Advanced Optical Materials
·
2016
·Vol. 4
·期 11
·1732-1737
·
IF 5.359
Wen-Gao Lu,Cheng Chen,Dengbao Han,Linhua Yao,Junbo Han,Haizheng Zhong,Yongtian Wang
Graphical The comparison between organic–inorganic CH 3 NH 3 PbBr 3 quantum dots and all inorganic halide perovskite CsPbBr 3 quantum dots allows to understand the structural difference and corresponding optical properties. Using Z-scan measurements, it is revealed that colloidal CH 3 NH 3 PbBr 3 exhibits enhanced two-photon absorption properties compared to those of CsPbBr 3 quantum dots due to their structural difference.
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Advanced Optical Materials
·
2024
·
IF 8
Xingyi He,Tianfeng Li,Zifan Liang,Renming Liu,Xia Ran,Xiaojuan Wang,Lijun Guo,Caofeng Pan
The emission of cyan light (470-500 nm) plays a vital role in the visible light spectrum and is essential for applications such as lighting, displays, and optical communication. Inorganic cesium lead bromide perovskite quantum dots (CsPbBr 3 PQDs) have made significant progress in the field of luminescence materials and devices, however, the lack of techniques to obtain highly emissive and stable cyan-emitting CsPbBr 3 PQDs has limited their device applications. Here, it is demonstrated that the complete surface passivation by treatment of didodecyldimethylammonium bromide (DDAB) and lead bromide, which can enhance the photoluminescence and stability of cyan emitting CsPbBr 3 PQDs. In particular, the photoluminescence quantum yield of CsPbBr 3 QDs can be greatly improved from 10.5% to 83.8%. Through an effective PMMA passivation, the obtained stable and bright CsPbBr 3 PQDs composite films as the cyan color converters can effectively emit the cyan light to fill the “cyan gap” of white light-emitting diode (WLED). The color rendering index value of such WLED is remarkably enhanced from 73.6 to 82.5. This study paves the way for the application of PQD color converters in the next generation of full-visible-spectrum WLED lighting.
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Light-Science & Applications
·
2024
·Vol. 13
·期 1
·1-13
·
IF 20.6
Huang Qianqian,Yin Wenxu,Gao Bo,Zeng Qingsen,Yao Dong,Zhang Hao,Zhao Yinghe,Zheng Weijia,Zhang Jiaqi,Yang Xuyong,Zhang Xiaoyu,Rogach Andrey L.
Quantum-confined CsPbBr 3 perovskites are promising blue emitters for ultra-high-definition displays, but their soft lattice caused by highly ionic nature has a limited stability. Here, we endow CsPbBr 3 nanoplatelets (NPLs) with atomic crystal-like structural rigidity through proper surface engineering, by using strongly bound N-dodecylbenzene sulfonic acid (DBSA). A stable, rigid crystal structure, as well as uniform, orderly-arranged surface of these NPLs is achieved by optimizing intermediate reaction stage, by switching from molecular clusters to mono-octahedra, while interaction with DBSA resulted in formation of a Cs x O monolayer shell capping the NPL surface. As a result, both structural and optical stability of the CsPbBr 3 NPLs is enhanced by strong covalent bonding of DBSA, which inhibits undesired phase transitions and decomposition of the perovskite phase potentially caused by ligand desorption. Moreover, rather small amount of DBSA ligands at the NPL surface results in a short inter-NPL spacing in their closely-packed films, which facilitates efficient charge injection and transport. Blue photoluminescence of the produced CsPbBr 3 NPLs is bright (nearly unity emission quantum yield) and peaks at 457 nm with an extremely narrow bandwidth of 3.7 nm at 80 K, while the bandwidth of the electroluminescence (peaked at 460 nm) also reaches a record-narrow value of 15 nm at room temperature. This value corresponds to the CIE coordinates of (0.141, 0.062), which meets Rec. 2020 standards for ultra-high-definition displays.
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ACS Applied Materials & Interfaces
·
2024
·
IF 8.3
Zhiwei Zeng,Yuhan Meng,Zunxian Yang,Yuliang Ye,Qiuxiang Lin,Zongyi Meng,Hongyi Hong,Songwei Ye,Zhiming Cheng,Qianting Lan,Jiaxiang Wang,Ye Chen,Hui Zhang,Yuting Bai,Xudong Jiang,Benfang Liu,Jiajie Hong,Tailiang Guo,Fushan Li,Yongyi Chen,Zhenzhen Weng
Perovskite nanocrystals have absorbed increasing interest, especially in the field of optoelectronics, owing to their unique characteristics, including their tunable luminescence range, robust solution processability, facile synthesis, and so on. However, in practice, due to the inherent instability of the traditional long-chain insulating ligands surrounding perovskite quantum dots (PeQDs), the performance of the as-fabricated QLED is relatively disappointing. Herein, the zwitterion 3-(decyldimethylammonio)propanesulfonate (DLPS) with the capability of double passivating perovskite quantum dots could effectively replace the original long-chain ligand simply through a multistep post-treatment strategy to finally inhibit the formation of defects. It was indicated from theexperimental results that the DLPS, as one type of ligand with the bimolecular ion, was very adavntageous in replacing long-chain ligands and further suppressing the formation of defects. Finally, the perovskite quantum dots with greatly enhanced PLQY as high as 98% were effectively achieved. Additionally, the colloidal stability of the corresponding PeQDs has been significantly enhanced, and a transparent colloidal solution was obtained after 45 days under ambient conditions. Finally, the as-fabricated QLEDs based on the ligand-exchanged PeQDs exhibited a maximum brightness of 9464 cd/m2 and an EQE of 12.17%.
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ACS Applied Materials & Interfaces
·
2024
·
IF 8.3
Chun Sun,Yiwei Zhao,Yelin Ding,Fuhao Zhang,Zhihui Deng,Kai Lian,Zhengtong Wang,Jiazhi Cui,Wengang Bi
A novel TiO2–CsPbBr3(Q) photocatalyst is proposed and rationally constructed, where CsPbBr3 perovskite quantum dots (QDs) of various sizes inside mesopore TiO2 (M-TiO2) are integrated. These perovskite QDs, generated in situ within M-TiO2, establish a type-II homojunction. Interestingly, a Z-scheme heterojunction is simultaneously formed at the interface between CsPbBr3 and TiO2. Due to the coexistence of the type-II homojunction and the Z-scheme heterojunction, photogenerated electrons are effectively transferred from TiO2 to CsPbBr3, thereby suppressing carrier recombination and thus enhancing the degradation of rhodamine B (RhB). Compared with pure CsPbBr3 and TiO2, TiO2–CsPbBr3(Q) shows significantly enhanced photocatalytic performance for RhB degradation. The degradation efficiency of RhB in the presence of the TiO2–CsPbBr3(Q) attains 97.7% in 5 min under light illumination, representing the highest efficiency observed among photocatalysts based on TiO2. This study will facilitate the development of superior semiconductor catalysts for photocatalytic applications.
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CHEMICAL ENGINEERING JOURNAL
·
2024
·
IF 13.3
Junyang Yin,Feng Wu,Jiangnan Dai,Changqing Chen
Perovskite quantum dots (PQDs) are emerging as promising nanomaterials for optoelectronic applications. However, developing a cost-effective green synthesis process that simultaneously possesses satisfactory photoluminescence quantum yield (PLQY) and stability remains a severe challenge. Here, CsPbBr 3 @PbSO 4 nanocomposites with a near-unity PLQY of 99.8 % and robust ambient stability are synthesized in situ in water via 4-Bromobenzenesulfonic acid and ditetradecylamine ligands. Notably, these nanocomposites show no decline in PLQY even after being immersed in water for over 250 days, and also exhibit superior stability against heating, ultrasonication, UV irradiation, anion exchange, and erosion by polar solvents. First-principles calculations reveal that CsPbBr 3 @PbSO 4 nanocomposites can form a natural quantum well structure, which effectively promotes the radiative recombination of carriers in CsPbBr 3 QDs. Meanwhile, the remarkable stability is attributed to the ultrahigh decomposition enthalpy of PbSO 4 that serves as a strong barrier preventing the invasion of anions and polar media into the embedded CsPbBr 3 QDs. Finally, besides the convenient application of green fluorescent paper, a fingerprint recognition is demonstrated by fabricating a bright-green LED integrated with the CsPbBr 3 @PbSO 4 nanocomposites powder and a commercial UV chip. This work provides a new strategy for green synthesis and practical application of high-efficient and ultrastable PQDs.
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JOURNAL OF COLLOID AND INTERFACE SCIENCE
·
2024
·
IF 9.4
Dong Li,Renyi Li,Yizhou Zhao,Kaixuan Wang,Ke Fan,Wei Guo,Qi Chen,Yujing Li
Perovskite CsPbBr 3 quantum dot shows great potential in artificial photosynthesis, attributed to its outstanding optoelectronic properties. Nevertheless, its photocatalytic activity is hindered by insufficient catalytic active sites and severe charge recombination. In this work, a CsPbBr 3 @Ag-C 3 N 4 ternary heterojunction photocatalyst is designed and synthesized for high-efficiency CO 2 reduction. The CsPbBr 3 quantum dots and Ag nanoparticles are chemically anchored on the surface of g-C 3 N 4 sheets, forming an electron transfer tunnel from CsPbBr 3 quantum dots to Ag nanoparticles via g-C 3 N 4 sheets. The resulting CsPbBr 3 @Ag-C 3 N 4 ternary photocatalyst, with spatial separation of photogenerated carriers, achieves a remarkable conversion rate of 19.49 μmol·g −1 ·h −1 with almost 100 % CO selectivity, a 3.13-fold enhancement in photocatalytic activity as compared to CsPbBr 3 quantum dots. Density functional theory calculations reveal the rapid CO 2 adsorption/activation and the decreased free energy (0.66 eV) of *COOH formation at the interface of Ag nanoparticles and g-C 3 N 4 in contrast to the g-C 3 N 4 , leading to the excellent photocatalytic activity, while the thermodynamically favored CO desorption contributes to the high CO selectivity. This work presents an innovative strategy of constructing perovskite-based photocatalyst by modulating catalyst structure and offers profound insights for efficient CO 2 conversion.
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Small
·
2024
·
IF 13
Yuan-Jun Cai,Qiu-Xia Luo,Qiao-Qiao Jiang,Xin Liu,Xiao-Juan Chen,Jin-Lan Liu,Xiang-Lan Mao,Jia-Xin Qi,Ru-Ping Liang,Jian-Ding Qiu
At present, poor stability and carrier transfer efficiency are the main problems that limit the development of perovskite-based photoelectric technologies. In this work, hydrogen-bonded cocrystal-coated perovskite composite (PeNCs@NHS-M) is easily obtained by inducing rapid crystallization of melamine (M) and N -hydroxysuccinimide (NHS) with PeNCs as the nuclei. The outer NHS-M cocrystal passivates the undercoordinated lead atoms by forming covalent bonds, thereby greatly reducing the trap density while maintaining good structure stability for perovskite nanocrystals. Moreover, benefiting from the interfacial covalent band linkage and long-range ordered structures of cocrystals, the charge transfer efficiency is effectively enhanced and PeNCs@NHS−M displays superior photoelectric performance. Based on the excellent photoelectric performance and abundant active sites of PeNCs@NHS−M, photocatalytic reduction of uranium is realized. PeNCs@NHS−M exhibits U(VI) reduction removal capability of up to 810.1 mg g −1 in the presence of light. The strategy of cocrystals trapping perovskite nanocrystals provides a simple synthesis method for composites and opens up a new idea for simultaneously improving the stability and photovoltaic performance of perovskite.
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JOURNAL OF ALLOYS AND COMPOUNDS
·
2024
·
IF 5.8
Zhou Yuan,Le Han,Yuchi Zhang,Lufang He,Peng Liu,Yan Xu
Self-assembled inorganic metal halide perovskite composites with high emitting efficiency, tunable multimode emission and stimuli-responsive luminescence demonstrated great potential in diversified luminescence applications. Here, a novel CsPbBr 3 /EuWO 4 (OH) composite was successfully prepared through the surface adsorption of Pb 2+ ions on hydroxylated EuWO 4 (OH) microsheets and subsequent nucleation of CsPbBr 3 peroviskite quantum dots (PQDs) by the anti-solvent crystallization in CsBr containing N,N-dimethylformamide (DMF) solution. Due to the distinct fluorescent thermochromic switching properties of temperature-insensitive Eu 3+ and sensitive CsPbBr 3 PQDs emitting centers, the resultant CsPbBr 3 /EuWO 4 (OH) composite exhibits excellent ratiometric temperature sensing performance. The CsPbBr 3 /EuWO 4 (OH) thermometer based on the fluorescence intensity ratio (FIR) technique originating from emissions of Eu 3+ to CsPbBr 3 PQDs was then explored with a high temperature sensitivity (S r ) of 5.8 % ℃ −1 at 54 ℃. In addition, a high-security-level information encryption scheme was proposed by utilizing the excitation-wavelength-dependent switchable fluorescence of CsPbBr 3 /EuWO 4 (OH) composite. This study provides a simple and feasible strategy for assembling dual-emission CsPbBr 3 /EuWO 4 (OH) composite, showing potential applications in optical ratiometric thermometry and information encryption fields.
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ELECTROCHIMICA ACTA
·
2024
·
IF 5.5
Yanting Li,Jiaying Li,Hua Yao,Lili Meng,Qian Chen
Carbon-based perovskite solar cells (PSCs) have attracted attention as low-cost and facile fabrication process. However, the ionic nature of perovskite and nonradiative recombination at perovskite/carbon interface are present inevitable obstacles in approaching their highly efficiency. Herein, the multifunctional molecules of zinc oxalate is implanted into the precursor of perovskite to passivate defects and narrowing the interface energy barrier, and a flexible method of screen-printing employed in prepare stacked structure device ITO/SnO 2 /CsPbBr 3 •x % ZnOX //CQDs/ITO. In this regard, CQDs are used as carbon electrodes to replace expensive materials of hole transport layer and precious metal electrode, in which CQDs extracted from sugarcane molasses, a cheap by-product of native sugar industry. Additionally, the stacked structure composed of a photoanode (ITO/SnO 2 /CsPbBr 3 •x % ZnOX) and back electrode (CQDs/ITO) exhibits a promising prospect in photovoltaic application. Finally, the power conversion efficiency of 2 % ZnOX modified PSCs increases to 1.96 %, and the improvement rate has reached 1.54 times. In addition, modified PSCs with a greater stability compared with that of the control device. This work presents a useful approach to passivate defects and provides a cost-effective option to fabricate devices with stacked structure.
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ADVANCED MATERIALS
·
2018
·Vol. 30
·期 44
·1802110
·
IF 21.95
Zheng Yang,Qian Xu,Xiandi Wang,Junfeng Lu,Hui Wang,Fangtao Li,Li Zhang,Guofeng Hu,Caofeng Pan
Stability is a key problem that hinders the practical application of lead halide perovskite. Therefore, all-inorganic perovskite CsPbX 3 monocrystalline films are urgently needed to fabricate photoelectric devices. Herein, a low-temperature and substrate-independent growth method is demonstrated to grow millimeter-level inorganic perovskite monocrystalline thin films. These films present good optical and electrical properties comparable to bulk ones. What is more, they exhibit excellent long-term stability toward humidity and thermal treatment. The as-grown CsPbBr 3 monocrystalline films are then fabricated into photodetectors with high photodetection performance. These results demonstrate that the CsPbBr 3 monocrystalline films have potential in fabricating high-performance optoelectronic devices.
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OPTICS EXPRESS
·
2024
·Vol. 32
·期 6
·9276-9286
·
IF 3.2
Shuya Ning,Shuya Ning,Zhihui Liu,Shuo Wang,Naming Zhang,Bin Yang,Xin Wang,Fanghui Zhang
All-inorganic halide perovskite quantum dots (QDs) have recently received much attention due to their excellent optoelectronic properties. And their emission properties still need to be improved for further applications. Here, we demonstrated a remarkable emission enhancement of the CsPbBr3 QDs based on an Ag nanoparticle-Ag film plasmonic coupling structure. Through precise control of the gap distance between Ag nanoparticle and Ag film, the localized surface plasmon resonance (LSPR) peak was tuned to match the emission wavelength of the CsPbBr3 QDs. We achieved a 30-fold fluorescence intensity enhancement and a lower lasing threshold, which is 25% of that of the CsPbBr3 QDs without plasmonic coupling structure. It is attributed to that the plasmonic coupling structure exhibits an extremely strong local electric field owing to the coupling between LSPR of Ag nanoparticle and surface plasmon polariton of Ag film. This work provides an effective way to enhance the optical emission of perovskite QDs and promotes the further exploration of on-chip light source.
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