The utility of optoelectronic materials can be greatly reduced by the presence of efficient pathways for nonradiative recombination (NRR). Lead halide perovskites have garnered much attention in recent years as materials for solar energy conversion, because they readily absorb visible light, are easy to synthesize, and have a low propensity for NRR. Here we report a theoretical study of the pathways for NRR in an archetypal lead halide perovskite: CsPbBr. Specifically, we identified a set of conical intersection (CIs) in both a molecule-sized cluster model (CsPbBr) and nanoparticle model (CsPbBr) of the CsPbBr surface. The energies of the minimal energy CIs, corrected for both dynamical electron correlation and spin-orbit coupling, are well above the bulk band gap of CsPbBr, suggesting that these intersections do not provide efficient pathways for NRR in this material. Analysis of the electronic structure at these intersections suggests that the ionic nature of the bonds in CsPbBr may play a role in the high energy of these CIs. The lowest-energy intersections all involve charge transfer over long distances, whether it be across a dissociated bond or between neighboring unit cells.
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http://dx.doi.org/10.1021/acs.jpca.9b00952 | DOI Listing |
ACS Nano
December 2024
Department of Materials Science and Engineering, Technion - Israel Institute of Technology, Haifa 32000, Israel.
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 PDFACS Nano
December 2024
Nanochemistry, Istituto Italiano di Tecnologia, Via Morego 30, Genova 16163, Italy.
We report the synthesis of ethylammonium lead iodide (EAPbI) colloidal nanocrystals as another member of the lead halide perovskites family. The insertion of an unusually large -cation (274 pm in diameter) in the perovskite structure, hitherto considered unlikely due to the unfavorable Goldschmidt tolerance factor, results in a significantly larger lattice parameter compared to the Cs-, methylammonium- and formamidinium-based lead halide perovskite homologues. As a consequence, EAPbI nanocrystals are highly unstable, evolving to a nonperovskite δ-EAPbI polymorph within 1 day.
View Article and Find Full Text PDFJ Am Chem Soc
December 2024
Univ Rennes, ENSCR, CNRS, ISCR-UMR6226, Université de Rennes, Rennes 35042, France.
Metal halide perovskites, including some of their related perovskitoid structures, form a semiconductor class of their own, which is arousing ever-growing interest from the scientific community. With halides being involved in the various structural arrangements, namely, pure corner-sharing MX (M is metal and X is halide) octahedra, for perovskite networks, or alternatively a combination of corner-, edge-, and/or face-sharing for related perovskitoids, they represent the ideal probe for characterizing the way octahedra are linked together. Well known for their inherently large quadrupolar constants, which is detrimental to the resolution of nuclear magnetic resonance spectroscopy, most abundant halide isotopes (Cl, Br, I) are in turn attractive for magnetic field-free nuclear quadrupolar resonance (NQR) spectroscopy.
View Article and Find Full Text PDFDalton Trans
December 2024
Department of Chemical Engineering, Indian Institute of Technology Madras, Adyar, Chennai, Tamil Nadu 600036, India.
Tuning the selectivity and improving the activity of photocatalysts are among the main bottlenecks for the conversion of CO to value-added chemicals. Recently, lead-free halide perovskites have been extensively investigated as photocatalysts for the photoreduction of CO. Herein, we report a composite photocatalyst using CsBiCl and Ir/IrO for the photoreduction of CO.
View Article and Find Full Text PDFAdv Sci (Weinh)
December 2024
State Key Laboratory of Supramolecular Structure and Materials, College of Chemistry, Jilin University, Changchun, 130012, P.R. China.
The filterless single-pixel imaging technology is anticipated to hold tremendous competitiveness in diverse imaging applications. Nevertheless, achieving single-pixel color imaging without a filter remains a formidable challenge. Here a lead-free perovskite hemispherical photodetector is reported for filterless single-pixel color imaging.
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