Lead-free halide double perovskite nanocrystals have emerged as one of the most promising alternatives to lead halide perovskite nanocrystals due to their non-toxicity, high stability, and outstanding optoelectronic properties. However, conventional synthesis methods often result in impurities due to increased constituent elements. In this study, an efficient water-oil biphasic interface-driven approach is introduced for synthesizing lead-free double perovskite nanocrystals, enabling controlled structural transformations from 0D to 2D and 3D structures. Starting from 0D CsBiBr, a gradual cation exchange is achieved, forming 3D CsAgBiBr. Real-time monitoring reveals the slow insertion of Ag ions as the key to the structural transformation. The resulting CsAgBiBr nanocrystals exhibit exceptional stability, maintaining their integrity for over 120 days under ambient conditions without significant degradation, showing no considerable material decomposition. Additionally, this method allows for the successful synthesis of 2D layered double perovskite CsZnBiBr, which has not previously been reported in experimental studies. This biphasic synthesis strategy provides a universal and reliable method for producing high-quality double perovskite nanocrystals while offering valuable insights into their structural dynamics and properties.
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http://dx.doi.org/10.1002/advs.202416046 | DOI Listing |
ACS Appl Mater Interfaces
March 2025
State Key Laboratory of Molecular Engineering of Polymers, Collaborative Innovation Center of Polymers and Polymer Composite Materials, Department of Macromolecular Science, Fudan University, Shanghai 200433, P. R. China.
Perovskite has attracted extensive attention in the realm of photovoltaic and light-emitting diodes (LEDs) on account of its outstanding photoelectric properties. Perovskite-type quantum wells (QW) have been developed for high-efficiency perovskite-type LEDs. However, there are few reports on the in situ quantum well structure formed by a bimetallic antiperovskite and its properties.
View Article and Find Full Text PDFChem Asian J
March 2025
Jawaharlal Nehru Centre for Advanced Scientific Research, New Chemistry Unit & Internation Centre for Materials Science, Jakkur P. O., 560064, Bangalore, INDIA.
TMA)2SnX6 (TMA = tetramethylammonium; X = Cl, Br, I) compounds form vacancy-ordered halide double perovskites (VODPs) with TMA+ cation in the A-site, Sn4+ cation in the M-site and X- anion in the halide site. This study reports the synthesis and structural phase transition of (TMA)₂SnCl₆, (TMA)2SnCl0.7Br5.
View Article and Find Full Text PDFSmall
March 2025
The State Key Laboratory of Luminescent Materials and Devices, Guangdong Provincial Key Laboratory of Fiber Laser Materials and Applied Techniques, Guangdong Engineering Technology Research and Development Center of Special Optical Fiber Materials and Devices, School of Physics and Optoelectronics, South China University of Technology, Guangzhou, 510641, China.
Temperature evolution is critical in monitoring the status of Li-ion batteries (LIBs), however, it is a challenge to develop precise thermometry down to the nanoscale regime and instantly detect the internal temperature of pouch-type LIBs. Herein, a Boltzmann type luminescence thermometry is designed and prepared in halide double perovskite CsNaLuCl:Yb/Er upconversion nanocrystals and further fabricate the flexible fluorescence polymer optical fiber (POF) sensor for their in situ and real-time temperature monitoring. The thermally enhanced upconversion luminescence of the nanocrystals thermometry ensures sensitive temperature sensing in a wide temperature range, and the POF sensor exhibits stable and repeatable responses to temperature with a deviation of ±0.
View Article and Find Full Text PDFJ Am Chem Soc
March 2025
Beijing National Laboratory for Condensed Matter Physics, Institute of Physics, Chinese Academy of Sciences, Beijing 100190, China.
Colossal magnetoresistance (CMR) effects have been extensively studied in ABO perovskite manganites where the Mn-O-Mn double-exchange mechanism plays a pivotal role. However, A-site-ordered AA'BO-type quadruple perovskite oxides exhibit significantly suppressed double exchange due to their extremely small B-O-B bond angles (≈140°), hindering the realization of intrinsic CMR effects. Here, we report the design and synthesis of a novel quadruple perovskite oxide Pb(PbHg)MnO (PPHMO) characterized by an unusually increased Mn-O-Mn bond angle of up to 153°.
View Article and Find Full Text PDFInorg Chem
March 2025
State Key Laboratory of Inorganic Synthesis and Preparative Chemistry, College of Chemistry, Jilin University, Changchun 130012, China.
Tunable multicolor luminescence materials can flexibly meet the needs of smart lighting, enabling efficient light energy use and minimizing waste. Lead-free hybrid double perovskites AMM(NO) hold great potential in luminescence, benefiting from their tunable composition, high light absorption, low synthesis cost, and environmental friendliness. However, achieving tunable multicolor emission within a single matrix of these materials has yet to be realized.
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