Two-dimensional tin(II) halide perovskites stand as an environmentally benign alternative to Pb(II) halide perovskites. However, they are often challenging to make due to the oxidation of Sn(II) ion to more stable Sn(IV) ion. Here we report hybrid tin bromide and iodide perovskites: (1,4-BDA)Sn(IV)Br and (1,4-BDA)Sn(II)X (where X = Br, I; 1,4-BDA = 1,4-diammoniumbutane) with 0D and 2D structures, respectively. Their synthesis, structural characterization and photophysical properties are reported. They show bandgaps in the 1.94-2.70 eV range.
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http://dx.doi.org/10.1039/d3dt03772j | DOI Listing |
Sci Rep
January 2025
Multifunctional Materials Laboratory, Department of Physics, Indian Institute of Technology Madras, Chennai, 600036, India.
The utilization of single crystals is exponentially growing in optoelectronic devices due to their exceptional benefits, including high phase purity and the absence of grain boundaries. However, achieving single crystals with a porous structure poses significant challenges. In this study, we present a method for fabricating porous single crystals (porous-SC) of CsAgBiBr and related halide double perovskites using an infrared-assisted spin coating technique.
View Article and Find Full Text PDFAdv Mater
January 2025
Department of Chemistry, City University of Hong Kong, Kowloon, 999077, Hong Kong.
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 PDFACS Appl Mater Interfaces
January 2025
State Key Laboratory of Rare Earth Resource Utilization, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Changchun, Jilin 130022, China.
Fluorescence thermometry based on metal halide perovskites is increasingly becoming a hotspot due to its advantages of high detection sensitivity, noninvasiveness, and fast response time. However, it still presents certain technical challenges in practical applications, such as complex synthesis methods, the use of toxic solvents, and being currently mainly based on the visible/first near-infrared light with poor penetration and severe autofluorescence. In this study, we synthesize the second near-infrared (NIR-II) luminescent crystals based on Yb/Nd-doped zero-dimensional CsScCl·HO by a simple "dissolve-dry" method.
View Article and Find Full Text PDFNat Commun
January 2025
State Key Laboratory of Silicon and Advanced Semiconductor Materials, School of Materials Science and Engineering, Zhejiang University, Hangzhou, Zhejiang, China.
The instability of hybrid wide-bandgap (WBG) perovskite materials (with bandgap larger than 1.68 eV) still stands out as a major constraint for the commercialization of perovskite/silicon tandem photovoltaics, yet its correlation with the facet properties of WBG perovskites has not been revealed. Herein, we combine experiments and theoretical calculations to comprehensively understand the facet-dependent instability of WBG perovskites.
View Article and Find Full Text PDFNat Commun
January 2025
Department of Chemistry and Biochemistry, The University of Oklahoma, Norman, OK, 73019, USA.
Surface defect-induced photoluminescence blinking and photodarkening are ubiquitous in lead halide perovskite quantum dots. Despite efforts to stabilize the surface by chemically engineering ligand binding moieties, blinking accompanied by photodegradation still poses barriers to implementing perovskite quantum dots in quantum emitters. To date, ligand tail engineering in the solid state has rarely been explored for perovskite quantum dots.
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