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CsPbX3
JOURNAL OF MATERIALS SCIENCE & TECHNOLOGY · 2024 · IF 11.2

TiO2 doping promoted nucleation of CsPbX3 (X = Cl, Br, I) quantum dots in glass with improved luminescent performance and stability

Xiaotu Yang,Zihao Yue,Ruixiang Deng,Zhengliang Zhang,Tao Zhang,Lixin Song

Stability hinders further development of all-inorganic CsPb X 3 ( X = Cl, Br, I) quantum dots (QDs) although they exhibit promising prospects in optoelectronic applications. Coating perovskite quantum dots (PQDs) with a glass network to form QD glass can significantly improve their stability. However, the dense glass network degrades their luminescent performance. In this work, the crystallization behavior of PQDs in glass and better luminescence properties are prompted by introducing titanium dioxide into borosilicate glass. The luminescence intensity of TiO 2 -doped CsPbBr 3 QD glass is increased by 1.6 times and the PLQY is increased from 49.8 % to 79 % compared to the undoped glass. Evidence proves that the improved properties are attributed to the enhanced nucleation effect of titanium dioxide during the annealing process. Benefiting from the densification of the glass network caused by titanium dioxide doping, the stability of the PQD glass is further improved. LED devices with an ultra-wide color gamut that fully covers the NTSC1953 standard and achieves 128.6 % of the NTSC1953 standard as well as 91.1 % of the Rec.2020 standard were fabricated by coupling PQD glass powder, demonstrating promising commercial applications of PQD glass in optoelectronic displays.

研究领域: 材料科学 · 光学工程
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CHEMISTRY OF MATERIALS · 2018 · IF 9.89

Synergetic Effect of Postsynthetic Water Treatment on the Enhanced Photoluminescence and Stability of CsPbX3 (X = Cl, Br, I) Perovskite Nanocrystals

Ying Liu,Fei Li,Quanlin Liu,Zhiguo Xia

All inorganic cesium lead halide CsPbX3 (X = Cl, Br, I) perovskite nanocrystals (NCs) are generally considered to be sensitive and even decompose when exposed to ambient humidity. Herein, we perform a well-controlled investigation of the effect of postsynthetic water treatment of the as-prepared CsPbX3 NCs on the photoluminescence quantum yields (PLQYs) and stability, and one can find that the surface defective layer of CsPbX3 NCs can be dissolved into water and we can further separate the supernatant CsPbX3 NCs hexane solution from the water, which improves the PLQYs of CsPbCl3, CsPbBr3, CsPbI3 from 5%, 69.3%, 68.1% to 78.5%, 95.5%, 91%, respectively. As a synergetic effect, a trace amount of residual water facilitated the hydrolysis of tetramethyl orthosilicate, leading to the formation of SiO2-coated CsPbX3 NCs with high stability. The stable green-emitting CsPbBr3/SiO2 composite is used as an example to combine with red K2SiF6:Mn4+ to fabricate the light-emitting diodes device on the blue InGaN chip, which displays wide color gamut (128% of National Television Standard Committee standard), providing the possibility for liquid-crystal display backlight utilization.

研究领域: 材料科学 · 光学工程 · 化学
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JOURNAL OF LUMINESCENCE · 2021 · IF 3.599

Photon upconversion of all-inorganic CsPbX3 quantum dots based on fluorescence resonance energy transfer in hetero-structured perovskite/upconversion nanocomposites

Yuhan Ma,Youchao Wei,Feilong Jiang,Yongsheng Liu,Maochun Hong

Photo upconversion that converts low-energy light into high-energy photons holds great promise for boosting the energy conversion efficiencies particularly for photovoltaic devices based on all-inorganic CsPbX 3 (X = Cl, Br, and I) perovskite quantum dots . However, the realization of nonlinear upconversion luminescence (UCL) from these all-inorganic CsPbX 3 perovskites has been met with very limited success until now. Herein, we propose a rational perovskite/upconversion hetero-structured design strategy to achieve excitonic UCL of all-inorganic CsPbX 3 perovskites based on fluorescence resonance energy transfer (FRET), where all-inorganic CsPbX 3 perovskites and upconverting CaF 2 :Ln (Ln = Yb 3+ /Er 3+ , Yb 3+ /Ho 3+ , and Yb 3+ /Tm 3+ ) nanocrystals are closely integrated with each other as a whole by using a modified two-step epitaxial growth approach, forming the unique upconverting CsPbX 3 /CaF 2 :Ln hetero-structured nanocomposites (HSNCs). Benefitting from the extremely high FRET efficiency of ∼99.7%, excitonic UCL from CsPbX 3 perovskites can be realized upon low-power density 980-nm diode laser irradiation. More importantly, all the HSNCs are found to outperform their pure CsPbX 3 counterparts in terms of air-stability, thermal-stability, and excitonic downconversion luminescence intensity, clearly demonstrating the overwhelming advantages of upconverting HSNCs we prepared over the pure CsPbX 3 perovskites for high-performance optoelectronic and photovoltaic applications.

CAS / MDL: 112-90-3 114460-21-8
研究领域: 材料科学 · 光学 · 光伏技术
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CERAMICS INTERNATIONAL · 2026 · IF 6

Controllable crystallization, luminescence, and self-calibrated temperature sensing properties of CsPbX3 quantum dot glasses and fibers via synergistic regulation of network structure

Zhousu Xu,Peng Wang,Minhao Fang,YuanHang Gao,Hong Jia,Beibei Xu,Xiaofeng Liu,Qifeng Qian,Jianrong Qiu

Encapsulation of metal halide perovskite quantum dots (QDs) inside an inorganic glass matrix offers an effective route to address the stability issue, while the tuning of the luminescence performance across the full series of CsPbX 3 (X = Cl, Br, I) QD in a single glass system remains challenging. Here, by tuning the fraction of the two-dimensional (2D) network structure in a borosilicate glass system, we demonstrate the growth of CsPbX 3 (X = Cl, Cl/Br, Br, Br/I, I) QDs with controllable optical properties. Results indicate that as the halide ion radius increases, the optimal B 2 O 3 concentration corresponding to the maximum fluorescence intensity gradually increases, with the proportion of 2D network structures in the glass rising accordingly. Furthermore, CsPbX 3 QD glass fibers were further fabricated via high-temperature melt-drawing process. By optimizing the heat treatment parameters and fiber length, the optimal light transmission performance was determined. Finally, a self-calibrated temperature sensor based on the fluorescence intensity ratio (FIR) technique was successfully developed by incorporating Sm 3+ ions. The sensor delivers exceptional sensitivity and stability, with a maximum relative sensitivity of 0.030 K −1  at 370 K. This study not only confirms the critical role of the glass network in glass design but also provides a feasible technical pathway for developing a new generation of stable and efficient perovskite optoelectronic devices.

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Nature Communications · 2025 ·Vol. 16 ·期 1 ·1-10 · IF 15.7

Intense upconverted ultraviolet emission of Er3+ through confined energy transfer in Yb3+/Er3+ co-doped Rb3InCl6

Zhang Wen,Zheng Wei,Huang Ping,Yang Dengfeng,Shao Zhiqing,Zhang Wei,Zhang Hao,Xie Zhi,Xu Jin,Chen Xueyuan

Yb 3+ /Er 3+ activated upconversion (UC) materials have been widely applied in many advanced technologies owing to their high UC efficiency in the visible region. However, it is challenging to achieve efficient ultraviolet (UV) UC luminescence (UCL) in Yb 3+ /Er 3+ system, due to the dense energy levels of Er 3+ that impose deleterious nonradiative relaxation. Herein, we report a strategy to liberate the UV-UCL of Er 3+ based on the confined energy transfer in Yb 3+ /Er 3+ co-doped 0D Rb 3 InCl 6 with a low phonon energy and a large interionic distance. This facilitates the population of Er 3+ at the 4 G 11/2 state, which yields intense upconverted UV emission at 384 nm, with a much higher UV-to-green ratio ( I 384 / I 554  = 0.864) than that of traditional UC materials ( < 0.1). By leveraging the intense upconverted UV emission of Er 3+ , we demonstrate the application of Rb 3 InCl 6 :Yb 3+ /Er 3+ nanocrystals as a NIR-to-UV transducer for NIR-triggered anion exchange of CsPbX 3 perovskite nanocrystals with high efficiency and good controllability. These findings offer an approach for the exploration of novel UC materials via energy transfer and crystal lattice engineering towards versatile applications.

研究领域: 材料科学 · 光学材料 · 光子学 · 纳米技术 · 固体物理 · 稀土材料 · 能量传递
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Science China-Materials · 2020 ·Vol. 64 ·期 1 ·158-168 · IF 6.098

Facial synthesis of highly stable and bright CsPbX3 (X=Cl, Br, I) perovskite nanocrystals via an anion exchange at the water-oil interface

Fang Cong,Li Ye,Cai Yuting,Zhou Tian-Liang,Tang Xueyuan,Xie Rong-Jun

Cesium lead halide perovskite nanocrystals (NCs) have attracted unprecedented attention owing to their compelling properties for optoelectronic applications. Compared with the classical hot-injection method, the room-temperature (RT) synthetic strategy is more facile and tender, but it is hard to obtain stable CsPbI 3 NCs and it usually uses polar solvents that sometimes reduce the stability and properties of NCs. Here, we reported a simple approach to synthesize highly efficient and stable CsPbI 3 as well as other color-tunable CsPbX 3 NCs with high quantum efficiency at room temperature via an anion exchange at the water-oil interface, in which the as-synthesized pristine CsPbBr 3 NCs in toluene were treated in aqueous solutions of HX (X=Cl, Br, and I) and protonated oleylamine (OAm) acted as a carrier. The synthesized CsPbI 3 NCs had an emission at 680 nm and even showed excellent colloidal stability after being stored for 32 d. The high efficiency and stability of the obtained CsPbX 3 NCs were ascribed to the facts that: (i) the polar reagents were almost removed from the surface of NCs; (ii) the defect-related nonradiative recombination was suppressed efficiently by surface passivation.

研究领域: 纳米材料 · 光电子学 · 钙钛矿化学 · 胶体合成
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CHEMICAL ENGINEERING JOURNAL · 2024 · IF 13.3

Ostwald ripening inhibition by a bipolar ligand achieves long-term-reaction and scalable synthesis of ultra-stable CsPbX3 perovskite quantum dots towards LEDs

Yongfeng Liu,Qingyu Xie,Yupeng Ying,Zhaoju Gao,Xiuwen Shao,Weizhi Xia,Min Zhou,Wei Pei,Xiaosheng Tang,Yusong Tu

All-inorganic perovskite quantum dots (PeQDs) hold immense potential for use in light-emitting diodes (LEDs) due to their excellent optoelectronic properties. However, the scalable synthesis and poor stability have severely hindered their application. Here, we solved both the two issues with “one stone”, namely a bipolar ligand 3-(N,N-dimethyloctadecylammonio) propane sulfonate (ASC18). ASC18 contains a positively charged quaternary ammonium group and a negatively charged sulfonic group, which enables for long-term reaction and gram-level synthesis of PeQDs with outstanding morphology, crystallinity, and optical properties. Density functional theory calculations and experimental studies show that these merits arise from the inhibition of Ostwald ripening by ASC18 due to their simultaneous interaction with undercoordinated Br – and Pb 2+ via a bidentate binding mode. Furthermore, ASC18 capped PeQDs present significantly improved stabilities against air, UV irradiation, heat, and polar solvent. Finally, both electroluminescent LEDs and down-conversion white LEDs fabricated with our PeQDs show significant operational stability. This presents a trustworthy avenue to obtain high-quality PeQDs for their practical applications.

CAS / MDL: 6080-56-4
研究领域: 材料科学 · 光电领域
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Analytical Methods · 2023 ·Vol. 15 ·期 8 ·1037-1046 · IF 3.1

Metal nanoprobe-decorated all-inorganic perovskite nanocrystal-based fluorescence-linked immunosorbent assay for the detection of tumor-derived exosomes

Zhaoyan Yang,Shenfei Zong,Guohua Jiang,Kai Zhu,Ziting Qian,Kuo Yang,Zhuyuan Wang,Yiping Cui

All-inorganic perovskite nanocrystals (CsPbX3 NCs, X = Cl, Br, I) are promising fluorescence materials for biological detection due to their excellent optical properties. However, there is still a challenge to obtain stable CsPbX3 NCs with more biofunctions. Here, we proposed a distinct strategy by absorbing the functionalized metal nanoprobes onto the phospholipid encapsulated CsPbX3 NCs to achieve CsPbX3-metal hybrids as probes for the detection of tumor-derived exosomes. Here, the metal nanoprobes have two functions: first, it endows phospholipid encapsulated CsPbX3 NCs with recognition ability; second, it avoids the fluorescence quenching of CsPbX3 NCs during the biological modification process by using metal nanoparticles as a bridge to connect with CsPbX3 NCs and various biomolecules. The obtained CPXD–AD exhibited a bright fluorescence signal, narrow full width at half-maximum (FWHM), and high specificity. Under optimal conditions, the CPXD–AD-based fluorescence-linked immunosorbent assay (FLISA) was successfully established and used for both qualitative and quantitative detection of tumor-derived exosomes.

CAS / MDL: 111-86-4
研究领域: 纳米技术 · 生物医学工程 · 材料科学 · 癌症研究 · 生物传感器
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Advanced Optical Materials · 2018 ·Vol. 7 ·期 4 ·1801323 · IF 7.43

One-Step Loading on Natural Mineral Halloysite Nanotube: An Effective Way to Enhance the Stability of Perovskite CsPbX3 (X = Cl, Br, I) Quantum Dots

Jiarui Hao,Xingyu Qu,Lei Qiu,Guogang Li,Yi Wei,Gongcheng Xing,Hongquan Wang,Chunjie Yan,Ho Seong Jang,Ziyong Cheng,Jun Lin

Currently, poor luminescence stability seriously impedes the practical application of inorganic halide perovskite (CsPbX 3 , X = Cl, Br, and I) quantum dots (QDs) in optoelectronic devices. In present work, CsPbX 3 QDs are successfully assembled on natural mineral halloysite nanotubes (HNTs) for improving the luminescence performances. Monodispersed CsPbX 3 QDs are arranged on two edges of HNTs in a highly ordered manner, which possibly originates from the electrostatic interaction between halogen ion and surface hydroxyl (Sur  OH 2 + ) on the section face of HNTs. As expected, the photoluminescence (PL) performances of CsPbX 3 @HNTs nanocomposites are obviously improved. The PL intensity still can be maintained even 80% when working at 100 °C. Almost no emission degradation is observed after storing in an open ambient condition for 28 days. Moreover, the PL intensity also maintains 82% of room temperature (RT) intensity after continuously being illuminated by 365 nm UV lamps for 144 h. Excellent white light with Commission Internationale de l'Eclairage (CIE) chromaticity coordinates (0.34, 0.32) of the white light-emitting diodes (w-LEDs) fabricated by CsPbBr 3 @HNTs, CsPbBr 1.2 Cl 1.8 @HNTs, and CsPbBr 1.2 I 1.8 @HNTs phosphors are achieved. This work opens up a new insight in achieving stable CsPbX 3 QD-based multifunctional materials by designing nanocomposites with natural clay mineral.

研究领域: 材料科学 · 光学 · 纳米技术
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CHEMISTRY OF MATERIALS · 2018 · IF 9.89

Postsynthetic Surface Trap Removal of CsPbX3 (X = Cl, Br, or I) Quantum Dots via a ZnX2/Hexane Solution toward an Enhanced Luminescence Quantum Yield

Fei Li,Ying Liu,Hongliang Wang,Qian Zhan,Quanlin Liu,Zhiguo Xia

The control of surface properties of all inorganic cesium lead halide perovskite (CsPbX3; X = Cl, Br, or I) quantum dots (QDs) is essential to achieve excellent stability and high photoluminescence quantum yields (PLQYs). Herein, a facile method was performed to simultaneously enhance the stability and PLQYs of CsPbX3 QDs by a ZnX2/hexane solution post-treatment. We show that the halogen defect on the surface of CsPbX3 QDs can be treated in a controlled way, whereby the “black dots” that adhered on the surface as observed by transmission electron microscopy have be completely removed, resulting in enhanced stability and photoluminescence. The PLQYs of CsPbCl3, CsPbBr3, and CsPbI3 increased from 4, 58, and 63% to 86, 93, and 95%, respectively, and the origin of the “black dots” as well as their transformation mechanism has been demonstrated. As a result, the poly(dimethylsiloxane) composite films created by encapsulating stable and nearly defect-free green-emitting CsPbBr3, the red-emitting K2SiF6:Mn4+ phosphor, and a blue emission GaN chip were prepared and used to fabricate a remote-type white light-emitting diode device, which exhibits a high luminescence efficiency (≤98 lm/W) and a wide color gamut (∼130% of the National Television Standard Committee standard), suggesting the potential for liquid crystal display backlight application.

研究领域: 材料科学 · 光学
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CHEMICAL ENGINEERING JOURNAL · 2025 · IF 13.2

Regulating the local glass networks to enhance the optical performance of CsPbX3 (X = Cl, Br, I) quantum dots embedded in zinc borosilicate glasses via GeO2

Shuailong Shen,Ziyi Guo,Wanmei Zhong,Jilin Zhang,Wenli Zhou,Liping Yu,Shixun Lian

All inorganic CsPbX 3 (X = Cl, Br, I) perovskite quantum dots (QDs) have excellent optical properties, and show great potential in optoelectronic devices, information storage, wide color gamut backlight display   and other fields. In previous work, embedding CsPbBr 3 QDs into glass matrix through in-situ crystallization has become an important strategy to improve the stability of quantum dots. However, few reports have been made on the synthesis of high-quality whole family CsPbX 3 QDs glass by melt-quenching method. Herein, CsPbX 3 QDs glasses with full visible spectrum were synthesized by a closed melt-quenching technique. And the precise content of GeO 2 was used to regulate the size of glass network gaps to accommodate different sizes of CsPbX 3 QDs. The deconvoluted infrared spectra confirmed that the introduction of GeO 2 was beneficial to the increase of non-bridging oxygen in the rigid structure, the number and percentage of [BO 3 ] triangular units increased correspondingly, and the glass network changed in a three-dimensional and looser benign way, which was beneficial to the growth of large-size QDs. Finally, the luminescent properties of CsPbCl 2 Br, CsPbBr 3 and CsPbBrI 2 QDs glasses were improved respectively. The optimized CsPbX 3 QDs glasses have tunable luminescence in the full visible spectrum (414–692 nm), improved photoluminescence quantum yield (PLQY, ∼53.06 %) and longer decay lifetime, and excellent stability. Finally, the construction of a white light-emitting diode (WLED) device shows that CsPbX 3 QDs glass has potential applications in solid-state lighting.

研究领域: 材料科学 · 光学工程
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Advanced Science · 2019 ·Vol. 6 ·期 22 ·1901694 · IF 15.804

Fiber-Spinning-Chemistry Method toward In Situ Generation of Highly Stable Halide Perovskite Nanocrystals

Xuan Lu,Yang Hu,Jiazhuang Guo,Cai-Feng Wang,Su Chen

All-inorganic halide perovskite nanocrystals (PNCs) have drawn increasing attention owing to their splendid optical properties. However, such nanomaterials suffer from intrinsic instability, greatly limiting their practical application. Meanwhile, environmental regulation has restricted the emissions of volatile organic compounds (VOCs), initiating a search for alternative approaches to PNC synthesis and film forming. Herein, fiber-spinning chemistry (FSC) is proposed for easy-to-perform synthesis of highly stable PNC fibrous films. The FSC process utilizes spinning fibers as reactors, reducing the generation of VOCs. This method enables the fabrication of CsPbX 3 (X = Cl, Br, I) PNCs/poly(methyl methacrylate)/thermoplastic polyurethanes fibrous films at room temperature in one step, exhibiting tunable emission between 450 and 660 nm. Significantly, the in situ generation of PNCs in hydrophobic core–shell nanofibers results in highly improved fluorescence stability. PNCs/polymer fibrous films keep constant in photoluminescence (PL) after storage at atmosphere for 90 d and retain 82% PL after water immersion for 120 h (vs fluorescence quenching in 10 d in air or 5 h in water for pristine PNCs). The PNCs/polymer fibrous films endowed with superior optical stability and great flexibility show promising potentials in flexible optoelectronic applications. This work paves a facile way toward high-performance nanoparticles/polymer fibrous films.

研究领域: 材料科学 · 纳米技术 · 光电子学 · 化学工程
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