In response to the toxic heavy metal absorbers in perovskite solar cells (PSCs), this work focuses on the development of an environmentally friendly simple solution-processed infrared (IR) absorber. In this work, a simple solution-crystallized IR-absorbing AgBiS film is reported by spin-coating silver, bismuth nitrates, and thiourea dissolved in dimethylformamide (DMF) to produce thick AgBiS film. Extensive optimization of the precursor concentrations thicknesses and conductive substrates used allow for obtaining 250 nm AgBiS film with different crystal sizes. When applied as an absorber in solar cells, solution-crystalized AgBiS thick film delivers an extraordinarily high current density of over 31 mA cm. The devices show high stability under continuous 100 mW cm illumination and when stored in the dark for more than six months. When the AgBiS layer is fabricated in a gradient fashion combining one layer of 0.25 m and three layers of 0.5 m precursor concentrations, the efficiency of 5.15% is registered which is the highest reported for the simple solution-crystallized AgBiS films.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11600239PMC
http://dx.doi.org/10.1002/advs.202406998DOI Listing

Publication Analysis

Top Keywords

solar cells
12
agbis film
12
solution-crystalized agbis
8
agbis films
8
density 31 ma
8
simple solution-crystallized
8
precursor concentrations
8
agbis
6
films solar
4
cells generating
4

Similar Publications

Recent advances in the development of enantiopure BODIPYs and some related enantiomeric compounds.

Chem Commun (Camb)

January 2025

Department of Chemistry, Khalifa University, SAN Campus, Abu Dhabi, United Arab Emirates.

During the process of developing smart chiroptical luminophores, small chiral organic dyes have emerged as candidates of utmost importance. In this regard, the chiral variants of boron dipyrromethene (BODIPY) serve as suitable molecules owing to their excellent photophysical properties such as high fluorescence quantum yields, narrow emission bandwidths with high peak intensities, high photo and chemical stability, and higher molar extinction coefficients. Thus, the last decade observed an influx of research from various research groups for the induction of chirality in originally achiral BODIPY.

View Article and Find Full Text PDF

Indium (In) reduction is a hot topic in transparent conductive oxide (TCO) research. So far, most strategies have been focused on reducing the layer thickness of In-based TCO films and exploring TCOs. However, no promising industrial solution has been obtained yet.

View Article and Find Full Text PDF

The advancement of tin-based perovskite solar cells (TPSCs) has been severely hindered by the poor controllability of perovskite crystal growth and the energy level mismatch between the perovskite and fullerene-based electron transport layer (ETL). Here, we synthesized three cis-configured pyridyl-substituted fulleropyrrolidines (PPF), specifically 2-pyridyl (PPF2), 3-pyridyl (PPF3), and 4-pyridyl (PPF4), and utilized them as precursor additives to regulate the crystallization kinetics during film formation. The spatial distance between the two pyridine groups in PPF2, PPF3, and PPF4 increases sequentially, enabling PPF4 to interact with more perovskite colloidal particles.

View Article and Find Full Text PDF

P-Dopant with Spherical Anion for Stable n-i-p Perovskite Solar Cells.

Angew Chem Int Ed Engl

January 2025

EPFL: Ecole Polytechnique Federale de Lausanne, Department of Chemistry, Rue de Industries 17, 1050, Sion, SWITZERLAND.

Li-TFSI/t-BP is the most widely utilized p-dopant for hole-transporting materials (HTMs) in state-of-the-art perovskite solar cells (PSCs). However, its nonuniformity of doping, along with the hygroscopicity and migration of dopants, results in the devices that exhibit limited stability and performance. This study reports the use of a spherical anion of the p-dopant, regulated by its radius and shape, as an alternative to the linear TFSI- anion.

View Article and Find Full Text PDF

Perovskite/silicon tandem solar cells (TSCs) are promising candidates for commercialization due to their outstanding power conversion efficiencies (PCEs). However, controlling the crystallization process and alleviating the phases/composition inhomogeneity represent a considerable challenge for perovskite layers grown on rough silicon substrates, ultimately limiting the efficiency and stability of TSC. Here, this study reports a "halide locking" strategy that simultaneously modulates the nucleation and crystal growth process of wide bandgap perovskites by introducing a multifunctional ammonium salt, thioacetylacetamide hydrochloride (TAACl), to bind with all types of cations and anions in the mixed halide perovskite precursor.

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!