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Solution-grown metal halide perovskite single crystals have been demonstrated as potential gamma-ray spectrometer. However, the energy resolution of the solution-grown formamidinum lead bromide (FAPbBr) single crystal spectrometer still suffers from strong bulk charge recombination. Here, it is identified that the high bulk charge recombination arises from a gradient Type-I band distribution throughout the crystal. This band distribution is attributed to the strong coordination of solvents with FA⁺ cations, which become incorporated into the perovskite lattice during crystal growth. It is selected a solvent that more easily decomplexed with FA, and successfully obtained FAPbBr single crystals without any trapped solvent molecules in the lattices. The FAPbBr single crystals exhibited a tenfold reduction in bulk charge recombination rate, and this enabled the FAPbBr gamma-ray spectrometer to achieve an energy resolution of 1.47 ± 0.05% for 662 keV Cs gamma rays, which is the best among solution-grown semiconductor detectors. The unencapsulated FAPbBr gamma-ray spectrometer exhibited more than three months of operational and storage stability.
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http://dx.doi.org/10.1002/smll.202503111 | DOI Listing |
J Phys Chem Lett
September 2025
Department of Chemistry and Chemical Biology, University of New Mexico, Albuquerque, New Mexico 87106, United States.
Defects significantly influence charge transport in CHNHPbI (MAPbI) perovskite solar cells, particularly at interfaces. Using quantum dynamics simulation, we reveal a distinct interstitial iodine (I) defect behavior at different positions in the TiO/MAPbI system. In the perovskite bulk-like region, I exhibits high mobility and dissociates detrimental iodine trimers, facilitating small-to-large polaron transition and promoting shallow trap formation.
View Article and Find Full Text PDFNanoscale
September 2025
School of Materials and Energy, University of Electronic Science and Technology of China, Chengdu 611731, China.
Although improving the charging cutoff voltage is an effective strategy to increase its capacity, LiCoO ("LCO") undergoes rapid capacity decay due to severe structural and interface degradations at high voltages. Herein, we proposed a multifunctional surface modification by coating nano-sized entropy materials (Li-La-Ti-Zr-Co-O, Nano-MEO). Nano-MEO rivets were constructed on the surface of LCO, which stabilized the fragile surface.
View Article and Find Full Text PDFNanoscale Horiz
September 2025
Department of Chemistry and Biochemistry, University of California, Los Angeles, California 90095, USA.
Nanostructuring, which shortens lithium-ion diffusion lengths, can help facilitate pseudocapacitive behavior in some battery materials. Here, nanostructured LiNiCoAlO (NCA), with porosity and decreased crystallite size compared to commercial bulk NCA, was synthesized using a colloidal polymer template. Small particles (∼150 nm) were obtained using rapid thermal annealing (RTA), while medium particles (∼300 nm) were obtained with conventional heating.
View Article and Find Full Text PDFNanoscale
September 2025
Institute of Pure and Applied Sciences, University of Tsukuba, 1-1-1 Tennodai, Tsukuba, Ibaraki, 305-8573, Japan.
[1]Benzothieno[3,2-][1]benzothiophene (BTBT)-based molecules exhibit remarkably high hole mobility, sparking interest in their charge transport mechanisms. However, for thin films, the theoretically proposed mixed-orbital charge transport (MOCT) mechanism, which involves the hybridization of different frontier orbitals between neighboring molecules in the bulk, remains unexplored both experimentally and theoretically. In this study, we prepared a monolayer of 2,7-diphenyl-BTBT (DPh-BTBT) with a unique one-dimensional structure and investigated its molecular-level structure and electronic state.
View Article and Find Full Text PDFJ Am Chem Soc
September 2025
Kathleen Lonsdale Materials Chemistry, Department of Chemistry, University College London, London WC1H 0AJ, U.K.
The exceptional performance of ceria (CeO) in catalysis and energy conversion is fundamentally governed by its defect chemistry, particularly oxygen vacancies. The formation of each oxygen vacancy (V) is assumed to be compensated by two localized electrons on cations (Ce). Here, we show by combining theory with experiment that while this 1 V: 2Ce ratio accounts for the global charge compensation, it does not apply at the local scale, particularly in nanoparticles.
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