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JOURNAL OF LUMINESCENCE · 2013 · IF 2.144

Spectroscopic investigations on the binding of leucomalachite green to bovine serum album

XiaoDan Zeng,Lin Zhu,FuSheng Zhang,LiYun Feng

The interaction of bovine serum with leucomalachite green (LMG) was investigated by spectroscopic methods . LMG was found to quench the intrinsic fluorescence of BSA by dynamic quenching. High quenching constant suggested that LMG can form a complex with BSA. Binding constant and number of binding site were determined. The thermodynamic parameters suggested the main interacting force is hydrophobic forces . The effect of LMG on the conformation of BSA was analyzed by synchronous fluorescence spectroscopy . RLS spectra were also used to reconfirm the formation of complex between BSA and LMG.

研究领域: 生物化学 · 分子生物学 · 光谱学 · 药物代谢 · 蛋白质-配体相互作用
✓ 已验证 DOI 高影响因子
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JOURNAL OF APPLIED POLYMER SCIENCE · 2012 ·Vol. 125 ·期 4 ·2867-2873 · IF 1.289

Synthesis of fluorescent poly(1-vinylimidazole-co-(1-pyrene) methyl 2-methyl-2-propenote) and determination of monomer reactivity ratios

Yehai Yan,Na Lu,Jian Cui,Jinfang Zhang

A new fluorescent copolymer, poly(1-vinylimidazole- co -(1-pyrene) methyl 2-methyl-2-propenote) (VI- co -PyMMP), has been designed and synthesized by a free-radical copolymerization of VI and PyMMP as well as characterized using ultraviolet (UV), Fourier transform infrared spectroscopy (FTIR), 1 H NMR, and fluorescence spectroscopies. The monomer reactivity ratios are determined by two methods of Fineman-Ross ( r 1 = 0.28 ± 0.04 for VI, r 2 = 1.32 ± 0.11 for PyMMP) and Kelen-Tüdös ( r 1 = 0.23 ± 0.05, r 2 = 1.22 ± 0.12). Based on the reactivity ratios, the monomer sequence lengths and Q and e for PyMMP monomer are further calculated. The results suggest that the copolymerization of VI and PyMMP is a nonideal copolymerization without an azeotropic point (i.e., r 1 < 1, r 2 > 1 and r 1 r 2 < 1) and has a low alternation tendency. The conclusions drawn in this work may not only direct the later synthesis of the copolymers but also enrich the database of free-radical copolymerization. © 2012 Wiley Periodicals, Inc. J Appl Polym Sci, 2012

研究领域: 高分子化学 · 功能高分子 · 荧光材料 · 聚合物合成 · 材料化学
✓ 已验证 DOI 高影响因子
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JOURNAL OF POWER SOURCES · 2016 · IF 6.333

Integrated plasmonic and upconversion starlike Y2O3:Er/Au@TiO2 composite for enhanced photon harvesting in dye-sensitized solar cells

Fanli Meng,Yi Luo,Yali Zhou,Jinwen Zhang,Yanzhen Zheng,Guozhong Cao,Xia Tao

A plasmon-enhanced upconversion composite Y 2 O 3 :Er/Au@TiO 2 (SYE/A@T) with a three-dimensional starlike morphology is prepared and then mixed with submicron TiO 2 (200 nm) to form a multifunctional scattering layer in TiO 2 -based dye-sensitized solar cells (DSSCs). In such starlike micronsized upconverter, Au nanoparticle-assisted plasmon effect can intensify the upconversion emission of Y 2 O 3 :Er, and simultaneously TiO 2 coating can improve the charge transport within SYE/A@T. Therefore, the SYE/A@T shows extended light-absorbing range to near-infrared region and improved light-scattering ability, leading to an improved photovoltaic performance of DSSCs. With the optimum mixing ratio, a conversion efficiency of 8.62% is attained, which is a significant improvement of 27.6% compared with the cell without adding SYE/A@T. Our work provides a feasible strategy to prepare an upconversion composite with plasmon-enhanced emission and enable this composite to accommodate the DSSCs system and improve the conversion efficiency of DSSCs.

研究领域: 材料科学 · 光伏技术 · 纳米光学 · 能源材料 · 表面等离激元
✓ 已验证 DOI 高影响因子
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CARBON · 2024 · IF 10.5

Combined laser-induced graphene and microcontact printing for processing scalable and stackable micro-stripe patterns toward multifunctional electronic devices

Boru Du,Jingyu Lu,Guantao Wang,Mingguang Han,Yan Gao,Sida Luo

Laser-induced graphene (LIG) is a highly promising technology for assembling thin-film electronics with miniaturized surficial patterns, although hard to guarantee both high-quality formation of raw materials and high resolution of feature size. In this study, a combined microcontact printing (μCP) and LIG protocol is creatively utilized to fabricate ultra-thin graphene films with highly ordered micro-stripe arrays. In addition to realize various patterned structures with unique scalable and stackable characteristics, PAA concentration (4–8 wt%) is systematically investigated as a critical parameter to precisely control the feature size of micro-patterns before and after the irradiation process, including line width (before: 5.37–22.44 μm, after: 4.83–22.32 μm) and average height (before: 69.81–187.39 nm, after: 5.72–48.61 nm). By further exploring a defocused multi-lasing strategy, sheet resistance of the graphene array could be optimized dramatically from 634.1 kΩ/sq to 1.9 kΩ/sq, while maintaining low ablation (45.38 % porosity) and high carbon content (84.2 wt%). Lastly, the process is demonstrated to assemble different graphene based electronic devices with miniaturized sizes, including liquid sensors with sensitivity of 2.7 % μL −1 and electrothermal heaters with temperature-ramping rate as high as 24.7 °C/s and working temperature as high as 248 °C.

研究领域: 材料科学 · 纳米科技 · 电子工程 · 生物医学工程 · 表面科学 · 柔性电子学
✓ 已验证 DOI 高影响因子
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JOURNAL OF APPLIED POLYMER SCIENCE · 2015 ·Vol. 132 ·期 20 · IF 1.768

Synthesis of hyperbranched polymers by free radical addition-coupling polymerization with A3/B2 and A2A′/B2 approaches

Yaobin Liu,Zhiqiang Fan

Two tribromide compounds, 1,3-(propanoic acid, 2-bromo-)-2-(2-bromo-1-oxopropylamino)propyl ester (A 1 ) and trimethylolpropane tris(2-bromopropionate) (A 2 ), were synthesized. By Cu/ N,N,N′,N′,N″ -pentamethyldiethylenetriamine (PMDETA)-mediated radical addition-coupling polymerization (RACP) of 2-methyl-2-nitrosopropane (MNP) with the tribromide compounds, two types of hyperbranched polymers were synthesized under mild conditions, respectively. Polymerization degrees of the polymers increased with time gradually, which is in line with a step-growth polymerization mechanism. By tracing the polymerization process by gel permeation chromatography and NMR analysis, proper reaction conditions to get hyperbranched polymers was obtained. Based on the results of NMR analysis on the polymer chain structure, mechanism of forming hyperbranched polymer has been proposed, which includes formation of carbon radicals from the tribromo monomer through single electron transfer, their reaction with MNP to form nitroxide radicals, and cross-coupling reaction of the nitroxide radicals with other carbon radicals. The gelation point of the A 2 -MNP system is larger than that of the A 1 -MNP system, indicating that probability of intramolecular cyclization in A 2 -MNP RACP system is higher than the A 1 -MNP system. The reactivity of —NHCOCH(CH 3 )Br group of A 1 is lower than its two —OCOCH(CH 3 )Br groups, and this resulted in longer distance between two adjacent branch points in the hyperbranched polymer of A 1 -MNP than the A 2 -MNP system. It is possible to adjust the chain structure of RACP-based hyperbranched polymer by changing the reactivity of the functional groups in A 3 monomer. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132 , 41972.

研究领域: 高分子化学 · 聚合物合成 · 功能高分子 · 材料化学 · 有机合成方法学
✓ 已验证 DOI 高影响因子
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Small · 2022 ·Vol. 18 ·期 29 ·2202622 · IF 15.153

Affinities and Kinetics Detection of Protein–Small Molecule Interactions with a Monolayer MoS2-Based Optical Imaging Platform

Hao Zhu,Zixuan Chen,Yun Chen,Jun-Jie Zhu

Quantifying the binding kinetics and affinities of protein–small molecule interactions is critical for biomarker validation, drug discovery, and deep understanding of various biological processes at the molecular-scale. Novel approaches are demanded as most common label-free techniques are mass-sensitive, which are not suitable for the detection of small molecule interactions. Here, an optical imaging platform is developed to measure the binding kinetics of both protein–small molecules and protein–ions based on monolayer MoS 2 , an ultra-thin 2D material whose optical absorption is extremely sensitive to charge. A model is established to calibrate the optical response due to the charged analyte binding and it is applied to quantify the interactions between abl1 kinase and different small-molecule inhibitors. Such a presented method is capable of distinguishing different inhibitors binding to a wild or mutated kinase, which provides guidance for drug evaluation and drug mechanism exploration. The binding kinetics of calcium ions to calmodulin is also measured, further broadening the application field of the method. In addition, the imaging capability allows mapping the local binding kinetics of the molecular interactions with a high resolution, which reveals visible spatial variability and offers a promising tool for studying heterogeneous local interfacial interactions.

研究领域: 分子生物学 · 药物发现 · 生物传感器 · 化学生物学 · 生物物理 · 转化医学 · 纳米生物技术
✓ 已验证 DOI 高影响因子
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APPLIED CATALYSIS B-ENVIRONMENTAL · 2014 · IF 6.007

Single-crystalline AgIn(MoO4)2 nanosheets grafted Ag/AgBr composites with enhanced plasmonic photocatalytic activity for degradation of tetracycline under visible light

Xu Yan,Xiyou Wang,Wei Gu,MiaoMiao Wu,Yan Yan,Bo Hu,Guangbo Che,Donglai Han,Jinghai Yang,Weiqiang Fan,Weidong Shi

Single-crystalline AgIn(MoO 4 ) 2 nanosheets have been successfully fabricated by facile hydrothermal method without any surfactants. Subsequently, Ag/AgBr-grafted AgIn(MoO 4 ) 2 nanosheets were synthesized by the in situ photoreduction of AgBr/AgIn(MoO 4 ) 2 composites prepared by a deposition–precipitation method. Under visible light irradiation. The Ag/AgBr/AgIn(MoO 4 ) 2 composites exhibit a strong absorbance in the visible region because of the surface plasmon resonance absorption of Ag nanocrystals. Compared with bare AgIn(MoO 4 ) 2 nanosheets, Ag/AgBr nanoparticles and Ag/AgIn(MoO 4 ) 2 composites, a dramatic enhancement in the degradation rate of tetracycline (TC) is observed over the Ag/AgBr/AgIn(MoO 4 ) 2 composites. The immense enhancement of the photocatalytic activity is attributed to the extended absorption in the visible-light region, effective charge separation, and synergistic enhancement induced by surface plasmon resonance (SPR) in the heterostructured Ag/AgBr/AgIn(MoO 4 ) 2 . This study provides new insight into the fabrication of highly efficient and stable ternary metal molybdate based plasmonic photocatalysts and facilitates their practical application to solve environmental issues. The mechanism for the photodegradation of TC over Ag/AgBr/AgIn(MoO 4 ) 2 is discussed in detail.

研究领域: 材料科学 · 环境化学 · 光催化 · 纳米材料 · 无机化学 · 物理化学
✓ 已验证 DOI 高影响因子
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JOURNAL OF ALLOYS AND COMPOUNDS · 2018 · IF 3.779

Pb8M(BO3)6 (M = Mg, Ca): Two new borates with large birefringence activated by the ∞[Pb8B6O18]2- double layers

Chen Zhou,Hui Zhang,Jianian Cheng,Hongyi Li,Sadeh Beysen

Two new isostructural lead borates , Pb 8 Mg(BO 3 ) 6 and Pb 8 Ca(BO 3 ) 6 , have been synthesized via high temperature solution method. The single crystal structures of title compounds contain ∞ [Pb 8 B 6 O 18 ] 2- double layers composed of planar BO 3 triangles, Pb(2)O 9 and distorted Pb(1)O 5 polyhedra, these layers condense in c -axis, and the MgO 6 (or CaO 6 ) polyhedra fill into the layers, forming a three-dimensional framework. The stereochemical activity of lone pair (SCALP) electrons were found in the Pb(1)O 5 polyhedra, which combine with the BO 3 units, generating strong optical anisotropy . The calculated birefringences of Pb 8 Mg(BO 3 ) 6 and Pb 8 Ca(BO 3 ) 6 using first-principles method are 0.15@1064 nm and 0.12@1064 nm, respectively, which are comparable to the commercial α -BaB 2 O 4 (α-BBO) crystal and imply that they probably can be used as birefringent materials. The electronic structures, density of states of title compounds were calculated by density functional theory (DFT). Meanwhile, the TG-DSC curves, infrared spectral and UV–Vis–NIR diffuse reflectance spectral were measured.

研究领域: 无机化学 · 材料科学 · 晶体工程 · 非线性光学材料 · 固体化学
✓ 已验证 DOI 高影响因子
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Journal of Materials Chemistry A · 2019 ·Vol. 7 ·期 37 ·21378-21385 · IF 10.733

Hollow TiN nanotrees derived from a surface-induced Kirkendall effect and their application in high-power supercapacitors

Wei Wen,Jincheng Yao,Hua Tan,Jin-Ming Wu

Electrode materials with hollow micro/nanostructures and high electrical conductivity are important for achieving high-power supercapacitors, especially those with super-fast charging/discharging. TiN, which can be easily obtained from TiO2, is regarded as a high-power supercapacitor material. Here, we report that a nanoscale Kirkendall effect is triggered by surface branches on TiO2 nanowires, which then transform into hollow TiN nanotrees during a thermal nitridation process. The surface branches play a key role in accelerating the initial reaction, which forms a uniform, continuous surface TiN layer and induces the Kirkendall effect via surface diffusion. The hollow TiN nanotrees have a high surface area, porous structure, and high electrical conductivity. The constructed symmetric supercapacitors exhibit high areal and volumetric energy density, super-fast charge/discharge ability, and good capacitance retention up to 350 000 cycles. This work provides a new method to synthesize hollow TiN nanostructures and demonstrates their advantages in achieving high-power energy storage devices.

研究领域: 材料科学 · 纳米科技 · 电化学 · 能源存储 · 功能材料
✓ 已验证 DOI 高影响因子
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OPTICAL MATERIALS · 2022 · IF 3.754

Enhancing performance of tin-based perovskite solar cells by polyvinyl pyrrolidone doping strategy

Ziang Xie,Ping Wu,Sen Chen,Shiping Zhang,Yili Pei,Li Li,Guodong Fu,Ying Xie,Haochen Guan,Yun Xing,Jianzhang Zhu,Xinran Wang

The power conversion efficiency (PCE) of tin-based perovskite solar cells (TPSCs) was significantly improved when polyvinyl pyrrolidone (PVP) was doped into the formamidinium tin iodide (FASnI 3 ) layer with an optimized doping mass. After doping, the FASnI 3 grain size, film smoothness and average carrier lifetime were largely enhanced, which demonstrate the crystallization quality improvement to FASnI 3 . The champion PCE of the enhanced TPSC was improved to 7.83%, which is relatively 27% larger than that of the control, 6.15%. After continuous storage for 15 days, the PCE of the enhanced TPSC remained 74.4% of its original value. Using the finite difference time domain (FDTD) simulation method, we demonstrated that the light absorption ratio of the FASnI 3 :PVP layer was larger than that of the FASnI 3 , and the photo-generated carrier density of the enhanced TPSC was approximately 2% ∼ 3% larger than that of the control. The ultimate efficiency of the enhanced TPSC was calculated to be 26.23%. It is potential to dope PVP into FASnI 3 to further enhance the device performance of TPSCs.

研究领域: 材料科学 · 光伏技术 · 纳米科技 · 表面化学 · 半导体器件
✓ 已验证 DOI 高影响因子
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JOURNAL OF POWER SOURCES · 2022 · IF 9.794

Promoting effective electrochemical oxidation of CO by Cu-doping for highly active hybrid direct carbon fuel cell anode

Xiao Yang,Minjian Ma,Chunming Xu,Rongzheng Ren,Jinshuo Qiao,Wang Sun,Kening Sun,Zhenhua Wang

Hybrid direct carbon fuel cells (HDCFCs) present its inherent and unparalleled advantages in converting chemical energy from organic waste, biomass, and coal directly into clean energy with high efficiency. However, the progress of HDCFC technology continues to be hampered by the sluggish anode reaction kinetics. Herein, an effective design strategy for HDCFC anode is proposed, a Cu-modified Sr 2 Fe 1.3 Cu 0.2 Mo 0.5 O 6-δ (SFCM) perovskite oxide is developed to meet the requirements of intermediate-temperature HDCFC anode. The Cu-doping SFCM anode demonstrates excellent redox structural stability and catalytic activity. In addition, the electrolyte-supported single cell with Cu-doping SFCM anode has improved the peak power density from 285.5 mW cm −2 to 489.3 mW cm −2 at 800 °C with activated carbon as the fuel. The significantly enhanced anode catalytic activity is primarily due to the improved interfacial activity and chemical adsorption of CO. Therefore, the present work shows an effective strategy for designing and developing novel high-performance HDCFCs anode materials .

研究领域: 能源材料 · 电化学 · 燃料电池 · 功能材料 · 催化化学
✓ 已验证 DOI 高影响因子
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Journal of Nanomaterials · 2018 ·Vol. 2018 ·期 1 ·1465760 · IF 2.207

Synthesis of Platinum Nanocrystals within Iodine Ions Mediated

Jiamao Li,Jingwei Hou,Yu Gong,Chengjian Xiao,Lei Yue,Linjie Zhao,Huan Ma,Heyi Wang,Shuming Peng,Chao Chen,Hongli Chen

A liquid-phase reducing method of synthesizing Pt nanocrystals was demonstrated, and dendrite-, cube-, and cuboctahedron-shaped Pt nanocrystals (NCs) with well-defined monomorphic were successfully synthesized through iodine ions mediated with the CTAB agent. When the KI concentration was increased to thirty times of K 2 PtCl 4 at the nucleation stage, the high-quality Pt nanodendrites could be obtained. However, no matter how many KI were added at the growth age, only cube- and cuboctahedron-shaped Pt nanocrystals formed. The results of high-resolution TEM, EDX, and XRD indicated that the size and shape of Pt NCs could be turned by changing the concentration and time of KI. In the nucleation stage, it might be due to that some iodine ions adsorb on the surfaces of Pt NCs, which probably cause the rapid growth process resulting in the formation of Pt nanodendrites. In the growth stage, although high concentrations of I − ions could contribute to the shape control and generate bigger particles of Pt NCs, small Pt particles do not grow into dendrites. The insight into the role of I − ions in synthesis of Pt NCs reported here provided a viewpoint for clearly understanding the formation mechanism of anisotropic platinum nanostructures.

研究领域: 纳米材料科学 · 物理化学 · 无机合成 · 催化化学 · 材料表征技术
✓ 已验证 DOI 高影响因子
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