Flexible and Printed Electronics
·
2023
·Vol. 8
·期 3
·035008
·
IF 3.1
Xianyao Wu,Kai Yin,Mu Yang,Yufeng Hu,Hongshang Peng
All-inorganic perovskite quantum dots (PQDs) have received considerable attentions due to their fascinating optical properties. However, the mainstream preparation methods rely on toxic solvents, raising significant environmental and safety concerns. In this work, ethyl acetate was chosen as the environmentally friendly anti-solvent to prepare silica-coated CsPbBr3 PQDs using a aminoalkoxysilane-assisted reprecipitation–encapsulation method. The as-prepared PQDs exhibited tunable emission wavelength and a medium photoluminescence quantum yield (PLQY) of 60%. Furthermore, CsPbBr3 PQDs were post-treated by different ligands with the aim of passivating surface defects. This strategy successfully mitigated the presence of surface defects and minimized non-radiative recombination losses in PQDs. As a result, the PLQY (achieving up to 73%) and stability of PQDs were substantially enhanced (luminescence stability improved by about 40% under the same test conditions). Our studies offer a novel approach for the environmentally friendly large-scale production of PQDs, opening up new possibilities for their practical applications.
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高影响因子
Advanced Optical Materials
·
2023
·
IF 9
Bing Tang,Shixun Wang,Haochen Liu,Nanli Mou,Arsenii S. Portniagin,Peigang Chen,Ye Wu,Xiaoqing Gao,Dangyuan Lei,Andrey L. Rogach
Owing to their attractive optical and chiroptical properties, chiral metal halide perovskites have received increasing attention, with potential applications ranging from photonics and optoelectronics to spintronics. Metal halide perovskite nanocrystals with either intrinsic or extrinsic (e.g., chiral ligand-induced) chirality have been reported recently, and the interplay between these two types of chirality has yet to be addressed. Herein, the inversion and tuning of excitonic optical activity is reported in intrinsically chiral perovskite nanoplatelets, originating from interactions between their structural chirality (due to the spontaneously formed screw dislocations in the crystalline lattice) and the surface enantiomeric (R/S) chiral ligands R/S-phenylethylammonium bromide. Through post-preparative exposure of the perovskite nanoplatelets to these R/S ligands of varied contents, either chiral ligand-induced intrinsic chirality inversion or negative and positive Cotton effects induced by the ligands via electronic coupling between the ligand and the nanoplatelets are identified. These findings deepen understanding of the modulation of excitonic optical activity in chiral perovskites and can guide the rational design and synthesis of novel chiral materials.
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高影响因子
OPTICAL MATERIALS
·
2023
·
IF 3.9
Lifang Wu,Jun Wang,Wenzhi Wu
In this work, photoluminescence (PL) intensity and stability of CsPbBr 3 /PbBrOH powders synthesized by one-pot method are enhanced through the encapsulation of poly (vinyl acetate) (PVA) in water. Understanding the function of PbBrOH and PVA matrix for photogenerated transition can be achieved through temperature-dependent steady-state and time-resolved PL. The enhanced PL quantum yield (65.9%) and longer lifetime indicate the strengthened structural stability and a significant reduction in nonradiative recombination of CsPbBr 3 . Negative thermal quenching can be observed and interpreted using a multilevel PL transition model. Through nanosecond time-resolved PL spectra under femtosecond laser excitation, it is revealed that the PL position shows a redshift (∼8 nm) with time delay due to the reduction of band-filling effect during the recombination of photoexcited carriers. PVA further encapsulates CsPbBr 3 /PbBrOH powders to form a flexible film, which exhibits excellent thermal and water stability due to the dual protective effects of PVA and PbBrOH. The experimental investigation demonstrates that CsPbBr 3 encapsulated by PbBrOH and PVA possesses excellent luminescent and water-resistant characteristics, making it a new choice for practical applications in LEDs and screen printing.
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JOURNAL OF ALLOYS AND COMPOUNDS
·
2023
·
IF 6.2
Yue Zhao,Shujie Jiao,Shuo Liu,Yimin Jin,Song Yang,Xianghu Wang,Tong Liu,Hongyan Jin,Dongbo Wang,Shiyong Gao,Jinzhong Wang
All-inorganic metal halide perovskite is considered as one of the most promising perovskite materials for photodetectors , because of its remarkable optoelectronic characteristics and stability. Whereas, it remains challenge to achieve both excellent photodetection performance and stability due to the multitudes of defects in perovskite films. Herein, an interface engineering based on surface passivation strategy to achieve high-quality CsPbBr 3 perovskite films by introducing thioacetamide (C 2 H 5 NS, abbreviated as TAA) as interface materials is reported. The interaction between TAA and perovskite passivates the uncoordinated Pb 2+ on the surface of CsPbBr 3 film, suppress carrier non-recombination and accelerates carriers transfer. The self-powered photodetector based on the passivated CsPbBr 3 film prefers the maximum responsivity of 0.26 A W −1 and detectivity of 8.39 × 10 12 Jones under 520 nm irradiation. In addition, the optimized photodetector exhibits excellent stability and maintains more than 98% of its initial photocurrent when operating over 8 h. This work demonstrates an alternative approach for the preparation of improved performance in CsPbBr 3 perovskite photodetectors and associated photoelectric devices.
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高影响因子
Materials Today Communications
·
2022
·
IF 3.662
Cong Zhou,Fanfan Xu,Wei Wang,Wendong Nie,Weixiong You,Xinyu Ye
As an emerging optical material, all-inorganic perovskite quantum dots (QDs) have been successfully applied in some fields. However, inherent ionic properties of perovskite QDs lead to poor stability of water and heat which severely hinders the further industrial applications. Therefore, the incorporation of Metal-Organic Framework (MOF) into QDs to obtain CsPbX 3 @MOF composite is developing to improve the stability of all-inorganic perovskite QDs. In this work, a simple and fast method was developed to synthesize a CsPbBr 3 @EuBTC composite. The water stability and thermal stability of the CsPbBr 3 @EuBTC composite have been improved compared to pure CsPbBr 3 QDs. Simultaneously, luminescent properties and promising latent fingerprints and optical anti-counterfeiting applications of the CsPbBr 3 @EuBTC composite are further explored. Under fluorescent interference, it still shows excellent luminescence sensitivity and anti-interference ability. The CsPbBr 3 @EuBTC composite displays dual-mode luminescence as excited under the 365 nm or 254 nm ultraviolet (UV) excitation wavelength. Adjusting the ratio of CsPbBr 3 QDs to EuBTC in the CsPbBr 3 @EuBTC composite can also achieve multi-color luminescence. Therefore, it is expected that CsPbBr 3 @EuBTC can be applied to latent fingerprints and multi-mode optical anti-counterfeiting materials.
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Journal of Materials Chemistry C
·
2022
·Vol. 10
·期 21
·8356-8363
·
IF 8.067
Ye Li,Miaoling Cai,Mengling Shen,Yuting Cai,Rong-Jun Xie
The stability of perovskite nanocrystals (NCs) is greatly limited due to highly dynamic binding of ligands, which hinders their applications in optoelectronic devices. In this paper, a new ligand strategy was employed to prepare CsPbBr3 NCs via a facile room temperature (RT) ligand-assisted reprecipitation (LARP) method, where N1.N2-didodecyl-N1.N1.N2.N2-tetramethylethane-1.2-diaminium bromide (DTDB) as the sole capping ligand and an additional Br resource was used. Compared to other ligands with one coordinating group, this class of bidentate ligand can be tightly anchored to the surface of NCs with double N+ sites. The as-synthesized DTDB-CsPbBr3 NCs exhibited a high photoluminescence quantum yield (PLQY) of 92.3% and also showed a superior colloidal stability even under intense purification for up to ten cycles. Compared to the dodecyltrimethyl ammonium bromide (DTAB) ligand capped-CsPbBr3 NCs, the DTDB-CsPbBr3 NCs display obviously enhanced stability to light, heat and water. X-ray photoelectron spectroscopy (XPS) results revealed that the DTDB-CsPbBr3 NCs have a Br− rich surface, which accounts for the high stability and PLQY. Hence, DTDB is a promising ligand to prepare perovskite NCs with higher optical performance.
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Laser & Photonics Reviews
·
2022
·Vol. 16
·期 7
·2100736
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IF 10.947
Baiqian Wang,Jiali Peng,Xin Yang,Wensi Cai,Hongbin Xiao,Shuangyi Zhao,Qianqian Lin,Zhigang Zang
Metal halide perovskite-based high-performance X-ray scintillator is considered as one of the most favorable candidates applied in the fields of medicine, industry, and science. However, the current X-ray scilltillators based on perovskites still suffer from the issue of poor stability, which impedes their further wide applications. Herein, a template assembled method to prepare large-size, flexible, and stable CsPbBr 3 @Polymethyl methacrylate composite films in ambient conditions is developed and their detection performance is studied. The composite films can maintain 94% and 81% of the initial PL intensity after 2000 cycles bending and storing in water over 2520 h, respectively. In addition, the prepared scintillators exhibit not only a low detection limit of 40.1 nGy air s −1 and a high spatial resolution of 8.0 lp mm −1 , but also an excellent tolerance against radiation (108 h). Thus, this simple but yet effective method would not doubt pave the way for further development of scintillators and might be well applicable to other metal halides.
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Nanoscale
·
2022
·Vol. 14
·期 17
·6392-6401
·
IF 8.307
Zhaoyan Yang,Yuhui Dong,Shenfei Zong,Lang Li,Kuo Yang,Zhuyuan Wang,Haibo Zeng,Yiping Cui
Single-molecule localization microscopy (SMLM) is one of the most promising super-resolution imaging techniques for visualizing ultrasmall cellular structures. Here, water-dispersed perovskite CsPbBr3 nanocrystals (CsPbBr3 NCs) fabricated by a one-step mechanochemical method are explored as a SMLM fluorophore for bioimaging. Due to their ultrahigh photoluminescence quantum yield (PLQY), inherent frequent fluorescence blinking, proper duty cycle and long-term photostability, an extremely high location precision of ∼3 nm was achieved, a sixfold enhancement than those reported previously. In addition, the spatial resolution of a SMLM image depends on the size of CsPbBr3 NCs, which is approximately 23 nm. Two closely spaced CsPbBr3 NCs with a gap of 40 nm can be clearly distinguished in the SMLM image. More importantly, unlike most perovskite quantum dots (QDs), one-step mechanochemically prepared CsPbBr3 NCs can retain their excellent fluorescence characteristics even after surface biofunctionalization, greatly reducing the current limitations of perovskite QDs on bioimaging. As an example, cell-derived exosomes (30–150 nm in diameter) labeled with CsPbBr3 NCs were easily identified by SMLM. In addition, after being functionalized with biotin, targeted SMLM imaging of the nuclear lamina or cell membranes of cells was achieved with an enhanced resolution. This work may open up a promising avenue to expand the field of perovskite QD-based SMLM to bioimaging with a high location accuracy.
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PubMed
高影响因子
Chemosensors
·
2022
·Vol. 10
·期 5
·170
·
IF 4.229
Henggan Li,Feiming Li,Yipeng Huang,Linchun Zhang,Min Ye,Jingwen Jin,Xi Chen
In this study, CsPbBr3@SiO2perovskite nanocrystal composites (CsPbBr3@SiO2PNCCs) were synthesized by a benzyl bromide nucleophilic substitution strategy. Homogeneous halide exchange between CsPbBr3@SiO2PNCCs and Cl−solution (aqueous phase) was applied to the determination of Cl−in sea sand samples. Fast halide exchange with Cl−in the aqueous phase without any magnetic stirring or pH regulation resulted in the blue shift of the photoluminescence (PL) wavelength and vivid PL color changes from green to blue. The results show that the PL sensing of Cl−in aqueous samples could be implemented by using the halide exchange of CsPbBr3@SiO2PNCCs. A linear relationship between the PL wavelength shift and the Cl−concentration in the range of 0 to 3.0% was found, which was applied to the determination of Cl−concentration in sea sand samples. This method greatly simplifies the detection process and provides a new idea for further broadening PL sensing using the CsPbBr3PNC halide.Keywords:CsPbBr3perovskite nanocrystal composites;colorimetric sensing;photoluminescence wavelength shift;sea sand;Cl−
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ACS Applied Nano Materials
·
2022
·
IF 6.14
Ru-Kun Ding,Xiao-Song Zhang,Lan Li,Jian-Ping Xu,Li-Na Kong,Xiao-Kai Gong,Hao Yin,Zhao-Wei Zhang,Qian Li,Long Liu
Lead halide perovskites have received extensive attention due to their excellent photoelectric and photonic properties. However, low stability is an obstacle to material production and optoelectronic applications. In this research study, CsPbBr3/Cs2SiF6:Mn4+ rivet nanostructured perovskites coated with ZnS and self-passivation layers have been synthesized. The rivet nanostructured perovskites are applied in tunable white light-emitting diode (WLED) devices and tunable flexible white electroluminescent (EL) devices. The red and green dual-wavelength tunable luminescence in the rivet nanostructured perovskites has been obtained via Cs ion sharing. Upon the addition of ZnS and a self-passivation aluminum layer coating on the surface of the rivet perovskites, the photoluminescence (PL) intensity and the stability increased by 588.7 and 323.6%, respectively. In addition, a series of spectrally tunable WLED devices with an InGaN blue LED chip and flexible white EL devices is fabricated using the CsPbBr3/Cs2SiF6:Mn4+/2ZnS/Al rivet nanostructured perovskites. The tunable WLED devices can produce standard white light and cold and warm white light. The tunable EL devices produce luminescence even at 60° bending. By studying the temperature-dependent PL spectra of CsPbBr3/Cs2SiF6:Mn4+/nZnS/Al rivet nanostructured perovskites, the energy transfer mechanism at cryogenic and room temperatures is analyzed. At the same time, the protection principle of the self-passivation coating on the CsPbBr3/Cs2SiF6:Mn4+ rivet nanostructured perovskites is discussed.
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CHEMICAL ENGINEERING JOURNAL
·
2022
·
IF 16.744
Yu Zhang,Guishun Li,Guangning Hou,Jianqiu Lin,Maosheng Chen,Shaohua Liu,Hechun Lin,Junfeng Fang,Chengbin Jing,Junhao Chu
Inorganic cesium lead halide perovskite nanocrystals (NCs) show promising application in the field of optoelectronic devices. However, the poor stability and low photoluminescence quantum yield (PLQY) have been a huge hurdle for practical applications. Ligand engineering strategy was proven to be an effective way to improve the stability and PLQY. Herein, we utilize a multidentate ligand of Boc-D-Glutamic acid (BDGA) to treat the perovskite NCs, enabling exceptional quantum yield approaching 100% and superior colloidal stability (about 10% reduction after 60 days storage at ambient conditions), as well as greatly enhanced resistance to thermal treatment and UV irradiation which can be ascribed to the surface defect passivation and an efficient ligand exchange with robust affinity and/or compensation. Besides, the as-fabricated white light-emitting diodes (WLEDs) exhibits a high luminous efficiency of 93.5 lm/W and a wide color gamut (128% of the National Television System Committee and 95% Rec. 2020). This work provides a facile route to realize high PLYQ and improve the challenging stability issue in perovskite NCs.
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Journal of Materials Chemistry C
·
2022
·Vol. 10
·期 10
·3729-3737
·
IF 8.067
Yi Huang,Pengfei Tang,Wenxia Zhang,Wensheng Yan,Bin Liu,Xiaosheng Tang,Zhen Wang,Yue Peng,Weiwei Chen
Metal halide perovskite quantum dots (QDs) are emerging as promising materials for illumination and display applications owing to their unique optical and electronic properties. However, research into the doping of perovskite QDs with alkali metal cations for use in light-emitting diode (LED) devices is limited. Herein, a facile and convenient room-temperature method for synthesizing Na+-ion-doped CsPbBr3 QDs is presented. Through the optimization of the Na+ doping concentration, the as-prepared Na+-doped CsPbBr3 QDs display a higher photoluminescence quantum yield of 94.74%, faster radiative recombination rate of 30.4 μs−1, and longer lifetime of 31.2 ns than their undoped counterparts, allowing the practical realization of high-efficiency electroluminescent QD LED (QLED) devices. As a result, a maximum luminance of 20 190 cd m−2, a peak current efficiency of 34.5 cd A−1, and an external quantum efficiency of 8.97% for as-fabricated QLEDs are obtained; all these characteristics are higher than those of the control device with undoped CsPbBr3 QDs. Experimental studies combined with auxiliary theoretical calculations indicate that the enhanced performance can be chiefly attributed to the decreased trap defect density of the perovskite upon sodium incorporation. This research indicates the immense potential of the Na+-doped CsPbBr3 QDs to act as an emission layer for use in the next-generation illumination and display fields.
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