JOURNAL OF POWER SOURCES
·
2016
·
IF 6.333
Gang Peng,Xiayin Yao,Hongli Wan,Bingxin Huang,Jingyun Yin,Fei Ding,Xiaoxiong Xu
An insightful study on the fundamental lithium storage behavior of all-solid-state lithium battery with a structure of LiNi 0.8 Co 0.15 Al 0.05 O 2 (NCA)/Li 10 GeP 2 S 12 /Li-In is carried out in this work. The relationship between electrochemical performances and particle size, surface impurities and defects of the NCA positive material is systematically investigated. It is found that a ball-milling technique can decrease the particle size and remove surface impurities of the NCA cathode while also give rise to surface defects which could be recovered by a post-annealing process. The results indicate that the interfacial resistance between the NCA and Li 10 GeP 2 S 12 is obviously decreased during the ball-milling followed by a post-annealing. Consequently, the discharge capacity of NCA in the NCA/Li 10 GeP 2 S 12 /Li-In solid-state battery is significantly enhanced, which exhibits a discharge capacity of 146 mAh g −1 at 25 °C.
研究领域:
材料科学
·
电化学
·
能源存储
·
固态离子学
·
电池技术
✓ 已验证
DOI
高影响因子
JOURNAL OF ELECTROANALYTICAL CHEMISTRY
·
2022
·
IF 4.598
Dexi Liu,Shichang Xu,Yanmeng Cai,Yue Wang,Jiaqi Guo,Youlin Li
The conventional separation technologies, like chemical precipitation and adsorption processes, cannot quickly and selectively separate and recycle heavy metal ions from waste. Due to its rich sulfur content and excellent electrical conductivity, vanadium disulfide is a potential material for effectively removing lead from wastewater. The vanadium disulfide material with selective adsorption ability was introduced into CDI technology to construct a coupling technology with both advantages. The N -doped modified ZIF@vanadium disulfide (ZAC@VS 2 ) composites were successfully synthesized by hydrothermal method. Electrosorption experiments show that ZAC@VS 2 material presents the remarkable saturated adsorption capacity to lead(II) ions (239.52 mg/g) in the 500 mg/L PbCl 2 solution. In the triplex blend system (Fe 3+ /Pb 2+ /Na + ) with each solute density of 100 mg/L, the saturated adsorption efficiency of 85.4% to Pb 2+ can still be maintained. In addition, compared with the Langmuir(R 2 =0.873) adsorption isotherm model, the Freundlich model (R 2 =0.922) can be better used to fit the adsorption process, which proves that the adsorption process is multilayered and heterogeneous. XPS tests and competitive adsorption experiments show that the electric double layer (EDL) and complexation together promote the selective adsorption of heavy metal ions by ZAC@VS 2 . ZAC@VS 2 composite electrode shows excellent performance in the removal of lead ions in battery waste liquid, indicating the potential of introducing ZAC@VS 2 into CDI to remove lead ions.
研究领域:
环境科学
·
材料科学
·
水处理技术
·
重金属污染控制
·
电化学工程
✓ 已验证
DOI
高影响因子
JOURNAL OF CHEMICAL THERMODYNAMICS
·
2017
·
IF 2.726
Dongshun Deng,Xiaobang Liu,Yanhong Cui,Yaotai Jiang
Solubilities of SO 2 have been determined in four biobased solvents (BBSs) at temperatures between 293.15 K and 323.15 K with 10 K intervals and pressure scope of (0–120.0) kPa using isochoric saturation method. The BBSs were selected from butyl lactate (BL), glyceryl triacetate (GT), triethyl citrate (TEC), and acetyl triethyl citrate (ATEC). Henry’s constants and thermodynamic properties such as Gibbs free energy , enthalpy and entropy of dissolution were derived from the solubility data. The gravimetric solubilities of SO 2 in BBSs were in the range of (0.07–8.52) mol.kg −1 and changed with the sequence of GT > BL > TEC ≈ ATEC. All the dissolution enthalpies were negative at each condition. The performances of SO 2 absorption in these solvents were further compared with those in some ionic liquids as well as common absorbents. The results illustrated that present BBSs possessed the potentiality as SO 2 absorbents due to their relatively large absorption ability, small absorption enthalpy, low toxicity, and biodegradability.
研究领域:
化学工程
·
环境化学
·
热力学
·
绿色溶剂
·
气体吸收
✓ 已验证
DOI
高影响因子
INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
·
2019
·Vol. 44
·期 39
·22250-22262
·
IF 4.084
Hongri Wan,Xiaofang Hu
Nitrogen/sulfur co-doped disordered porous biocarbon was facilely synthesized and applied as anode materials for lithium/sodium ion batteries. Benefiting from high nitrogen (3.38 wt%) and sulfur (9.75 wt%) doping, NS 1-1 as anode materials showed a high reversible capacity of 1010.4 mA h g −1 at 0.1 A g −1 in lithium ion batteries . In addition, it also exhibited excellent cycling stability, which can maintain at 412 mAh g -1 after 1000 cycles at 5 A g −1 . As anode materials of sodium ion batteries , NS 1-1 can still reach 745.2 mA h g −1 at 100 mAg -1 after 100 cycles. At a high current density (5 A g -1 ), the reversible capacity is 272.5 mA h g −1 after 1000 cycles, which exhibits excellent electrochemical performance and cycle stability. The preeminent electrochemical performance can be attributed to three effects: (1) the high level of sulfur and nitrogen; (2) the synergic effect of dual-doping heteroatoms; (3) the large quantity of edge defects and abundant micropores and mesopores , providing extra Li/Na storage regions. This disordered porous biocarbon co-doped with nitrogen/sulfur exhibits unique features, which is very suitable for anode materials of lithium/sodium ion batteries.
研究领域:
材料科学
·
电化学
·
能源存储
·
纳米材料
·
功能碳材料
✓ 已验证
DOI
高影响因子
JOURNAL OF MATERIALS CHEMISTRY
·
2011
·Vol. 21
·期 18
·6569-6575
·
IF 5.101
Xintao Luo,Jishu Han,Yang Ning,Zhe Lin,Hao Zhang,Bai Yang
1-Thioglycerol (TG)-stabilized quantum dots (QDs) are good candidate for performing a stepwise polymerization reaction with polyurethane (PU) prepolymers, but their use is limited by their worse photoluminescence (PL) in comparison to QDs stabilized by other mercapto-ligands. To overcome this problem, TG-stabilized CdTe QDs with enhanced PL were synthesized in water through a N2H4-promoted growth approach. The current synthesis significantly shortened the duration of the size evolution of QDs, particularly for obtaining samples with orange and red emissions. It also permitted QD growth at low temperatures, such as room temperature, which avoided the decomposition of TG and subsequent embedment of sulfur into the QDs as occurs in the conventional synthesis. Most importantly, the TG ligand endowed the QDs with hydroxyl coverage, making the QDs miscible with PU prepolymers in dimethyl sulfoxide, and therefore overcoming the main problem in fabricating PU-based nanocomposites of eliminating water. The hydroxyl coverage further allowed for the linkage of PU on the surface of the QDs through the reaction between –OH and –NCO, producing CdTe QD–PU bulk nanocomposites. Systematic characterization indicated that the QDs were well dispersed in the PU medium, and the size-dependent PL of QDs was also maintained.
研究领域:
材料科学
·
纳米科技
·
高分子化学
·
光电子学
·
胶体与界面化学
✓ 已验证
DOI
高影响因子
Small
·
2024
·Vol. 20
·期 26
·2310387
·
IF 13
Wei Luo,Yanli Yu,Yucheng Wu,Wenbin Wang,Yimin Jiang,Wei Shen,Rongxing He,Wei Su,Ming Li
Rational design of heterostructure catalysts through phase engineering strategy plays a critical role in heightening the electrocatalytic performance of catalysts. Herein, a novel amorphous/crystalline (a/c) heterostructure (a-CoS/Ni 3 S 2 ) is manufactured by a facile hydrothermal sulfurization method. Strikingly, the interface coupling between amorphous phase (a-CoS) and crystalline phase (Ni 3 S 2 ) in a-CoS/Ni 3 S 2 is much stronger than that between crystalline phase (c-CoS) and crystalline phase (Ni 3 S 2 ) in crystalline/crystalline (c/c) heterostructure (c-CoS/Ni 3 S 2 ) as control sample, which makes the meta-stable amorphous structure more stable. Meanwhile, a-CoS/Ni 3 S 2 has more S vacancies (S v ) than c-CoS/Ni 3 S 2 because of the presence of an amorphous phase. Eventually, for the oxygen evolution reaction (OER), the a-CoS/Ni 3 S 2 exhibits a significantly lower overpotential of 192 mV at 10 mA cm −2 compared to the c-CoS/Ni 3 S 2 (242 mV). An exceptionally low cell voltage of 1.51 V is required to achieve a current density of 50 mA cm −2 for overall water splitting in the assembled cell (a-CoS/Ni 3 S 2 || Pt/C). Theoretical calculations reveal that more charges transfer from a-CoS to Ni 3 S 2 in a-CoS/Ni 3 S 2 than in c-CoS/Ni 3 S 2 , which promotes the enhancement of OER activity. This work will bring into play a fabrication strategy of a/c catalysts and the understanding of the catalytic mechanism of a/c heterostructures.
研究领域:
材料科学
·
电化学
·
催化化学
·
纳米材料
·
能源材料
✓ 已验证
DOI
高影响因子
POLYMERS FOR ADVANCED TECHNOLOGIES
·
2017
·Vol. 29
·期 1
·463-469
·
IF 1.907
Xiaoxia Jian,Yiwen Hu,Weiliang Zhou,Leqin Xiao
Tough and transparent polyurethane networks with self-healing capability at mild temperature conditions were successfully prepared in a 1-pot procedure. The self-healing ability of synthesized polyurethane comes from the covalent disulfide metathesis and non-covalent H-bonding. The mechanical testing indicates that disulfide metathesis reforms the covalent bonds on a longer time scale, while H-bonding gives rise to a healing efficiency of around 46% in the early healing processing. The compromise between mechanical performance and healing capability is reached by tailoring the concentration of disulfide. The tensile strength of the sample with 100% self-heal efficiency can get to 5.01 MPa, which can be explained by higher mobility of polymer chain under ambient temperature from creep testing.
研究领域:
高分子材料科学
·
功能材料
·
软物质物理
·
化学工程
·
纳米复合材料
✓ 已验证
DOI
高影响因子
CATALYSIS LETTERS
·
2023
·Vol. 154
·期 5
·2182-2196
·
IF 2.8
Liu Jialu,Song Zhi,Liu Boxia,Zhang Xiayan,Huang Yeqiong,Han Dongxu
Because of its high toxicity and severe degradation, phenol has caused serious environmental pollution, and it is urgent to explore a stable and efficient degradation method of phenol. In this study, Ni/Fe bimetallic atomic cluster composite catalyst activated peroxymonosulfate (PMS) to degrade phenol efficiently. The experimental results show that the phenol degradation rate can reach 100% in a wide range of pH (3–11), and the system offers good stability in repeated experiments. The free radical quenching investigation and electrochemical characterization showed that the non-free radical pathway dominated the degradation system, and a large amount of singlet oxygen and rapid electron transfer promoted the efficient degradation of phenol in wastewater. This study opens up a new way for bimetallic atom cluster catalysts to activate PMS to degrade organic pollutants. Graphical
研究领域:
环境科学
·
催化
·
化学工程
·
材料科学
✓ 已验证
DOI
高影响因子
MICROCHIMICA ACTA
·
2015
·Vol. 182
·期 7
·1337-1344
·
IF 3.741
Cui Yang,Liu Sheng,Wei Kaiju,Liu Yangzhong,Hu Zhangjun
We describe a method for magnetic solid phase extraction of trace-levels of Hg(II) ions by using Fe 3 O 4 nanoparticles (NPs) covered with a shell of silica and modified with the chelator N-(2-acetylaminoethyl)-N′-(3-triethoxysilylpropyl)thiourea. The new magnetic NPs enable rapid magnetic separation, thus leading to higher efficiency and accuracy. The extracted Hg(II) ions on the NPs were directly quantified using a mercury analyzer. Possible interferents are widely eliminated in this highly selective extraction process, and the NPs are not exerting an interfering effect either. The method has an enrichment factor of 100, and extraction recoveries are between 95 and 107 % when using 10 mg of the extracting NPs. The method works over a wide range of pH values and can be applied to even complex natural samples. The effects of pH value, extraction time, sample volume and adsorbent amount on the extraction efficiency were optimized. Under the optimal conditions, the detection limit is as low as 17 ng L −1 . The method was applied to the preconcentration and detection of Hg(II) in three natural water samples using the standard addition method.
A facile magnetic solid phase extraction using surface decorated nano-scale magnetic core-shell nanoparticles coupled with a direct mercury analyzer is proposed for trace-level mercury ions detection.
研究领域:
环境化学
·
分析化学
·
纳米材料科学
·
生物医学分析
·
重金属检测
✓ 已验证
DOI
高影响因子
WATER SCIENCE AND TECHNOLOGY
·
2021
·Vol. 84
·期 12
·3616-3628
·
IF 1.915
Li Xiaoyan,Wang Hongwei,Zhang Guozhen,Zhou Tianhong,Wu Fuping
Advanced oxidation process (AOP) has attracted widespread attention because it can effectively remove antibiotics in water, but its practical engineering application is limited by the problems of the low efficiency and difficult recovery of the catalyst. In the study, nano-spinel CoFe 2 O 4 was prepared by hydrothermal method and served as the peroxymonosulfate (PMS) catalyst to degrade antibiotic amoxicillin (AMX). The reaction parameters such as CoFe 2 O 4 dosage, AMX concentration, and initial pH value were also optimized. The reaction mechanism was proposed through free radical capture experiment and possible degradation pathway analysis. In addition, the magnetic recovery performance and stability of the catalyst were evaluated. Results showed that 85.5% of AMX could be removed within 90 min at optimal conditions. Sulfate radicals and hydroxyl radicals were the active species for AMX degradation. Moreover, the catalyst showed excellent magnetism and stability in the cycle experiment, which has great potential in the AOP treatment of antibiotic polluted wastewater. Magnetic nano-CoFe 2 O 4 was fabricated by hydrothermal process. High activity of removing AMX in the CoFe 2 O 4 /PMS system. The recovery of nano-CoFe 2 O 4 was convenient due to strong magnetics. The nano-CoFe 2 O 4 exhibited good stability and reusability.
研究领域:
环境科学
·
材料化学
·
催化化学
✓ 已验证
DOI
高影响因子
Desalination and Water Treatment
·
2024
·
IF 1
Jian-jun Lian,Meng Wu,Bo Chen,Lin Zhang,Fan-jie Zhou,Qiao-ping Kong,Jing Wu
Although iron sulfide (FeS) has been used to remove heavy metals from the environment, its capability for remediation of molybdenum (Mo) contaminated soil and some important influencing factors are still unclear. The purpose of this study was to investigate whether soil Mo(VI) contamination could be immobilized by using nano-FeS. The effects of FeS dosage, natural organic matter (NOM), and inorganic salts on soil Mo(VI) immobilization properties were compared and analyzed. The results showed that the addition of FeS significantly reduced the leaching of Mo in the soil. The amount of Mo leaching dropped from 87.66 to 2.20 mg/L when the molar ratio of FeS to Mo(VI) increased from 1:1 to 50:1. It was discovered that the major two mechanisms for the immobilization of soil Mo(VI) by FeS were adsorption and reduction. Soil Mo leaching was promoted with the existence of NOM, but the addition of SO 4 2– and H 2 PO 4 – prevented soil Mo(VI) leaching. Mo leaching from soil that was polluted with Mo(VI) and included humic acid, salicylic acid, SO 4 2– , or H 2 PO 4 – was reduced by 116.41–77.54 mg/L, 116.41–112.72 mg/L, 116.41–72.45 mg/L, and 116.41–84.39 mg/L, respectively, after FeS treatment. Meanwhile, the cabbage mustard growth experiments findings indicated that FeS particles have a significant field application potential for Mo(VI) contaminated soil remediation due to their high Mo(VI) immobilization efficiency.
研究领域:
环境科学
·
纳米技术
·
土壤修复
·
重金属污染
·
环境化学
✓ 已验证
DOI
高影响因子
Materials Science & Engineering C-Materials for Biological Applications
·
2018
·
IF 5.08
Huikang Yang,Nianhua Wang,Lei Mo,Mei Wu,Ruimeng Yang,Xiangdong Xu,Yugang Huang,Jiantao Lin,Li-Ming Zhang,Xinqing Jiang
Tumor-targeted multifunctional nanocarriers play an important role in tumor diagnosis and treatment. Herein, disulfide bonds linked amphiphilic hyaluronan-SS-poly(ε-caprolactone) diblock copolymers (HA-SS-PCL) were synthesized and studied as theranostic nanocarriers for tumor diagnosis and treatment. The chemical structure of HA-SS-PCL was confirmed by Fourier transform infrared spectroscopy (FTIR) and proton nuclear magnetic resonance ( 1 H NMR). The self-assembling behavior of the HA-SS-PCL into GSH-responsive micelles and their degradation were characterized by fluorescence spectroscopy, dynamic light scattering (DLS) and transmission electron microscopy (TEM). Theranostic nanocarriers encapsulating doxorubicin (DOX) and superparamagnetic iron oxide (SPIO) were formed via a dialysis. In vitro drug release results suggested that the HA-SS-PCL micelles possessed reductant-triggered doxorubicin release ability, which was confirmed by 100% of DOX release from HA-SS-PCL micelles within 12 h under 10 mM of glutathione (GSH), whereas about 40% of DOX was released under non-reductive condition within 24 h. Both flow cytometry and confocal laser scanning microscopy (CLSM) analysis revealed that the HA-SS-PCL micelles loaded with DOX were internalized in HepG2 cell via a receptor mediated mechanism between hyaluronan and the CD44 receptor. Furthermore, the MTT assay and cell apoptosis analysis revealed that the DOX-loaded HA-SS-PCL micelles exhibited pronounced antitumor ability towards HepG2 cells compared with that of the reduction-insensitive HA-PCL micelles at the same DOX dosage. The r 2 relaxivity value of the DOX/SPIO loaded HA-SS-PCL micelles was up to 221.2 mM −1 s −1 (Fe). Thus, the obtained HA-SS-PCL block copolymers demonstrate promising potential as tumor targeting theranostic nanocarriers in the field of tumor diagnosis and treatment.
研究领域:
生物材料
·
肿瘤学
·
药剂学
✓ 已验证
产品关联
DOI
PubMed
高影响因子
危险品化学品经营许可证（带存储）