ACS Applied Nano Materials
·
2026
·
IF 5.8
Yan Yuxin,Zou Ailing,Wang Yiyan,Zhang Yanjie,Yu Jingjie,Xiao Zhiguo
CsPbX 3 (X = I, Br, Cl) perovskite quantum
dots (PQDs)
are promising for optoelectronic applications owing to their tunable
bandgap, high photoluminescence (PL) quantum yield, and narrow emission
bandwidth. However, CsPbBr 3 PQDs exhibit a large Stokes
shift (>155 nm) and are mainly excited by near-ultraviolet light
(∼365
nm), resulting in substantial energy loss and limiting their compatibility
with blue light-emitting diodes (LEDs) excitation. Herein, Sr 2+ /Cl – codoped CsPbBr 3 PQDs embedded
in zinc borosilicate (ZBS) glass powders were developed to regulate
the band structure. Sr 2+ incorporation significantly enhances
PL performance. Notably, CsPb 0.5 Sr 0.5 Br 3 PQDs exhibit ∼1.6 times higher PL intensity than undoped
samples with a slight red-shift (∼5 nm). Meanwhile, the bandgap
of CsPb 0.1 Sr 0.9 Br 3 PQDs is widened
to 3.12 eV compared to 2.36 eV for CsPbBr 3 . Totally different
with undoped PQDs, the excitation peak of CsPb 0.1 Sr 0.9 Br 3 PQDs covers the desired blue-violet region
in the range of 400–480 nm and the maximum peak is located
at 414 nm, which displays a narrow Stokes shift of 106 nm. Further,
Cl – ions substitution in Sr-doped host materials
enables the blueshift of the PL emission from 521 nm (green light)
to 448 nm (blue light) via bandgap engineering accompanied by ultranarrow
Stokes shift of ∼34 nm for CsPb 0.1 Sr 0.9 BrCl 2 sample. The Sr-doped PQDs embedded in ZBS glass
also demonstrate excellent water resistance, retaining ∼96%
of their initial PL intensity after immersion in deionized water for
more than 60 days. Thus, the ultrastable PQDs glass powders can be
effectively excited by the blue-violet light chip (410 nm-460 nm)
via bandgap engineering possess and demonstrate promising application
potential in color-conversion display devices, wide-color-gamut backlight
systems and screen-printable emissive display films.
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ACS Applied Materials & Interfaces
·
2022
·
IF 10.383
Jiejun Ren,Andries Meijerink,Xiaopeng Zhou,Jiapeng Wu,Gangyi Zhang,Yuhua Wang
All-inorganic perovskite quantum dots (PQDs), which possess outstanding photophysical properties, are regarded as promising materials for optoelectronic applications. However, the poor light conversion efficiency and severe stability problem hinder their widespread applications. In this work, a novel encapsulation strategy is developed through the in situ growth of CsPbX3 PQDs in presynthesized mesoporous cerium-based metal organic frameworks (Ce-MOFs) and further silane hydrolysis–encapsulation, generating stable CsPbX3@Ce-MOF@SiO2 composites with greatly enhanced light conversion efficiency. Moreover, the simulation results suggest that the pore boundary of Ce-MOFs has a strong waveguide effect on the incident PQD light, constraining PQD light inside the bodies of Ce-MOFs and suppressing reabsorption losses, thus increasing the overall light conversion efficiency of PQDs. Meanwhile, the Ce-MOF@SiO2 protective shell effectively improves the stability by blocking internally embedded PQDs from the harmful external environment. Further, the obtained white-light-emitting diode shows an ultrahigh luminous efficiency of 87.8 lm/W, which demonstrates their great potential in optoelectronic applications.
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Advanced Science
·
2021
·Vol. 8
·期 19
·2101418
·
IF 16.806
Qingwei Zhou,Jialong Duan,Jian Du,Qiyao Guo,Qiaoyu Zhang,Xiya Yang,Yanyan Duan,Qunwei Tang
The crystal distortion such as lattice strain and defect located at the surfaces and grain boundaries induced by soft perovskite lattice highly determines the charge extraction-transfer dynamics and recombination to cause an inferior efficiency of perovskite solar cells (PSCs). Herein, the authors propose a strategy to significantly reduce the superficial lattice tensile strain by means of incorporating an inorganic 2D Cl-terminated Ti 3 C 2 (Ti 3 C 2 Cl x ) MXene into the bulk and surface of CsPbBr 3 film. Arising from the strong interaction between Cl atoms in Ti 3 C 2 Cl x and the under-coordinated Pb 2+ in CsPbBr 3 lattice, the expanded perovskite lattice is compressed and confined to act as a lattice “tape”, in which the Pb Cl bond plays a role of “glue” and the 2D Ti 3 C 2 immobilizes the lattice. Finally, the defective surface is healed and a champion efficiency as high as 11.08% with an ultrahigh open-circuit voltage up to 1.702 V is achieved on the best all-inorganic CsPbBr 3 PSC, which is so far the highest efficiency record for this kind of PSCs. Furthermore, the unencapsulated device demonstrates nearly unchanged performance under 80% relative humidity over 100 days and 85 °C over 30 days.
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Journal of Materials Chemistry A
·
2020
·Vol. 8
·期 23
·11859-11866
·
IF 11.301
Yafeng Xu,Jialong Duan,Xiya Yang,Jian Du,Yudi Wang,Yanyan Duan,Qunwei Tang
The electron-transporting layer (ETL) plays a non-negligible role in determining the charge extraction and transfer behaviors from perovskite films under solar irradiation for high efficiency perovskite solar cells. A suitable band structure, good conductivity, high electron mobility and low trap state density are preferred for the desired ETL to maximize the electricity generation and minimize the charge recombination. Herein, we have demonstrated that the incorporation of antimony (Sb) dopants into the lattice of low-temperature processed TiO2 nanocrystals can effectively suppress the formation of under-coordinated Ti3+ and oxygen vacancies, leading to improved electronic conductivity and mobility. When assembling into all-inorganic, carbon-based CsPbBr3 planar perovskite solar cells free of noble metal electrodes, an enhanced efficiency of 8.91% with an ultra-high open-circuit voltage of 1.654 V and reduced hysteresis from 32% to 15% is achieved based on the Sb-doped TiO2 ETL. The mechanism behind this phenomenon is mainly attributed to the improved perovskite film quality and significantly reduced charge recombination. Taking the advantages of low temperature, low defect state density, high electrical conductivity and mobility into consideration, the Sb-doped TiO2 ETL demonstrates great potential in advanced perovskite solar cells even in flexible devices.
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ACS Applied Materials & Interfaces
·
2018
·
IF 8.097
Ya-Meng Chen,Yang Zhou,Qing Zhao,Jun-Ying Zhang,Ju-Ping Ma,Tong-Tong Xuan,Shao-Qiang Guo,Zi-Jun Yong,Jing Wang,Yoshihiro Kuroiwa,Chikako Moriyoshi,Hong-Tao Sun
All-inorganic perovskites have emerged as a new class of phosphor materials owing to their outstanding optical properties. Zero-dimensional inorganic perovskites, in particular the Cs4PbBr6-related systems, are inspiring intensive research owing to the high photoluminescence quantum yield (PLQY) and good stability. However, synthesizing such perovskites with high PLQYs through an environment-friendly, cost-effective, scalable, and high-yield approach remains challenging, and their luminescence mechanisms has been elusive. Here, we report a simple, scalable, room-temperature self-assembly strategy for the synthesis of Cs4PbBr6/CsPbBr3 perovskite composites with near-unity PLQY (95%), high product yield (71%), and good stability using low-cost, low-toxicity chemicals as precursors. A broad range of experimental and theoretical characterizations suggest that the high-efficiency PL originates from CsPbBr3 nanocrystals well passivated by the zero-dimensional Cs4PbBr6 matrix that forms based on a dissolution–crystallization process. These findings underscore the importance in accurately identifying the phase purity of zero-dimensional perovskites by synchrotron X-ray technique to gain deep insights into the structure–property relationship. Additionally, we demonstrate that green-emitting Cs4PbBr6/CsPbBr3, combined with red-emitting K2SiF6:Mn4+, can be used for the construction of WLEDs. Our work may pave the way for the use of such composite perovskites as highly luminescent emitters in various applications such as lighting, displays, and other optoelectronic and photonic devices.
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高影响因子
SENSORS AND ACTUATORS B-CHEMICAL
·
2024
·
IF 8
Jingcheng Zheng,Jie Chen,Ruifen Sun,Weiwei Zhang,Yun Huang,Jiwei Shao,Yuwu Chi
Fluorescent immunochromatographic test (FICT) strips have received extensive attention due to their virtue of simple operation, low cost, and a point-of-care (POC) assay. In recent years, people are constantly seeking new labels to improve the sensitivity of immunosensors. Perovskite nanocrystals (PNCs) possess strong fluorescence and a narrow emission peak, making them an excellent choice as a new fluorescent signal label. Herein, we have developed a simple, fast, and environmentally friendly method to synthesize CsPbBr 3 /CsPb 2 Br 5 @SiO 2 with the good water stability and high biocompatibility. These CsPbBr 3 /CsPb 2 Br 5 @SiO 2 have been applied to construct FICT strips. To achieve the quantitative determination of human chorionic gonadotropin (HCG), a lab-made FICT strips detection system was established. The FICT strips had a good linear relationship to HCG in the range of 5–500 ng/mL, and the detection limit was 2.09 ng/mL. In addition, the recovery results of HCG detection in human urine samples also proved the feasibility of this FICT strips. CsPbBr 3 /CsPb 2 Br 5 @SiO 2 can also be modified with different biomarkers for functionalization, which exhibits a promising application in the development of sensing platform of FICT strips.
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Analytical Methods
·
2024
·Vol. 16
·期 15
·2267-2277
·
IF 2.7
Yang He,Yangjie Li,Han Wang,Site Luo,Haihu Yu
The weakly bound organic ligand shells around perovskite quantum dots (QDs) are easily decomposed and cannot provide sufficient stability in polar solvents, which greatly obstructs their applications in sensing. Herein, a fluorescent sensor based on CsPbBr3/CdS core/shell QDs was developed for the detection of tetracycline (TC) in the polar solvent-ethanol. Pristine CsPbBr3 QDs were treated with cadmium diethyldithiocarbamate (Cd(DDTC)2) to form a shell on the surface at 110 °C, while extra oleylammonium bromide (OAmBr) was added to inhibit the phase transformation of CsPbBr3 into a Cs4PbBr6 impurity phase during high-temperature processing. And finally CsPbBr3/CdS core/shell QDs were successfully synthesized. The capping with the CdS inorganic shell remediated surface defects and improved the stability in ethanol without affecting the emission properties of the parent CsPbBr3 QDs. The results showed that the fluorescent sensor detected TC in the range of 0.05–25 μM with a low detection limit of 22.6 nM, whereas it had high selectivity and anti-interference ability for TC. And the fluorescence quenching mechanism of the sensor was mainly photoinduced electron transfer between TC and CsPbBr3/CdS QDs. Our research provides a unique way to improve the stability of perovskite QDs in polar solvents and applications in fluorescence detection.
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Advanced Energy Materials
·
2018
·Vol. 8
·期 31
·1802346
·
IF 21.875
Jialong Duan,Yuanyuan Zhao,Xiya Yang,Yudi Wang,Benlin He,Qunwei Tang
All-inorganic cesium lead bromide (CsPbBr 3 ) perovskite solar cells have attracted enormous attention owing to their outstanding stability in comparison with organic–inorganic hybrid devices. The greatest weakness for inorganic CsPbBr 3 solar cells is their lower power conversion efficiencies, mainly arising from inferior light-absorbance range and serious charge recombination at interfaces or within perovskite films. To address this issue, the lattice doping of lanthanide ions (Ln 3+ = La 3+ , Ce 3+ , Nd 3+ , Sm 3+ , Eu 3+ , Gd 3+ , Tb 3+ , Ho 3+ , Er 3+ , Yb 3+ , and Lu 3+ ) into CsPbBr 3 films for all-inorganic solar cells free of hole-transporting materials and precious metal electrodes is presented. Arising from the enlarged grain size and prolonged carrier lifetimes upon incorporating Ln 3+ ions into perovskite lattice, the performances of these inorganic CsPbBr 3 solar cell devices are significantly enhanced, achieving a champion efficiency as high as 10.14% and an ultrahigh open-circuit voltage of 1.594 V under one sun illumination. Meanwhile, the nearly unchanged efficiency upon persistent attack by 80% RH in air atmosphere over 110 d and enhanced thermal stability at 80 °C over 60 d provide new opportunities of promoting commercialization of all-inorganic CsPbBr 3 perovskite solar cells.
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CHEMISTRY OF MATERIALS
·
2022
·
IF 10.508
Fucai Cui,Peng Zhang,Longzhen Zhang,Yunqiu Hua,Xue Sun,Xiang Li,Guodong Zhang,Xutang Tao
Metal halide perovskites have emerged as next-generation semiconductors for X-ray detection because of their excellent photoelectric properties. However, severe ion migration in three-dimensional (3D) halide perovskites usually causes dark current drift in radiation detectors, especially in high electric fields. Here, we report a liquid-phase epitaxial method based on inverse-temperature crystallization (ITC), with which a hybrid/all-inorganic 3D perovskite single-crystal heterojunction is constructed, using an orientated CsPbBr3 single crystal as a substrate. MAPbBr3–nCln/CsPbBr3 single-crystal heterojunctions and single-crystal arrays (through the addition of a mask onto the substrate) with good lattice matching were successfully constructed, laying the foundation for high-performance X-ray detectors. In particular, the MAPbBr3/CsPbBr3 heterojunction drastically enhances the X-ray response of the CsPbBr3 single crystal, with a record-high sensitivity of 2.0 × 105 μC Gyair–1 cm–2 and lowest detection limit of 96 nGyair s–1 for 120 keV hard X-ray detection. Moreover, the dark current drift caused by ion migration is suppressed to 3.92 × 10–4 nA cm–1 s–1 V–1 even in a high reverse electric field of −125 V mm–1. Based on the superior detection performance, it is confirmed that a robust and uniform X-ray imaging detector with good resolution was successfully devised using the heterojunction. Our study provides a simple strategy for constructing perovskite single-crystal heterojunction films and arrays that effectively suppress ion migration that otherwise occurs in 3D halide perovskite single crystals to enable the creation of robust ultrasensitive X-ray detection and imaging systems.
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高影响因子
JOURNAL OF LUMINESCENCE
·
2019
·
IF 2.961
Run Wang,Yue Zhang,Fu-Xing Yu,Yajie Dong,Ya-Lan Jia,Xing-Juan Ma,Qiang Xu,Yanhong Deng,Zu-Hong Xiong,Chun-Hong Gao
An efficient perovkite light-emitting diode (PeLED) is fabricated by incorporating 1,3,5-tri (m-pyrid-3-yl-phenyl)benzene (TmPyPB) between the emitting layer (EML) and the electron transporting layer (ETL), where TmPyPB plays an indispensable blocking effect on both excitons and holes. It shows a maximum current efficiency of 9.37 cd/A, and the corresponding external quantum efficiency (EQE) of 2.42% with a saturated green color Commission International de I'Eclairage (CIE1993) coordinated of (0.1279, 0.7951) under a driving voltage of 6 V. Meanwhile, the operational lifetime of the TmPyPB-based PeLED is improved to about 2.6-fold to that of the one with only the traditional ETL of aluminum 8-hydroxyquinolinate (Alq 3 ). The enhancements of electroluminescence (EL) performance are mainly attributed to better confinement of both the holes and the excitons in the EML, and more balanced carrier transportation in the TmPyPB-based PeLED. This work offers a feasible strategy to develop high performance optoelectronic devices.
研究领域:
材料科学
·
光电子学
·
纳米技术
·
半导体器件
·
功能材料
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DALTON TRANSACTIONS
·
2023
·Vol. 52
·期 42
·15353-15359
·
IF 4
Peng Zhang,Liming Chen,Xiaoyan Cai,Binbin Luo,Tianju Chen,Haini Chen,Guoliang Chen,Feiming Li
A traditional fluorescence–scattering intensity based ratiometric sensing system utilizes both inherent scattering and fluorescence intensity and has drawn extensive attention owing to its simplicity and self-calibration properties. In this work, we propose a novel ratiometric fluorescence sensing system that combines a fluorescence wavelength shift and scattering in a single window, using second-order scattering (SOS) as the representative scattering signal based on the halide exchange of CsPbBr3@SiO2 perovskite nanocrystal composites. We observe a fast halide exchange within 10 seconds, resulting in an identifiable fluorescence wavelength blue shift, while the scattering wavelength remains relatively constant for self-correction. This system could be applied for ratiometric sensing of Cl− in the serum without any sample treatment. The established wavelength-based ratiometric system demonstrates high reliability and reproducibility, paving a new way for fluorescence sensing.
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ACS Applied Materials & Interfaces
·
2018
·
IF 8.097
Yang Li,Ying Lv,Ziquan Guo,Liubing Dong,Jianghui Zheng,Chufen Chai,Nan Chen,Yijun Lu,Chao Chen
CsPbBr3 perovskite quantum dots (PQDs)/ethylene vinyl acetate (EVA) composite films were prepared via a one-step method; on the basis of this, both supersaturated recrystallization of CsPbBr3 PQDs and dissolution of EVA were realized in toluene. The prepared films display outstanding green-emitting performance with high color purity of 92% and photoluminescence (PL) quantum yield of 40.5% at appropriate CsPbBr3 PQD loading. They possess long-term stable luminescent properties in the air and in water, benefiting from the effective protection of CsPbBr3 PQDs by the EVA matrix. Besides, the prepared CsPbBr3 PQDs/EVA films are flexible enough to be repeatedly bent for 1000 cycles while keeping unchanged the PL intensity. The optical properties of the CsPbBr3 PQDs/EVA films in white light-emitting diodes were also studied by experiments and theoretical simulation. Overall, facile preparation process, good long-term stability, and high flexibility allow our green-emitting CsPbBr3 PQDs/EVA films to be applied in lighting applications and flexible displays.
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