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International Journal of Electrochemical Science · 2023 ·Vol. 7 ·期 6 ·5172-5184 · IF 1.5

Reduction of Graphene Oxide Via Ascorbic Acid and Its Application for Simultaneous Detection of Dopamine And Ascorbic Acid

Xu Zhu,Qin Liu,Xiaohua Zhu,Chunlan Li,Maotian Xu,Yong Liang

A new approach to synthesize graphene was applied by reduction of graphene oxide using ascorbic acid. Chitosan/graphene modified electrode could be employed for simultaneous determination of dopamine and ascorbic acid. The modified electrode showed excellent electrocatalytic activity towards the oxidation of DA and AA. The calibration curves for DA and AA were obtained in the range of 0.3-1067.5μM and 0.6-1378.1μM, respectively. Detection limits were 0.1μM and 0.01μM for DA and AA, respectively. The present method was applied to the determination of AA and DA in human serum samples and the results were quite promising.

研究领域: 分析化学 · 电化学 · 生物传感器 · 纳米材料 · 临床检验 · 神经化学 · 药物分析
✓ 已验证 DOI 高影响因子
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CERAMICS INTERNATIONAL · 2018 ·Vol. 44 ·期 17 ·21000-21003 · IF 3.057

MgTiO3/TiO2/MgTiO3: An ultrahigh-Q and temperature-stable microwave dielectric ceramic through cofired trilayer architecture

Jie Zhang,Zhenxing Yue,Yu Luo,Longtu Li

A cofired trilayer ceramic architecture showing as MgTiO 3 /TiO 2 /MgTiO 3 was designed to realize temperature-stable and ultrahigh- Q microwave dielectrics in the typical MgTiO 3 -TiO 2 system. The effects of TiO 2 content on the microwave dielectric properties of cofired trilayer ceramics were studied. Through the design of cofired trilayer architecture, the chemical reactions between MgTiO 3 and TiO 2 were limited within a narrow region of MgTiO 3 /TiO 2 interfaces (~ 15 µm in width), which could be beneficial for optimizing the microwave dielectric properties. Excellent characteristics of ε r ~ 18.38, Q×f value ~ 169,900 GHz and τ f ~ − 1 ppm/°C were gained for the MgTiO 3 /TiO 2 /MgTiO 3 ceramic architectures stacked with 1.63 vol% TiO 2 . The current work could serve as new strategies to develop high-performance dielectric resonators and multilayers for 5G wireless communication applications.

研究领域: 材料科学 · 无机非金属材料 · 电子陶瓷 · 微波介质材料 · 功能陶瓷
✓ 已验证 DOI 高影响因子
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MATERIALS & DESIGN · 2017 · IF 4.364

In-situ synthesis of crystalline Ag-Nb2O5 nanobelt clusters with enhanced solar photo-electrochemical performance for splitting water

Puhong Wen,Lili Ai,Fenyan Wei,Dengwei Hu,Jingjing Guo,Fangyi Yao,Taotao Liu

The crystalline hexagonal Nb 2 O 5 (H-Nb 2 O 5 ) nanobelt clusters dominantly exposed (−   110) facet are firstly synthesized by a hydrothermal topological reaction with a precursor of fiber-like K 2 Nb 2 O 6 ·H 2 O. The structure and morphology of samples obtained at different temperatures and times are investigated. There are two steps in the synthesis process. One is the acid-exchanging reaction transforming into amorphous phase protonated niobate (HNO), and the other is dehydration reaction transforming into H-Nb 2 O 5 , and simultaneous dissolution reaction which forms nanobelt cluster morphology from the fiber-like particle. The formation mechanism of H-Nb 2 O 5 nanobelt clusters has been proposed in detail. After photo-reduced reaction between the H-Nb 2 O 5 nanobelt clusters and AgNO 3 solution, the dominantly exposed (−   110) facet of H-Nb 2 O 5 nanobelt is homogeneously covered by Ag nanoparticles . The photo-electrochemical performance of the obtained H-Nb 2 O 5 nanobelt clusters and Ag deposited H-Nb 2 O 5 (Ag-Nb 2 O 5 ) nanobelt clusters as photocatalysts are evaluated by splitting water under simulated sunlight illumination, and the generated photocurrent of Ag-Nb 2 O 5 sample is 10.73   μA, which is 535 times that of the H-Nb 2 O 5 sample. The results demonstrate that the Ag-Nb 2 O 5 nanobelt clusters have a high photo-electrochemical performance as well as good sunlight photoelectric conversion efficiency.

研究领域: 材料科学 · 纳米科技 · 光催化 · 能源化学 · 半导体材料 · 电化学 · 太阳能转换
✓ 已验证 DOI 高影响因子
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SENSORS AND ACTUATORS B-CHEMICAL · 2018 · IF 5.667

Electrochemical immunosensor for HBe antigen detection based on a signal amplification strategy: The co-catalysis of horseradish peroxidase and nanoporous gold

Yachao Zhang,Yan Gao,Xueli Zhang,Huiming Wang,Tian Xia,Congcong Bian,Shuang Liang,Xiaozhi Tang,Xia Wang

The amplification of the electrochemical signal is crucial to improving the sensing performance of an immunosensor. In this study, a signal amplification strategy based on the co-catalysis of horseradish peroxidase (HRP) and nanoporous gold (NPG) was used to fabricate an electrochemical immunosensor for the determination of Hepatitis B e antigen (HBeAg). For the resulting immunosensor, HRP catalyzed catechol and thus served as a signal label of secondary antibody. NPG with unique properties was selected as a carrier for capture antibody immobilization. Further, NPG had an efficient electrocatalytic activity towards catechol (the substrate of HRP), which thus significantly enhanced the electrochemical signal produced by the HRP-labeled secondary antibody. Based on the co-catalysis of HRP and NPG, the immunosensor exhibited a good linear relationship between peak current density and HBeAg concentration in a wide HBeAg detection range from 1 pg mL −1 to 1 ng mL −1 with a high sensitivity of 23.51 μA mL ng −1  cm −2 as well as a low detection limit of 0.064 pg mL −1 (S/N = 3). Additionally, the immunosensor presented a strong anti-interference capability against human serum, human serum/dopamine, human serum/tryptophan, human serum/NO 2 − , human serum/D-glucose, and human serum/IgG. For the detection of HBeAg in human serum, the concentrations detected by the immunosensor were in good agreement with the standard concentrations that added in the human serum samples. These unique properties potentially make the proposed immunosensor a good choice for HBeAg detection.

CAS / MDL: 51-61-6
研究领域: 生物医学工程 · 分析化学
✓ 已验证 产品关联 DOI 高影响因子
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DRUG DELIVERY · 2019 · IF 3.829

Albumin-bioinspired iridium oxide nanoplatform with high photothermal conversion efficiency for synergistic chemo-photothermal of osteosarcoma

Wenguang Gu,Tao Zhang,Junsheng Gao,Yi Wang,Dejian Li,Ziwen Zhao,Bo Jiang,Zhiwei Dong,Hui Liu

Protein-based nanocarriers with inherent biocompatibility have been widely served as building blocks to construct versatile therapeutic nanoplatforms. Herein, bovine serum albumin-iridium oxide nanoparticles (denoted BSA-IrO2 NPs) are successfully synthesized via one-step biomineralization approach. The BSA-IrO2 NPs exhibits uniform size (40 nm), superb biocompatibility and high drug loading capacity for doxorubicin (27.4 wt%). Under near-infrared (NIR) laser irradiation, the as-prepared BSA-IrO2 NPs exhibited high photothermal conversion ability (54.3%) and good photostability. The in vitro drug release experiments displayed pH and NIR laser -triggered DOX release profiles, which could enhance the therapeutic anticancer effect. By utilizing this DOX loaded nanoplatform, effective synergistic chemo-photothermal therapy against human osteosarcoma can be realized, which has been systematically verified both in vitro and in vivo. Notably, in vivo pharmacokinetics studies showed that BSA-IrO2@DOX had prolonged blood circulation time due to the BSA component can improve the stealthiness of the nanoparticles during the blood circulation. Meanwhile, in vitro and in vivo toxicity studies demonstrated that the BSA-IrO2 NPs can act as biocompatible agents for drug delivery and cancer therapy. Therefore, this work presents a biomineralized iridium-based NPs with remarkable features and be used as a very potential therapeutic nanoplatform for cancer treatment.

CAS / MDL: 10025-83-9
研究领域: 生物医学工程 · 肿瘤学 · 材料科学
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Journal of Materials Chemistry A · 2021 ·Vol. 9 ·期 38 ·22064-22071 · IF 12.732

Phase formation and ionic conduction in Na-doped Sr2MgSi2O7 melilite-type silicate

Wenda Zhang,Jie Feng,Fengqi Lu,Alberto J. Fernández-Carrión,Hui Fu,Xiaojun Kuang

Na-doped melilite-type silicate Sr2MgSi2O7 was reported to display high oxide ion conductivity. In this work, through multiple complementary techniques including X-ray diffraction, scanning electron microscopy, transmission electron microscopy, solid-state 29Si and 23Na nuclear magnetic resonance spectroscopy, and DFT calculations of defect formation energies, we found that it is hard to replace Sr with Na in Sr2MgSi2O7, and the Sr2−xNaxMgSi2O7−0.5x compositions formed mixed crystalline Sr2MgSi2O7 and Na-containing glassy phases. AC impedance spectroscopy measurements indicated that the ionic conduction in Sr2−xNaxMgSi2O7−0.5x could be from Na+ ions in the glassy phase, instead of the oxide ions.

研究领域: 材料科学 · 固体离子导体 · 无机非金属材料 · 能源材料 · 电化学
✓ 已验证 DOI 高影响因子
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DALTON TRANSACTIONS · 2014 ·Vol. 44 ·期 1 ·237-246 · IF 4.097

Multicolor (Vis-NIR) mesoporous silica nanospheres linked with lanthanide complexes using 2-(5-bromothiophen)imidazo[4,5-f][1,10]phenanthroline for in vitro bioimaging

Ying Liu,Lining Sun,Jinliang Liu,Yu-Xin Peng,Xiaoqian Ge,Liyi Shi,Wei Huang

A novel mesoporous nanosphere functionalized with 3-(aminopropyl)triethoxysilane (APTES) and 2-(5-bromothiophen)imidazo[4,5-f][1,10]phenanthroline (5-Br-Tip) was synthesized (denoted as Tip-MSS). With the coordinating function of the 5-Br-Tip to lanthanide (Ln) ions, for the first time, LnL3(5-Br-Tip) complexes were linked to the mesoporous nanospheres. The derived materials, named Ln-Tip-MSS (Ln = Eu, Tb, Sm, Nd, Yb), were characterized by Fourier-transform infrared (FT-IR) spectroscopy, TEM, XRD (wide-angle and small-angle), N2 adsorption/desorption analysis, and fluorescence spectroscopy. Upon excitation in the ligand absorption, the Ln-Tip-MSS nanomaterials show characteristic visible (Eu, Tb, Sm) and NIR (Sm, Nd, Yb) luminescence (multicolor emission covered from 450 nm to 1400 nm spectral region). Of importance is that, with low cytotoxicity and good biocompatibility given by the methyl thiazolyl tetrazolium (MTT) assay, the Eu-Tip-MSS was successfully applied to cell imaging in vitro based on the Eu3+ luminescence (under 405 nm excitation).

研究领域: 纳米医学 · 生物成像 · 材料科学 · 分子探针 · 化学生物学
✓ 已验证 DOI 高影响因子
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JOURNAL OF ALLOYS AND COMPOUNDS · 2024 · IF 5.8

Fe2AlB2@FeAl layered double hydroxides with core-shell heterostructures for electromagnetic wave absorption

Peng Hou,Ke Chen,Xudong Wang,Xiaofei Hu,Bing Li,Ming Liu,Xiao (Matthew) Hu,Yujie Song

The rapid development of high-performance materials has garnered considerable attention in addressing electromagnetic pollution . The construction of core-shell heterostructures is an effective approach for regulating the electromagnetic parameters of absorbers. However, these heterostructures usually lack a direct channel for charge transport between the core phase and the adhesive shell phase. Herein, Fe 2 AlB 2 @FeAl-layered double hydroxides with core-shell heterostructures were prepared using a top-down approach. The tightly connected FeAl-LDHs nanosheets to the Fe 2 AlB 2 parent phase improved electronic transport. Compared with raw Fe 2 AlB 2 , the spherical absorber with an embroidered structure demonstrated stronger reflection loss (-15.6 dB for Fe 2 AlB 2 , −58.6 dB for Fe 2 AlB 2 @FeAl-LDHs) and a broader effective absorption bandwidth (2.2 GHz for Fe 2 AlB 2 , 3.6 GHz for Fe 2 AlB 2 @FeAl-LDHs) due to the enhanced dielectric and magnetic losses. This study presents a practical method for designing new controllable core-shell heterostructures for electromagnetic wave-absorbing materials.

研究领域: 材料科学 · 电磁学 · 纳米材料 · 功能材料 · 复合材料
✓ 已验证 DOI 高影响因子
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INTERNATIONAL JOURNAL OF HYDROGEN ENERGY · 2022 ·Vol. 47 ·期 83 ·35352-35364 · IF 7.139

Remarkable kinetics of novel Ni@CeO2–MgH2 hydrogen storage composite

Zhichao Yu,Wei Zhang,Yongxi Zhang,Yaokun Fu,Ying Cheng,Sanyang Guo,Yuan Li,Shumin Han

Magnesium hydroxide (MgH 2 ) has excellent reversibility and high capacity, and is one of the most promising materials for hydrogen storage in practical applications. However, it suffers from high dehydrogenation temperature and slow sorption kinetics. Rare earth hydrides and transition metals can both significantly improve the de/hydrogenation kinetics of MgH 2 . In this work, MgH 2 –Mg 2 NiH 4 –CeH 2.73 is in-situ synthesized by introducing Ni@CeO 2 into MgH 2 . The unique coating structure of Ni@CeO 2 facilitates homogeneous distribution of synergetic CeH 2.73 and Mg 2 NiH 4 catalytic sites in subsequent ball milling process. The as-fabricated composite MgH 2 -10 wt% Ni@CeO 2 powders possess superior hydrogenation/dehydrogenation characteristics, absorbing 4.1 wt% hydrogen within 60 min at 100 °C and releasing 5.44 wt% H 2 within 10 min at 350 °C. The apparent activation energy of MgH 2 -10 wt% Ni@CeO 2 is determined to be 84.8 kJ/mol and it has favorable hydrogen cycling stability with almost no decay in capacity after 10 cycles.

研究领域: 材料科学 · 无机化学 · 能源化学 · 纳米催化 · 氢能源存储
✓ 已验证 DOI 高影响因子
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POLYMERS FOR ADVANCED TECHNOLOGIES · 2023 ·Vol. 34 ·期 6 ·1918-1932 · IF 3.4

Effective hybridization of SiO2 microsphere and graphene with tannic acid interface modifier for fabrication of multifunctional natural rubber/graphene nanocomposites

Yuqian Du,Xueya Wang,Ziwen Zhou,Feng Zhao,Song Li,Zhihua Liu,Zhengyu Wu,Shuai Zhao,Lin Li

Nowadays, although highly conductive polymer composites filled with two-dimensional graphene-based nano-fillers have been explored extensively, constructing nanocomposites with high performance, industrial feasibility, and more efficient conductive networks at lower nano-filler contents remains a challenge. To achieve the above objectives, industrial wastes microsilica powder (N98) with amorphous spherical structure and large particle size is employed in this work. And the hybrids (TGN) are obtained between N98 and graphene (GE) by the effective bridging and interface coupling of tannic acid, which can achieve the purpose of obtaining conductive composites with low-filler contents by traditional polymer processing technologies. The volume exclusion effect of N98 and its own assisted dispersion effect can prevent and attenuate graphene agglomeration, enabling the formation of a dense, complete and uniform conductive network in natural rubber (NR) matrix based on a small amount of graphene addition (parts per thousand). Thus, it give the nanocomposite highly functional, especially electric property. The results show that when the ratio of GE to N98 hybridization is 1:20, N98 and graphene are more uniformly hybridized together, and the volume exclusion effect is best matched with the rubber composites, and the comprehensive performance is optimal. Moreover, the electrical conductivity of NR/TG 1 N 20 nanocomposite can reach the balanced value of 10 −3 S·cm −1 with the GE loading of 0.48 phr, which shows the effectiveness of the prepared hybrids.

研究领域: 高分子科学 · 纳米复合材料 · 功能高分子 · 材料化学 · 导电聚合物
✓ 已验证 DOI 高影响因子
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JOURNAL OF ELECTROANALYTICAL CHEMISTRY · 2018 · IF 3.235

Identification of four isomers of Dihydroxynaphthalene by using a Briggs-Rauscher oscillating system

Wangning Zhang,Waqar Uddin,Gang Hu,Lin Hu,Zhaohui Fang

A novel method for identification of four isomers of dihydroxynaphthalene (DHN) was reported by their different perturbation effects on a Briggs-Rauscher (BR) oscillating system. In the system, macrocyclic nickel (II) complex NiL(ClO 4 ) 2 is used as the catalyst, where the ligand L in the complex is 5,7,7,12,14,14‑hexemethyl‑1,4,8,11‑tetraazacyclotetradeca‑4,11‑diene. By putting equal amount of the same concentrations of four isomers (1,4‑dihydroxynaphthalene (1,4-DHN), 1,5‑dihydroxynaphthalene (1,5-DHN), 2,3‑dihydroxynaphthalene (2,3-DHN) and 2,7‑dihydroxynaphthalene (2,7-DHN)) into BR system, the system could or couldn't be perturbed, being reflected in quite different oscillating behaviors after addition of isomers. These four isomers were identified in their concentration range of 5.0 × 10 −6 to 2.5 × 10 −4  mol/L. An explanation of such perturbation mechanism is that, 1,4-DHN couldn't be oxidized by BR matrix, but 1,5-DHN, 2,3-DHN and 2,7-DHN could be oxidized by HOO to yield 5‑Hydrox‑1,4‑naphthoquinone, phthalic acid and 6,7‑dihydroxyperylene‑1,12‑quinone (DHPQ), respectively.

研究领域: 分析化学 · 物理化学 · 化学生物学 · 反应动力学 · 分子识别
✓ 已验证 DOI 高影响因子
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CARBOHYDRATE POLYMERS · 2015 · IF 4.074

Antimicrobial and antioxidant surface modification of cellulose fibers using layer-by-layer deposition of chitosan and lignosulfonates

Hui Li,Lincai Peng

To confer cellulose fibers antimicrobial and antioxidant activities, chitosan (CS)/lignosulfonates (LS) multilayers were constructed on fibers surfaces through layer-by-layer deposition technique. The formation of CS/LS multilayers on cellulose fibers surfaces was verified by X-ray photoelectron spectroscopy (XPS) and zeta potential measurement. The surface morphologies of CS/LS multilayers on fibers surfaces were observed by atomic force microscopy (AFM). The results showed that characteristic element (i.e. N and S element) content increased with increasing bilayers number, the surface LS content increased linearly as a function of bilayers. Zeta potential of modified fibers was inversed after deposition of each layer. AFM phase images indicated that the cellulose microfibrils on fibers surfaces were gradually covered by granular LS aggregate. The antimicrobial testing results demonstrated that CS/LS multilayers modified fibers with CS in the outermost layer exhibited higher antimicrobial activity against Escherichia coli . The antioxidant testing results showed that antioxidant activity of CS/LS multilayers modified fibers was better than that of original fibers under the same oxidation conditions.

研究领域: 高分子材料 · 表面科学 · 生物医学工程 · 功能材料 · 纳米技术
✓ 已验证 DOI 高影响因子
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