Lead halide perovskites are widely recognized for their exceptional defect tolerance, setting the benchmark for high-performance optoelectronic applications. Conversely, low-toxicity perovskite-inspired materials (PIMs) typically exhibit suboptimal optoelectronic performance, primarily due to their intrinsic susceptibility to defects. In this study, we address this limitation by exploring the effects of halide vacancies in PIMs through the synthesis of non-stoichiometric CsBiBrI microcrystals (MCs) with a trigonal crystal structure, incorporating iodine vacancies. Density functional theory simulations reveal that these iodine vacancies introduce benign mid-gap states that facilitate charge transport without perturbing band-edge excitons. As a result, the MCs exhibit sharp photoluminescence emission with a linewidth of 140 meV and a minimal Stokes shift of 147 meV, indicative of efficient band-edge recombination. Transient absorption measurements confirm photo induced mid-gap absorption, while space charge limited current measurements demonstrate low trap densities of 1.1 × 10 cm, despite the presence of iodine vacancies. We further fabricated self-driven broadband photodetectors using 2D-CsBiBrI MCs, achieving a high responsivity of 0.9 A W with a photoresponse extending to 800 nm. While ultrafast carrier localization remains a performance-limiting factor, the room-temperature carrier mobility exceeds 1 cm V s, positioning Cs-Bi-Br-I as a highly promising low-toxicity absorber for advanced optoelectronic and light-harvesting applications.
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http://dx.doi.org/10.1039/d4mh01532k | DOI Listing |
Mater Horiz
March 2025
School of Applied & Interdisciplinary Sciences, Indian Association for the Cultivation of Science, Jadavpur, Kolkata 700032, India.
Lead halide perovskites are widely recognized for their exceptional defect tolerance, setting the benchmark for high-performance optoelectronic applications. Conversely, low-toxicity perovskite-inspired materials (PIMs) typically exhibit suboptimal optoelectronic performance, primarily due to their intrinsic susceptibility to defects. In this study, we address this limitation by exploring the effects of halide vacancies in PIMs through the synthesis of non-stoichiometric CsBiBrI microcrystals (MCs) with a trigonal crystal structure, incorporating iodine vacancies.
View Article and Find Full Text PDFAdv Colloid Interface Sci
March 2025
School of Advanced Chemical Sciences, Faculty of Basic Sciences, Shoolini University, Solan, HP 173229, India. Electronic address:
Defect engineering represents a paradigm shift in tailoring nanomaterials for enhanced catalytic performance across various applications. This manuscript succinctly highlights the significance of defect engineering in improving the catalytic performance of BiOI nanoparticles for multiple applications, particularly in photocatalysis. The photocatalytic process of BiOI semiconductor is intricately linked to its indirect bandgap and layered crystalline structure.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
March 2025
College of Materials Science and Engineering, Beijing University of Technology, No.100 Pingleyuan, Chaoyang District, Beijing, 100124, P.R. China.
Hydrogen vacancies (V) were considered major non-radiative recombination centers in hybrid perovskites. By employing a multiscale approach that combines first-principles calculations and molecular dynamics (MDs) simulations, our findings indicated that the V impact was overestimated due to the previous metastable V configurations. The organic molecules with V located on either the nitrogen or carbon atom act as the ligands that form energetically stable dimers with Pb cations.
View Article and Find Full Text PDFPhys Chem Chem Phys
March 2025
Chair of Computational Materials Design, Faculty of Materials Science, Kim Il Sung University, Ryongnam-Dong, Taesong District, Pyongyang, Democratic People's Republic of Korea.
Halide perovskite (HP) composites with transition metal dichalcogenides (TMDs) have attracted attention as promising photocatalysts for hydrogen production through solar-driven water splitting but their working mechanism is yet unclear. Here, we propose novel heterostructures composed of all-inorganic HP β-CsPbI and metallic TMD 1T-MoS and investigate the influence of interfacial vacancies on their interfacial properties using first-principles calculations. Using CsPbI(001)/MoS(001) interface slab models with a minimal lattice mismatch, we calculate the interface formation and interlayer binding energies, finding that the PbI-terminated interfaces have better stability and stronger binding strength than the CsI-terminated ones and iodine vacancy enhances the binding properties.
View Article and Find Full Text PDFAdv Mater
February 2025
Australia Institute for Bioengineering and Nanotechnology (AIBN), The University of Queensland, Brisbane, QLD, 4072, Australia.
The electrostatic interaction between zinc ions and the host structure significantly limits the practicality of vanadium-based cathodes in aqueous zinc-ion batteries (AZIBs). Herein, an anion doping strategy is demonstrated to mitigate electrostatic resistance and steric hindrance during zinc ion insertion by incorporating iodine atoms into the lattice of the cathode material, NaVO·3HO. Iodine doping reduces the adsorption energy at the most stable site, thereby weakening the Zn-host interaction and lowering the Zn diffusion energy barrier, resulting in a one-order-of-magnitude increase in the diffusion coefficient.
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