CsPbBr is a stable, water-resistant, material derived from CsPbBr perovskite and featuring two-dimensional Pb-Br framework separated by Cs layers. Both compounds can coexist at nanolength scale, which often produces conflicting optical spectroscopy results. We present a complete set of polarized Raman spectra of nonluminescent CsPbBr single crystals that reveals the symmetry and frequency of nondegenerate Raman active phonons accessible from the basal (0 0 1) plane. The experimental results are in good agreement with density functional perturbation theory simulations, which suggests that the calculated frequencies of yet unobserved double degenerate Raman and infrared phonons are also reliable. Unlike CsPbBr, the lattice dynamics of CsPbBr is stable as evidenced by the calculated phonon dispersion. The sharp Raman lines and lack of a dynamic-disorder-induced central peak in the spectra at room temperature indicate that the coupling of Cs anharmonic motion to Br atoms, known to cause the dynamic disorder in CsPbBr, is absent in CsPbBr.
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http://dx.doi.org/10.1088/1361-648X/aadeb4 | DOI Listing |
Nanoscale
January 2025
Department of Chemistry, Maulana Azad National Institute of Technology, Bhopal-462003, India.
Mixing different metal ions at the B site of ABX perovskites offers a promising approach for addressing challenges related to toxicity, stability and performance in optoelectronic applications. One such example is CsPbSnBr which addresses the toxicity issue posed by lead while allowing us to tune optoelectronic properties such as the band gap. In this work, nearly monodisperse CsPbSnBr quantum dots (QDs) were synthesized with variable Pb/Sn compositions, CsPbBr, CsPbSnBr and CsPbSnBr.
View Article and Find Full Text PDFACS Nano
January 2025
Key Laboratory of Bioinorganic and Synthetic Chemistry of Ministry of Education, LIFM, GBRCE for Functional Molecular Engineering, School of Chemistry, IGCME, Sun Yat-Sen University, Guangzhou 510275, China.
Lead halide perovskite nanocrystal materials such as CsPbX (X = Cl, Br, and I) have triggered an intense research upsurge due to their excellent scintillation performance. Herein, an crystallization strategy is developed to grow CsPbBr nanocrystals (NCs) within a low-melting-point (280 °C) coordination polymer (CP) glass. The viscosity of coordination glass is reduced through a low-temperature (e.
View Article and Find Full Text PDFSmall
January 2025
Department of Chemistry, National Taiwan University, Taipei, 10617, Taiwan.
Addressing the challenges of the efficiency and stability of red perovskite nanocrystals is imperative for the successful deployment of these materials in displays and lighting applications. the structural dynamic changes of red perovskite quantum dots (PQDs) are explored using a flow chemistry system to solve the above hurdles. First, the ultrabright red-emitting PQDs of CsPb(Br,I) are achieved by adjusting ligand distribution (oleic acid and oleyamine) in combination with different flow rates and equivalence ratios.
View Article and Find Full Text PDFMaterials (Basel)
January 2025
Hainan Engineering Research Center of Tropical Ocean Advanced Optoelectronic Functional Materials, Hainan International Joint Research Center of Marine Advanced Photoelectric Functional Materials, Key Laboratory of Laser Technology and Optoelectronic Functional Materials of Hainan Province, Key Laboratory of Functional Materials and Photoelectrochemistry of Haikou, College of Chemistry and Chemical Engineering, Hainan Normal University, Haikou 571158, China.
The CsPbBr perovskite exhibits strong environmental stability under light, humidity, temperature, and oxygen conditions. However, in all-inorganic perovskite solar cells (PSCs), interface defects between the carbon electrode and CsPbBr limit the carrier separation and transfer rates. We used black phosphorus (BP) nanosheets as the hole transport layer (HTL) to construct an all-inorganic carbon-based CsPbBr perovskite (FTO/c-TiO/m-TiO/CsPbBr/BP/C) solar cell.
View Article and Find Full Text PDFJ Phys Chem Lett
January 2025
Institut de Ciència de Materials de Barcelona, ICMAB-CSIC, Campus UAB, 08193 Bellaterra, Spain.
So far, the striking sign reversal in the near-ambient slope of the gap temperature dependence of colloidal CsPbCl perovskite nanocrystals (NCs) compared to its Br counterpart remains unresolved. Pure bromide NCs exhibit a linear gap increase with increasing temperature, to which thermal expansion and electron-phonon interaction equally contribute. In contrast, the temperature slope for the chlorine compound gap is clearly negative.
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