing (3-aminopropyl)-triethoxysilane (APTS).

View Article and Find Full Text PDF

Research on perovskite light-emitting diodes (PeLEDs) has primarily focused on modulating crystal growth to achieve smaller grain sizes and defect passivation using organic additives. However, challenges remain in controlling the intermolecular interactions between these organic additives and perovskite precursor ions for precise modulation of crystal growth. In this study, we synthesize two triphenylphosphine oxide (TPPO)-based multidentate additives: bidentate hexane-1,6-diyl-bis(oxy-4-triphenylphosphine oxide) (2-TPPO) and tetradentate pentaerythrityl-tetrakis(oxy-4-triphenylphosphine oxide) (4-TPPO).

View Article and Find Full Text PDF

Collective optical properties can emerge from an ordered ensemble of emitters due to interactions between the individual units. Superlattices of halide perovskite nanocrystals exhibit collective light emission, influenced by dipole-dipole interactions between simultaneously excited nanocrystals. This coupling changes both the emission energy and rate compared to the emission of uncoupled nanocrystals.

View Article and Find Full Text PDF

Graphdiyne (GDY) alone as a photocatalyst is unsatisfactory because of its low crystallinity, limited regulation of the band gap, weak photogenerated charge separation, , and heterojunctioning with other materials is necessary to activate the photocatalytic activity of GDY. Through elaborate design, a diacetylene-rich linker (S2) was prepared and employed to construct a crystalline and structurally well-defined GDY-like covalent organic framework (COF, namely S2-TP COF) which merges the merits of both COF and GDY to boost the photocatalytic hydrogen evolution reaction (HER). By theoretical prediction on the donor-acceptor (D-A) pair, two other monoacetylene-bridged COFs (S1-TP COF and S3-TP COF) were prepared for comparison.

View Article and Find Full Text PDF

Carbon nitride grafted with single-atom manganese and 2-hydroxy-4,6-dimethylpyrimidine: A visible-light-driven photocatalyst for enhanced ozonation of organic pollutants.

J Colloid Interface Sci

December 2024

State Key Laboratory of Photocatalysis On Energy and Environment, College of Chemistry, Fuzhou University, Fuzhou 350108, PR China. Electronic address:

The development of durable and highly efficient visible-light-driven photocatalysts is essential for the photocatalytic ozonation process towards degrading organic pollutants. This study presents CN-MA, a novel photocatalyst synthesized by grafting carbon nitride (CN) with single-atom Mn and 2-hydroxy-4,6-dimethylpyrimidine (HDMP) via one-step thermal polymerization. Experimental characterization and theoretical calculation results reveal that incorporating single-atom Mn and HDMP into CN alters the charge density distribution on the heptazine rings.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!