APPLIED SURFACE SCIENCE
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2022
·
IF 7.392
Hongwei Ding,Jingjing Yang,Rui Liu,Yan Li,Xueliang Liu,Xiangyue Wang,Lin Jin
Driven by clean solar energy, photocatalytic technology can effectively degrade organic pollutants and kills pathogenic bacteria. Researchers are always devoted to developing more economical and efficient photocatalysts. In this work, mesoporous TiO 2 nanoparticles (MTN) with controlled diameters (100–200 nm) and large specific surface areas (∼112 m 2 /g) were prepared via a simple sol–gel method. Then, 10 wt% Ag nanocrystals (∼5 nm) were in situ generated in the MTN via solvothermal process, Ti 3+ and oxygen vacancies also been introduced on their surface, thereby leading to a narrowed bandgap (∼2.9 eV) and strong absorption in the visible region. Finally, polydopamine (PDA) was decorated on the surface of Ag/bMTN to further improve their dispersity and photocatalytic activity. The degradation rate of tetracycline and the bactericide rate of E. coli could surpass 90 % and 99 %, which were mainly attributed to the generated O 2 − and the released Ag ions.
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NANO
·
2022
·
IF 1.438
Zhenyang Yao,Yali Yin,Yu Xia,Haitao Chen
All-inorganic halide perovskite (CsPbX 3 ) is a photoelectric material with great potential. However, the Pb element in CsPbX 3 is toxic, which affects the further use of these materials. The toxicity problem can be solved by adding Zn ions into CsPbBr 3 . In this work, Zn-doped cesium lead bromide perovskites (CsPbBr 3 ) nanocrystals (NCs) were synthesized by thermal injection method, and their optical properties were also studied. When Zn was introduced into CsPbBr 3 , its exciton emission summit shifts slightly. By changing the concentration of Zn 2 + , the size and optical properties of Zn:CsPbBr 3 NCs can be controlled. We also study the decay lifetime of its emission peak, and the results showed that Zn:CsPbBr 3 had a longer PL decay lifetime than undoped CsPbBr 3 . This indicated that the incorporation of CsPbBr 3 into Zn 2 + had a good application prospect in the optical field.
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INORGANIC CHEMISTRY
·
2022
·
IF 5.436
Dayu Huang,Qiuyun Ouyang,Jinjiang Wu,Youchao Kong,Bo Wang,Hongzhou Lian,Jun Lin
Broadband emission with a large Stokes shift is important to obtain an excellent color rendering index of the solid-state lighting device. Among low-dimensional material and perovskite-like phosphors with broadband self-trapped emission, Sn-based phosphors have attracted much attention due to their high photoluminescence quantum yield (PLQY). However, the disadvantage is that the synthesis of Sn-based phosphors needs to be performed in a glovebox. Upon photoexcitation, the broadband emission of self-trapped excitons results from exciton–phonon coupling induced by the transient distortion of the lattice. Low-dimensional material structures often promote self-trapped emission because of more vibrational degrees of freedom and easier polarization under photoexcitation. Here, zero-dimensional (0D) SnX2 (X = Br, I) single crystals are synthesized by the solvent evaporation method in the air. SnX2 emits blue light, broadband yellow light, and deep red light, among which SnBr2 has the best luminescence performance. The photoluminescence quantum yield (PLQY) of SnBr2 reaches 85% and the Stokes shift reaches 265 nm. The PL intensity of SnX2 is linearly related to excitation power, which preliminarily indicates that the origin of SnX2 luminescence is attributed to self-trapped emission (STE). The white light-emitting diodes (WLEDs) were fabricated using yellow-emitting SnBr2 and blue-emitting BaMgAl10O17:Eu2+, which has a low correlated color temperature (3160 K) and a relatively common color rendering index (79).
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高影响因子
APPLIED SURFACE SCIENCE
·
2022
·
IF 7.392
Yanzhao Wu,Xiaoyang Yue,Jiajie Fan,Xiaoming Hao,Quanjun Xiang
In recent years, the semimetal bismuth with surface plasmon resonance (SPR) effect has attracted great attention due to its application in enhancing photocatalytic activity. Herein, we developed a novel plasma-enhanced Bi/CsPbBr 3 composite photocatalyst by in situ growth method (BCPB-IS) using the fabricated CsPbBr 3 nanosheets (CPB) as the substrate for subsequent growth of Bi nanoparticles. Without the addition of any sacrificial agent, the CO yield of BCPB-IS reaches 76.4 µmol g −1 with an over 97% selectivity of CO under 4 h visible light irradiation. Such remarkable CO 2 reduction activity far exceeds that of pure CPB. The enhanced activity can be attributed to these factors: (1) The SPR effect from the loading of Bi NPs enhances the light response performance of BCPB; (2) The simultaneously generated hot electrons leads to rising ambient temperature, which promotes the electron transfer efficiency and photoreduction reaction efficiency; (3) The energy band bending effect at the interface of BCPB further improves the carrier separation and transfer performance. The enhanced separation and transfer performance of photogenerated carriers were investigated in detail by X-ray photoelectron spectroscopy (XPS), Infrared thermograms and Time-resolved photoluminescence spectra (TRPL).
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Advanced Fiber Materials
·
2022
·Vol. 5
·期 1
·183-197
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IF 12.958
Hu Xiaobo,Xu Yanqiao,Wang Jiancheng,Ma Jiaxin,Wang Lianjun,Jiang Wan
All-inorganic CsPbX 3 (X = Cl, Br, I) perovskite nanocrystals (NCs) are emerging as promising candidate materials for optoelectronic devices due to their splendid optical and electrical properties. However, the intrinsic instability greatly limits their practical application. Herein, a feasible strategy is proposed for fabricating highly stable and luminescent CsPbBr 3 @PVDF-HFP/PS nanofibers by combining one-step electrospinning method with 1 H ,1 H ,2 H ,2 H -perfluorodecyltrimethoxysilane (PFDTMS)-assisted post-treatment. The bright-emitting CsPbBr 3 NCs can be effectively encapsulated within polymer nanofibers, which exhibit ultrafine diameter of only 88.1 ± 2.8 nm and high photoluminescence quantum yield (PLQY) of 87.9% via rationally optimizing the electrospinning parameters, concentration of perovskite precursors and ligands. Most importantly, the superhydrophobic surface structures of nanofibers are formed by the hydrolysis and condensation of PFDTMS under moist environment. Benefiting from the double effective protection of polymer matrices and hydrophobic PFDTMS oligomers against moisture erosion, the CsPbBr 3 @PVDF-HFP/PS nanofibers present an obviously improved stability, which can retain 90% initial PL intensity after water immersion for 70 days. Furthermore, an efficient white light-emitting diode with wide color gamut covering 117% of National Television System Committee (NTSC) standard is successfully fabricated based on the composite nanofiber membranes, suggesting their promising prospect for solid-state lighting and display applications. Graphical Abstract Superfine perovskite nanofibers with efficient fluorescence and ultrahigh stability are fabricated by combining one-step electrospinning method with PFDTMS-assisted post-treatment.
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Journal of Materials Chemistry A
·
2022
·Vol. 10
·期 42
·22468-22476
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IF 14.511
Guilin Yin,Xiaosi Qi,Yanli Chen,Qiong Peng,Xingxing Jiang,Qinglong Wang,Wenhua Zhang,Xiu Gong
Metal halide perovskite quantum dots (QDs) are regarded as one of the promising photocatalysts for CO2 reduction because of their unique optoelectronic properties. However, severe charge recombination and insufficient CO2 absorption/activation have limited photocatalytic CO2 reduction. Herein, we report an efficient 0D/0D CsPbBr3/CdSe heterojunction consisting of CdSe QDs in situ grown on CsPbBr3 QDs for high-performance photocatalytic CO2 reduction using water as the electron donor in organic solution. The type-II 0D/0D heterojunction with the strong electronic coupling of Pb–Se and Br–Cd bonds between CdSe and CsPbBr3 facilitates fast electron transfer. Moreover, the specific abundant edge- and corner-sites of CdSe accelerate the CO generation by forming a Cd–C2O4− adduct, enabling superior CO2 activation capacity and efficient CO2 conversion into CO. Consequently, assisted by water to provide electrons and protons, the yield of main product CO reaches 115.26 μmol g−1, which is 4.6-fold higher than that of pristine CsPbBr3. This study is expected to provide a new way to fabricate high-performance perovskite-based catalysts in the field of photocatalysis.
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CHEMICAL ENGINEERING JOURNAL
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2022
·
IF 16.744
Xiaobo Hu,Yanqiao Xu,Jiancheng Wang,Jiaxin Ma,Lianjun Wang,Wan Jiang
CsPbX 3 (X = Cl, Br, I) perovskite nanocrystals (NCs) are emerging as promising candidates for fluorescence sensors due to their superior optoelectronic properties. However, the poor stability restricts their practical applications in aqueous fluorescent detection. Herein, we report in-situ encapsulation of CsPbX 3 NCs into uniform PVDF-HFP/PS polymer nanofibers with fine diameter of only 49.9 ± 2.2 nm by one-step electrospinning process. The as-fabricated CsPbX 3 @PVDF-HFP/PS nanofibers exhibit high photoluminescence quantum yield (PLQY) of 90%, tunable emission wavelength covering the whole visible range of 451.5–650.8 nm. Most importantly, the water stability of nanofiber membranes can be significantly improved by introducing the 1H,1H,2H,2H-perfluorodecyltrimethoxysilane (PFDTMS) as hydrophobic additives, in which their PL intensity can retain 88% initial value after water immersion for up to 100 days. The universality of this fabrication strategy for the stable nanofibers is demonstrated by utilizing different types of polymers and perfluorosilanes (PFSs). Taking advantage of excellent optical properties, fine diameter and high hydrophobicity of PFDTMS-modified CsPbBr 3 @PVDF-HFP/PS nanofibers, the detection for rhodamine 6G (R6G) and rhodamine B (RhB) in aqueous solution with maximum fluorescence resonance energy transfer (FRET) efficiency up to 80.9% and 69.7% are realized, respectively. Notably, these electrospun nanofiber membranes possess outstanding durability and recyclability, indicating their great potential in multifunctional photoelectric applications.
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Nanoscale
·
2022
·Vol. 14
·期 37
·13779-13789
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IF 8.307
Yanqiao Xu,Xiaobo Hu,Haijie Chen,Huidong Tang,Qing Hu,Ting Chen,Weihui Jiang,Lianjun Wang,Wan Jiang
A great hurdle restricting the optoelectronic applications of cesium lead halide perovskite (CsPbX3) nanocrystals (NCs) is due to the uncoordinated lead atoms (Pb0) on the surface, where most attempts to address the challenges in the literature depend on complicated post-treatment processes. Here we report a simple in situ surface engineering strategy to obtain highly fluorescent and stable perovskite NCs, wherein the introduction of the multifunctional additive 1-butyl-3-methyl-imidazolium tetrafluoroborate ([Bmim]BF4) can significantly eliminate the Pb0 traps. The photoluminescence quantum yield (PLQY) of the as-synthesized NCs was improved from 63.82% to 94.63% due to the good passivation of the surface defects. We also confirm the universality of this in situ passivation pathway to remove Pb0 deep traps by using fluoride acid-based ionic liquids (ILs). Due to the high hydrophobicity of the cations of ILs, the as-prepared CsPbBr3 NCs exhibit robust water resistance stability, maintaining 67.5% of the initial photoluminescence (PL) intensity after immersion in water for 21 days. A white light emitting diode (LED), assembled by mixing the as-synthesized CsPbBr3 NCs and red K2SiF6:Mn4+ phosphors onto a blue chip, exhibits high luminous efficiency (100.07 lm W−1) and wide color gamut (140.64% of the National Television System Committee (NTSC) standard). This work provides a promising and facile technique to eliminate the Pb0 traps and improve the optical performance and stability of halide perovskite NCs, facilitating their applications in optoelectronic fields.
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高影响因子
SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY
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2022
·
IF 4.831
Peng Zhang,Shufen Zhang,Xiaoxi Hu,Maosheng Zhang,Chaoyu You,Guoliang Chen,Wenli Yang,Wei Huang,Tianju Chen,Feiming Li
Determination of cesium ion in soybean oil is of high importance since the increasing risk from releasing of main component of nuclear waste cesium 137. The complex composition and high viscosity of soybean oil make it necessary to convert it into water phase by nitration before detection, so developing a simple, accurate and sensitive method for on-site sensing of Cs + in soybean oil is still a big challenge. In this work, we report a traffic light-type ratiometric fluorescence strategy for the visual sensing of Cs + in soybean oil based on dimensional regulation of two dimensional (PEA) 2 PbI 4 perovskite nanosheets (NSs). The PEA + in (PEA) 2 PbI 4 NSs exchanged with Cs + and lead to dimension of partial (PEA) 2 PbI 4 NSs progressively increase from 2D to 3D CsPbI 3 NCs. Resultantly, the fluorescence of (PEA) 2 PbI 4 NSs decreases with a concomitant fluorescence enhancement of CsPbI 3 NCs upon increasing the concentrations of Cs + , and the emission accordingly change from green, yellow to red with a high fluorescence colorimetric resolution up to 5.0 μM, make it successful to achieve on-site sensing of Cs + in soybean oil just with naked eye in 5 min without any nitration, demonstrating a bright application future for determination of Cs + in the soybean oil.
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Nanomaterials
·
2022
·Vol. 12
·期 17
·2994
·
IF 5.719
Daojun Zhang,Bei Jiang,Chengxiang Li,Hao Bian,Yang Liu,Yingping Bu,Renchun Zhang,Jingchao Zhang
Electrochemical energy storage devices (EESDs) have caused widespread concern, ascribed to the increasing depletion of traditional fossil energy and environmental pollution. In recent years, nickel cobalt bimetallic sulfides have been regarded as the most attractive electrode materials for super-performance EESDs due to their relatively low cost and multiple electrochemical reaction sites. In this work, NiCo-bimetallic sulfide NixCo3−xS4particles were synthesized in a mixed solvent system with different proportion of Ni and Co salts added. In order to improve the electrochemical performance of optimized Ni2.5Co0.5S4electrode, the Ni2.5Co0.5S4particles were annealed at 350 °C for 60 min (denoted as Ni2.5Co0.5S4-350), and the capacity and rate performance of Ni2.5Co0.5S4-350 was greatly improved. An aqueous NiCo-Zn battery was assembled by utilizing Ni2.5Co0.5S4-350 pressed onto Ni form as cathode and commercial Zn sheet as anode. The NiCo-Zn battery based on Ni2.5Co0.5S4-350 cathode electrode delivers a high specific capacity of 232 mAh g−1at 1 A g−1and satisfactory cycling performance (65% capacity retention after 1000 repeated cycles at 8 A g−1). The as-assembled NiCo-Zn battery deliver a high specific energy of 394.6 Wh kg−1and long-term cycling ability. The results suggest that Ni2.5Co0.5S4-350 electrode has possible applications in the field of alkaline aqueous rechargeable electrochemical energy storage devices for supercapacitor and NiCo-Zn battery.Keywords:NixCo3−xS4structures;micro/nanostructures;supercapacitors;Ni-Zn batteries
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高影响因子
Nano Today
·
2022
·
IF 18.962
Di Liu,Hongliang He,Fei Kong,Yixiang Cao,Fengchao Zang,Ming Ma,Ning Gu,Yu Zhang
Currently, multimodal synergistic nanoplatform emerges as an important cancer therapy paradigm, however, multimodal synergistic theranostic nanoplatform remains to be developed. Herein, using the mouse model of breast cancer, a versatile multimodal synergistic theranostic nanoplatform is rationally designed and synthesized for enhancing chemodynamic therapy (CDT), overcoming immunosuppression within tumor microenvironment , and inhibiting metastasis as well as tracking tumor. To fulfill our design, a composite Fe/Mn magnetic nanoparticle is first synthesized by loading with Fe 3 O 4 and BMS-202 (PD-L1 inhibitor) within a poly(lactide-co-glycolide)-based nanoparticle core, which are further modified with in situ synthesis of MnO 2 layer. Then, the composite metal-organic nanoparticle is coated with two targeting moieties hyaluronic acid (HA) and AMD3100 (CXCR4 antagonist), respectively, to achieve the multimodal synergistic theranostic nanoplatform ( [email protected] +AMD). With surface targeting modification, [email protected] +AMD exhibits enhanced tumor accumulation, where it effectively consumes endogenous glutathione to generate Mn 2+ allowing for the enhanced CDT effect, alleviates tumor hypoxia by O 2 generation and reverses the tumor immunosuppression. [email protected] +AMD blocks CXCR4 receptor on cancer cells, thus suppressing the CXCR4-mediated cancer metastasis and invasion. Additionally, [email protected] +AMD would synchronously be achieving tumor tracking by T 1 -T 2 dual-mode magnetic resonance imaging. Collectively, this strategy holds a novel multimodal synergistic theranostics for effective cancer management.
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JOURNAL OF ALLOYS AND COMPOUNDS
·
2022
·
IF 6.371
Yanping Liu,Yan Zhan,Beata Szreniawa,Katarzyna Matras-Postolek,Ping Yang
Perovskite nanomaterials with highly stable and bright emission were requested for white light emitting diodes (LEDs). In this paper, superior thin CsPbBr 3 nanoplates (NPLs) with an average thickness of 1.9 nm were synthesized via solvothermal reactions. A bright blue-emitting peak at 455 nm with a photoluminescence (PL) quantum yield of 89 % was observed. The high PL efficiency was kept after storing for 90 days at ambient condition. This supplied an efficient approach to solve the problem of low PL efficiency and poor stability of blue-emitting perovskite nanocrystals . The thickness of CsPbBr 3 NPLs was adjusted by changing preparation conditions. The PL peak wavelength of CsPbBr 3 NPLs was adjusted in a region of 455–465 nm. Through dynamic anion exchange promoted cation exchange reactions, Mn ions were introduced in the lattice of CsPbBr 3 NPLs to generate bright orange emitting to create dual-luminescent CsPbBr 3 :Mn NPLs. A white emitting sample with a color coordinate of (0.304, 0.325) was finally fabricated using bright CsPbBr 3 :Mn NPLs and green-emitting CsPbBr 3 nanocrystals. This work broadened the application of perovskite for display and lighting.
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