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CHINESE PHYSICS LETTERS · 2017 ·Vol. 34 ·期 6 ·068103 · IF 0.8

A Simple Deposition Method for Self-Assembling Single Crystalline Hybrid Perovskite Nanostructures

Wen-Rong Xie,Bin Liu,Tao Tao,Guo-Gang Zhang,Bao-Hua Zhang,Zi-Li Xie,Peng Chen,Dun-Jun Chen,Rong Zhang

A sequential deposition method is developed, where the hybrid organic–inorganic halide perovskite (CH3NH3Pb (I1−xBrx)3) is synthesized using precursor solutions containing CH3NH3I and PbBr2 with different mole ratios and reaction times. The perovskite achieved here is quite stable in the atmosphere for a relatively long time without noticeable degradation, and the perovskite nanowires are proved to be single crystalline structure, based on transmission electron microscopy. Furthermore, strong red photoluminescence from perovskite is observed in the wavelength range from 746 nm to 770 nm with the increase of the reaction time, on account of the exchanges between I− ions and Br− ions in the perovskite crystal. Lastly, the influences of concentration and reaction time of the precursor solutions are discussed, which are important for evolution of hybrid perovskite from nanocuboid to nanowire and nanosheet.

研究领域: 材料科学 · 纳米技术
✓ 已验证 DOI 高影响因子
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ADVANCED FUNCTIONAL MATERIALS · 2019 ·Vol. 30 ·期 6 ·1906232 · IF 15.621

Boosting Photocurrent via Heating BiFeO3 Materials for Enhanced Self-Powered UV Photodetectors

Rudai Zhao,Nan Ma,Kai Song,Ya Yang

BiFeO 3 (BFO) is a potentially important Pb-free ferroelectric with a narrow bandgap and is expected to become a novel photodetector. The photocurrent in BFO 3 strongly depends on the temperature but only a few studies have investigated in detail the relationships between photocurrent and temperature. Here, the temperature-dependent photocurrent and the corresponding photosensing properties of a Ag/BFO/indiumtin oxide (ITO) photodetector based on an optimized planar-structured electrode configuration are investigated. The photocurrent and responsivity of the BFO 3 -based photodetector can first be increased and then be decreased with increasing temperature. The largest photocurrent and responsivity can reach 51.5 µA and 6.56 × 10 −4 A W −1 at 66.1 °C, which is enhanced 126.3% as compared with that at room temperature. This may be caused by the temperature-modulated bandgap and barrier height in Ag/BFO/ITO device. This study clarifies the relationship between photosensing performance and the operating temperature of BFO-based photodetector and will push forward the application of ferroelectric materials in photoelectric field.

研究领域: 材料科学 · 光电领域
✓ 已验证 DOI 高影响因子
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INORGANIC CHEMISTRY · 2020 · IF 4.825

Thermally Stable Phosphor KBa2(PO3)5:Eu2+ with Broad-Band Cyan Emission Caused by Multisite Occupancy of Eu2+

Dan Zhao,Shi-Rui Zhang,Yan-Ping Fan,Bao-Zhong Liu,Rui-Juan Zhang

The relationship between the structure and properties is always a hot topic in the luminescent material field. In this work, a new phosphor KBa2(PO3)5:Eu2+ (KBP:Eu) was prepared by a high-temperature solid-state reaction method and characterized by X-ray diffraction, energy-dispersive X-ray spectroscopy, photoluminescence (PL), and electroluminescence studies. The polyphosphate host KBP offers three lattice environments (K1, Ba1, and Ba2) for Eu2+ ions to realize broad-band emission from 380 to 700 nm under 345 nm excitation. The distributions of Eu2+ in the three lattice sites can be proven by low-temperature PL and transient fluorescence spectroscopy. Furthermore, temperature-dependent luminescence studies for phosphor KBP:0.02Eu reveal that its luminescence intensity at 150 °C retains about 97% of the initial value at 25 °C. By composing a 365 nm UV chip and KBP:0.02Eu, CaAlSiN3:Eu2+ phosphors, a warm white-light-emitting diode (WLED) was obtained with a correlated color temperature of 5146 K and chromaticity coordinates (0.3404, 0.3384). Therefore, KBP:Eu phosphor is a potential cyan-emitting phosphor used for high-power WLEDs.

研究领域: 材料科学 · 光学
✓ 已验证 DOI 高影响因子
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ChemistrySelect · 2022 ·Vol. 7 ·期 33 ·e202202124 · IF 2.307

Construction of Excellent Visible Light Absorption Heat Storage Slurry Using Phase Change Microcapsules for Solar Thermal Utilization

Qingqing Zhang,Zhicheng Sun,Qingwei Guo,Yang Zhou,Zhenzhen Li,Jinyue Wen,Furong Li,Yuanyuan Liu,Shouzheng Jiao

Graphical The combination of photosensitive dyes and phase change microcapsules significantly improves the efficiency of photothermal conversion. The dye converts light energy into heat, which is stored in phase-change microcapsules and released when needed. The heat storage slurry doped with copper phthalocyanine and MXene have the best photothermal conversion performance and are expected to become a novel kind of heat collecting medium. Most solar thermal utilization materials can only absorb ultraviolet irradiation rather than visible-light, limiting the photothermal conversion efficiency of corresponding devices. In this work, a functional thermal slurry system with excellent visible-light absorption and high photothermal conversion performance is developed based on the phase change microcapsules, incorporating the visible-light absorption antenna in the shell structure. Specifically, a phase change microcapsule with paraffin as the core material and silica as the wall material is prepared by the in-situ polymerization method, in which the shell layer is doped with various photosensitive molecules. The photothermal conversion efficiency of copper phthalocyanine and MXene can reach 98 % and 85.3 % respectively. The corresponding conversion efficiency could reach up to more than 80 % in a long temperature range. Therefore, the doping of photosensitive molecules with visible-light absorption can promote the solar energy conversion efficiency of these solar thermal utilization materials.

研究领域: 材料科学 · 太阳能利用
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ACS Applied Optical Materials · 2024 · IF 0

Achieving High Luminescence Thermal Stability in Sm3+-Doped Sc(NbO4)x(TaO4)1–x Orange-Reddish Phosphors by Cosubstitution Component Regulation

Yuhang Zheng,Shoujun Ding,Yong Zou,Xubing Tang,Wenpeng Liu

Sc(NbO4)x(TaO4)1–x is composed of ScNbO4 and ScTaO4 matrices, containing [NbO4]3– and [TaO4]3– self-activating luminescent groups, and is a series of potential high-performance luminescent matrixes. In this work, trivalent samarium (Sm3+)-doped Sc(NbO4)x(TaO4)1–x (SNTO) phosphors have been synthesized through a traditional solid-state reaction method. The quenching concentration of Sm3+ in the SNTO matrix was 2 atom %, and the quenching mechanism was analyzed. Especially, the effects of [NbO4]3–/[TaO4]3– component ratios on luminescent properties and thermal stability were studied. The temperature-dependent fluorescence spectra and decay curves of Sm:SNTO phosphors, spanning from 300 to 510 K, have unveiled their luminescent thermal stability. The activation energy Ea representing luminescent thermal stability was found to be sensitive to the [NbO4]3–/[TaO4]3– component ratios, and the maximum Ea value was 0.272 eV. The findings suggest that the luminescent thermal stability of Sm3+-doped Sc(NbO4)x(TaO4)1–x orange-reddish phosphors can be regulated by the host component. Thus, this study can provide a reference for achieving high luminescent thermal stability phosphors through cosubstitution component regulation.

研究领域: 材料科学 · 无机化学 · 光学
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Advanced Optical Materials · 2024 · IF 8

Multicolor and Hydrochromic Luminescence of Alloyed Cs2CdCl4 for Advanced Information Encryption

Chao Wang,Zhengguang Yan,Lin Ma,Jiawen Xiao

Advanced optical information encryption usually relies on the integration of multicolor, stimulus-responsive, and afterglow luminescence. However, achieving these simultaneously within a single-phase system has posed challenges, complicating the design process. In this study, an advanced 3D information encryption strategy is presented based on undoped and alloyed Cs₂CdCl₄, encrypted through three distinct channels: emission wavelength, water stimulation, and afterglow time. Specifically, Mn 2+ , Sb 3+ , and Ag + doped Cs₂CdCl₄ single crystals are successfully synthesized via a modified hydrothermal method, which exhibit bright orange, green, and blue emissions, respectively. Decryption of specific information can be achieved by employing corresponding narrowband filters. Furthermore, the Cs₂CdCl₄ system demonstrates hydrochromism, attributed to water-induced sequential phase transitions. Upon water treatment, the 2D Cs₂CdCl₄ will undergo a phase transition to Cs 3 Cd 2 Cl 7 , and finally to cubic CsCdCl 3 . Interestingly, the resultant CsCdCl 3 exhibits pronounced afterglow, originating from the triplet emission of Cd ions. Leveraging these unique properties, a highly secure and adjustable 3D encrypted quick response code is designed. The encrypted information is encoded in coordinates, and decrypted information can be retrieved in both compressed and decompressed modes as required. These findings pave the way for the development of novel smart photonic materials and multimodal optical information encryption.

研究领域: 材料科学 · 光学
✓ 已验证 DOI 高影响因子
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CHEMICAL ENGINEERING JOURNAL · 2024 · IF 13.3

Visualization of strain rate based on mechanoluminescence tailing

Man Wang,Jianqiang Xiao,Jian Zhang,Lei Zhao,Yingdan Song,Zhichao Liu,Ting Wang,Xuhui Xu,Jie Yu

Mechanoluminescence (ML) materials have the ability to emit light under mechanical force, allowing for visible mechanical force distribution and making them valuable for applications in smart textiles and wearable sensors. Detecting the force rate is crucial for applications, such as haptic feedback devices and mechanical monitoring, but visualizing the speed of strain has not been achieved yet. In this study, we have successfully visualized the strain rate by monitoring the ML tailing lengths of red, green, and blue (RGB) ML materials, including CaF 2 : Tm 3+ , CaF 2 : Eu 3+ , and CaF 2 : Tb 3+ phosphors. These materials exhibit varying ML tailing lengths at identical rotation speed of friction force, due to their distinct lifetime of the emitting centers. By incorporating these RGB ML phosphors into a composite film, the discrepancies in ML tailing lengths across different colors become visible, with these differences becoming more pronounced as the rotation speeds rise. Ultimately, the visualization of rotational speed in bearings was achieved successfully based on the vivid color changes in the ML tailing length at different speeds.

研究领域: 材料科学 · 光学
✓ 已验证 DOI 高影响因子
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Journal of Materials Chemistry C · 2024 ·Vol. 12 ·期 32 ·12571-12581 · IF 5.7

“Cage-confinement” controlled dimensionality conversion of Bi2O2Se crystals towards high-performance phototransistors

Kaiyi Zhang,Fang Wang,Lei Zheng,Junqing Wei,Yongxu Hu,Yangyang Xie,Hongling Guo,Fengpu Zhang,Xin Lin,Zewen Li,Tianling Ren,Zhitang Song,Kailiang Zhang

2D Bi2O2Se is an intriguing building block for next-generation optoelectronic devices owing to its ultrahigh electron mobility and ultrabroadband photodetection capability. However, fully exploiting its advantages in advanced optoelectronic applications remains greatly challenging owing to the lack of in-depth understanding of the morphological evolution of Bi2O2Se crystals and efficient methods for enhancing their photoresponse. Herein, we developed a novel “cage-confinement” technique to achieve dimensionality-tunable growth of Bi2O2Se crystals in a space-confined CVD system. It can effectively control the key parameter of determining the dimensionality of crystals, referred to as the elastic strain energy of nucleation (ΔGs), by tuning the active area size of Bi2O3 seeds at a suitable flow rate of carrier gas. Furthermore, based on an optimized van der Waals transfer technique of crystals and electrodes, a sheet-shaped phototransistor of Bi2O2Se has a high responsivity (R) of ∼74 000 A W−1 and detectivity (D*) of ∼4.0 × 1011 Jones. Meanwhile, a wire-shaped device demonstrates an impressive R value of 300 000 A W−1, D* value of 3.9 × 1012 Jones and photoconductance gain (Gph) of 1.2 × 105. These results surpass most reported Bi2O2Se-based detectors and pave the way for the applications of 2D layered semiconductors in advanced optoelectronic devices and technologies.

研究领域: 材料科学 · 光电子学
✓ 已验证 DOI 高影响因子
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ACS Applied Materials & Interfaces · 2024 · IF 8.3

Photoconductivity and Photovoltaic Effect Strengthened via Microstructural Cotuning in Ferroelectrics: Intuitively Assessed by Macroscopic Transparency

Xiao Wu,Peng Wang,Xingan Jiang,Shuyao Cao,Jinfeng Lin,Rui Xiong,Zhenhuan Zheng,Min Gao,Chunlin Zhao,Tengfei Lin,Cong Lin,Baisheng Sa

Photoferroelectrics that involve strong light-matter coupling are regarded as promising candidates for realizing bulk photovoltaic and photoelectric effects via light absorption. Nonetheless, understanding the photoresponse mechanism or modulation of performance from a microscopic point of view is scarcely explored through quantification of macroscopic properties. Herein, we design a model material, Gd3+-doped (K0.5Na0.5)NbO3 ferroelectric-transparent ceramics, and present an advantageous strategy to enhance the optoelectronic coupling through joint modulations of lattice distortion and oxygen vacancies, along with inner defects and ferroelectric domains. Significantly, their microcosmic manipulation can be intuitively and facilely evaluated by the optical transparency of each ceramic. An approximately 104 fold increase in conductivity under ultraviolet irradiation was produced. Under the cocoupling between external physical fields, the synergy of photoelectric stimulation increased the photoconductivity of the ceramics by 13.89 times. Additionally, a significant increase (4.5-fold) in the current output from the photovoltaic effect was achieved via ferroelectric domains of moderate size, whose size could be easily assessed by optical transmittance. In situ microscopic observations confirmed that the configuration of oxygen vacancy-dependent ferroelectric domains contributes to the enhanced optoelectronic response. This research provides a distinct way to develop inexpensive optocoupler devices and meet the requirements for multifunctional integration in single photoferroelectrics.

研究领域: 材料科学 · 光学 · 电子工程
✓ 已验证 DOI 高影响因子
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MACROMOLECULAR CHEMISTRY AND PHYSICS · 2020 ·Vol. 221 ·期 6 ·1900557 · IF 2.335

Polythioethers with Controlled α,ω-End Groups Prepared by Visible Light Induced Thiol–Ene Click Polymerization of Dithiol and Divinyl Ether with 4-(N,N-diphenylamino)benzaldehyde as Organocatalyst

Yiran Wang,Xianhong Zhang,Yuhong Ma,Dong Chen,Changwen Zhao,Wantai Yang

This study reports a step-growth click-polymerization of 1,4-benzenedimethane (BDMT) and diethylene glycol divinyl ether (DEGVE) with 4-( N,N -diphenylamino)-benzaldehyde (DPAB) as a photoredox catalyst under irradiation of visible light. DPAB exhibits a strong UV–vis absorption at 350 nm and a strong fluorescence emission at 480 nm in anisole. There is a strong fluorescence quenching between BDMT and DPAB. The molecular weight of the polythiolether can be controlled by reaction time and monomer feed ratios. More importantly, α,ω-dithiol and α,ω-divinyl telechelic polythiolether oligomers are successfully synthesized by simply changing the molar ratios of BDMT to DEGVE. 1 H NMR and MALDI-TOF MS spectra demonstrate that the oligomers have high end group fidelity. In addition, strong fluorescence is observed when the α,ω-dithiol terminated polythiolether adds with N -(1-pyrenyl) maleimide, indicating that the as-prepared polythiolether bears reactive thiol end groups. Furthermore, high molecular weight polythiolether are prepared by chain extension with reactive polythiolether oligomers as macro-monomers. For example, α,ω-divinyl oligomer ( M n = 2000 g mol −1 ) could further react with α,ω-dithiol oligomer ( M n = 2400 g mol −1 ) to form high molecular weight polythiolether ( M n = 6000 g mol −1 ).

研究领域: 材料科学 · 化学工程 · 高分子化学
✓ 已验证 DOI 高影响因子
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Nature Communications · 2019 ·Vol. 10 ·期 1 ·1-10 · IF 11.878

A chloroplast structured photocatalyst enabled by microwave synthesis

Xiao Shuning,Zhang Dieqing,Pan Donglai,Zhu Wei,Liu Peijue,Cai Yong,Li Guisheng,Li Hexing

Photosynthesis occurs through the synergistic effects of the non-ncontinuously distributed components in the chloroplast. Inspired by nature, we mimic chloroplast and develop a generic approach to synthesize non-continuously distributed semiconductors threaded by carbon nanotubes. In the synthesis, carbon nanotubes serve as microwave antennas to produce local super-hot dots on the surface, which might induce and accelerate various organic/inorganic semiconductors assembly. With the unique nanoscale designed bionic architecture, a chloroplast structured photocatalyst with 3−dimentional dual electron transfer pathways facilitate enhanced photocatalytic performance. The as-synthesized carbon nanotubes-titanium oxide achieves a record-breaking efficiency of 86% for nitric oxide treatment under ultraviolet light irradiation. As a general strategy, a wide variety of carbon nanotubes threaded chloroplast structured nanomaterials can be synthesized and these nanomaterials could find applications in energy chemistry, environmental science and human health.

研究领域: 材料科学 · 环境科学 · 生物仿生学
✓ 已验证 DOI 高影响因子
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CRYSTENGCOMM · 2017 ·Vol. 19 ·期 6 ·982-993 · IF 3.474

Fabrication of novel Z-scheme InVO4/CdS heterojunctions with efficiently enhanced visible light photocatalytic activity

Yadong Meng,Yuanzhi Hong,Changyou Huang,Weidong Shi

Novel Z-scheme InVO4/CdS heterojunction photocatalysts have been successfully synthesized for the first time via a microwave-assisted process, followed by a mild hydrothermal method. The crystal structures, morphologies and sizes, chemical compositions and optical properties of the prepared photocatalysts were characterized via X-ray diffraction (XRD), field emission scanning electron microscopy (FESEM), high-resolution transmission electron microscopy (HRTEM), X-ray photoelectron spectroscopy (XPS), UV-vis diffuse reflectance spectroscopy (DRS), and photocurrent measurements. Results showed that the prepared InVO4/CdS heterojunctions were composed of about 15 nm InVO4 nanoparticles and 1.5 μm CdS microspheres, and all heterojunctions exhibited good photoabsorption in the visible light region. The photocatalytic activity of the obtained samples was carefully evaluated via the degradation of rhodamine B (RhB) and ciprofloxacin (CIP) under visible light irradiation (λ > 420 nm). Compared to that of bare InVO4 and CdS, the InVO4/CdS heterojunctions exhibited significantly enhanced photocatalytic activity for RhB and CIP degradation. Moreover, the 40 wt% InVO4-coupled CdS composite displayed the highest catalytic efficiency for RhB photodegradation, which is about 59.4 and 4.8 times higher than that of pure InVO4 and CdS, respectively. In addition, the active species trapping experiment and electron spin resonance (ESR) measurement demonstrated that h+ and ˙O2− radicals were the predominant active species in the photocatalytic reaction process. Furthermore, the possible enhanced photocatalytic mechanism of InVO4/CdS heterojunctions was also proposed based on the band position measurements and ESR analysis.

研究领域: 材料科学 · 纳米技术 · 环境化学 · 光催化 · 无机合成
✓ 已验证 DOI 高影响因子
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