CHINESE JOURNAL OF ANALYTICAL CHEMISTRY
·
2015
·Vol. 43
·期 10
·1569-1572
·
IF 0.754
Ming-Yan LUO,Bei LÜ,Guo-Bin SHEN,Fei-Fang ZHANG,Bing-Cheng YANG
Electrodialytic eluent generator, one of the key components of ion chromatography system, was fabricated and evaluated. The data achieved indicated that its performance could be comparable to that of commercial one. The maximal operation pressure was over 20 MPa, the generated KOH concentration was up to 100 mM, and the designed usage lifetime was about 354 day (take 8 h working time per day). This device will be helpful to the improvement of domestic instruments of ion chromatography.
研究领域:
分析化学
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仪器科学与技术
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分离科学
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离子色谱技术
✓ 已验证
DOI
高影响因子
Journal of Chemistry
·
2010
·Vol. 9
·期 1
·435-442
·
IF 0
Yabin Wang,Yanni Li,Fang Wang
The protective performances of coating formed by organo-silane with a linear alkyl chain for promoting aluminum alloy corrosion protection were evaluated by electrochemical techniques. The coatings were self-assembled in the hydrolyzed hydroalcoholic bath of n -octyltriethoxysilane (OS) and cured at hot air oven by different time. The coatings prepared by the less self-assembled number and shorter cured time, were always porous and scarcely protective. On the contrary, those built by the more self-assembled number and the longer cured time had higher coverage on aluminum surface and favorable corrosion resistant property. The best results were obtained when n -octyltri-ethoxysilane (OS) was hydrolyzed 25 h, self-assembling of OS was conducted for five times and the multi-layers were cured at 120 for 1∼2 hours. In this case, the thicker, high cross-linked and more scarcely defective layer was formed on aluminum alloy surface.
研究领域:
材料科学
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表面工程
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腐蚀与防护
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高分子化学
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电化学
✓ 已验证
DOI
ENVIRONMENTAL POLLUTION
·
2018
·
IF 4.358
Zhaocheng Zhang,Dongyang He,Haiyang Liu,Miao Ren,Yanan Zhang,Jiao Qu,Nan Lu,Jiunian Guan,Xing Yuan
Black phosphorus (BP), a superior two-dimensional (2D) semiconductor, has attracted much attention due to its unique properties. The graphene (GR)-BP hybrid was synthesized through one pot chemical vapor transport (CVT) approach. The characterization results indicated that P atom was successfully incorporated into GR by the formation of P-C bond. Remarkably, the newly-synthesized GR-BP represented high photocatalytic activity towards 2-chlorophenol (2-CP) degradation, due to the high efficiency of charge separation and transformation caused by the direct band gap of BP and carrier mobility of GR. The removal efficiency for 2-CP reached up to 87.08% within visible light irradiation for 180 min ( λ > 420 nm). The degradation rate of GR-BP hybrid for 2-CP was approximately 7.29-fold than that of BP within 30 min. In addition, the little increasing of the peak for P-O bond in GR-BP hybrid was observed after being exposed in air for 15 days, meant that the stability of BP was significantly enhanced. It was caused by the decreasing of the oxidation sites in BP due to the formation of P-C bond in hybrid. In brief, our synthetic method for GR-BP not only provides a novel route for the improvement of the stability of BP, but also constitutes an insight into the promising practical application of BP in the photocatalysis field.
研究领域:
材料科学
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纳米科技
·
光催化
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半导体材料
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环境化学
✓ 已验证
DOI
高影响因子
Journal of Energy Chemistry
·
2022
·
IF 13.599
Xi Wang,Yong Wang,Yiyu Wu,Yunmiao Fan,Yang Tian
Li 6.4 La 3 Zr 1.4 Ta 0.6 O 12 (LLZTO) solid garnet-type electrolyte has been widely reported due to its outstanding safety and electrochemical stability. However, the inherent rigidity and brittleness of LLZTO lead to poor contact with anode/cathode and the operation failure of full cells. Herein, the dual-interlayers are constructed as the fast interfacial ion-migration channel by using Ti 3 C 2 T x (MXene, T x is –O, –OH, –F) with trace ionic liquid (IL), which promote the intimate contact between LLZTO and anode/cathode and suppress Li-dendrites growth. Notably, IL can wet the cathode to promote intimate interface contact and be decomposed into some inorganic compounds (such as Li 3 N, LiF, and Li 2 S x ), resulting in reduced interfacial resistance and fast Li-ion transportation. Consequently, in the prepared Li-symmetric cell, the interfacial resistance on the anode side plunges to 33.1 Ω cm −2 , and stably maintains over 1000 h without short circuit at 0.05 mA cm −2 . The full cell of Li|LiFePO 4 delivers a high initial capacity of 158.52 mA h g −1 and outstanding retention of 90.18% after 100 cycles at 60 °C and 0.2 C. Our work provides an efficient strategy to design dual-interlayers between LLZTO and anode/cathode for the interfacial modification to enhance the performance of solid garnet batteries.
研究领域:
材料科学
·
电化学
·
固态电池
·
界面工程
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能源材料
✓ 已验证
DOI
高影响因子
OPTICAL MATERIALS
·
2016
·
IF 2.183
Renping Cao,Xiangfeng Ceng,Jijun Huang,Hui Ao,Guotai Zheng,Xiaoguang Yu,Xinqin Zhang
A double perovskite Sr 2 ZnMoO 6 :Mn 4+ (SZM:Mn 4+ ) phosphor is synthesized by high-temperature solid-state reaction method in air. Emission band peaking at ∼705 nm of SZM:Mn 4+ phosphor in the range of 650–790 nm is attributed to the 2 E → 4 A 2 transition of Mn 4+ ion with activated different lattice vibration modes. Three excitation bands in the range of 210–610 nm are assigned to the O 2− → Mn 4+ charge transfer and the 4 A 2 → ( 4 T 1 , 2 T 2 , and 4 T 2 ) transition of Mn 4+ ion. The optimal Mn 4+ ion concentration is ∼0.8 mol% in SZM:Mn 4+ phosphor. Fluorescence lifetime of SZM:Mn 4+ phosphor decreases from ∼132 μs to 108 μs with increasing Mn 4+ ion concentration in the range of 0.2–1.0 mol%. Time-resolved spectra and fluorescence lifetime data indicate that luminescent center is caused by Mn 4+ ion. The luminous mechanism of SZM:Mn 4+ phosphor is explained by Tanabe-Sugano energy level diagram of Mn 4+ ion. The results are useful to understand the influences of the neighboring coordination environment around Mn 4+ and host crystal structure to the luminescence properties of Mn 4+ ion and develop other novel Mn 4+ -doped materials.
研究领域:
材料科学
·
无机化学
·
固体物理
·
发光材料
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光电功能材料
✓ 已验证
DOI
高影响因子
JOURNAL OF ELECTRONIC MATERIALS
·
2022
·Vol. 51
·期 9
·4846-4854
·
IF 2.047
Bo Lin,Wang Lei,Hou Yangbo,Li Fujin,Liu Sida,Zhang Ruipeng,Zuo Min,Zhao Degang
Ternary Cu 3 SbSe 4 thermoelectric material with a diamond-like structure exhibits good thermoelectric performance in the middle-temperature region. In this study, Cu 2.98 Co 0.02 SbSe 4 material with intrinsically low thermal conductivity was prepared by a melting–ball milling–hot pressing process. The maximum zT value for the Cu 2.98 Co 0.02 SbSe 4 sample was 0.7 at 650 K, which was about 190% higher than that of the pristine sample. The improvement in thermoelectric performance was ascribed to the realization of multi-scale features induced by ball milling. It was found that multiple scattering centers of phonons were formed via interfacial engineering, including dislocations, nano-holes and grain boundaries, which offers an applicable pathway for the reduction of lattice thermal conductivity. Graphical
研究领域:
材料科学
·
凝聚态物理
·
功能材料
·
能源材料
·
半导体物理
✓ 已验证
DOI
高影响因子
Small
·
2019
·Vol. 15
·期 12
·1805474
·
IF 10.856
Yi Jiang,Xingqiao Wu,Yucong Yan,Sai Luo,Xiao Li,Jingbo Huang,Hui Zhang,Deren Yang
Developing an efficient electrocatalyst for the hydrogen evolution reaction (HER) working in both acidic and alkaline solutions is highly desirable, but still remains challenging. Here, Pt x Ni ultrathin nanowires (NWs) with tunable compositions ( x = 1.42, 3.21, 5.67) are in situ grown on MXenes (Ti 3 C 2 nanosheets), serving as electrocatalysts toward HER. Such Pt x Ni@Ti 3 C 2 electrocatalysts exhibit excellent HER performance in both acidic and alkaline solutions, with the Pt 3.21 Ni@Ti 3 C 2 being the best one. Specifically, Pt 3.21 Ni@Ti 3 C 2 achieves record-breaking performance in terms of lowest overpotential (18.55 mV) and smallest Tafel slope (13.37 mV dec −1 ) for HER in acidic media to date. Theory calculations and X-ray photoelectron spectroscopy analyses demonstrate that the coupling of MXenes with the NWs not only approaches the Gibbs free energy for hydrogen adsorption close to zero through the electron transfer between them in acidic media, but also provides additional active sites for water dissociation in alkaline solution, both of them being beneficial to the HER performance.
研究领域:
材料科学
·
电化学
·
纳米催化
·
能源材料
·
物理化学
✓ 已验证
DOI
高影响因子
ELECTROCHIMICA ACTA
·
2016
·
IF 4.803
M.Y. Gao,C. Yang,Q.B. Zhang,Y.W. Yu,Y.X. Hua,Y. Li,P. Dong
Porous Ni-Cu alloy films composed of nanosheets are directly fabricated on Cu substrate using a facile potentiostatic electrodeposition approach from a 1:2 choline chloride-ethylene glycol eutectic solvent (ethaline) containing nickel chloride and copper chloride. Electrochemical co-deposition of Ni-Cu alloy in ethaline is found to be thermodynamically favorable in comparison to conventional aqueous solutions. The deposition process occurs via an instantaneous nucleation and growth of nanoparticles at the initial stage and develops vertically to form nanoporous structures arrayed with nanosheets over deposition time . The as-prepared porous Ni-Cu alloy nanosheet arrays exhibit enhanced electrocatalytic activity for the hydrogen evolution reaction (HER) in alkaline media , which displays a small Tafel slope of 57.2 mV dec −1 with a low onset potential of −48 mV vs. RHE at an optimal condition. It requires small overpotentials of −128 and −150 mV to drive catalytic current densities of 10 and 20 mA cm −2 , respectively. This facile electrodeposition method performed in ethaline provides an efficient way to fabricate porous Ni-based alloy nanosheets directly on a current collector, which is a promising technology for the synthesis of earth-abundant HER electrocatalysts .
研究领域:
电催化
·
材料科学
·
能源化学
·
纳米材料
·
电化学
✓ 已验证
DOI
高影响因子
RSC Advances
·
2019
·Vol. 9
·期 1
·498-506
·
IF 3.049
Wei Wang,Ang Zheng,Yifan Jiang,Dongsheng Lan,Fenghua Lu,Lelin Zheng,Lin Zhuang,Ruijiang Hong
Monodisperse colloidal particles have promising applications in electrophoretic displays with vivid colors, reversibility and low switching times. In this study, a facile, effective and large-scale strategy for preparing size-controlled Fe3O4@SiO2 particles is reported. Multiple Fe3O4 particles were synthesized by a modified solvothermal method using sodium citrate as a surface modifier with a binary solvent, and were then coated with a SiO2 layer to obtain a highly negatively charged surface via a modified Stöber method. Owing to the easily controlled sizes and sufficient surface charges, Fe3O4@SiO2 particles can be assembled into colloidal amorphous arrays with the balance of electrostatic repulsion and electrophoretic forces. The reflections cover wavelengths ranging from 802 to 453 nm, and were optimized by investigating the dependence of the particles on variables such as particle size, particle volume fraction, and electric field intensity. The large-scale preparation of electrically responsive Fe3O4@SiO2 particles facilitates an electrophoretic display with broad-range colors, showing the practical potential in industrial application.
研究领域:
材料科学
·
纳米技术
·
显示技术
✓ 已验证
产品关联
DOI
PubMed
高影响因子
APPLIED SURFACE SCIENCE
·
2019
·
IF 5.155
Xingchao Zhang,Ruoyu Zhang,Siying Niu,Jiming Zheng,Chongfeng Guo
The MoS 2 /g-C 3 N 4 heterojunction composite (marked as MoS 2 /g-C 3 N 4 -H) was successfully prepared via calcining the melamine coated MoS 2 nano-sphere, where the thin g-C 3 N 4 nano-sheets were tightly grown on the surface of MoS 2 nano-sphere to form MoS 2 inlaying in g-C 3 N 4 heterostructure. The detailed charge transfer mechanism was discussed by combining theoretical calculation and experiments, in which the intrinsic cause of photo-generated charge separation and transfer was determined as the directional built-in electric field driven by different Fermi levels of MoS 2 and g-C 3 N 4 . Comparatively, the enhanced photo-catalytic performance and stability of the sample were assessed by degrading the Rhodamine (RhB) and reducing the Dichromate (Cr 6+ ) solutions under the irradiation of the simulated sunlight, which could be attributed to the widened spectral absorption range and improved electron-hole separation rate. Based on above results, the photo-catalytic mechanism involving redox reactions was also clearly proposed.
研究领域:
材料科学
·
环境科学
✓ 已验证
产品关联
DOI
高影响因子
PRECISION ENGINEERING-JOURNAL OF THE INTERNATIONAL SOCIETIES FOR PRECISION ENGINEERING AND NANOTECHNOLOGY
·
2016
·
IF 1.914
Kun Shan,Ping Zhou,Yunsheng Zuo,Renke Kang,Dongming Guo
Electrogenerated chemical polishing (EGCP) had been proved effective in improving both the smoothness and the flatness of copper surface in our previous work. In this paper the polishing ability, defined as the ratio between the material removal rate at the peak and at the valley of a rough surface, is studied theoretically and experimentally. In a mathematical model, the effects of the special wavelength L , the peak-to-valley height h of the workpiece surface profile and the working distance d between working electrode and workpiece surface on the polishing ability are studied. The results show that the polishing ability decreases with increasing the working distance and finally approaches the value ( d + h )/ d , if L is much larger than d . However, the effect of the working distance on polishing ability is negligible, if L is close to or less than d . The polishing ability also decreases with h decreasing. Based on the above analysis, an analytical expression of the polishing ability of EGCP is given. For validating the theoretical analysis, a copper surface is polished by EGCP and the change of the surface profile is measured and analyzed using the analytical expression. The measured polishing ability agrees well with the simulation results.
研究领域:
材料科学
·
表面工程
·
电化学
✓ 已验证
DOI
高影响因子
Sustainable Energy & Fuels
·
2017
·Vol. 2
·期 2
·444-454
·
IF 0
Xiaohong Xia,Chunming Wang,Lang Liu,Yonglin Du,Weichun Ye
Transition metal dichalcogenides for electrocatalytic water splitting are important in renewable energy research, with studies showing that the edge structure and specific surface area are crucial to their electrocatalytic activity. Herein, the design and construction of yolk–shell nanospheres based on molybdenum diselenide-encapsulated molybdenum oxide are reported. Their structures were characterized using various techniques, which showed that the void space between the interior core and outer shell increased the number of active sites. This yolk–shell structure exhibited enhanced and stable electrocatalytic activity in the hydrogen evolution reaction (HER). The HER current density at −0.5 V vs. the reversible hydrogen electrode was increased by 95% (to −256 mA cm−2) compared to that of traditional flower-like molybdenum diselenide. The overpotential of this yolk–shell structure, which was required to drive a current density of −10 mA cm−2, was 65 mV lower than that of flower-like molybdenum diselenide (286 mV). Furthermore, long-term potential cycling and potentiostatic measurement of this catalyst showed favorable stability and durability of electrocatalytic activity. This yolk–shell structure plays a key role in energy conversion processes central to several renewable energy technologies.
研究领域:
材料科学
·
纳米科技
·
电化学
·
能源化学
·
催化化学
✓ 已验证
DOI
危险品化学品经营许可证（带存储）