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APPLIED SURFACE SCIENCE · 2024 · IF 6.3

ZIF-8-CdS photonic crystal beads for slow photon effect induced enhanced photocatalysts

Tianyi Zhang,Da Teng,Jiaojiao Zhang,Zihui Meng,Lili Qiu

The unique periodic structure of photonic crystals demonstrates an effective slow photon effect that enhances the interaction between light and matter. This study designed and prepared MOF photonic crystal beads, and significantly improved the photocatalytic efficiency by utilizing the slow light effect. Utilizing microfluidic technology, ZIF-8 was self-assembled to form photonic crystal beads (PCB-Z) to enhance adsorption properties and light absorption. The surface of PCB-Z is modified with CdS to form a heterostructure (PCB-ZC), which widens the absorption spectrum, reduces the carrier recombination rate, and increases the specific surface area, while the photocurrent intensity of PCB-ZC is about 1.8 and 29 times that of CdS and PCB-Z. Under the combined effect of photonic crystal structure, ZIF-8/CdS heterojunction and slow photon effect, the degradation rate of Rhodamine B by PCB-ZC was 15.22 times higher than the disordered ZIF-8 powder, and the photocatalytic performance was significantly improved. The dominant role of holes in Rhodamine B degradation was confirmed by free radical trapping experiments and EPR tests. This research confirms that MOF-based photonic crystals can be assembled into periodic structures to enhance adsorption properties and light absorption, which provides a new paradigm for the development of MOF-based photocatalysts.

CAS / MDL: 57-09-0
研究领域: 材料科学 · 光化学
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DALTON TRANSACTIONS · 2020 ·Vol. 49 ·期 11 ·3606-3614 · IF 4.174

Novel Mn4+ doped red phosphors composed of MgAl2O4 and CaAl12O19 phases for light-emitting diodes

Yibing Wu,Yixi Zhuang,Rong-Jun Xie,Kaibin Ruan,Xinhua Ouyang

Red emitters based on CaAl12O19:Mn4+ have been attracting extensive attention due to their advantages of being rare-earth-free and chemically stable. However, their relatively low luminescence efficiencies will seriously hinder their application in light-emitting diodes (LEDs). In this regard, the promising red phosphors of CaAl12O19:Mn4+ were synthesized with enhanced luminous efficiency by introducing the coexisting phase of MgAl2O4. Importantly, an approximately 5 times enhancement of integrated intensity in the emission spectrum was observed for the phosphor with the coexisting phase compared to that with a single phase. Their crystal structures, morphologies and photoluminescence properties and the mechanism of improved luminescence were systematically investigated. Upon exciting them by using near-ultraviolet or blue LEDs, an efficient red emission was achieved with a maximum peak at ∼658 nm. In order to evaluate their potential application, a warm white LED and a plant growth LED were fabricated by using the prepared phosphors in combination with YAG:Ce3+ and InGaN-based blue chips.

研究领域: 材料科学 · 光学工程
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JOURNAL OF NANOPARTICLE RESEARCH · 2016 ·Vol. 18 ·期 2 ·1-11 · IF 2.101

Low toxic and highly luminescent CdSe/Cd x Zn1−x S quantum dots with thin organic SiO2 coating for application in cell imaging

Du Yingying,Yang Ping,Matras-Postolek Katarzyna,Wang Junpeng,Che Quande,Cao Yongqiang,Ma Qian

A silanization process was employed to transfer hydrophobic quantum dots (QDs) prepared via an organic route at high temperature into water phase. The QDs were further coated with a thin organic SiO 2 shell to form QDs@SiO 2 composite nanoparticles by ligand exchange or remaining initial organic ligands on the surface. In this study, QDs with different ligands, either trioctylphosphine oxide (TOPO) or oleic acid (OA), were employed to investigate the effects of ligands on the reverse micelles in preparing QDs@SiO 2 nanoparticles. In the preparing process, hydrophobic QDs were silanized by partially hydrolyzed tetraethyl orthosilicate (TEOS). For TOPO-capped CdSe QDs, surface TOPO ligands were completely replaced by partially hydrolyzed TEOS. As for OA-capped CdSe/Cd x Zn 1− x S QDs, surface OA ligands were partially replaced. It was found that the ligand exchange drastically reduced the photoluminescence (PL) efficiency of CdSe QDs. Furthermore, the cytotoxicity studies of QDs@SiO 2 have been carried out in detail. The results indicate that CdSe/Cd x Zn 1− x S QDs@SiO 2 composite nanoparticles exhibit lower cytotoxicity compared with CdSe QDs@SiO 2 , because the SiO 2 shell and remained OA ligand layer can effectively prevent the leakage of toxic Cd 2+ ions. Meanwhile, it was found that these CdSe/Cd x Zn 1− x S QDs@SiO 2 nanocomposites could keep excellent PL properties even for 24 h incubating with Siha cells, which indicating that our prepared composite nanoparticles are potentially applicable for cell imaging in biological systems.

CAS / MDL: 7782-49-2
研究领域: 生物医学 · 材料科学
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CERAMICS INTERNATIONAL · 2022 · IF 5.532

SrLaNaTeO6:Eu3+ red-emitting phosphors with high luminescence efficiency and high thermal stability for high CRI white LEDs

Yuan Wang,Zhikai Liang,Kezhou Jiang,Yifang Lin,Daomiao He,Jinhui Liu,Weixian Wang,Jingfei Wang,Bin Deng,Dan Zhang,Ruijin Yu

A novel single-phase trivalent europium activated red-emitting SrLaNaTeO 6 phosphor was first synthesized in a process of traditional high-temperature solid-state. The phase purity, morphology, and spectroscopy of the prepared phosphor were analyzed. Under 395 nm excitation, the photoluminescence (PL) spectra of the SrLaNaTeO 6 :Eu 3+ products mainly contained five dominant sharp peaks. The intense red emission peak at 615 nm was the typical 5 D 0 → 7 F 2 electric dipole transition of Eu 3+ . The optimum product of high quenching concentration was the SrLaNaTeO 6 :0.90Eu 3+ , which reached a high internal quantum efficiency (IQE) of 90.6%. The SrLaNaTeO 6 :0.90Eu 3+ was estimated to have R c of 6.57 Å and possessed high color purity of 100.0%. The phosphors exhibited excellent thermal stability and high activation energy ( E a  = 0.29 eV). The prepared white light-emitting diode (WLED) had a high color rendering index (CRI) R a of 92 and a low correlated color temperature (CCT) of 5008 K. In conclusion, the phosphors have potential as red components for WLEDs.

研究领域: 材料科学 · 光学
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Crystals · 2017 ·Vol. 8 ·期 1 ·4 · IF 1.566

Improved Stability and Photoluminescence Yield of Mn2+-Doped CH3NH3PbCl3 Perovskite Nanocrystals

Xianli Li,Yan Guo,Binbin Luo

Organic–inorganic CH3NH3PbCl3perovskite nanocrystals (PNCs) doped with Mn2+, CH3NH3PbxMn1−xCl3, have been successfully prepared using a reprecipitation method at room temperature. Structural and morphological characterizations reveal that the CH3NH3PbxMn1−xCl3PNCs with cubic phase transforms from particles to cubes and increases in size from 16.2 ± 4.4 nm in average diameter to 25.3 ± 7.2 nm in cubic length after the addition of Mn2+precursor. The CH3NH3PbxMn1−xCl3PNCs exhibit a weak exciton emission at ~405 nm with a low absolute quantum yield (QY) of around 0.4%, but a strong Mn2+dopant emission at ~610 nm with a high QY of around 15.2%, resulting from efficient energy transfer from the PNC host to the Mn2+dopant via the4T1→6A1transition. In addition, the thermal and air stability of CH3NH3PbxMn1−xCl3PNCs are improved due to the passivation with (3-aminopropyl) triethoxysilane (APTES), which is important for applications such as light emitting diodes (LEDs).Keywords:perovskite;Mn2+doping;CH3H3PbCl3;stability

研究领域: 材料科学 · 光学
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Nanoscale Research Letters · 2018 ·Vol. 13 ·期 1 ·1-7 · IF 3.125

Dual-Emissive and Color-Tunable Mn-Doped InP/ZnS Quantum Dots via a Growth-Doping Method

Zhang Guilin,Mei Shiliang,Wei Xian,Wei Chang,Yang Wu,Zhu Jiatao,Zhang Wanglu,Guo Ruiqian

In this letter, dual-emissive and color-tunable Mn-doped InP/ZnS quantum dots (Mn:InP/ZnS QDs) with the absolute photoluminescence quantum yield (PL QY) up to 78% were successfully synthesized via a growth-doping method. The dual emission of Mn:InP/ZnS QDs is composed of intrinsic emission and Mn-doped emission, which can be tuned by different Mn/In ratios. With the increase of Mn dopant concentration, the intrinsic emission shows a red shift from 485 to 524 nm. The new class of dual-emissive QDs provides potential for future application in white LED.

研究领域: 材料科学 · 纳米技术
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Nano Research · 2024 · IF 9.5

Bright InP quantum dots by Ga-doping for red emitters

Song Kai-Zheng,He Xiao-Hang,Chen Zhe-Yong,Tang Ge,Huang Jin-Zhao,Jiang Feng-Lei

Environment-friendly indium phosphide (InP)-based quantum dots (QDs) with efficient red-emitting properties are sufficiently needed to satisfy the requirement of burgeoning display and lighting technology. Currently, the syntheses of InP QDs using tris(trimethylsilyl)phosphine as the precursor are highly toxic and expensive. Herein, we successfully introduced gallium (Ga) ions into tris(dimethylamino)phosphine-based red InP cores through thermally-promoted cation exchange, and the obtained Ga-doped InP cores exhibited significantly increased photoluminescence quantum yields (PLQY) of up to 26%. The existence of Ga was directly confirmed by energy-dispersive X-ray spectroscopy and X-ray photoelectron spectroscopy, and the functions of Ga were systematically studied. After subsequent coating of Ga-doped InP cores with ZnSeS and ZnS shells, the resulting Ga-InP/ZnSeS/ZnS QDs achieved a high PLQY of 62% with an emission maximum at 640 nm. In contrast, without Ga-doping, the PLQY only attained 36% using the same synthetic approach. This indicated an approximate 1.7-fold increase in PLQY. The enhancement of photoluminescence was related to the Ga 3+ , as it not only passivated surface defects of InP cores but also reduced core-shell interface stress. The Ga-InP/ZnSeS/ZnS QDs exhibited good stability towards heat treatment and ultraviolet (UV) irradiation. Moreover, the red light-emitting diode (LED) based on Ga-InP/ZnSeS/ZnS QDs performed well in a wide injected current range of 2 to 200 mA, with a maximum power efficiency of 0.68 lm/W. This work showcases Ga-doping through cation exchange as a promising strategy for enhancing the efficiency of InP-based red emitters.

研究领域: 材料科学 · 纳米技术
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Science China-Chemistry · 2025 · IF 9.7

A facile ligand engineering strategy to achieve ultra-highly efficient afterglow luminescence of ordinary metal salts

Liang Li Ya,Wang Xiao Yuan,Gao Ya Ting,Wu Da Jun,Li Da Wei,Chen Bin Bin

Ordinary metal salts have become a promising afterglow material because of the characteristics of wide sources, low cost, and easy availability. However, their extremely weak afterglow efficiency makes them rarely used in practical applications. In this study, we proposed a ligand engineering strategy to greatly enhance the afterglow efficiency of metal salts. Al 2 (SO 4 ) 3 , as a typical metal salt, has only a photoluminescence quantum yield (PL QY) as low as 0.1% and an unmeasurable phosphorescent QY. After doping with dual organic ligands, the PL QY of Al 2 (SO 4 ) 3 has increased by nearly 200 times, reaching 19.90%. Meanwhile, the afterglow intensity of Al 2 (SO 4 ) 3 has increased by approximately 20 times, accompanied by a great increase in phosphorescent lifetime from 416.15 to 2870.08 ms (a about 7-time increase). The enhancement mechanism of afterglow efficiency is ascribed to the fact that the excited electrons from the dual ligands can be directly captured by oxygen defects (trap), then transferred to the emitters (Al 3+ ions), and ultimately achieving efficient afterglow luminescence. This study utilizes ligand engineering strategy to improve the afterglow luminescence efficiency of metal salts, achieving their applications in deep ultraviolet (UV)-excited light emitting devices and visual ethylene glycol recognition.

CAS / MDL: 141-78-6 78525-34-5
研究领域: 材料科学 · 化学
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Coatings · 2021 ·Vol. 11 ·期 5 ·581 · IF 2.881

Synthesis of Highly Luminescent InP/ZnS Quantum Dots with Suppressed Thermal Quenching

Linyuan Lian,Youyou Li,Daoli Zhang,Jianbing Zhang

InP quantum dots (QDs) are promising down-conversion phosphors for white light LEDs. However, the mainstream InP QDs synthesis uses expensive phosphorus source. Here, economic, in situ-generated PH3is used to synthesize InP QDs and a two-step coating of ZnS shells is developed to prepare highly luminescent InP/ZnS/ZnS QDs. The QDs show a photoluminescence quantum yield as high as 78.5%. The emission can be tuned by adjusting the halide precursor and yellow emissive InP/ZnS/ZnS QDs are prepared by judiciously controlling the synthetic conditions. The yellow QDs show suppressed thermal quenching and retain >90% room temperature PL intensity at 150 °C for the growth solution. Additionally, the PL spectrum matches with the eye sensitivity function, resulting in efficient InP QD white light LEDs.Keywords:InP;quantum dots;core/shell;InP/ZnS;thermal quenching

研究领域: 材料科学 · 光学工程
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JOURNAL OF NANOPARTICLE RESEARCH · 2013 ·Vol. 15 ·期 8 ·1-11 · IF 2.175

Water-soluble CdSe/CdS and CdSe/Cd x Zn1−x S quantum dots with tunable and narrow luminescent spectra and high photoluminescence efficiency

Zhang Qiang,Cao Yongqiang,Shen Jianxing,Yang Ping

Nearly monodisperse CdSe/CdS and CdSe/Cd x Zn 1− x S core–shell quantum dots (QDs) were synthesized by the epitaxial growth of CdS or Cd x Zn 1– x S shells on pre-synthesized CdSe cores through a facile organic route. The thickness effect of CdS and Cd x Zn 1− x S shells on the properties of resulting core–shell QDs, such as the photoluminescence (PL) efficiency, PL full width at half-maximum (fwhm), and PL decay lifetime, were investigated. The PL efficiency is greatly enhanced from 9 % of CdSe cores to 64 % of CdSe/Cd x Zn 1− x S core–shell QDs. The PL spectra are narrowed after coating (fwhm ~28–32 nm). The alloy Cd x Zn 1− x S shell is especially effective to enhance the PL efficiency, and it leads to a smaller red-shift in PL spectra compared with that of the CdS shell. The water-soluble CdSe/Cd x Zn 1− x S core–shell QDs were obtained by the encapsulation of amphiphilic poly(styrene-co-maleic anhydride) (PSMA)–ethanolamine (EA) polymers, which was initially dispersed in oil phase. It was found that the CdSe/Cd x Zn 1− x S QDs in water still retained a high PL efficiency as well as a small value in fwhm after encapsulating the CdSe/Cd x Zn 1− x S QDs with PSMA–EA polymers, expanding the applications of these core–shell QDs in aqueous environment.

CAS / MDL: 7782-49-2
研究领域: 材料科学 · 纳米技术 · 光学
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NANOTECHNOLOGY · 2018 ·Vol. 30 ·期 7 ·075704 · IF 3.404

Tunable dual emission in Mn2+-doped CsPbX3 (X = Cl, Br) quantum dots for high efficiency white light-emitting diodes

Weiwei Chen,Xiaosheng Tang,Zhigang Zang,Yue Shi,Zhaoqi Yang,Juan Du

Doping of Mn2+ into semiconductor nanocrystals has been demonstrated to endow them with novel electronic, optical and magnetic functionalities. In this paper, Mn-doped CsPbX3 (X = Br, Cl) quantum dots (QDs) were synthesized at room temperature via a facile strategy by introducing dimethyl sulfoxide (DMSO)-MnBr2/PbX2 composite as a precursor. The excitonic emission spectra of the as-obtained Mn-doped CsPbX3 QDs can be tuned from 517 nm to 418 nm by adjusting the ratio of PbBr2/PbCl2 precisely, and the luminescence mechanism of the doped QDs is discussed in detail. Moreover, the highest photoluminescence quantum yield of the Mn2+ emission achieves 36.7%, which is comparable with QDs prepared by the conventional hot-injection method. Depending on the ratios of PbPb2/PbCl2, the energy transfer rate from the band-edge to Mn2+ excited state is in the range of 0.006–20.42 × 107 s−1. Furthermore, white light-emitting diodes (LEDs) were successfully fabricated by combining the as-prepared Mn-doped CsPbX3 QDs with commercial UV GaN chips, and the high luminous efficiency of the as-prepared white LEDs was developed to 55.9 lm W−1. This work strongly supports the fact that Mn-doped CsPbX3 QDs are promising materials for application in lighting and displaying fields.

研究领域: 材料科学 · 光学 · 纳米技术
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JOURNAL OF MATERIALS SCIENCE · 2022 ·Vol. 57 ·期 9 ·5374-5383 · IF 4.682

Rapid anti-solvent vapor-assisted synthesis of CsPbBr3/Cs4PbBr6 microcrystals with high brightness and stability of green light emission

Qin Wenjing,Zheng Kai,Liu Hengchao,Chu Jingting

The CsPbBr 3 /Cs 4 PbBr 6 perovskite composite material has received wide attention due to its good stability and photoelectric properties, and it is promising to appear in various photoelectric applications. However, there are still some challenges in how to control the synthesis of this material and obtain the balance between high fluorescence efficiency and well stability. In this study, we proposed a rapid anti-solvent vapor-assisted method to prepare CsPbBr 3 /Cs 4 PbBr 6 microcrystals (MCs) with hexagonal tower structure. It is found that oleic acid and oleamine can effectively control the morphology, grain size and optical properties of the material. This unique hexagonal tower structure CsPbBr 3 /Cs 4 PbBr 6 MCs has excellent optical properties, showing strong green emission at 514 nm and PLQY of 78.4 ± 4.3%, with a narrow full width at half maximum value of 20 nm. In addition, environmental stability experiments have shown that after 6 months of storage under 50% relative humidity, the PL strength loss is lower than 20%. Graphical Abstract

CAS / MDL: 112-90-3 112-80-1
研究领域: 材料科学 · 光电材料
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