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CHINESE JOURNAL OF ANALYTICAL CHEMISTRY · 2015 ·Vol. 43 ·期 10 ·1569-1572 · IF 0.754

Development and Evaluation of On-line Eluent Generator

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 · 仪器科学与技术 · 分离科学 · 离子色谱技术
✓ 已验证 DOI 高影响因子
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Journal of Energy Chemistry · 2022 · IF 13.599

Dual-interlayers constructed by Ti3C2Tx/ionic-liquid for enhanced performance of solid garnet batteries

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 · 能源材料
✓ 已验证 DOI 高影响因子
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CHEMICAL ENGINEERING JOURNAL · 2019 · IF 8.355

Ultrafast kinetics net electrode assembled via MoSe2/MXene heterojunction for high-performance sodium-ion batteries

Enze Xu,Yan Zhang,Hui Wang,Zhifeng Zhu,Junjie Quan,Yajing Chang,Pengcheng Li,Dabin Yu,Yang Jiang

Establishing advanced sodium-ion batteries (SIBs) with high energy density and eco-friendly electrode materials are still far from satisfactory due to the large-size of sodium-ions and sluggish redox kinetics during electrochemical processes. Herein, a novel ultrafast kinetics net electrode assembled via MoSe 2 /MXene heterojunction is synthesized by a simple hydrothermal method followed by thermal annealing. Featuring the Van der Waals force interaction between MoSe 2 and MXene , the volumetric change during the sodium ions insertion/extraction courses is effectively restrained, and the reaction kinetics is greatly enhanced further. Meanwhile, both the high electrical and ion conductivity (lower diffusion barrier between Na + /MXene ~0.066 eV) provided by the unique MXene based net heterostructure of our hybrid materials, as evidenced by DFT calculations, are beneficial to the transportation of sodium ions, thus enabling an outstanding rate and long-cycling capability. As a result, the fabricated cells exhibit high reversible capacities of 490 mAh g −1 at 1 A g −1 , as well as 250 mAh g −1 at a high current of 10 A g −1 with a coulombic efficiency of 99.8%, indicating the excellent electrochemical performance of our hybrid materials, especially at high current. This novel net MoSe 2 /MXene heterostructure, combined with our simple synthesis strategy together, are expected to have great potential in sodium-ions storage application.

研究领域: 材料科学 · 电化学 · 能源存储 · 纳米材料 · 固态物理
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JOURNAL OF CHEMICAL AND ENGINEERING DATA · 2018 · IF 2.196

A Novel Amino and Carboxyl Functionalized Mesoporous Silica as an Efficient Adsorbent for Nickel(II)

Li Zhang,Fangxiang Song,Yonggui Wu,Liang Cheng,Jin Qian,Shuai Wang,Qianlin Chen,Yan Li

In this study, the as-prepared spherical mesoporous silica was modified by amino and cyano groups via grafting, and the amino and carboxyl functionalized adsorption materials (MSS@NH2@COOH) were obtained after cyano group hydrolysis. The introduction of amino and carboxyl groups increases the surface active sites of the materials. The materials were characterized by SEM, TEM, XRD, N2 adsorption/desorption, XPS, etc. BET analysis revealed the amino and carboxyl functionalized mesoporous silica maintained their mesostructure nature and its specific surface area was 113 m2·g–1. TG-DTA and FT-IR confirmed effective grafting on the surface of mesoporous silica with functionalized groups. The simulated wastewater of Ni(II) was carried out to test the adsorption properties of the materials, and several influential factors (pH, initial nickel ion concentration, adsorbent dose) were discussed. The saturated adsorption capacity increased clearly from 46.55 mg·g–1 of MSS to 125.57 mg·g–1 of MSS@NH2@COOH. Even recycling three times, the removal rate of Ni(II) ions using MSS@NH2@COOH as an adsorbent could still be over 75%. Adsorption isotherms, kinetics, and thermodynamics of adsorption were taken to clarify the adsorption process. This newly developed adsorbent material does exhibit good reusable performance and effective removal of the heavy metal ions of Ni(II).

CAS / MDL: 108-67-8
研究领域: 环境科学 · 材料科学
✓ 已验证 产品关联 DOI 高影响因子
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MICROCHEMICAL JOURNAL · 2014 · IF 3.583

Determination of Zr, Nb, Mo, Sn, Hf, Ta, and W in seawater by N-benzoyl-N-phenylhydroxylamine extraction chromatographic resin and inductively coupled plasma-mass spectrometry

Shengling Sun,Jie Li

A method has been developed for the determination of zirconium (Zr), hafnium (Hf), niobium (Nb), tantalum (Ta), molybdenum (Mo), tungsten (W), and tin (Sn) in seawater by quadrupole inductively coupled plasma-mass spectrometry (Q-ICP-MS). The method is based on separation of the seven elements by extraction chromatography using N-benzoyl-N-phenylhydroxylamine (BPHA) supported on a microporous acrylic ester polymeric resin. The optimized procedure indicates that the BPHA resin has high selective adsorption for Zr, Nb, Mo, Sn, Hf, Ta, and W (known as fluoride soluble elements), whereas other interference and matrix elements are minimally adsorbed. The optimized eluent mixture with their molarity gives satisfactory recoveries for all analytes. The recovery can be achieved 99% for Zr, 97% for Nb, 97% for Mo, 99% for Sn, 99% for Hf, 95% for Ta, and 98% for W, respectively, by eluting with 6   mL of 6   mol   L −   1 HF/1   mol   L −   1 HCl. Furthermore, the technique for separation and enrichment of these elements provides a low total method blank. The detection limits for this method are 0.5   ppt for Zr, 0.2   ppt for Nb, 1.7   ppt for Mo, 1.0   ppt for Sn, 0.1   ppt for Hf, 0.1   ppt for Ta, and 0.3   ppt for W, respectively. The validity of the method is evaluated by replicate analyses of seawater reference materials; the precision of the results is better than 3% (RSD, n   =   4), and the results are in good agreement with certified values. The established procedure has proved to be both practical and effective for seawater sample analyses.

研究领域: 分析化学 · 海洋化学 · 环境地球化学 · 痕量元素检测 · 质谱分析
✓ 已验证 DOI 高影响因子
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NEW JOURNAL OF CHEMISTRY · 2022 ·Vol. 46 ·期 19 ·9432-9439 · IF 3.925

A scalable ball milling strategy to endow SnS anode electrodes with free volume property for enhanced electrochemical performance

Huibin Guan,Dong Feng,Qi Liu,Tianbiao Zeng

Among the tin-based composites, stannous sulfide (SnS) is a prospective material to serve as an anode for lithium-ion batteries (LiBs) owing to its high theoretical-capacity, layer-structure for fast Li+ diffusion paths, and low toxicity. However, severe volume expansion/shrinkage exfoliates the electrode coating, leading to the severe loss of active materials. Herein, free volume was introduced into SnS to relieve the sequelae of volume expansion/shrinkage creatively, which effectively improved the cyclability of the SnS-based anode. The as-synthesized SnS/G-15% exhibited overall optimal electrochemical performances, i.e., the highest reversible capacity and best cyclability over pure SnS, SnS/G-5% and SnS/G-25%. Ex situ scanning electron microscopy images also illustrated that no cracks were generated in the cycled SnS/G-15% electrode. This work highlights an efficient and cost effective approach for the synthesis of long-cycle life and high-cyclability anodes.

研究领域: 材料科学 · 电化学 · 纳米材料 · 能源存储 · 电池技术
✓ 已验证 DOI 高影响因子
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JOURNAL OF ALLOYS AND COMPOUNDS · 2015 · IF 2.999

Carbon nanotubes modified for ZnCo2O4 with a novel porous polyhedral structure as anodes for lithium ion batteries with improved performances

Qiang Ru,Xiong Song,Yudi Mo,Lingyun Guo,Shejun Hu

Carbon nanotubes (CNTs) are adopted to modify ZnCo 2 O 4 (ZCO) electrode, and a novel porous polyhedral structure ZCO/CNTs composites are prepared by a facile and scalable hydrothermal process, and the pure ZCO with cubic structure is also synthesized for comparison. The as-prepared materials are characterized by field emission scanning electron microscopy (FESEM). The results demonstrate that the introduced of CNTs has great effects on the nanostructure and electrochemical performance of the samples. The CNTs among the polyhedral structure ZCO/CNTs composites can provide better mechanical robustness, more contact between Li + and electrodes, and more effective electron transmission than the pure ZCO with cubic structure. When tested as anode materials for lithium ion batteries , the ZCO/CNTs composites exhibit a high initial coulombic efficiency of 83.9%, a high specific capacity of ∼864.6 mAh g −1 at a current rate of 100 mA g −1 after 150 cycles, as well as a good rate capability at elevated current rates, such as, ∼924.3 and ∼605.7 mAh g −1 at current rates of 500 and 2000 mA g −1 , respectively. This work would be meaningful in the preparation of complex oxides/carbon composites with porous nanostructure as anodes for LIBs.

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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Energy & Environmental Materials · 2020 ·Vol. 5 ·期 1 ·245-252 · IF 0

Carbon Supported MoO2 Spheres Boosting Ultra-Stable Lithium Storage with High Volumetric Density

Chunli Wang,Lianshan Sun,Bingbing Tian,Yong Cheng,Limin Wang

As important ingredients in lithium-ion battery, the Coulombic efficiency and power density greatly impact the electrochemical performances. Although recent literatures have reported nano-porous materials to enhance the specific capacities, intrinsic drawbacks such as poor initial Coulombic efficiency and low volumetric capacity could not be avoided. Herein, we propose a strategy to prepare carbon supported MoO 2 spheres used for lithium-ion battery with high volumetric capacity density. A high initial Coulombic efficiency of 76.5% is obtained due to limited solid electrolyte interface film formed on the exposed surface. Meantime, the sample with an optimal carbon content and a proper structural strength reveals a higher reversible capacity of 956 mA h g −1 than the theoretical capacity of crystalline MoO 2 (838 mA h g −1 ) and a high capacity retention ratio of 96.4% after 100 cycles at 0.5 A g −1 . And an effective compaction capacity density (under 5 MPa) of 670 mA h cm −3 of the spheres proves its potential value in practical applications.

研究领域: 材料科学 · 电化学 · 能源存储 · 纳米材料 · 电池技术
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RSC Advances · 2015 ·Vol. 5 ·期 118 ·97435-97445 · IF 3.84

Selective adsorption of Cu(II) from an aqueous solution by ion imprinted magnetic chitosan microspheres prepared from steel pickling waste liquor

Yuling Cai,Liuchun Zheng,Zhanqiang Fang

To reduce costs and improve practicability, an ion imprinted magnetic chitosan (IMCS) was synthesized through co-precipitation using steel pickling waste liquor and chitosan and Cu(II) as template ions, which was then characterized by TEM, SEM, EDX, FTIR, XRD and VSM. The batch experiments were carried out for its potential application and high selectivity of Cu(II) removal, which were observed due to the paramagnetic properties and coordination reactions in the imprinted cavities. Kinetic studies revealed that the adsorption process followed a pseudo second-order model and the equilibrium data fit perfectly with the Langmuir isotherm model. The maximum adsorption capacity was 109.89 mg g−1. Negative values for ΔH0 and ΔG0 indicated an exothermic and spontaneous adsorption process. The adsorption process was found to be a chemical reaction and coordination complexes were formed between the metal ions and the groups of chitosan binding mainly in the “bridge model”. Moreover, 0.2 mol L−1 HCl solution was considered as the most appropriate eluent for regeneration. It showed a great performance in the experiments for practical copper wastewater and the process was considerably cost-effective.

研究领域: 环境化学 · 材料科学 · 污染控制工程 · 资源循环利用 · 吸附技术
✓ 已验证 DOI 高影响因子
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JOURNAL OF POWER SOURCES · 2024 · IF 8.1

Study on the influence of different manganese sources on the formation of P2/β Bi-phase cathode materials for sodium ion batteries

Yixuan Zhang,Guo-Qiang Liu,Danlei Qiao,Jiaguan Chen,Qiang Sun,Lei Wen

This work focuses on the effect of the of Mn 3+ /Mn 4+ ratio in the reactants on the structure and electrochemical properties of NaMn 0.9 Cu 0.1 O 2 cathode materials for sodium-ion batteries. By systematically varying the manganese valence states in the reactants, we observed a phase transition from the β-phase to the P2-phase with increasing Mn 3+ concentrations in the reactants, contrary to the expected favorability of the β-phase at higher Mn 3+ levels. This finding suggests a complex interplay between the valence states of the reactants and phase formation mechanisms, which needs further investigation. Additionally, electrochemical testing indicated that the phase composition significantly impacts the electrochemical performance of the material. Specifically, the M0 sample, possessing the optimal P2/β ratio, exhibited excellent electrochemical performances, achieving a high initial discharge capacity of 155.1 mA h g −1 and remains 88.1 % after 40 cycles. These results emphasize the importance of precursor selection and valence management in the development of high-performance cathode materials for sodium-ion batteries.

研究领域: 材料科学 · 电化学 · 能源存储 · 无机化学 · 固态化学
✓ 已验证 DOI 高影响因子
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JOURNAL OF MATERIALS SCIENCE-MATERIALS IN ELECTRONICS · 2018 ·Vol. 29 ·期 16 ·13925-13930 · IF 2.324

Structure, morphology and electrical conductivity of Sm and Bi co-doped CeO2 electrolytes synthesized by co-precipitation method

Li Tianjing,Shi Qingle

In this paper, explain a new relationships between Bi 3+ content, the phase crystal, microstructure and conductivity for Sm and Bi co-doped Ce 0.8− x Sm 0.2 Bi x O 1.9−1/2 x ( x  = 0, 0.05, 0.1, 0.15, 0.2) electrolytes prepared by co-precipitation method. The XRD patterns showed that this compounds exhibit a fluorite-type cubic structure after the samples calcined at 700 °C for 4 h and the cell volumes of increased when the Bi content increased. In addition, for the samples sintered at 1400 °C for 4 h, the Bi doping improves the relative density, the grain size and the average thermal expansion coefficient (TEC). More in details, the relative density and TEC increase with the Bi content. Form the AC impedance spectroscopy measurements, the conductivity of the sintered samples is found to improve with the increasing of Bi content (for x  ≤ 0.15), which is ascribed to the increasing of the number of oxygen ion vacancies and the increase in the unit cell volume. However, the conductivity decreases when the Bi content is further increased (0.15 <  x  ≤ 0.2), which is ascribed the reduction of the number of free oxygen vacancies. The highest conductivity at 800 °C is 5.6 × 10 −2  S/cm and the activation energy is 0.83 eV for Ce 0.65 Sm 0.2 Bi 0.15 O 1.825 , indicating that this would be a promising electrolyte for the intermediate temperature-solid oxide fuel cell applications.

研究领域: 材料科学 · 无机非金属材料 · 固态离子学 · 能源材料 · 燃料电池
✓ 已验证 DOI 高影响因子
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CHINESE JOURNAL OF ANALYTICAL CHEMISTRY · 2022 ·Vol. 50 ·期 7 ·100101 · IF 1.193

Boosting the performances of water-processable LiNi0.5Co0.2Mn0.3O2 cathode with conventional white latex as binder ingredient

Ranehipura Dewage Lahiru SANDARUWAN,Bo-Yu WANG,Suwanda Arachchige Don Rumesh MADHUSANKA,Shun-Chao MA,Hong-Yu WANG

Transition to aqueous electrode fabrication of lithium ion batteries (LIBs) with green binder is certainly profitable and imperative in terms of economic benefit and environmental wellness. However, aqueous processing of cathode in LIB, especially the ternary LiNi x Co y Mn z O 2 (NCM), is still problematic and novel water-soluble binder should be developed to boost the electrochemical performances of cathode. In this regard, commercially available white latex (WL), cooperating with CMC (carboxymethyl cellulose), is employed as water-processable binder mixture for manufacturing NCM cathode. Interestingly, the prepared NCM cathode assisted by WL/CMC mixture exhibits improved electrochemical performances including better initial reversible capacity of 161.7 mAh g −1 at 0.5 C current density, long-term cyclability with a reversible capacity of 155 mAh g −1 along with high-capacity retention of around 96% after cycling 200 times, and even excellent rate capability, which are superior to those of the conventional counterpart base on polyvinylidene fluoride (PVdF). Moreover, the NCM|graphite full cell, which is absolutely based on this novel WL binder, also demonstrates the outstanding electrochemical behaviors.

研究领域: 电化学 · 能源材料 · 锂电池技术 · 高分子材料科学
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