The open circuit voltage (V) losses at multiple interfaces within perovskite solar cells (PSCs) limit the improvements in power conversion efficiency (PCE). Herein, a tailored strategy is proposed to reduce the energy offset at both hetero-interfaces within PSCs to decrease the V losses. For the interface of perovskite and electron transport layer where exists a mass of defects, it uses the pyromellitic acid to serve as a molecular bridge, which reduces non-radiative recombination and energy level offset. For the interface of perovskite and hole transport layer, which includes a passivator of PEAI, the detrimental effect (negative shift of work function) of PEAI passivation and optimizing the interface energy level alignment are neutralized by incorporating (2-(4-(bis(4-methoxyphenyl)amino)phenyl)-1-cyanovinyl)phosphonic acid. Owing to synergistically reduced hetero-interface energy offset, the PSCs achieve a PCE of 25.13%, and the V is increased from 1.134 to 1.174 V. In addition, the resulting PSCs possess enhanced stability, the unencapsulated PSCs can maintain ≈96% and ≈97% of their initial PCE after 2000 h of aging under ambient conditions and 210 h under operation conditions.

Download full-text PDF

Source
http://dx.doi.org/10.1002/smll.202312067DOI Listing

Publication Analysis

Top Keywords

energy offset
12
voltage losses
8
hetero-interface energy
8
perovskite solar
8
solar cells
8
interface perovskite
8
transport layer
8
energy level
8
energy
5
pscs
5

Similar Publications

The growing demand for efficient, stable, and environmentally friendly photovoltaic technologies has motivated the exploration of nontoxic perovskite materials such as KGeCl. However, the performance of KGeCl-based perovskite solar cells (PSCs) depends heavily on the compatibility of charge transport layers (CTLs) and optimization of device parameters. In this study, six PSC configurations were simulated using SCAPS-1D software, incorporating CTLs such as Alq, CSTO, VO, PB, and SbS.

View Article and Find Full Text PDF

Perovskite solar cells are commonly employed in photovoltaic systems because of their special characteristics. Perovskite solar cells remain efficient, but lead-based absorbers are dangerous, restricting their manufacture. Therefore, studies in the field of perovskite materials are now focusing on investigating lead-free perovskites.

View Article and Find Full Text PDF

Boosting Multicolor Emission Enhancement in Two-Dimensional Covalent-Organic Frameworks via the Pressure-Tuned π-π Stacking Mode.

Nano Lett

January 2025

Synergetic Extreme Condition High-Pressure Science Center, State Key Laboratory of Superhard Materials, College of Physics, Jilin University, Changchun 130012, China.

Covalent-organic frameworks (COFs) are dynamic covalent porous organic materials constructed from emissive molecular organic building blocks. However, most two-dimensional (2D) COFs are nonemissive or weakly emissive in the solid state owing to the intramolecular rotation and vibration together with strong π-π interactions. Herein, we report a pressure strategy to achieve the bright multicolor emission from yellow to red in the 2D triazine triphenyl imine COF (TTI-COF).

View Article and Find Full Text PDF

Objective: Timing calibration is essential for positron emission tomography (PET) system as it enhances timing resolution to improve image quality. Traditionally, positron sources are employed for timing calibration. However, the photons emitted by these sources travel in opposite directions, necessitating that positrons annihilate at multiple locations to collect coincidence data across a greater number of lines of response (LORs).

View Article and Find Full Text PDF

Stack bonding in pentacene and its derivatives.

Phys Chem Chem Phys

January 2025

Department of Chemistry and Biochemistry, Old Dominion University, Norfolk, Virginia 23529, USA.

Understanding the nature of π-stacking interactions is important to molecular recognition, self-assembly, and organic semiconductors. The stack bond order (SBO) model of π-stacking has shown that the conformations of dimers are found at orientations where the combinations of monomer MOs are overall bonding within the stack. DFT calculations show that parallel displaced minima found on the potential energy surface for the π-stacked dimers of pentacene and perfluoropentacene occur when the dimer MOs are constructed from combinations of monomer MOs with an allowed SBO.

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!