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JOURNAL OF MATERIALS SCIENCE-MATERIALS IN ELECTRONICS · 2023 ·Vol. 34 ·期 24 ·1707 · IF 2.8

Enhancement of electrochemical properties of porous rGO by controlled growth CoFe2O4 nanoparticles

Van Ngo Hoanh,Nguyen Hung Tran,Le Hieu Trung,Le Thanh Huu,Vu Thien Tri,Pham Kien Trung,Phung Thinh Xuan

A study area in supercapacitor research is the design and manufacturing of composite electrode materials that combine the advantages of various materials. The rGO/CoFe 2 O 4 composite material is produced by growing cobalt ferrite particles on the surface of rGO using a simple and highly efficient thermal reduction technique. The results show that the electrochemical properties of rGO are significantly improved by the incorporation of cobalt ferrite. rGO sheets are used as supporting frameworks for the CoFe 2 O 4 nanoparticles, while the CoFe 2 O 4 particles provide more active sites for redox reactions. The prepared rGO/CoFe 2 O 4 show excellent electrochemical properties, with a high specific capacitance of 283 F/g at a current density of 0.1 A/g and a specific capacitance retention of 90.5% after 1000 cycles. The attractive performances exhibited by rGO/CoFe 2 O 4 composites make them potential electrode materials for supercapacitors in future.

研究领域: 材料科学 · 电化学 · 纳米科技 · 能源存储 · 功能材料
✓ 已验证 DOI 高影响因子
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CERAMICS INTERNATIONAL · 2021 ·Vol. 48 ·期 6 ·8579-8588 · IF 4.527

Anisotropic binary TiB2–SiC composite powders: Synthesis and microwave absorption properties

Sunyi Shen,Shaolei Song,Jinming Wang,Rong Li,Xingchao Li,Qiang Zhen

Microstructure control and multiple compounding methods in the synthesis stage can enhance microwave absorption performance of microwave absorbents. In this work, we successfully synthesized binary TiB 2 –SiC (TsBC) powders with hexagonal sheet (TiB 2 ) and particle (SiC) interlocking structures by sol-gel carbothermal reduction method. We investigated the effect of raw material ratio and synthesis temperature on the synthesized powders and evaluated the microwave absorption properties of the synthesized TsBC powders. It was found that the TsBC absorber exhibited excellent microwave adsorption properties with the minimum Reflection Loss ( R L ) reached −21.8 dB at 17.4 GHz corresponding to the thickness of 4 mm. This excellent performance was attributed to the interfacial polarization between TiB 2 –SiC interfaces and the multiple reflections between the sheet-particle interlocking structures.

研究领域: 材料科学 · 功能材料 · 复合材料 · 电磁学 · 无机非金属材料
✓ 已验证 DOI 高影响因子
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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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JOURNAL OF ALLOYS AND COMPOUNDS · 2009 · IF 1.51

Electrochemical behavior of nanoporous/nanofibrous Si anode materials prepared by mechanochemical reduction

Rongguan Lv,Jun Yang,Pengfei Gao,Yanna NuLi,Jiulin Wang

A mixture of nanoporous and nanofibrous silicon (NPNF-Si) is prepared by the mechanochemical reduction of SiCl 4 using Li 13 Si 4 as reducing agent in the presence of Super P carbon (SP) and the following thermal treatment and washing process. Morphologies and structures of the as-obtained composites are investigated using scanning electron microscopy (SEM), transmission electron microscopy (TEM) and X-ray diffraction (XRD). After carbon coating via pyrolysis of polyvinyl chloride (PVC), the resulting NPNF-Si/SP/C composite is evaluated for the use as anode material in lithium-ion battery. It exhibits the first discharge capacity of 746.6   mAh   g −1 at current density of 0.2   mA   mg −1 and capacity retention of 91.1% after 30 cycles. The good electrochemical performance arises from the particular Si nano-structure, which can alleviate the volume effect during lithium insertion and extraction.

研究领域: 材料科学 · 电化学 · 纳米科技 · 能源存储 · 锂离子电池
✓ 已验证 DOI 高影响因子
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JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY · 2015 ·Vol. 53 ·期 12 ·1457-1463 · IF 3.113

Investigation of Suzuki–Miyaura catalyst-transfer polycondensation of AB-type fluorene monomer using coordination-saturated aryl Pd(II) halide complexes as initiators

Zilong Zhang,Pan Hu,Xiao Li,Hongmei Zhan,Yanxiang Cheng

Novel triarylamine-based coordination-saturated aryl Pd(II) halide complexes ligated by PEt 3 , PCy 3 , and P( o -tol) 3 were successfully synthesized by direct oxidative addition of aryl halide to the corresponding Pd(0) precursors. Suzuki–Miyaura coupling polymerization of 2-(7-halide-9,9-dioctylfluoren-2-yl)−1,3,2-dioxaborinane with these Pd(II) complexes as initiators was investigated for the synthesis of poly(fluorene)s with triarylamine end group. Pd(II) complexes with PCy 3 or P( o -tol) 3 exhibited catalytic activity and realized the catalyst-transfer polycondensation at 75 °C and room temperature, respectively, while the polymerization using Pd(II) catalyst ligated by PEt 3 did not proceed, which indicated that the bulky phosphine ligands could facilitate the reductive elimination and further promote the polymerization. In addition, the dimeric Pd(II) complex with P( o -tol) 3 can convert into monomeric Pd(II) intermediate with an open coordination site, which had a higher activity. The end groups of the afforded polyfluorene were analyzed by matrix-assisted laser desorption ionization time-of-flight (MALDI-TOF) mass spectrometry, in which the Ar/H end groups are indicative of the catalyst-transfer polymerization. © 2015 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2015 , 53 , 1457–1463

研究领域: 高分子化学 · 有机合成 · 金属有机化学 · 功能材料 · 聚合反应机理
✓ 已验证 DOI 高影响因子
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CHINESE JOURNAL OF CHEMISTRY · 2014 ·Vol. 33 ·期 1 ·125-130 · IF 1.04

Carboxylatopillarene-Modified Reduced Graphene Oxides with High Water Dispersibility for Fluorescent Dye Sensing

Ting Zhou,Hao Yu,Mingqiang Liu,Ying-Wei Yang

Carboxylated pillar[5]arene (CP5) macrocycles were modified onto the surface of reduced graphene oxide (RGO) via covalent bonds to form new pillarene-functionalized RGO nanosheets, i.e. , RGO-CP5. The obtained RGO-CP5 nanosheets capable of molecular recognition exhibited much better water-dispersibility and enhanced fluorescence-quenching property as compared with native RGO. This new sensing platform holds great potentials in the sensing and detection of analytes, such as organic dye molecules and pesticides, in aqueous solutions.

研究领域: 分析化学 · 纳米材料科学 · 传感器技术 · 环境监测 · 分子识别
✓ 已验证 DOI 高影响因子
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NEW JOURNAL OF CHEMISTRY · 2023 ·Vol. 47 ·期 26 ·12109-12116 · IF 3.3

A Y-doped P2-Na0.6Li0.11Fe0.27Mn0.62O2 cathode with improved high-rate capability and cycling stability for Na-ion batteries

Ming-Hui Cao,Ren-Yan Li,Fen-Fen Huang,Xin-Yin Cai,Miao Cui,Shi-Ya Lin,Jing-Yang Tian,Yuan-Ping Jiang,Zulipiya Shadike,Zheng-wen Fu

P2-Na0.6Li0.11Fe0.27−xMn0.62YxO2 (x = 0, 0.5%, 1%, and 2%) cathode materials were successfully prepared using a traditional solid-state method with ball milling-assisted modification. The effect of Y-doping on the crystal structure, grain size, morphology and sodium storage performance of Na0.6Li0.11Fe0.27Mn0.62O2 was investigated using X-ray diffraction (XRD), scanning electron microscopy (SEM), galvanostatic charge–discharge cycling tests, cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS). The results demonstrated that the ball-milling pre-treatment method could effectively reduce the grain size and mitigate the aggregation of Na0.6Li0.11Fe0.27Mn0.62O2. Additionally, reasonable Y-doping (x = 1%) significantly enhances the rate capability and cycling stability of Na0.6Li0.11Fe0.27Mn0.62O2via improving the Na+ diffusion kinetics and the reversibility of the oxygen redox reaction. These results indicate that Na0.6Li0.11Fe0.26Mn0.62Y0.01O2 is a promising candidate material for high-rate and long-life cathodes for Na-ion battery application.

研究领域: 材料科学 · 电化学 · 能源存储 · 无机固体化学 · 电池技术
✓ 已验证 DOI 高影响因子
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ELECTROCHIMICA ACTA · 2015 · IF 4.504

Novel graphite-carbon encased tungsten carbide nanocomposites by solid-state reaction and their ORR electrocatalytic performance in alkaline medium

K. Huang,K. Bi,J.C. Xu,C. Liang,S. Lin,W.J. Wang,T.Z. Yang,Y.X. Du,R. Zhang,H.J. Yang,D.Y. Fan,Y.G. Wang,M. Lei

Novel nanocomposites of spherical graphite-carbon encased tungsten carbide (GC-WC) are synthesized by solid state reaction with melamine and WO 3 as precursors under N 2 atmosphere. The diameters of the GC-WC composites range from 50 to 200   nm and the WC nanoparticles inside with an average size of ca. 15   nm distribute uniformly. The characterization results indicate that the GC-WC is composed of few layers of graphite carbon and WC nanoparticles with high crystallization and purity. Moreover, the electrocatalytic performance of GC-WC for the oxygen reduction reaction (ORR) in alkaline medium is further investigated by cyclic voltammetry (CV), rotating disk electrode (RDE) and chronoamperometry test with or without 3   M methanol. The results show that GC-WC has a considerable performance for ORR in the view of activity, stability and methanol tolerance, which may further used as proper supports for noble-metal based ORR catalysts in alkaline fuel cell . The synergetic interaction between the carbide nanoparticles and graphite carbon, which means that the surface graphite carbon layers are activated by WC nanoparticles for ORR and in turn protect inner WC from highly oxidizing environments has also been verified.

研究领域: 材料科学 · 纳米科技 · 电化学 · 能源材料 · 催化化学
✓ 已验证 DOI 高影响因子
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RSC Advances · 2018 ·Vol. 8 ·期 44 ·24900-24905 · IF 2.936

Porous carbon adsorption layer enabling highly reversible redox-reaction of a high potential organic electrode material for sodium ion batteries

Yanjie Wang,Chun Fang,Ying Huang,Qing Liu,Ruirui Zhao,Xuli Ding,Yunhui Huang

Organic compounds have been utilized in rechargeable batteries as electrode materials on account of their designable structures and reversible redox properties. However, most of them suffer from problems with dissolution resulting in poor electrochemical performance. In this work, we adapt a sodium salt of tetracyanoquinodimethane (NaTCNQ) to work as a high redox potential cathode material in sodium ion batteries (SIBs). A porous carbon coated separator is demonstrated to be an adsorption layer and prevents the dissolved active material from migrating to the anode side. The NaTCNQ cell assembled with a carbon layer containing 5% activated carbon (AC) exhibits a higher initial capacity and greatly improved cycling stability. Using a conductive adsorption layer in organic redox batteries is a promising pathway to develop high performance organic electrode materials for SIBs.

研究领域: 电化学 · 能源材料 · 纳米材料 · 电池技术 · 功能材料
✓ 已验证 DOI 高影响因子
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RSC Advances · 2021 ·Vol. 11 ·期 16 ·9450-9458 · IF 3.361

Phosphorus modification of cobalt–iron nanoparticles embedded in a nitrogen-doped carbon network for oxygen reduction reaction

Rui Zhang,Zheng Wang,Lin Zhu,Weixin Lv,Wei Wang

For the electrochemical reduction of oxygen the development of heteroatom-doped carbon-based transition metal catalysts has become a recognized strategy to replace traditional noble metal catalysts. In this work a catalyst consisting of CoFe nanoparticles encapsulated in N-doped carbon-based materials (NC) supported by carbon nanotubes (CNTs), i.e. Fe3Co1@NC/CNTs, was modified via treatment with a phosphate salt to synthesize a P-Fe3Co1@NC/CNTs catalyst. The P-Fe3Co1@NC/CNTs exhibits with 5.29 mA cm−2 an enhanced current density which is comparable to a Pt/C catalyst. In addition, a stability and methanol resistance better than the Pt/C catalyst were observed which is ascribed to the carbon encapsulation and the synergies between the two transition metals. Finally, the reaction mechanism of P-doping was studied and discussed. These results provide possible directions for carbon-based catalysts and doping with heteroatoms for the improvement of catalytic activity. Moreover, the zinc–air battery assembled with P-Fe3Co1@NC/CNTs as the air-cathode exhibited a high-power density of 73 mW cm−2, which is comparable to that of Pt/C (71 mW cm−2) and a specific capacity of 763 mA h g−1. The prepared catalyst could potentially serve to take the place of precious metal catalysts in rechargeable Zn–air batteries.

研究领域: 电催化 · 材料化学 · 能源化学 · 纳米材料 · 电化学能源存储 · 燃料电池 · 金属-空气电池
✓ 已验证 DOI 高影响因子
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CHINESE JOURNAL OF CATALYSIS · 2022 ·Vol. 43 ·期 9 ·2443-2452 · IF 12.92

Carbon dots-derived carbon nanoflowers decorated with cobalt single atoms and nanoparticles as efficient electrocatalysts for oxygen reduction

Yaojia Cheng,Haoqiang Song,Jingkun Yu,Jiangwei Chang,Geoffrey I.N. Waterhouse,Zhiyong Tang,Bai Yang,Siyu Lu

The sluggish kinetics of oxygen reduction reaction (ORR) hinders the commercialization of Zn-air batteries (ZABs). Manipulating the electronic structure of electrocatalysts to optimize the adsorption energy of oxygen-containing intermediates during the 4e − ORR offers a practical route toward improving ORR kinetics. Herein, we designed a novel ORR electrocatalyst containing Co single atoms and nanoparticles supported by carbon dots-derived carbon nanoflowers (Co SAs/NPs CNF). Co SAs/NPs CNF possessed a very high ORR activity ( E 1/2 of the Co SAs/NPs CNF catalyst is 0.83 V ( vs. RHE)), and outstanding catalytic performance and stability when used as the air-electrode catalyst in rechargeable ZABs (152.32 mW cm −2 , 1000.58 mWh g Zn −1 , and over 1300 cycles at a current density of 5 mA cm −2 ). The Co SAs and Co NPs cooperated to improve electron and proton transfer processes during ORR. Theoretical calculations revealed that the presence of adjacent Co NPs optimized the electronic structure of the isolated Co-N 4 sites, significantly lowering the energy barriers for the rate-determining step in ORR (adsorption of *OOH) and thereby delivering outstanding ORR performance. This work reveals that the combination of supported single-atom sites and metal nanoparticles can be highly beneficial for ORR electrocatalysis , outperforming catalysts containing only Co SAs or Co NPs.

研究领域: 电化学 · 纳米材料科学 · 能源化学 · 催化化学 · 先进电池技术
✓ 已验证 DOI 高影响因子
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CHINESE JOURNAL OF CHEMISTRY · 2013 ·Vol. 31 ·期 3 ·371-376 · IF 0.917

Study of the Transient Reactive Pd(IV) Intermediate in the Pd(OAc)2-Catalyzed Oxidative Coupling Reaction System by Electrospray Ionization Tandem Mass Spectrometry

Wei Zhu,Haoyang Wang,Haihui Peng,Guosheng Liu,Yinlong Guo

Pd-catalyzed oxidative coupling reaction was of great importance in the aromatic C  H activation and the formation of new C  O and C  C bonds. Sanford has pioneered practical, directed C  H activation reactions employing Pd(OAc) 2 as catalyst since 2004. However, until now, the speculated reactive Pd(IV) transient intermediates in these reactions have not been isolated or directly detected from reaction solution. Electrospray ionization tandem mass spectrometry (ESI-MS/MS) was used to intercept and characterize the reactive Pd(IV) transient intermediates in the solutions of Pd(OAc) 2 -catalyzed oxidative coupling reactions. In this study, the Pd(IV) transient intermediates were detected from the solution of Pd(OAc) 2 -catalyzed oxidative coupling reactions by ESI-MS and the MS/MS of the intercepted Pd(IV) transient intermediate in reaction system was the same with the synthesized authentic Pd(IV) complex. Our ESI-MS(/MS) studies confirmed the presence of Pd(IV) reaction transient intermediates. Most interestingly, the MS/MS of Pd(IV) transient intermediates showed the reductive elimination reactivity to Pd(II) complexes with new C  O bond formation into product in gas phase, which was consistent with the proposed reactivity of the Pd(IV) transient intermediates in solution.

研究领域: 有机化学 · 金属有机化学 · 分析化学 · 催化化学 · 质谱学
✓ 已验证 DOI 高影响因子
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