文献检索

查找使用阿拉丁产品的科研文献

检索与阿拉丁产品相关的同行评审论文、DOI、PubMed 编号、期刊、作者、CAS 号及研究领域。

科研影响力快照

与阿拉丁产品相关的已发表科研成果

在搜索之前,这些指标可帮助访客快速了解产品关联科研的规模与质量。

346,364+ SCI 论文 与阿拉丁产品引用相关
2,295,288.15 总影响因子 匹配文献记录中影响因子的总和
81.20 最高期刊影响因子 匹配期刊中的最高 IF
6.63 平均期刊影响因子 匹配文献的平均 IF

参考指标 指标基于阿拉丁文献引用数据库及期刊影响因子记录。文献关联仅供科研参考,请以原始文献为准。

热门产品

视图 列表 网格

9 项

设置提升方向
Co3V2O8
COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS · 2023 · IF 5.2

Co3V2O8 nanoparticle-assembled porous sphere as a new electrocatalyst for sensitive nonenzymatic sensing of H2O2

Chengcheng Qi,Wei Xiang,Yongping Dong,Wangbing Zhang

The development of new highly active electrocatalysts is one of the key factors to improve the performance of enzyme-free electrochemical sensors . In this paper, Co 3 V 2 O 8 was proposed as a new electrocatalyst for nonenzymatic oxidation of H 2 O 2 . A facile self-templating strategy was adopted for the synthesis of Co 3 V 2 O 8 nanomaterial which was further characterized by transmission electron microscopy (TEM), powder X-ray diffractometry (XRD), fourier translation infrared spectroscopy (FTIR), X-ray photoelectron spectroscopy (XPS), and electrochemical techniques . The results showed that porous Co 3 V 2 O 8 sphere was constructed from interconnected nanoparticle with a three-dimensional porous structure. Such unique structure made the sensor based on Co 3 V 2 O 8 exhibit good electrocatalytic activity toward H 2 O 2 oxidation, and could detect H 2 O 2 with a low detection limit of 0.34 µM, a wide linear range of 2.0 µM to 6.1 mM and a high sensitivity of 541.4 µA mM −1 cm −2 . This work demonstrated an effective new sensing platform for nonenzymatic detection of H 2 O 2 .

CAS / MDL: 7803-55-6
研究领域: 材料科学 · 分析化学 · 电化学
✓ 已验证 产品关联 DOI 高影响因子
查看原文 查看 PubMed
SEPARATION AND PURIFICATION TECHNOLOGY · 2024 · IF 8.1

Hydrogen storage properties of MgH2 modified by efficient Co3V2O8 catalyst

Shiteng Long,Yang Qin,Huafeng Fu,Jia Hu,Hansong Xue,Yu'an Chen,Fusheng Pan

Developing medium temperature hydrogen storage materials is important for the practical application of the Studies have demonstrated that V-based catalysts exhibit exceptional catalytic activity in the dehydrogenation of MgH 2 at medium levels. However, the V-base catalysts primarily concentrates on hydrogen desorption, and there is a necessity for further enhancement of hydrogen absorption properties. To solve this problem, herein we prepared a bimetallic oxide. Co can enhance the hydrogen absorption and desorption properties of MgH 2 as the catalyst and it influences the performance of hydrogen absorption more obviously than the hydrogen desorption performance. It is found that MgH 2 catalyzed by Co 3 V 2 O 8 can absorb 1.31 wt% hydrogen within 30 min even under room temperature and can release 3.41 wt% hydrogen within 120 min at temperatures as low as 225 °C. The activation energy of MgH 2 -6 wt.%Co 3 V 2 O 8 is determined to 68.5 kJ/mol, which is 50.2 % lower than that of Ball-MgH 2 . XRD combined with TEM measurements revealed that the in-situ formed Co and V 2 O 3 can weaken the H H and Mg H bonds respectively to improve the hydrogen storage properties of MgH 2 . These discoveries provide guideline of the further design of high efficiency catalysts for Mg-based hydrogen storage materials.

研究领域: 材料科学 · 化学工程 · 催化 · 能源存储
✓ 已验证 DOI 高影响因子
查看原文 查看 PubMed
Nano Materials Science · 2023 · IF 9.9

Double enzyme mimetic activities of multifunctional Ag nanoparticle-decorated Co3V2O8 hollow hexagonal prismatic pencils for application in colorimetric sensors and disinfection

Ying Gao,Peng Ju,Yu Zhang,Yuxin Zhang,Xiaofan Zhai,Jizhou Duan,Baorong Hou

Since the catalytic activity of most nanozymes is still far lower than the corresponding natural enzymes, there is urgent need to discover novel highly efficient enzyme-like materials. In this work, Co 3 V 2 O 8 with hollow hexagonal prismatic pencil structures were prepared as novel artificial enzyme mimics. They were then decorated by photo-depositing Ag nanoparticles (Ag NPs) on the surface to further improve its catalytic activities. The Ag NPs decorated Co 3 V 2 O 8 (ACVPs) showed both excellent oxidase- and peroxidase-like catalytic activities. They can oxidize the colorless 3,3’,5,5’-tetramethylbenzidine rapidly to induce a blue change. The enhanced enzyme mimetic activities can be attributed to the surface plasma resonance (SPR) effect of Ag NPs as well as the synergistic catalytic effect between Ag NPs and Co 3 V 2 O 8 , accelerating electron transfer and promoting the catalytic process. ACVPs were applied in constructing a colorimetric sensor, validating the occurrence of the Fenton reaction, and disinfection, presenting favorable catalytic performance. The enzyme-like catalytic mechanism was studied, indicating the chief role of ⋅O 2 - radicals in the catalytic process. This work not only discovers a novel functional material with double enzyme mimetic activity but also provides a new insight into exploiting artificial enzyme mimics with highly efficient catalytic ability.

研究领域: 材料科学 · 生物化学 · 分析化学
✓ 已验证 产品关联 DOI 高影响因子
查看原文 查看 PubMed
Nanomaterials · 2020 ·Vol. 10 ·期 4 ·740 · IF 4.324

Co3V2O8 Nanoparticles Supported on Reduced Graphene Oxide for Efficient Lithium Storage

Le Hu,Chaoqun Shang

Co3V2O8(CVO) with high theoretical specific capacity derived from the multiple oxidation states of V and Co is regarded as a potential electrode material for lithium-ion batteries (LIBs). Herein, reduced graphene oxide (rGO)-supported ultrafine CVO (rGO@CVO) nanoparticles are successfully prepared via the hydrothermal and subsequent annealing processes. The CVO supported on 2D rGO nanosheets possess excellent structural compatibility for the accommodation of volume variation to maintain the structural integrity of an electrode during the repeated lithiation/delithiation process. On the other hand, the rGO, as a highly-conductive network in the rGO@CVO composite, facilitates rapid charge transfer to ensure fast reaction kinetics. Moreover, the CV kinetic analysis indicates that the capacity of rGO@CVO is mainly dominated by a pseudocapacitive process with favorable rate capability. As a result, the rGO@CVO composite exhibits improved specific capacity (1132 mAh g−1, 0.1 A g−1) and promising rate capability (482 mAh g−1, 10 A g−1).Keywords:rGO@CVO;anode materials;rate performance;cycling stability;lithium-ion batteries

CAS / MDL: 10026-22-9
研究领域: 材料科学 · 电化学 · 能源存储
✓ 已验证 产品关联 DOI PubMed 高影响因子
查看原文 查看 PubMed
JOURNAL OF COLLOID AND INTERFACE SCIENCE · 2022 · IF 9.965

Efficient purification of tetracycline wastewater by activated persulfate with heterogeneous Co-V bimetallic oxides

Chuanyi Xu,Guanrong Yang,Jie Li,Shanqing Zhang,Yueping Fang,Feng Peng,Shengsen Zhang,Rongliang Qiu

The persistence and wide dispersion of antibiotics have a severe impact on the ecological environment. Developing an effective method with universal applicability to remove pollutants is pretty necessary. Herein, a bimetallic oxides (Co 3 V 2 O 8 ) heterogeneous material was successfully prepared and used to activate the persulfate (PS) for purification of tetracycline (TC) wastewater. By exploring the reaction conditions and influencing factors, the removal rate of 50 mg⋅L -1 TC reached 87.1% by Co 3 V 2 O 8 /PS system, and the reaction rate constant was up to 0.0271 min −1 . As a highly efficient catalyst for the activation of PS, Co 3 V 2 O 8 /PS system produces radicals of SO 4 •− , •OH, •O 2 – and 1 O 2 in the reaction process due to the Co(II) and V(IV) exchange electrons with S 2 O 8 2- and O 2 . Simultaneously, the internal electron exchange occurs between Co(II)/Co(III) and V(IV)/V(V), which stabilizes the content of Co(II) and V(IV). This work provides a novel activator for PS activation to degrade contaminants and contributes to a better understanding of the PS activation mechanism by transition compound.

研究领域: 环境科学 · 催化化学 · 污染治理
✓ 已验证 产品关联 DOI PubMed 高影响因子
查看原文 查看 PubMed
SOLID STATE SCIENCES · 2024 · IF 3.4

Ultra-thin g-C3N4-Modified Co3V2O8 hollow spheres for enhanced photocatalytic degradation of MB

Xiangyu Cao,Guoyu Liu,Jianhua Zheng,Zhihui Sui,Shunji Zheng,Qi Zhang

Considering the important role of morphology and interface during the photocatalytic process, the g-C 3 N 4 @Co 3 V 2 O 8 Z-scheme heterojunction photocatalyst was successfully prepared by a facile hydrothermal method and subsequent wet-impregnation treatment. The sample synthetic method allowed ultra-thin g-C 3 N 4 nanosheets to uniformly adhere on the surface of Co 3 V 2 O 8 hollow spheres, which not only avoided the aggregation of g-C 3 N 4 nanosheets but also benefited from forming a multidirectional contact interface to short the transfer distance of photoelectrons between g-C 3 N 4 and Co 3 V 2 O 8 . Benefitting from the unique hollow structure and Z-scheme configuration, g-C 3 N 4 @Co 3 V 2 O 8 composite with 10 % g-C 3 N 4 showed a better photocatalytic degraded performance, achieving 93.7 % degradation efficiency of methylene blue (MB) in water within 60 min, which was 3.1 and 1.9 times higher than these of pristine Co 3 V 2 O 8 and g-C 3 N 4 , respectively. The active species analysis demonstrated that ·O 2− and ·OH played a pivotal role in the photocatalytic degradation of MB. Based on the experimental results a comprehensive photocatalytic degradation mechanism was proposed. Our work provided an opportunity to design Z-scheme heterojunction photocatalysts for pollutant degradation in wastewater.

研究领域: 材料科学 · 环境催化 · 光催化 · 纳米材料 · 废水处理
✓ 已验证 DOI 高影响因子
查看原文 查看 PubMed
JOURNAL OF SOLID STATE CHEMISTRY · 2023 · IF 3.3

With the synergistic effect of MnCo2O4/Co3V2O8 composite nanomaterials for high performance supercapacitor electrodes

Rui Yu,Zhaokuan Li,Qing Wang

In this work, MnCo 2 O 4 /Co 3 V 2 O 8 composite nanomaterials were synthesized using a straightforward secondary hydrothermal and calcination process. Importantly, Co 3 V 2 O 8 as a pseudocapacitive material with unique intercalation/delamination reaction, and the stored charge behavior of MnCo 2 O 4 material is a battery-like behavior. These two different reaction mechanisms, when working in parallel, can produce an interfacial and synergistic effect, thus providing high reversible capacity and better electrochemical activity, and the composite has good electronic conductivity and superior electrochemical properties. The prepared MnCo 2 O 4 /Co 3 V 2 O 8 nanomaterial provides a high specific capacitance of 1460 F g −1 at 1 A g −1 and an excellent capacitance retention of 84.61 % (3500 cycles even at 10 A g −1 ). Hybrid supercapacitors consisting of MnCo 2 O 4 /Co 3 V 2 O 8 and activated carbon (AC) have a great energy density of 37.5 mAh g −1 . After 28,000 turns of uninterrupted constant current charging and discharging, it had an initial capacity ratio of 98.6 %. The electrochemical performance showed that the MnCo 2 O 4 /Co 3 V 2 O 8 nanometer material has broad prospects and can provide a new idea for the electrode materials of supercapacitors.

✓ 已验证 产品关联 DOI 高影响因子
查看原文 查看 PubMed
INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH · 2023 · IF 4.2

Constructing Defective Co3V2O8 Hexagonal Prism for Solvent-free Selective Oxidation of Cyclohexane: Strategy of Ionic Liquid Mediation

Hao Li,Yingwei Li,Ruirui Wang,Sheng Zhong,Ruirui Zhang,Ruixia Liu

Oxygen vacancies (OVs) engineering is essential in the regulation of the structure and properties of the catalysts for selective oxidation. In this work, the strategy of ionic liquid (IL) mediation was successfully developed in constructing the OV-rich defective Co3V2O8 (CVO), exhibiting excellent performance in cyclohexane oxidation. Coupling the prepotency of the heating treatment, ILs constructed optimal [Bmim][Ac]-CVO-700 possesses the highest OV concentration and catalytic activity with 12.7% cyclohexane conversion accompanied by 89.6% KA oil (cyclohexanol and cyclohexanone) selectivity. Experimental investigation reveals that ILs not only regulates the morphology structure as structure-directing agents but also benefits the formation of OVs through coordination with the Co2+ and V5+. The redox cycle between Co3+/Co2+ and V5+/V4+ was accelerated via the constructed OVs, enhancing the activation of substrates and the transfer of electrons. The distinguished performance is attributed to the rich OVs, porous structure, and synergistic effect between the active metals. The structure–activity relationship between OVs concentration and cyclohexane conversion further indicated that OVs facilitate the essential steps for the generation of targeted products. The possible reaction pathway of cyclohexane oxidation over the OV-rich CVO catalyst was also suggested regarding the radical trapping experiment. This design not only presents a facile and effective strategy for constructing OVs using ILs but also provides an in-depth insight into OV-rich mixed metal oxides in selective oxidation.

研究领域: 催化化学 · 材料科学 · 能源化学
✓ 已验证 产品关联 DOI 高影响因子
查看原文 查看 PubMed
ADVANCED FUNCTIONAL MATERIALS · 2025 · IF 19

Controllable Synthesis and “Fast-charging” Mechanism of Hollow-Micropencil Co3V2O8 from Perspective of Ion Diffusion in Crystal Structure

Rui Wang,Rong Zhang,Yixin Yan,Gaoyang Li,Yuan Li,Fujuan Wang,Youzhi Wu,Fen Ran

Co 3 V 2 O 8 as a bimetallic oxide with “fast-charging” capacity presents some potential advantages, comprising decent theoretical specific capacity, favorable crystal structure, and intrinsic safety. Presently, although extensive research of Co 3 V 2 O 8 as an anode material are reported, the formed Co° from Co 3 V 2 O 8 after the initial discharging is not oxidized to CoO during the charging process, and the ion diffusion mechanism are not well clarified. The lithium-storage process of Co 3 V 2 O 8 and the diffusion mechanism of lithium ion in Co 3 V 2 O 8 are studied in detail in this work. A hollow-micropencil Co 3 V 2 O 8 prepared through the hydrothermal method without using surfactants or templates demonstrates a high “fast-charging” capability even at the current densities as high as 1.0–2.0 A g −1 . The electrochemical kinetic results illustrate that the hollow-micropencil Co 3 V 2 O 8 presents low charge transfer resistance. The distinctive lithium ion storage sites as well as diffusion paths are predicted. The in situ X-ray diffraction analysis is adopted to confirm that the formed Co° after the initial discharging is not oxidized to CoO during the delithiation process. The work not only helps to understand the lithium insertion mechanisms of Co 3 V 2 O 8 but also offers new means to develop “fast-charging” anode material for lithium-ion batteries with remarkable electrochemical performance.

CAS / MDL: 7803-55-6 7791-13-1
研究领域: 材料科学 · 电化学 · 能源存储
✓ 已验证 产品关联 DOI 高影响因子
查看原文 查看 PubMed
已复制

文献关联基于可获得的产品、CAS、DOI 及引用记录。收录不代表作者或出版方对阿拉丁产品的背书,请以原始文献为准。