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CHEMICAL ENGINEERING JOURNAL · 2019 · IF 8.355

Environmentally friendly synthesis of Co-based zeolitic imidazolate framework and its application as H2O2 sensor

Yuhua Dong,Jianbin Zheng

The work presented that by regulating the proportion between cobalt and 2-methylimidazole in distilled water, a series of Co-based imidazolate framework compounds with diverse shapes were synthesized at ambient temperature. The morphology and structural characteristics of the compounds were surveyed by scanning electron microscope, energy disperse spectra, powder X-ray diffraction and N 2 absorption-desorption. It was found by cyclic voltammetry that the zeolitic imidazolate framework compound synthesized at a ratio of 1:20 had the best electrocatalytic activity to H 2 O 2 reduction, therefore, the compound was chosen to fabricate a H 2 O 2 electrochemical sensor. Electrochemical studies indicated that the sensor had a determination limit of 0.7 μM and short response time within 3 s. The catalytic current was linear with H 2 O 2 concentration from 2.5 to 212.5, 212.5 to 1662.5 and 1662.5 to 6662.5 μM and the sensitivity were 12.2, 5.3 and 2.4 μA mM −1  cm −2 , respectively. Furthermore, the proposed sensor showed a good anti-interference capacity, repeatability and stability.

研究领域: 分析化学 · 材料科学 · 电化学 · 生物传感器 · 纳米材料 · 环境监测
✓ 已验证 DOI 高影响因子
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POLYMER TESTING · 2020 · IF 3.275

Epoxy nanocomposites with high thermal conductivity and low loss factor: Realize 3D thermal conductivity network at low content through core-shell structure and micro-nano technology

Rui Wang,Congzhen Xie,Bin Gou,Huasong Xu,Shoukang Luo,Jiangang Zhou,Leilei Zeng

Dielectric polymers with high thermal conductivity are very promising in the fields of aerospace and electronic device packaging. However, composites with excellent dielectric properties usually have low thermal conductivity. It is usually to fill the polymer with thermal conductivity particles to improve the thermal conductivity, but the high content of filler often reduces the mechanical properties of the polymer. In this paper, the traditional insulating polymer epoxy resin was used as the matrix, by covering the surface of silicon carbide with graphene to form a core-shell structure and co-filled with nano diamonds to achieve the preparation of high-performance epoxy resin at low content. The results showed that at the filling content of 30 wt%, the thermal conductivity of epoxy nanocomposites showed a dramatic thermal conductivity enhancement of 1263%, the energy storage modulus increased by 1.1 GPa, and the dielectric loss remained unchanged at 50 Hz. The advantages of the composite are the structural design and surface modification of the filler, which not only take advantage of its inherent advantages, but also improve the interface area with the epoxy matrix. The composite materials with excellent properties are expected to provide theoretical guidance for the application of high thermal conductivity dielectric materials.

研究领域: 材料科学 · 高分子化学 · 复合材料工程 · 电子封装材料 · 介电材料 · 热管理材料
✓ 已验证 DOI 高影响因子
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INTERNATIONAL JOURNAL OF HYDROGEN ENERGY · 2019 ·Vol. 44 ·期 12 ·6148-6159 · IF 4.084

Enhanced anhydrous proton conductivity of SPEEK/IL composite membrane embedded with amino functionalized mesoporous silica

Xiaoyu Zhang,Shiyuan Yu,Qian Zhu,Lianhua Zhao

The novel SP/IL/AMS composite membrane doped with amino-functionalized mesoporous silica (AMS) was successfully prepared. Sulfonated poly ether ether ketone (SPEEK, SP) was used as the polymer matrix and the ionic liquid (IL) was N -ethylimidazolium trifluoromethanesulfonate (EIm[Tfo]). Its properties were compared with SP/IL/NMS composite membrane doped with non-functionalized mesoporous silica (NMS). Fourier transform infrared spectroscopy (FT-IR) analysis indicated that the components in the composite membrane were bound by intermolecular forces. In addition, an acid-base interaction was formed between -NH 2 in AMS and -SO 3 H in SPEEK. The acid-base pair is beneficial to proton conduction. The anhydrous proton conductivity of SP/IL/3-AMS-7.5 composite membrane is about 4 times higher than that of the SP/IL/NMS-7.5. In addition, the good interfacial compatibility between AMS and polymer matrix is conducive for creation continuous proton transfer channel. Thermogravimetric analysis (TG) showed that all composite membranes were stable at 270 °C. The leaching of IL data indicated that IL can be effectively retained due to the presence of -OH and -NH 2 on the NMS and AMS surfaces. The SP/IL/AMS composite membrane could be used in proton exchange membrane fuel cells under medium temperature and anhydrous conditions.

研究领域: 材料科学 · 高分子化学 · 能源材料 · 燃料电池 · 膜科学
✓ 已验证 DOI 高影响因子
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Small · 2023 ·Vol. 19 ·期 40 ·2303227 · IF 13.3

Sodium-Ion Substituted Water Molecule in Layered Vanadyl Phosphate Enhancing Electrochemical Kinetics and Stability of Zinc Ion Storage

YuanZhe Wu,Quan Zong,Chaofeng Liu,Yanling Zhuang,Daiwen Tao,Jiangying Wang,Jingji Zhang,Qilong Zhang,Guozhong Cao

Vanadyl phosphate (VOPO 4 ·2H 2 O) has been regarded as one of the most promising cathode materials for aqueous Zn-ion batteries due to its distinct layered structure. However, VOPO 4 ·2H 2 O has not yet demonstrated the exceptional Zn ion storage performance owing to the structural deterioration during repeated charging/discharging process and poor intrinsic conductivity. In this work, 2D sodium vanadyl phosphate (NaVOPO 4 ·0.83H 2 O, denoted as NaVOP) is designed as a cathode material for Zn-ion batteries, in which sodium ions are preinserted into the interlayer, replacing part of water. Benefiting from the in situ surface oxidization, improved electronic conductivity, and increased hydrophobicity, the NaVOP electrode exhibits a high discharge capacity of 187 mAh g −1 at 0.1 A g −1 after activation, excellent rate capability and enhanced cycling performance with 85% capacity retention after 1500 cycles at 1 A g −1 . The energy storage mechanism of the NaVOP nanoflakes based on the rapid Zn 2+ and H + intercalation pseudocapacitance are investigated via multiple ex situ characterizations.

研究领域: 材料科学 · 电化学 · 能源存储 · 无机化学 · 纳米材料
✓ 已验证 DOI 高影响因子
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CHEMICAL ENGINEERING JOURNAL · 2021 · IF 13.273

Multi-functional silk fibers/fabrics with a negligible impact on comfortable and wearability properties for fiber bulk

Zihui Liang,Zezhu Zhou,Jing Li,Shiliang Zhang,Binghai Dong,Li Zhao,Congcong Wu,Huiyu Yang,Fengxiang Chen,Shimin Wang

As a luxurious textile for more than five thousand years, silk fibers/products have always been favored by consumers and the markets, but the poor photostability seriously hinders its utilization in fashionable apparel. Even if enduing the functionality of silk fiber through surface modification, it is often at the expense of its comfort. Here, an ultra-thin amorphous titanium dioxide nano-film with a thickness of only five in a thousand of fiber diameter and the add-on percentage ≤ 5.33% was prepared on the surface of silk fibers/fabrics by atomic layer deposition (ALD) methods. The tensile strength of the modified silk fiber maintains 89.17% of the original fiber after exposure to UV light for 672 h. They can also withstand multi-cycle laundering and accelerate light-aging, which exhibiting an excellent UV resistance. Most importantly, the functional coating has a negligible impact on the comfortable and wearability performance of silk fibers/fabrics. In addition, ALD-coated silk fabric is also further used as an outdoor reflective cooling material and achieving a superior thermal insulation effect with the temperature reduction up to 10.1 °C.

研究领域: 材料科学 · 纺织工程 · 纳米技术 · 表面科学 · 功能纺织品 · 光稳定性 · 生物医学材料
✓ 已验证 DOI 高影响因子
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ELECTROCHIMICA ACTA · 2017 · IF 4.798

Chemical integration of reduced graphene oxide sheets encapsulated ZnCo2O4 quantum dots achieving excellent capacity storage for lithium-ion batteries

Chang Chen,Kwok-ho Lam,Bao-jun Liu,Xian-hua Hou,Yu-ping Wu

Chemically integrated hybrid quantum dots ZnCo 2 O 4 /reduced graphene oxide (QDs ZCO/rGO) sheets nanocomposites are synthesized through polyol processes. rGO sheets grow and interweave to form basic skeletons. Ultrafine ZCO particles with a size of around 3.66   nm grow and embed on both sides of the rGO sheets, and the rGO sheets restrain the reunion of ZCO nanoparticles . The existence of rGO sheets and ZCO nanoparticles can engender the mutual synergistic effects so that hybrid QDs ZCO/rGO electrodes exhibit the excellent electrochemical properties . Owing to this special nanoparticles-on-sheets structure, the hybrid QDs ZCO/rGO electrodes exhibit an excellent initial discharge capacity for rechargeable lithium-ion batteries (1325.9   mAh   g −1 at the current density of 200   mA   g −1 ), high rate stability (532.3/566.1   mAh   g −1 at 4000   mA   g −1 ) and outstanding electrochemical cyclic stability (657.6/668.2   mAh   g −1 at 2000   mA   g −1 after 2000 cycles with a capacity retention of 68.6%). For full-cells, high initial reversible discharging capacity (646   mAh   g −1 at 200   mA   g −1 ) and good cyclic stability (514   mAh   g −1 at 200   mA   g −1 after 100 cycles) are obtained. The superior performance of the as-prepared electrodes is ascribed to the advantage of nano-sized particles. With the successful synthesis of hybrid QDs ZCO/rGO nanocomposites, the facile synthetic route and unique growth of nanostructuring method can be extended to high electrochemical performance electrodes for commercial lithium-ion batteries.

研究领域: 材料科学 · 电化学 · 纳米科技 · 能源存储 · 功能材料 · 先进电池技术
✓ 已验证 DOI 高影响因子
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PHYSICAL CHEMISTRY CHEMICAL PHYSICS · 2018 ·Vol. 20 ·期 27 ·18455-18462 · IF 3.906

The stabilization mechanism and size effect of nonpolar-to-polar crystallography facet tailored ZnO nano/micro rods via a top-down strategy

Xiangyang Duan,Chao Ma,Wentao Jin,Xiaoman Ma,Lu’an Guo,Su-Huai Wei,Jinying Yu,Yelong Wu

A simple and efficient top-down strategy, the chemical vapor etching method, is reported for synthesizing corrugated ZnO nano/micro rods (NRs). The stabilization mechanism of this unique nanostructure has been determined through a combination of aberration-corrected field emission scanning electron microscopy, high-resolution transmission electron microscopy, and first-principles calculations. The experimental data are in good agreement with the theoretical calculations, and a remarkable nonpolar-to-polar surface faceting transition is demonstrated. The corrugated-shaped structure results from the remarkable stability of the defect-induced reconstructions (O vacancy, Zn–Zn dimer), which makes the high-index polar {301} and {10} planes lower in energy compared to the nonpolar {100} plane. Based on the results of first-principles surface calculations, a general formula is established to provide an accurate description of the unusual size effect of the length of the corrugated unit vs. the NR diameter, and it also offers direct explanations for certain experimental observations. The present study deepens our atomic-level understanding of the detailed structure and stability of polar surface decorated corrugated ZnO NRs, and points to a viable path towards designing polar-stable wurtzite structures.

研究领域: 材料科学 · 纳米科技 · 表面科学 · 凝聚态物理 · 计算材料学
✓ 已验证 DOI 高影响因子
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APPLIED CATALYSIS B-ENVIRONMENTAL · 2019 · IF 14.229

In-situ synthesis of monodispersed CuxO heterostructure on porous carbon monolith for exceptional removal of gaseous Hg0

Liyuan Zhang,Shu Yang,Yuekun Lai,Hui Liu,Yiang Fan,Cao Liu,Haiying Wang,Liyuan Chai

Gaseous Hg 0 is one of the most deadly and hard-to-dispose pollutants. The oxidation of Hg 0 is a promising route, but the rational design and synthesis of highly efficient catalysts still remain grand challenges. Herein, CuO@Cu 2 O (or Cu x O) heterostructured nanoparticles uniformly monodispersing on porous carbon monolith were designed and successfully synthesized using oligo( m -phenylenediamine)-Cu 2+ complex as raw material. The Cu x O-carbon catalyst contains ∼28 wt% of Cu. Based on density functional theory calculation, the CuO@Cu 2 O junction interfaces can accelerate the Hg 0 oxidation by significantly reducing the energy barriers of reaction. Only 1 mg of the catalyst can catalyze the oxidation of more than 90 % of Hg 0 with [HCl] = 0.5 ppm, [O 2 ] = 6 vol%, T = 150 °C. The poisoning effect of either SO 2 or H 2 O on the catalysts is weak. Moreover, a long-term test confirmed that the Hg 0 oxidation rate can maintain more than 90 % even in the co-presence of SO 2 (5000 ppm) and H 2 O (10 vol%).

研究领域: 环境催化 · 材料化学 · 大气污染控制 · 纳米材料 · 表面科学
✓ 已验证 DOI 高影响因子
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Journal of Energy Storage · 2024 · IF 8.9

Control the explosive polymerization of 1,3-dioxolane in LiPF6 electrolyte by Lewis acid-base interactions

Xueting Yang,Haoyu Deng,Jie Xu,Dezhan Ye,Xiancai Jiang,Yazhou Chen,Ke Sun,Zengjin Liu

1,3-dioxolane (DOL) shows low interfacial impedance and high Coulombic efficiency, thus its polymer electrolytes have attracted extensive attention. In order to initiate DOL polymerization, catalyst amount of LiPF 6 is usually used rather than as the main lithium salt . Totally replacement of LiTFSI with low cost of LiPF 6 could bring the heat explosion and high viscosity when mixing DOL with 0.9 M LiPF 6 electrolyte (carbonate ester solvent). Here, based on the Lewis acid-base interaction, a new type of Lewis base, pyridine, is added to control the explosive polymerization of 1,3-dioxolane in LiPF 6 electrolyte. Through tuning the pyridine content, the gelling process and electrochemical properties could be controlled. It is demonstrated that the optimized monomer conversion and electrochemical window are up to 85.2 % and 4.6 V; meanwhile, the optimized conductivity and transfer number are 0.99 × 10 −3  S/cm (25 °C) and 0.68, respectively. The stable interface between PDOL and lithium metal anode could be proved by the stable over-potential (50mv, 700 h) at current density of 0.5 mA cm −2 . After 500 cycles at 2C, the assembled Li/PDOL@py 0.125 /LiFePO 4 battery delivers 115 mAh/g and 90 % capacity retention, with high average Coulombic efficiency of 99.83 %. The present results demonstrate the heat suppression role of pyridine toward mixing DOL with 0.9 M LiPF 6 electrolyte, which solves the heat and viscosity problems for PDOL based gelling polymer electrolytes .

研究领域: 电化学 · 高分子化学 · 能源材料 · 锂离子电池 · 界面化学 · 功能材料
✓ 已验证 DOI 高影响因子
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JOURNAL OF POWER SOURCES · 2017 · IF 6.395

High hydrogen desorption properties of Mg-based nanocomposite at moderate temperatures: The effects of multiple catalysts in situ formed by adding nickel sulfides/graphene

Xiubo Xie,Ming Chen,Peng Liu,Jiaxiang Shang,Tong Liu

Nickel sulfides decorated reduced graphene oxide (rGO) has been produced by co-reducing Ni 2+ and graphene oxide (GO), and is subsequently ball milled with Mg nanoparticles (NPs) produced by hydrogen plasma metal reaction (HPMR). The nickel sulfides of about 800 nm completely in situ change to MgS, Mg 2 Ni and Ni multiple catalysts after first hydrogenation/dehydrogenation process at 673 K. The Mg-5wt%NiS/rGO nanocomposite shows the highest hydrogen desorption kinetics and capacity properties, and the catalytic effect order of the additives is NiS/rGO, NiS and rGO. At 573 K, the Mg-NiS/rGO nanocomposite can quickly desorb 3.7 wt% H 2 in 10 min and 4.5 wt% H 2 in 60 min. The apparent hydrogen absorption and desorption activation energies of the Mg-5wt%NiS/rGO nanocomposite are decreased to 44.47 and 63.02 kJ mol −1 , smaller than those of the Mg-5wt%rGO and Mg-5wt%NiS samples. The best hydrogen desorption properties of the Mg-5wt%NiS/rGO nanocomposite can be explained by the synergistic catalytic effects of the highly dispersed MgS, Mg 2 Ni and Ni catalysts on the rGO sheets, and the more nucleation sites between the catalysts, rGO sheets and Mg matrix.

研究领域: 材料科学 · 纳米科技 · 能源化学 · 催化化学 · 储氢材料
✓ 已验证 DOI 高影响因子
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JOURNAL OF MEMBRANE SCIENCE · 2013 · IF 4.093

Plasma activation of porous polytetrafluoroethylene membranes for superior hydrophilicity and separation performances via atomic layer deposition of TiO2

Qiang Xu,Yang Yang,Jie Yang,Xiaozu Wang,Zhaohui Wang,Yong Wang

Conformal and smooth TiO 2 thin layers were coated on the surface of porous PTFE membranes subjected to a plasma activation process by atomic layer deposition (ALD). In contrast, TiO 2 was deposited on the PTFE surface as globular particulates without plasma activation due to the inert chemical nature of PTFE surface. X-ray photoelectron spectrometry confirmed the formation of functional groups on the plasma-activated PTFE surface which served as active sites for the homogeneous adsorption and reaction of ALD precursors. Scanning and transmission electron microscopy revealed the uniformity of the deposited layer and the precise control of its thickness by changing ALD cycle numbers. The water contact angle measurement showed that the hydrophobic surface gradually turned to be near superhydrophilic with the increment of ALD numbers. Also, the membrane mean pore size was progressively reduced by simply altering the ALD numbers. At proper deposition conditions , the modified membranes gained an increase of pure water flux of more than 150% and simultaneously a doubled retention compared to the original unmodified membrane. This research provides an efficient approach devoid of any harsh treatments to modifying PTFE membranes for achieving specific functions, which also can be applied to other organic materials especially with chemical inert surface.

研究领域: 材料科学 · 膜科学与技术 · 表面工程 · 高分子化学 · 环境工程 · 纳米科技
✓ 已验证 DOI 高影响因子
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JOURNAL OF ALLOYS AND COMPOUNDS · 2022 · IF 6.371

Using tetramethylammonium hydroxide electrolyte to inhibit corrosion of Mg-based amorphous alloy anodes: A route for promotion energy density of Ni-MH battery

Jianling Huang,ChengWei Liao,Hui Wang,YuJun Zhao,Liuzhang Ouyang,Jiangwen Liu,Min Zhu

Mg-based alloy anodes suffer from severe corrosion in conventional electrolytes (KOH solution) and this substantially obstructs the cycle life, which is a great challenge for using them in the Ni-MH battery. Herein, a high concentration tetramethylammonium hydroxide (TMAH) aqueous electrolyte with a special hydrate structure is explored and enables excellent cycle stability and high capacity for Mg-based alloy anodes. In this electrolyte, the Mg 0.4 Ti 0.1 Ni 0.5 alloy anode delivers a maximum discharge capacity of 466 mAh g −1 , and maintains 210 mAh g −1 after 100 cycles owing to the reduced corrosion rate , which are much better than that in 6 M KOH electrolyte, being 425 mAh g −1 and 69 mAh g −1 , respectively. Furthermore, by in-situ forming Cu coating on the Mg 0.4 Ti 0.1 Ni 0.5 electrode surface during charging process with the adding 0.01 M of Cu(OH) 2 in TMAH electrolyte, the corrosion of the electrode is further suppressed and the reversible capacity can reach 313 mAh g −1 after 100 cycles. The high conducting Cu coating can also increase the rate capability of the electrode by promoting the charge transfer. Thus, using TMAH electrolytes provides a new approach to promote the electrochemical performances of Ni-MH batteries with Mg-based alloy anodes.

研究领域: 材料科学 · 电化学 · 能源存储 · 金属腐蚀与防护 · 功能材料 · 电池技术
✓ 已验证 DOI 高影响因子
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