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Cs3Cu2X5
PHYSICAL CHEMISTRY CHEMICAL PHYSICS · 2024 · IF 2.9

Ultrasound-assisted nucleation and growth of hydroxyl-protected and ligand-free Cs3Cu2X5 nanocrystals with bright luminescence

Zhiqun Xu,Dengfeng Luo,Pei Wu,Bo Hou,Zhihao Zhang,Shuqiang Wang,Teng Gao,Guobin Huang,Lan Fang

The commercial applications of lead halide perovskites are hindered by their negative environmental impact and inherent instability. Consequently, developing environmentally friendly copper-based perovskite materials is crucial for future solid-state lighting and display applications. In this study, an ultrafast high-power ultrasonic synthesis strategy was utilized to achieve uniform nucleation and growth of Cs3Cu2X5 (X = Cl, Br, I) nanocrystals (NCs) that possess remarkable luminescence properties, hydroxyl protection, and ligand-free characteristics. These Cs3Cu2X5 NCs exhibited a tunable spectral range spanning from 446 to 525 nm, accompanied by photoluminescence quantum yields (PLQYs) varying from 0.2% to 79.2%. The spectral attributes of the NCs were effectively controlled by modulating the halide type and composition. It is worth noting that density functional theory (DFT) calculations offer valuable insights into the synthesis of NCs and the selection of suitable alcohol solvents. Moreover, we successfully fabricated an efficient and stable white light-emitting diode (WLED) with a high luminous efficiency of 23 lm W−1 and CIE color coordinates of (0.3266, 0.3487). Our work provides a new strategy to synthesize Cs3Cu2X5 NCs and holds promise for their potential application in display and lighting devices.

研究领域: 材料科学 · 光学工程 · 环境科学
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CHEMISTRY OF MATERIALS · 2020 · IF 9.567

Photophysics in Cs3Cu2X5 (X = Cl, Br, or I): Highly Luminescent Self-Trapped Excitons from Local Structure Symmetrization

Linyuan Lian,Moyan Zheng,Peng Zhang,Zhi Zheng,Kang Du,Wen Lei,Jianbo Gao,Guangda Niu,Daoli Zhang,Tianyou Zhai,Shengye Jin,Jiang Tang,Xiuwen Zhang,Jianbing Zhang

Self-trapped excitons (STEs) in metal halide materials are attracting an increasing level of interest due to their unique light emission properties. Light emission from STEs in metal halides is usually associated with excited-state structural deformation, which lowers the symmetry of local structures, as seen for the STEs in a wide range of materials systems. Here, we reveal a prototypic STE-associated structural “distortion” that, however, enhances the symmetry of local structures, in a series of all-inorganic copper(I)-based halides Cs3Cu2X5 (X = Cl, Br, or I). We further find that the emission peaks of Cs3Cu2X5 blue-shift when the halogen changes from Cl to Br to I, which is the opposite of the trends found in traditional halide perovskites. This phenomenon is attributed to a synergetic combination of the significant change in band gap associated with structural deformation and a strong excitonic effect. Due to the highly localized electron and hole upon photoexcitation, Cs3Cu2Cl5 shows an extremely long and temperature-sensitive photoluminescence (PL) lifetime among metal halide materials with STEs. Remarkably, strong green emission with a PL quantum yield exceeding 90% is found in Cs3Cu2Cl5, opening the way to designing light emission compounds based on local symmetry-enhancing STE mechanisms.

研究领域: 材料科学 · 光电学 · 光物理
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Journal of Materials Chemistry C · 2023 ·Vol. 12 ·期 3 ·922-929 · IF 6.4

Fast solution-phase growth of centimeter-sized Cs3Cu2X5 (X = Cl, I) single crystals for high-performance scintillators

Xiangshi Bin,Jiaxing Liu,Ruosheng Zeng,Hongbang Liu,Jialong Zhao,Tao Lin

Fast and convenient synthesis of zero-dimensional (0D) cesium-copper(I) halide (Cs3Cu2X5 (X = Cl, I)) single crystals (SCs) is critical to achieve practical radiography. In this study, rapid growth of high-quality Cs3Cu2X5 (X = Cl, I) SCs with sizes reaching centimeter scale were achieved within 24 hours using scalable solution-phased methods. These crystals exhibited highly effective emission with large Stokes shifts, excellent PL linearity, and PLQYs exceeding 86%. Additionally, post-treated Cs3Cu2X5–PMMA films demonstrated outstanding scintillation performance, including excellent stabilities, light yield surpassing 36 000 photons per MeV, and spatial resolution up to 6.5 lp per mm in X-ray imaging tests. The high scintillation efficiency can be attributed to their compact 0D crystalline structure, resulting in a small defect density and strong exciton localization.

研究领域: 材料科学 · 晶体生长 · 放射学 · 光学
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JOURNAL OF ALLOYS AND COMPOUNDS · 2022 · IF 6.371

Double passivation of alkali metal ion and organic ligand towards enhanced photoluminescence and stability of Cs3Cu2X5 (XCl, Br and I) nanocrystals

Yanmei Zhou,Shaoru Wu,Guobin Huang,Jingbin Zeng,Benjamin Edem Meteku,Xiaohong Tan,Heng Lu,Feiming Li,Zhixiong Cai,Xudong Wang,Maosheng Zhang

Intrinsic and surface defects are the crucial factors that affect the stability and luminescence efficiency of nanocrystals (NCs). Ion-doping and surface passivation are considered as the most effective strategies to suppress the intrinsic and surface defects of NCs, respectively. Herein, an efficient and facile double passivation process, simultaneously realizes ion-doping and surface passivation, for Cs 3 Cu 2 X 5 (X Cl, Br and I) NCs is developed by using potassium oleate (K-OA) as passivator. K ion is used as ion-doping passivation and OA ion is used as the organic ligand for surface passivation of NCs. Compared to the free passivated NCs, the Photoluminescence quantum yield (PLQYs) of dual-passivated Cs 3 Cu 2 X 5 (X Cl, Br and I) NCs increase significantly from 2.87%, 11.6% and 49.4–31%, 69.9%, and 97.2%, respectively. Moreover, the stability of proposed NCs is greatly improved (Cs 3 Cu 2 Cl 5 NCs maintain 63% of PL efficiency after 100 h, Cs 3 Cu 2 Br 5 and Cs 3 Cu 2 I 5 NCs maintain 65% and 97% of PL efficiency after 100 days, respectively) at 50–86% relative humidity and room temperature under ambient atmosphere.

研究领域: 材料科学 · 光学
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