Nano Energy
·
2014
·
IF 10.211
Xiaolei Jiang,Huayun Xu,Jing Liu,Jian Yang,Hongzhi Mao,Yitai Qian
Hierarchical mesoporous Li 2 Mn 0.5 Fe 0.5 SiO 4 consisted of nanoparticles or nanoplates has been successfully synthesized for the first time by a hydrothermal method . Their carbon-coated composites are obtained by a heat treatment in the presence of citric acid. These composites were characterized by powder X-ray diffractometry, scanning and transmission electron microscopy , Raman spectroscopy , and thermogravimetric analysis . The lithium storage capacity and cycling performance of the optimized Li 2 Mn 0.5 Fe 0.5 SiO 4 /C composite are greatly enhanced when tested as a cathode material in lithium-ion batteries (LIBs). It exhibits a discharge capacity of 125 mAh g −1 after 60 cycles at a rate of 0.1 C. This superior electrochemical property could be ascribed to high purity and mesoporous structure of Li 2 Mn 0.5 Fe 0.5 SiO 4 , which greatly enhances the electronic conductivity as well as the diffusion coefficient of lithium ions .
研究领域:
材料科学
·
电化学
·
能源存储
·
纳米材料
·
固体化学
✓ 已验证
DOI
高影响因子
International Journal of Electrochemical Science
·
2023
·Vol. 12
·期 8
·6930-6939
·
IF 1.5
Wei Su,Kaiqi Xu,Guobin Zhong,Zengfu Wei,Chao Wang,Yuezhong Meng
Titanium and nitrogen codoped LiFePO 4 was synthesized via a simple solid state reaction using TiN as the dopant source. The morphology, structure, valence state and electrochemical performance of all the samples were investigated and compared with the undoped LiFePO 4 . The results showed that the codoped samples maintained an olivine structure with modified lattice parameters and exhibited a prominent improved electrochemical performance. Among all the codoped samples, LiFe 0.94 Ti 0.04 PO 4-σ N 0.04 showed the best rate capability of 108.1 mAh g -1 even at a high rate of 5 C and exhibited a capacity retention of about 94% after 100 cycles at 1 C.
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
JOURNAL OF ALLOYS AND COMPOUNDS
·
2017
·
IF 3.133
Yanrong Wang,Hui Huang,Qingshui Xie,Yuanpeng Wang,Baihua Qu
Sodium-ion batteries (SIBs) have gained more and more interest for grid-level energy storage applications compared with current lithium-ion batteries (LIBs). In this paper, well-uniform and dispersed spindle-shaped NiCo 2 O 4 particles were synthesized by solvothermal method, and then graphene-encapsulated NiCo 2 O 4 (NiCo 2 O 4 @G) was formed core-shell nanostructures , which greatly enhanced the electronic and ionic (electro-active) conduction and also effectively buffering to accommodate the strain. Benefit from its structure feature, the prepared NiCo 2 O 4 @G core-shell nanostructures composite shows good cycling with a capacity of up to ∼400 mAh g −1 (100 mA g −1 ) in 100 cycles for NIBs anode. The facile synthesis process and excellent SIBs behaviors in this paper are expected to be extended in developing other anode materials in battery system.
研究领域:
材料科学
·
电化学
·
能源存储
·
纳米材料
·
电池技术
✓ 已验证
DOI
高影响因子
BULLETIN OF MATERIALS SCIENCE
·
2016
·Vol. 39
·期 1
·187-193
·
IF 0.895
CAO RENPING,QIN ZHENGDONG,JIANG SHENHUA,LIANG AIHUI,LUO ZHIYANG,YU XIAOGUANG
A series of CaNb 2 O 6 : x Sm 3+ (0 ≤
x
≤ 10 mol%) and CaNb 2 O 6 : Sm 3+ , Na + /B 3+ phosphors were synthesized by the solid-state reaction method in air. Their crystal structures and luminescence properties were investigated and analysed, respectively. Host CaNb 2 O 6 emitted blue light with excitation 270 nm. CaNb 2 O 6 : x Sm 3+ phosphors showed a systematically varied hue from blue to white by changing Sm 3+ ion concentration from 0 to 10 mol% with excitation of 270 nm and their chromaticity coordinates were the regions from (0.1665, 0.1767) to (0.2484, 0.2260). Luminescence properties of CaNb 2 O 6 : Sm 3+ phosphor were tuned and improved significantly by codoping B 3+ or Na + ions. Energy transfer between Nb \(_{\mathbf {2}}\textit {O}_{\mathbf {6}}^{\boldsymbol {2-}}\) group and Sm 3+ ion was observed and analysed via luminescence properties. The luminous mechanism was explained by energy level scheme and energy transfer process in CaNb 2 O 6 : Sm 3+ phosphor. The strong excitation band peaking at ∼ 407 nm indicated that the CaNb 2 O 6 : Sm 3+ , Na + /B 3+ phosphor has a potential application in white light-emitting diodes based on near-UV LED chip.
研究领域:
材料科学
·
无机化学
·
发光材料
·
固体物理
·
光电子学
✓ 已验证
DOI
高影响因子
IONICS
·
2019
·Vol. 25
·期 10
·4567-4576
·
IF 2.289
Xu Chun-Sheng,Yu Hai-Tao,Guo Chen-Feng,Xie Ying,Ren Ning,Yi Ting-Feng,Zhang Guo-Xu
To improve the stability and performance of the cathode materials, an ionic conductor layer was coated successfully on the surface of Li 1.2 Mn 0.54 Ni 0.13 Co 0.13 O 2 (LMNC) microspheres. The structural analysis confirmed that LiV 3 O 8 coating did not change the basic structure of LMNC, and all obtained materials are solid solutions with a good-layered structure and a good crystallinity. The microscopy measurement showed that the thickness of the coating layer for the LV-3 sample is about 2.5 nm. This appropriate layer is helpful for improving the surface stability of LMNC and the diffusion of lithium, leading to an obvious enhancement of the electrochemical performance. Our result confirmed that the average discharge specific capacities for LV-3 sample at 0.1 C, 0.2 C, 0.5 C, 1 C, and 3 C are respectively 265.9, 219.1, 188.0, 156.3, and 121.5 mAh g −1 , which are much larger than the values of other samples. After 50 cycles at a 1 C rate, the capacity retentions for different samples are 60.7%, 74.0%, 87.6%, and 70.4%, indicating that LV-3 sample exhibits the best performance. Furthermore, EIS measurements showed that the diffusion coefficient for LV-3 sample is calculated to be 1.26 × 10 −15 cm 2 s −1 , which is also the largest value among all considered samples. Our experiments identified that coating an ionic conductive layer on the cathode material surface will significantly improve their rate capacity and cycling stability.
研究领域:
材料科学
·
电化学
·
能源存储
·
无机化学
·
固态离子学
✓ 已验证
DOI
高影响因子
CHINESE JOURNAL OF CHEMISTRY
·
2016
·Vol. 34
·期 12
·1329-1334
·
IF 1.872
Keli Zhong,Jie Zhao,Xue Zhou,Shuhua Hou,Yanjiang Bian,Jianrong Li,Lijun Tang
A new (8-hydroxyquinolin-2-yl)methylene picolinohydrazide derivative ( L ) has been successfully synthesized and characterized. The probe L displays high selectivity to Co 2+ in CH 3 CN/HEPES (1:1, Ｖ / Ｖ , 10 mmol·L −1 , pH=7.4) with a fluorescence "ON-OFF" response. The Co 2+ ion recognition event possesses some distinct features including rapid response, high selectivity and sensitivity, good anti-interference ability and being applicable within a wide pH range. Based on job's plot and ESI-MS studies, the 1:1 binding mode was proposed. The binding constant of L and Co 2+ is 1.63×10 8 L·mol −1 and the detection limit is 1.15 µmol·L −1 . Natural water samples experiments revealed that probe L can be potentially applied to the detection of Co 2+ in real environment.
研究领域:
分析化学
·
生物无机化学
·
分子探针
·
环境监测
·
荧光传感
✓ 已验证
DOI
高影响因子
JOURNAL OF APPLIED POLYMER SCIENCE
·
2015
·Vol. 132
·期 17
·
IF 1.768
Ronglan Wu,Lingyuan Tian,Wei Wang,Xiaolin Man
In this article, we report a study of the design and synthesis of a bifunctional cellulose derivative on the removal of phenols and heavy-metal ions in wastewater treatment. A radical polymerization was performed in an ionic liquid, 1-allyl-3-methylimidazolium chloride, to graft two monomers, butyl methacrylate and 4-vinyl pyridine, on the backbone of cellulose. The effects of the five reaction conditions on the yield of final products were evaluated. The grafted celluloses were characterized by means of Fourier transform infrared spectroscopy, scanning electron microscopy, and thermogravimetric analysis. Adsorption experiments were carried out on the cellulose- g -poly(butyl methacrylate- co -4-vinyl pyridine) to evaluate the capacity of the removal of 2,4-dichlorophenol (2,4-DCP) and Cu(II) in water. The adsorption isotherms were measured at five temperatures and interpreted by a Langmuir model of adsorption. The thermodynamics of the adsorption suggested that the binding process was mildly exothermic for Cu(II) and endothermic for 2,4-DCP. Kinetic studies were interpreted with a pseudo-second-order adsorption model. The process of the adsorption of 2,4-DCP could be described overall by the model, whereas the adsorption of Cu(II) involved two processes. This was due to adsorption both on the surface and inside the adsorbent. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132 , 41830.
研究领域:
环境化学
·
高分子材料科学
·
水处理技术
·
吸附分离
·
绿色化学
✓ 已验证
DOI
高影响因子
INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
·
2015
·Vol. 41
·期 3
·1550-1558
·
IF 3.313
Meilin Lv,Shuang Ni,Zhuo Wang,Tongcheng Cao,Xiaoxiang Xu
Doping has generally been served as one of the most efficient strategies for the improvement of wide band gap semiconductor photocatalysts . However, atomic arrangements of doped elements in the host crystal structure have often been overlooked, particularly during the investigation and evaluation of dopant functionality. It is known that electronic structures of a semiconductor are profoundly controlled by atomic occupancies in different crystallographic positions. Knowledge about dopant accommodations in the crystal structure and their influence towards photocatalytic performance is highly desired. Here, we investigated four compositional and structural relevant compounds CrNbO 4 , CrTaO 4 , Sr 2 CrNbO 6 and Sr 2 CrTaO 6 with the aim to study the effects of cation ordering/disordering upon their photocatalytic activity . Our results showed that ordered cations, namely Cr and Nb/Ta, are detrimental to the photocatalytic performance. Theoretical calculations indicate that cation ordering would enlarge the band gap and inhibit charge transfer between Cr and Nb/Ta. Our findings imply that ordered dopants in photocatalytic materials would severely offset the benefits of doping and might be a reason for the decreased activity at high doping levels often encountered.
研究领域:
材料科学
·
半导体物理
·
光催化
·
固体化学
·
能源材料
✓ 已验证
DOI
高影响因子
JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS
·
2018
·
IF 2.831
Xiaoping Liang,Ping Hu,Hongyang Zhang,Wen Tan
In this work, hypercrosslinked strong anion-exchange polymer resins (HXLPP-SAX) were synthesized and evaluated as solid-phase extraction (SPE) sorbents for extracting fluoroquinolones (FQs) in milk samples. These particles were prepared using a protocol that was facile and cost-effective by combining hypercrosslinking reactions and quaternisation reactions in one step. After the synthesis, the morphological properties and anion-exchange, adsorption, and selectivity performances of the HXLPP-SAX resins were characterized and evaluated. It was shown that the polymers were monodisperse microspheres, with the mean diameters of 2–4 μm, ion-exchange capacity (IEC) of 0.311 meq/g, and specific surface area more than 1000 m 2 /g. The resins applied as SPE sorbents possessed high selectivity in the extraction of amphoteric compounds (enoxacin and enrofloxacin as the representatives) followed by HPLC-UV analysis, as compared to commercially available strong anion-exchange sorbents (Oasis MAX). The SPE-HPLC-UV method was fully validated and exhibited good linearity (10–2000 ng/g, R 2 ≥ 0.997), low limits of detection (2.8–5.1 ng/g), good recoveries (85.8%–117.9%, RSDs ≤ 7.1%) and precisions (intra-day RSDs ≤ 7.7% and inter-day RSDs ≤ 9.4%). Then the method was performed the selective enrichment of six FQs (enoxacin, norfloxacin, ciprofloxacin, lomefloxacin, enrofloxacin, and sparfloxacin) in milk samples. The present results demonstrated that the proposed resins exhibited a promising potential for the enrichment and determination of FQ residues in milk samples as well as in other samples with complex matrices.
研究领域:
分析化学
·
食品科学
✓ 已验证
产品关联
DOI
PubMed
高影响因子
ANALYTICA CHIMICA ACTA
·
2019
·
IF 5.256
Xiaoxiao Wei,Yuzhi Wang,Jing Chen,Panli Xu,Wei Xu,Rui Ni,Jiaojiao Meng,Yigang Zhou
Novel polymeric deep eutectic solvents (PDES) based on 3-acrylamidopropyl trimethylammonium chloride/D-sorbitol functionalized amino-magnetic (Fe 3 O 4 NH 2 ) metal-organic framework (HKUST-1-MOF) composites (Fe 3 O 4 NH 2 @HKUST-1@PDES) were synthesized and characterized by field emission transmission electron microscope (FE-SEM), transmission electron microscope (TEM), X-ray diffraction (XRD), fourier transform infrared spectrometry (FT-IR), thermal gravimetric analysis (TGA), vibrating sample magnetometer (VSM) and zeta potentials . Then the composites were firstly utilized to selectively separate malachite green (MG) and crystal violet (CV) coupled with magnetic solid-phase extraction (MSPE). A response surface methodology (RSM) based on Latin hypercube sampling (LHS) was selected to analytically optimize the extraction parameters including initial concentration of dyes, extraction time, pH value and extraction temperature. The maximum extraction amount and optimal extraction conditions predicted by the RSM model matched well with the actual experimental results, and the extraction amount was 966.93 mg g −1 for MG and 788.90 mg g −1 for CV,respectively. The results indicated that the model possessed higher calculation accuracy through analyzing fewer sample points, thereby achieving theoretical prediction of extraction amount and conditions and being a prefect supplementary to actual experiments. The electrostatic interaction between the composites and cationic dyes played the main roll in the extraction process. The proposed extraction method exhibited lower limit of detection (98.19 ng mL −1 for MG and 23.97 ng mL −1 for CV) and preeminent precision (RSD ˂ 0.4%). Spiked recoveries of fish samples at three spiking levers ranged from 89.43% to 100.65% for MG and 95.29%–98.03% for CV. All results highlighted the excellent potential of Fe 3 O 4 NH 2 @HKUST-1@PDES-MSPE strategy in selective separation of cationic dyes in complex medium.
研究领域:
分析化学
·
材料科学
✓ 已验证
产品关联
DOI
PubMed
高影响因子
SOLID STATE IONICS
·
2014
·
IF 2.112
Jing Yang,Zhen Huang,Bingxin Huang,Jing Zhou,Xiaoxiong Xu
NASICON-type structure lithium ion conductors have been considered as promising solid electrolytes due to its very high Li + -ion conductivity and chemical stability. In this paper, NASICON-type structured Li 1.5 Al 0.5 Ge 1.5 (PO 4 ) 3 (LAGP) glass–ceramics are prepared from crystallization of glass powders, which are obtained by a simple melt-quench method. NH 4 H 2 PO 4 , H 3 PO 4 , P 2 O 5 and H 3 PO 4 &Al(PO 3 ) 3 are used as phosphorus sources, respectively. The obtained LAGP glass–ceramics are systematically characterized with X-ray diffraction, field emission scanning electron microscopy , differential scanning calorimetry and AC impedance spectroscopy . The different impurities are formed depending on the phosphorus sources, which further influence the microstructure. As a result, the lithium ion conductivity is significantly affected by the phosphorus sources. The highest conductivity of 5.21 × 10 − 4 S·cm − 1 is obtained when H 3 PO 4 is used as the phosphorus source under optimum conditions.
研究领域:
材料科学
·
固态离子学
·
无机非金属材料
·
能源材料
·
电化学
✓ 已验证
DOI
高影响因子
JOURNAL OF POWER SOURCES
·
2017
·
IF 6.395
Haoxiang Yu,Minghe Luo,Hua Lan,Lei Yan,Shangshu Qian,Wuquan Ye,Miao Shui,Nengbing Long,Jie Shu
The preparation and characterization of Pb 1- x Ba x Li 2 Ti 6 O 14 ( x = 0, 1/4, 1/2, 3/4, 1) as anode materials for lithium ion batteries are investigated in this research. The structure, morphology and electrochemical properties are compared with each other by changing the Pb/Ba atomic ratio in Pb 1- x Ba x Li 2 Ti 6 O 14 . It can be observed that each sample shows the same orthorhombic structure with Cmca space group. Moreover, it can also be found that the working potential, conductivity, cycling and rate performances of as-received samples gradually change along with the evolution of x in Pb 1- x Ba x Li 2 Ti 6 O 14 ( x = 0, 1/4, 1/2, 3/4, 1). Electrochemical evaluation shows that the operating potential of the as-received sample gradually decreases with increasing x value in Pb 1- x Ba x Li 2 Ti 6 O 14 and its initial charge capacity increases reversely. Moreover, different Pb/Ba atomic ratio also brings different cycling stability for Pb 1- x Ba x Li 2 Ti 6 O 14 . Especially for Pb 3/4 Ba 1/4 Li 2 Ti 6 O 14 , it presents better electrochemical properties than other samples. After 120 cycles, the reversible capacity of Pb 3/4 Ba 1/4 Li 2 Ti 6 O 14 is maintained at 129.7 mAh g −1 with capacity retention of 88.3%. In addition, its electrochemical reversibility is also demonstrated by in-situ X-ray investigation.
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
危险品化学品经营许可证（带存储）