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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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BIOSENSORS & BIOELECTRONICS · 2017 · IF 7.78

Electrochemical immunosensor with nanocellulose-Au composite assisted multiple signal amplification for detection of avian leukosis virus subgroup J

Chao Liu,Jing Dong,Geoffrey I.N. Waterhouse,Ziqiang Cheng,Shiyun Ai

A sensitive sandwich-type electrochemical immunosensor was developed for the detection of avian leukosis virus subgroup J (ALV-J), which benefitted from multiple signal amplification involving graphene-perylene-3,4,9,10-tetracarboxylic acid nanocomposites (GR-PTCA), nanocellulose-Au NP composites (NC-Au) and the alkaline phosphatase (ALP) catalytic reaction . GR-PTCA nanocomposites on glassy carbon electrodes served as the immunosensor platform. Due to their excellent electrical conductivity and abundant polycarboxylic sites, the GR-PTCA nanocomposites allowed fast electron transfer and good immobilization of primary antibodies, thereby affording a strong immunosensor signal in the presence of ALV-J. The detected signal could be further amplified by the introduction of NC-Au composites as a carrier of secondary antibodies (Ab 2 ) and by harnessing the catalytic properties of Au and ALP. Under optimized testing conditions, the electrochemical immunosensor displayed excellent analytical performance for the detection of ALV-J, showing a linear current response from 10 2.08 to 10 4.0 TCID 50 /mL (TCID 50 : 50% tissue culture infective dose) with a low detection limit of 10 1.98 TCID 50 /mL (S/N = 3). In addition to high sensitivity, the immunosensor showed very good selectivity, reproducibility and operational stability, demonstrating potential application for the quantitative detection of ALV-J in clinical diagnosis.

研究领域: 免疫学 · 生物传感器 · 分子诊断 · 兽医病毒学 · 纳米医学
✓ 已验证 DOI 高影响因子
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Journal of Materiomics · 2022 ·Vol. 9 ·期 3 ·568-576 · IF 8.589

Synergistically enabling the interface stability of lithium metal batteries with soft ionic gel and garnet-type Li6.4La3Zr1.4Ta0.6O12 ceramic filler

Qiujun Wang,Weiqi Zhu,Ya Su,Di Zhang,Zhaojin Li,Huan Wang,Huilan Sun,Bo Wang,Dan Zhou,Li-Zhen Fan

Lithium metal batteries based on solid electrolytes are considered as promising candidates with high energy density and safety. However, the weak solid-solid contact between electrolyte and electrode can easily lead to interface instability and lithium ions discontinuous migration, which seriously reduces the electrochemical performance of the battery. Herein, we construct a soft gel interfacial layer to improve the stability of the solid-solid interface between electrolyte and electrode by means of polyester-based monomers and imidazole-based ionic liquids. Based on this, garnet-type Li 6.4 La 3 Zr 1.4 Ta 0.6 O 12 (LLZTO) particles as inorganic ceramic filler were introduced in the layer to obtain composite electrolytes with high ionic conductivity (up to 1.1 × 10 −3  S/cm at 25 °C). As a result, the assembled lithium symmetric battery of Li|THCE-15%LLZTO|Li suggests excellent cycling stability with 700 h at 0.1 mA/cm 2 at 50 °C, and the lithium metal batteries of LFP|THCE-15%LLZTO|Li delivers high initial discharge capacity of 128.2 mA ·h/g with capacity retain of 75.48% after 150 cycles at 2 C. This work paves a new route to build safe and stable lithium metal batteries with synergistic introduction of composite electrolytes between electrolyte and electrode using soft gel interfacial layer and inorganic filler.

研究领域: 电化学 · 材料科学 · 能源存储 · 固体离子学 · 界面工程
✓ 已验证 DOI 高影响因子
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ELECTROCHIMICA ACTA · 2020 · IF 6.215

A dendrite-suppressed flexible polymer-in-ceramic electrolyte membrane for advanced lithium batteries

Shi Wang,Qingyuan Li,Minglei Bai,Jixin He,Chongyang Liu,Zengxi Li,Xiangfeng Liu,Wen-yong Lai,Liaoyun Zhang

Lithium-ion batteries (LIBs) using solid-state electrolytes (SSEs) can improve safety and energy density comparable with the liquid electrolytes (LE)-based counterparts. Especially, employing garnet-type SSEs to prepare solid-state LIBs are promising to achieve high-energy cells. However, the unbending and brittle issues of the inorganic SSE films are not suitable to fabricate flexible and stretchable energy storage devices. Here, We find that introducing specific polymer (30 wt%) into Li 6.75 La 3 Zr 1.75 Ta 0.25 O 12 (LLZTO) can strongly increase the strength of the composite polymer-in-inorganic electrolyte (CIE) film. Both in-situ and ex-situ characterizations demonstrate that CIE delivers an excellent ability to suppress the growth of Li dendrites due to the close packing of LLZTO and effective filled grain boundaries and voids inside the CIE film by the polymer. The CIE inherits impressive electrochemical performance from LLZTO. As a result, the assembled LiFePO 4 (LFP)/CIE/Li cell delivers better cell performance than LFP/LE-separator/Li cell at ambient temperature (AT). The assembled high-voltage cathode (Li 1.2 Mn 0.6 Ni 0.2 O 2 , 4.8 V)/CIE/Li cell also displays an excellent cell performance at AT. The present study offers new insights into exploring of flexible polymer-in-ceramic electrolytes for high-voltage LIBs with improved safety and energy density .

研究领域: 材料科学 · 电化学 · 能源存储 · 固态电池 · 纳米复合材料 · 界面工程
✓ 已验证 DOI 高影响因子
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JOURNAL OF POWER SOURCES · 2022 · IF 9.794

Improving interfacial stability by in situ protective layer formation in 4.2V poly(ethylene oxide) based solid state lithium batteries

Wei Feng,Huirong Liu,Mingliang Zhao,Jianling Li,Feiyu Kang

The poly(ethylene oxide) based composite solid electrolyte(PEO-CSE) is an effective solution for developing high-performance solid-state lithium battery . However, the poly(ethlene oxide)(PEO) based solid-state lithium battery using 4.0 V cathode suffers from severe interfacial instability problems. In this work, we add additive lithium difluorophosphate(LiPO 2 F 2 ) into the PEO-CSE to form a stable and low resistance interphase at the cathode/electrolyte interface during charge/discharge process. The electrochemical stability window of PEO-CSE increases to ∼5.0 V. Besides, the electrochemical performance of PEO based solid-state lithium battery with LiCoO 2 as cathode is excellent. The discharge capacity of LiCoO 2 /Li cell with LiPO 2 F 2 reaches 108.5 mAh g −1 at 1.0C. In contrast, the discharge capacity that without LiPO 2 F 2 is only 60.0 mAh g −1 . Meanwhile, the PEO-CSE with LiPO 2 F 2 cell delivers stable cycle performance at 4.2 V. The capacity retention maintains 88.5% compared with 16.1%(without LiPO 2 F 2 ) after 100 cycles. Furthermore, it's still maintains 83.3% after 150 cycles. In addition, the cathode/electrolyte interface is analyzed by transmission electron microscope(TEM) and X-ray photoelectron spectroscopy(XPS). Galvanostatic intermittent titration test(GITT) is used to analyze the dynamic diffusion performance. This strategy provides a simple and effective way to improve the high voltage stability of the cathode/electrolyte interface.

研究领域: 电化学 · 材料科学 · 能源存储 · 固态电池 · 界面工程
✓ 已验证 DOI 高影响因子
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CARBOHYDRATE POLYMERS · 2018 · IF 5.158

Dopamine-induced functionalization of cellulose nanocrystals with polyethylene glycol towards poly(L-lactic acid) bionanocomposites for green packaging

Le Li,Rui-Ying Bao,Tao Gao,Zheng-Ying Liu,Bang-Hu Xie,Ming-Bo Yang,Wei Yang

Improving the physical properties of biobased polymers using bionanofillers is essential to preserve its biodegradability. This work presents a dopamine-induced functionalization of cellulose nanocrystals (CNCs) with polyethylene glycol (PEG), to enhance the crystallization, mechanical and barrier properties of poly( L -lactic acid) (PLLA) bionanocomposites. The effect of molecular weight of grafted PEG on the properties of PLLA is also studied. PEGylation of CNCs significantly enhance the crystallization of PLLA, especially for CNCs functionalized with PEG of lower molecular weight, which lead to balanced strength and ductility, and 66.4% reduction in the oxygen permeability coefficient at a low content of 0.5 wt %. Moreover, 168% improvement of ductility for PLLA can be obtained by CNCs functionalized with longer PEG chains. The surface functionalization of CNCs proposed here opens up a green avenue towards designing and fabricating fully bio-based, high-barrier and low-cost polymer nanocomposites for packaging applications.

研究领域: 高分子材料 · 纳米复合材料 · 生物基包装 · 材料科学 · 聚合物改性 · 结晶动力学
✓ 已验证 DOI 高影响因子
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COMPOSITES PART A-APPLIED SCIENCE AND MANUFACTURING · 2018 · IF 4.514

Micro-crack behavior of carbon fiber reinforced Fe3O4/graphene oxide modified epoxy composites for cryogenic application

Yuxin He,Qiuyu Chen,Song Yang,Chang Lu,Mengting Feng,Yuanli Jiang,Guoxi Cao,Jianping Zhang,Chuntai Liu

The epoxy nanocomposites with Fe 3 O 4 modified graphene oxide (Fe 3 O 4 /GO) were used to influence the micro-cracks resistance of carbon fiber reinforced epoxy (CF/EP) laminate at 77 K. Fe 3 O 4 /GO with good paramagnetic properties were prepared by co-precipitation method and used to modify epoxy for cryogenic applications. Fe 3 O 4 /GO modified CF/EP laminates were also prepared through vacuum-assisted resin transfer molding (VARTM). The results show that the Fe 3 O 4 /GO can effectively improve the mechanical properties of epoxy (EP) matrix at 77 K and reduce the coefficient of thermal expansion (CTE) of EP matrix. It also can obviously improve the micro-cracks resistance of CF/EP composites at 77 K. Compared to neat EP, the CTE of Fe 3 O 4 /GO modified EP composite is decreased 51.6%. Compared to CF/EP composite, the micro-cracks density of Fe 3 O 4 /GO modified CF/EP composite at 77 K is decreased 60.0%.

研究领域: 材料科学 · 高分子复合材料 · 低温工程 · 纳米复合材料 · 力学性能
✓ 已验证 DOI 高影响因子
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IONICS · 2022 ·Vol. 29 ·期 2 ·505-518 · IF 2.961

Fe-doped Sn@ 3D carbon lithium-ion battery anode mesoporous material with sodium alginate as the carbon source

Yang Dongping,Xiong Deping,Feng Zuyong,Wen Kunhua,Wu Kaidan,He Miao,Feng Yefeng

Sn-based materials receive a lot of attention because of their high theoretical specific capacity, acceptable price, and good electrical conductivity. However, Sn-based materials have a large volume expansion in the circulation process, leading to the rapid decay of capacity. According to the ion diffusion time formula: t  = L2/2D, where L is the diffusion length or the particle size, and D is the diffusion constant of the ions and the electrons. It can be seen that reducing the particle size can significantly improve the multiplier performance of the material. At present, the main methods for preparing nano-sized metal/carbon composites are the high-energy ball grinding method, hydrothermal method, calcined metal, and organic matter precursor. In this paper, sodium alginate was used as a precursor system for the Fe-doped Sn @3D carbon composite material, which was applied to the lithium-ion battery anode to obtain excellent electrochemical performance (1133.5 mAhg −1 after 200 cycles at 0.2 Ag −1 ). The increase in the specific surface area of Fe-doped Sn @3D carbon also increases the charge transfer efficiency and further improves the multiplier performance of the electrode. Meanwhile, the nano-size and structure can better buffer the volume expansion and protect the structure of the electrode.

研究领域: 材料科学 · 电化学 · 纳米材料 · 能源存储 · 功能材料 · 复合材料
✓ 已验证 DOI 高影响因子
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MATERIALS SCIENCE AND ENGINEERING A-STRUCTURAL MATERIALS PROPERTIES MICROSTRUCTURE AND PROCESSING · 2021 · IF 5.234

Optimizing phase interface of titanium carbide-reinforced copper matrix composites fabricated by electropulsing-assisted flash sintering

Siqi Xiang,Xingjian Du,Yihan Liang,Mengcheng Zhou,Xinfang Zhang

Full density TiC reinforced Cu matrix composites are fabricated by electropulsing-assisted flash sintering within 40 s. The addition of TiC significantly increases the hardness of the sintered sample. However, liquid Cu does not wet stoichiometric TiC, leading to a poor interface bonding strength between TiC and Cu, thus the tensile strength of the sintered sample is destroyed. By adding a small amount of Ti, the bonding strength of the interface between TiC and Cu can be effectively optimized, thereby the mechanical strength of the samples is improved, showing an increased hardness and tensile strength . Skillfully use the relationship between hardness and tensile strength curve to intuitively show the bonding strength of the micro interface from the macro characteristics. The reaction between dissolved Ti and stoichiometric TiC and the decomposition of stoichiometric TiC cause the formation of near-surface non-stoichiometric TiC x ( x  < 1) with a marked metal-like electronic structure, which is the fundamental reason for the optimization of the interface bonding between TiC particles and Cu matrix. In the process of powder metallurgy , it is a promising strategy to enhance the composite materials by adjusting the stoichiometry of ceramic to form metal-like electronic structure and alter the bonding strength of ceramic/metal interface.

研究领域: 材料科学 · 粉末冶金 · 金属基复合材料 · 界面工程 · 固态加工
✓ 已验证 DOI 高影响因子
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JOURNAL OF ALLOYS AND COMPOUNDS · 2022 · IF 6.371

Low-temperature monitoring of SF6 decomposition products based on CeO2@MWCNTs composite sensor

Dan Baohui,Mahmood ul Haq,Salah Ud Din,Shabab Hussain,Shao Wenyi,Wu Jingmin,Chi Hanwen,Zhizhen Ye,Liping Zhu

The SF 6 gas in gas-insulated switchgear (GIS) systems decomposes into SO 2 F 2 , SOF 2 , SO 2 , and H 2 S under abnormal conditions such as partial discharge. The detection of these decomposition gases with high sensitivity is essential for the safe operation of GIS devices. Herein, we report the synthesis of cerium oxide and multiwalled carbon nanotube composite (CeO 2 @MWCNTs). The CeO 2 @MWCNTs composite was characterized by X-ray diffraction, scanning electron microscopy, energy-dispersive X-ray spectroscopy, transmission electron microscopy , X-ray photoelectron spectroscopy, and Brunauer–Emmett–Teller analysis. The CeO 2 @MWCNTs composite sensor provided a response value of 7.7 at 100 ppm of SO 2 F 2 at a low operating temperature (50 °C), and the response and recovery features of the CeO 2 @MWCNTs composite sensor were recorded at 43 and 28 s, respectively. Moreover, the composite sensor exhibited excellent stability after two months. The developed CeO 2 @MWCNTs composite sensor can offer an exceptional platform for gas sensing applications in diverse fields.

研究领域: 材料科学 · 气体传感技术 · 电力设备监测 · 纳米复合材料 · 环境监测
✓ 已验证 DOI 高影响因子
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POLYMERS FOR ADVANCED TECHNOLOGIES · 2019 ·Vol. 30 ·期 9 ·2313-2320 · IF 2.162

Synthesis and characterization of waterborne polyurethane/polyhedral oligomeric silsesquioxane composites with low dielectric constants

Hui Zhao,Si-Qi Zhao,Guo-Hua Hu,Qun-Chao Zhang,Yang Liu,Chong-Xing Huang,Wei Li,Tao Jiang,Shuang-Fei Wang

A facile method was developed to synthesize a new type of polyhedral oligomeric silsesquioxane (POSS). It contained a single amine group and seven aliphatic moieties on its corners. FT-IR, 1 H-NMR, 13 C-NMR, 13 C- 1 H COSY, and 1 H- 1 H COSY confirmed that cages with eight corners were the main part of the product. This new POSS was used to modify the structure of hexamethylene diisocyanate trimer and then copolymerized with hexamethylene diisocyanate and poly (tetramethylene glycol) to get a serious of waterborne polyurethane (WPU)/POSS hybrid materials with low dielectric constants for microelectronics applications. The results showed that POSS particles were uniformly dispersed in the WPU dispersions. The WPU/POSS films did not show any macrophase separation, even when the POSS content was as high as 16%. As the POSS content increased from 0% to 16%, the tensile strength was increased from 2.3 to 7.3 MPa, the dielectric constant was decreased from about 2.9 to 2.0, and the thermal stability of the WPU/POSS was also improved.

研究领域: 高分子科学 · 材料化学 · 纳米复合材料 · 电子封装材料 · 功能高分子
✓ 已验证 DOI 高影响因子
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THIN SOLID FILMS · 2018 · IF 1.939

Yttrium-doped TiO2 nanorod arrays and application in perovskite solar cells for enhanced photocurrent density

Yanqi Lv,Yanhong Li,Hongxia Sun,Yi Guo,Yanmei Li,Jinkun Tan,Xingfu Zhou

Crystalline yttrium-doped rutile TiO 2 nanorod arrays were synthesized and successfully implemented as a photoanode of perovskite solar cells . Study shows that yttrium was successfully doped and TiO 2 band gap changes from 3.07 eV to 3.02 eV. A positive shift of 100 mV in the flat-band potential (V fb ) was observed in Y-doped rutile TiO 2 nanorods. A power conversion efficiency of 7.95% and a photocurrent density of 15.13 mA/cm 2 were obtained for the doped sample. The photocurrent density is 1.47 times higher than that of the un-doped device. Incident photon-to-current conversion efficiency shows Y-doped device has a clear increase in quantum efficiency in the visible light range from 450 and 750 nm. Open circuit voltage decay measurements demonstrate the superior ability of Y-doped TiO 2 nanorod for separating electrons and holes and decreasing the recombination events. The improved performance is possibly attributed to the enhanced electron injection and transfer efficiency caused by a positive shift in V fb and a reduction in charge recombination. This study opens a door toward the improvement of photocurrent density of perovskite solar cell via an element doping route.

研究领域: 材料科学 · 纳米科技 · 能源化学 · 光电子学 · 半导体物理 · 可再生能源
✓ 已验证 DOI 高影响因子
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