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

显示第253至264个,产品总数689个

设置提升方向
⋅O2-
INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH · 2019 · IF 3.375

Coral-like CoMnOx as a Highly Active Catalyst for Benzene Catalytic Oxidation

Qun Li,Tareque Odoom-Wubah,Yaping Zhou,Rafal Mulka,Yanmei Zheng,Jiale Huang,Daohua Sun,Qingbiao Li

The search for efficient and durable catalysts for volatile organic compounds oxidation is essential for environmental remediation. Herein, porous coral-like cobalt–manganese oxide (CoMnOx) catalyst was synthesized through annealing Co–Mn–1,3-propanediol precursors at 300 °C in air and applied for the catalytic oxidation of benzene. The as-prepared CoMnOx exhibited uniform porous coral-like structure, with an improved benzene catalytic abatement performance as compared to those of Mn3O4 and Co3O4 samples prepared by the same method, respectively. According to BET, H2-TPR, O2-TPD, and XPS analysis, the as-obtained CoMnOx catalyst showed the highest BET surface area, better low-reducibility temperature, and high content of absorbed oxygen groups when compared to Mn3O4 and Co3O4, which makes significant contribution to its catalytic benzene oxidation activity. Moreover, a plausible surface reaction mechanism for benzene oxidation over CoMnOx catalyst was also proposed through the in situ DRIFTS study.

CAS / MDL: 6147-53-1 6156-78-1
研究领域: 环境科学 · 催化 · 材料科学
✓ 已验证 产品关联 DOI 高影响因子
查看原文 查看 PubMed
JOURNAL OF POWER SOURCES · 2022 · IF 9.794

PVDF-based electrolyte decorated by Li29Zr9Nb3O40 Li-ion conductor and electrochemical performance of related solid-state batteries

Jiahao Chen,Hong Zhang,Hongzhu Chen,Enjie Xia,Yanmei Wu,Zhicheng Li

Solid-state Li-ion batteries (LIBs) have recently attracted much attention for their high safety and energy density . Polyvinylidene fluoride (PVDF) is as a potential electrolyte for solid-state LIBs due to its high permittivity, wide voltage window and excellent thermal stability. Here, Y 3+ -doped Li 29 Zr 9 Nb 3 O 40 (LZNO) Li-ionic conductor with room temperature conductivity (σ 25 ) of 1.26 × 10 −4  S cm −1 is prepared. LZNO decorated PVDF-based composite solid electrolytes (CSEs) are fabricated. The PVDF-based CSE with 10% (mass ratio) of LZNO shows σ 25 of 2.34 × 10 −4  S cm −1 , and has thermal stability with melting temperature up to 332 °C and voltage window of 4.8 V. The assembled Li ( Ni 0.8 Co 0.1 Mn 0.1 ) O 2 |CSE|Li cells show initial specific discharge capacity of 216.7 mAh g −1 at 0.1 C, and exhibit high capacity and cycle performance. LiFePO 4 |CSE|Li cells display initial specific discharge capacity of 137.4 mAh g −1 at 0.5 C and high cycle performance. Addition of LZNO powder in CSEs can inhibit the dehydrofluorination of PVDF during the charge-discharge of cells, alleviate the deterioration of interface resistance, and greatly improve the specific discharge capacity of cells at high rates.

CAS / MDL: 90076-65-6 7585-20-8
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
MICROCHEMICAL JOURNAL · 2023 · IF 4.8

Fabrication of dendrite PtPd bimetallic nanocomposites modified carbon fiber microelectrodes for detecting superoxide anion released from living cells

Ziyue Sun,Hongli Zhao,Kaicha Chen,Fangfang Zhou,Minbo Lan

In this work, the carbon fiber microelectrode (CFME) coated by ERGO-CNT network was used as a substrate to support dendrite PtPd nanoclusters. An enzyme-free O 2 − electrochemical sensor (PtPd@ERGO-CNT-CFME) was prepared based on this strategy. Due to the brilliant loading and dispersing abilities of the substrate and the excellent electrochemical activity of the dendrite PtPd alloy, PtPd@ERGO-CNT-CFME demonstrated outstanding detection ability towards O 2 − . The as-constructed sensor showed a wide-linear range of 16–744 μM and 744–3064 μM with high sensitivity of 6967.3 μA mM −1 cm −2 and 4124.3 μA mM −1 cm −2 , and the detection limit was 5.07 μM. Furthermore, PtPd@ERGO-CNT-CFME was successfully applied to monitor O 2 − released from living cells. This phenomenon indicated the application potential for O 2 − detection in biological samples.

研究领域: 电化学 · 纳米材料 · 生物传感器 · 分析化学
✓ 已验证 产品关联 DOI 高影响因子
查看原文 查看 PubMed
NEW JOURNAL OF CHEMISTRY · 2024 ·Vol. 48 ·期 6 ·2558-2568 · IF 2.7

Structure induced activity enhancement of tungsten oxide for tetrabromobisphenol A photodegradation under visible light illumination

Shiman Zhou,Qianqian Zhu,Denan Li,Lifeng Zhang,Yanshuo Li,Zhenxin Zhang

Tetrabromobisphenol A (TBBPA), a prevalent brominated flame retardant, poses significant environmental and health risks, necessitating its removal. In this study, WO3 with different structures was synthesized for TBBPA photodegradation under visible light using H2O2 and O2 as oxidants. The catalyst exhibited robust stability and reusability, rendering it suitable for practical applications. The crystalline structure and surface structure of WO3 controlled its catalytic activity towards TBBPA photodegradation. Monoclinic WO3 with the (022) plane was found to be the most active for ˙O2− active species generation from H2O2 and thus active for TBBPA degradation. Degradation product analysis showed that the catalyst was active not only for the removal of TBBPA, but also for the debromination of TBBPA. Nearly 100% debromination was achieved.

CAS / MDL: 12333-11-8
研究领域: 环境科学 · 材料科学 · 化学工程
✓ 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

PDMS-based artificial lung membranes with enhanced permeation to overcome the bottleneck in CO2/O2 selectivity

Jiaming Wang,Feifei Kang,Yifei Chen,Xiujuan Zhang,Xiaobin Jiang,Gaohong He,Xuehua Ruan

Artificial lung membranes are the heart for extracorporeal oxygenation. Hereinto, the nonporous PDMS-based membranes have excellent biocompatibility, and also isolation ability to both blood and harmful matters. Nevertheless, their CO 2 /O 2 selectivity, in the conventional cases using pure-oxygen sweeping stream, is not enough to accomplish sufficient CO 2 removal in balance with O 2 addition. In this work, the oxygenation mode using oxygen-enriched stream, faithfully based on the permeation mechanism, is established to overcome this bottleneck. To neutralize the negative impacts caused by lowering oxygen content and its partial pressure, PDMS-based composite membranes with ultra-thin selective layer to enhance mass transfer have been fabricated successfully. The experiments manifest that the selective layer, on the basic condition that the composite structure is stable enough to make surface modification and realistic utilization, is decreased to 376 nm on the porous substrates. O 2 and CO 2 permeation rates through the ultimate membrane samples have been enhanced to 502 GPU and 4117 GPU, respectively. In this instance, the essential oxygenation could be sustained with O 2 partial pressure less than 446 mmHg in the sweeping stream. The minimum membrane area for a common treatment case is 0.05 square meters. Once the membrane area is increased to 0.18 square meters, the sterile air after purification could be directly used for oxygenation. In comparison to the oxygenation devices being used currently, membrane area can be saved by about 90 %, which is highly significant to reduce the injuring influence on blood cells. All in all, the artificial lung membranes with ultra-thin PDMS coating layer have promising future in realistic utilization.

CAS / MDL: 1401-55-4
研究领域: 生物医学工程 · 材料科学
✓ 已验证 产品关联 DOI 高影响因子
查看原文 查看 PubMed
JOURNAL OF MATERIALS SCIENCE & TECHNOLOGY · 2024 · IF 11.2

Pauling-type adsorption of O2 induced by S-scheme electric field for boosted photocatalytic H2O2 production

Shuang Zhou,Da Wen,Wei Zhong,Jianjun Zhang,Yaorong Su,Aiyun Meng

The effective adsorption of oxygen (O 2 ) molecules over photocatalysts is a critical step in promoting the performance of photocatalytic H 2 O 2 production. However, g-C 3 N 4 usually features a Yeager-type (side-on) adsorption configuration of O 2 molecules, which causes the breaking of O–O bonds and severely hinders the H 2 O 2 production activity. Herein, we synthesized an oxygen-vacancy-rich TiO 2– x /g-C 3 N 4 step-scheme (S-scheme) heterojunction to regulate the oxygen adsorption configuration and improve the 2e – ORR selectivity of H 2 O 2 production. In-situ X-ray photoelectron spectroscopy (in-situ XPS) and density functional theory (DFT) calculations reveal that the S-scheme heterojunction is formed between TiO 2– x and g-C 3 N 4 . The difference between their Fermi levels leads to the electron flow from g-C 3 N 4 to TiO 2– x , which increases the electron-deficient sites in g-C 3 N 4 . As a result, the cleavage of O–O bonds on the surface of g-C 3 N 4 is avoided and the oxygen adsorption configuration is tuned from Yeager-type to Pauling-type (end-on). Consequently, the photocatalytic H 2 O 2 production rate is dramatically improved to 1780.3 μmol h –1 , which is about 5 times higher than that of pristine g-C 3 N 4 . This work paves a new way to tailor the oxygen adsorption configuration by rationally designing S-scheme heterojunction photocatalysts.

CAS / MDL: 57-13-6
研究领域: 材料科学 · 催化化学
✓ 已验证 产品关联 DOI 高影响因子
查看原文 查看 PubMed
JOURNAL OF COLLOID AND INTERFACE SCIENCE · 2025 · IF 9.7

Surface organic phosphates enhance mild oxidation of toluene by O2 to benzaldehyde over VTiOx/γ-Al2O3

Changshun Deng,Xiaorong Zhu,Jun Yao,Yibo Wang,Chenyang Shen,Bingqing Ge,Chaoxiang Li,Nianhua Xue,Luming Peng,Xuefeng Guo,Yan Zhu,Yafei Li,Weiping Ding

The direct oxidation of toluene by O 2 to benzaldehyde with high efficiency is a bright route for the green production of benzaldehyde but still a significant challenge. In this study, we develop a ligand modification strategy by bonding organophosphonic acid (OPA) to VTiO x /γ-Al 2 O 3 to restructure its interface microenvironment for enhancement of toluene oxidation to benzaldehyde. The as-prepared catalyst exhibits excellent selectivity over 99 % under mild conditions. Results of comprehensive characterizations and calculations reveal that the OPA bonding in bidentate with the V 6-coordinated species causes noticeable phase reconstruction between VO x and TiO 2 , thereby generating nearby new reactive oxygen species, which is responsible for the conversion of toluene to benzaldehyde at temperatures as low as ∼50 °C, much lower than that over VO x /TiO 2 (>130°C). The interface microdomain around the bonding site of OPA helps to significantly weaken the methyl C H bond of toluene molecule in reaction manifested as the significant decrease in apparent activation energy. Hence, the current work reveals a novel mechanism of the typical catalyst VO x /TiO 2 under OPA bonding, which is useful to solve the classic difficult reaction of toluene to benzaldehyde by O 2 oxidation.

研究领域: 催化化学 · 绿色化学
✓ 已验证 产品关联 DOI PubMed 高影响因子
查看原文 查看 PubMed
JOURNAL OF THE ELECTROCHEMICAL SOCIETY · 2017 ·Vol. 164 ·期 6 ·A1321 · IF 3.259

Enhanced Electrochemical Performance of Non-Aqueous Li-O2 Batteries with Triethylene Glycol Dimethyl Ether-Based Electrolyte

Chaolumen Wu,Taoran Li,Chenbo Liao,Qingkai Xu,Yuancheng Cao,Lei Li,Jun Yang

Triethylene glycol dimethyl ether (G3) is evaluated as an electrolyte solvent for non-aqueous lithium-oxygen (Li-O2) batteries. A liquid electrolyte of 1 M LiTFSI in G3 shows lower viscosity, higher oxygen solubility and diffusion, higher ionic conductivity and lithium ionic transference number compared to the conventional liquid electrolyte of 1 M LiTFSI in tetraethylene glycol dimethyl ether (G4). Then the Li-O2 battery using the G3-based electrolyte shows better cycling stability and higher rate capability compared to the battery using the G4-based electrolyte. At a higher current density of 2.5 A gcarbon−1, the discharge capacity of the battery using the G3-based electrolyte is about 1472 mAh gcarbon−1, which is about four times higher than that of the battery using the G4-based electrolyte. At current density of 1 A gcarbon−1 with a fixed capacity of 1000 mAh gcarbon−1, the battery using the G3-based electrolyte can be operated stably for 80 cycles, while only 20 cycles are achieved by using the G4-based electrolyte. Therefore, we think the G3-based electrolyte could be a proper alternative electrolyte to the conventional G4-based electrolyte for the development of Li-O2 batteries.

研究领域: 材料科学 · 电化学
✓ 已验证 DOI 高影响因子
查看原文 查看 PubMed
APPLIED CATALYSIS B-ENVIRONMENTAL · 2018 · IF 11.698

Persian buttercup-like BiOBrxCl1-x solid solution for photocatalytic overall CO2 reduction to CO and O2

Meichao Gao,Jinxiang Yang,Tao Sun,Zizhong Zhang,Dafeng Zhang,Huijuan Huang,Huaxiang Lin,Yi Fang,Xuxu Wang

The photocatalytic overall conversion of CO 2 with H 2 O to chemical fuel and oxygen mimicking natural photosynthesis is a huge challenge in photocatalysis. This work shows the achievement of the solar-driven photocatalytic overall CO 2 reduction with H 2 O to CO and O 2 over a Persian buttercup-like BiOBr x Cl 1-x solid solution. A CO generation rate of 15.86 μmol g −1  h −1 with the approximate stoichiometric O 2 evolution is yielded on BiOBr 0.6 Cl 0.4 solid solution under simulated solar light irradiation, which was about 7.5 and 10.2 times higher than that of pure BiOCl (2.11 μmol g −1  h −1 ) and BiOBr (1.55 μmol g −1  h −1 ), respectively. The enhanced photoactivity is contributed to the mediate band gap and energy level tuned by the formation of BiOBr x Cl 1-x solid solution to facilitate the separation of photogenerated charges. Besides the unique electron structure, the photoinduced oxygen vacancy (O V ) formed on BiOBr x Cl 1-x solid solution also plays an important role in the CO 2 reduction.

研究领域: 化学 · 材料科学 · 环境科学
✓ 已验证 DOI 高影响因子
查看原文 查看 PubMed
CHINESE JOURNAL OF CHEMICAL ENGINEERING · 2020 · IF 2.627

A design of Nafion-coated bilayered quasi-solid electrolyte for lithium-O2 batteries with high performance

Yingfei Hou,Lin Jiang,Yaoyao Zhang,Zhiwen Qin,Chi Jiang,Ming Wang

Lithium-air (also known as lithium-oxygen) batteries have attracted considerable global attention in recent years due to their extremely high energy density (11,140 W·h·kg −1 ). The electrolyte is a key element in lithium-air batteries and the traditional organic electrolyte has great safety risk due to leakage. On the contrary, the polymer electrolyte has the advantages of high safety, high stability and easy processing comparing with the organic liquid electrolytes. In this paper, a new idea was proposed to coat the Nafion membrane on a layer of polymer for blocking the oxidation reduction electric (RM) and Li based on the selective permeability on lithium ion of the Nafion membrane. Self-made thickness-controllable Nafion membrane, polyvinylidene fluoride-hexafluoropropylene copolymer (PVDF-HFP) and 2,2,6,6-tetramethylpiperidinooxy (TEMPO) were used to prepare a quasi solid polymer electrolyte (NSPE). Electrochemical workstation and LAND battery testing system were used to perform a galvanostatic charge/discharge test on Li-O 2 . The ionic conductivity of NSPE was 4.3 × 10 −4 S·cm −1 at room temperature and the discharge platform was 2.6 V and the charging voltage was 3.7 V after 50 cycles with the cut-off capacity of 500 mA·h·g −1 .

研究领域: 材料科学 · 电化学
✓ 已验证 DOI 高影响因子
查看原文 查看 PubMed
ELECTROCHIMICA ACTA · 2022 · IF 7.336

A hybrid bioelectrochemical device based on glucose/O2 enzymatic biofuel cell for energy conversion and storage

Panpan Zhao,He Zhang,Xiaoxuan Sun,Shuai Hao,Shaojun Dong

In this work, combining poly (methylene green)/glucose dehydrogenase (PMG/GDH) bioanode with Prussian blue/glucose oxidase (PB/GOD) biocathode, we developed a hybrid bioelectrochemical device based on glucose/O 2 enzymatic biofuel cell (EBFC) to achieve energy conversion and storage. Depending on the reversible redox behaviors, PMG and PB play roles of dual-functional nanomaterials , not only as mediators to accelerate electrons transport between enzymes and electrodes surface, but also as pseudocapacitive materials to achieve energy storage. As a result, this hybrid device exhibited superior performance towards energy storage with a specific capacitance of 158.5 mF cm −2 at the current density of 1 mA cm −2 . Meanwhile, a maximum output power density of 783.5 μW cm −2 in the pulse mode could be obtained, which had a prominent increment than that of the prototypical EBFC (87.5 μW cm −2 ) in the steady state. Furthermore, this hybrid device also exhibited better operational stability in long-term charge/discharge cycles test, at the current pulse of 1 mA cm −2 . Through the combination of bioelectrocatalysis and capacitive energy storage, this developed hybrid device achieves effective energy conversion and storage, and provides a high output power to address the insufficient power supply of traditional EBFCs, which may enlarge the practical application of EBFCs in self-powered implantable and wearable devices .

研究领域: 生物电化学 · 能量存储 · 材料科学 · 生物医学工程
✓ 已验证 DOI 高影响因子
查看原文 查看 PubMed
JOURNAL OF THE AMERICAN CERAMIC SOCIETY · 2025 ·Vol. 109 ·期 1 ·e70407 · IF 3.8

Preparation and properties of novel (Y, Yb, Zr, Hf, Sn, W)O2−δ high-entropy ceramics

Yuwei Zhang,Cuiwei Li,Guangjin Chen,Chenran Zhao,Zhikun Song,Kepi Chen,Haoran Sun,Linghao Wu,Junhui Xiang

A series of (Y, Yb, Zr, Hf, Sn, W)O 2−δ high-entropy ceramics with varying mole fraction of main elements were synthesized for the first time through the solid-state reaction synthesis method. The microstructure, phase composition, and properties of the prepared materials were thoroughly analyzed and tested. The results indicate that the phase composition transformed from a single-phase fluorite structure to a single-phase C-type rare earth sesquioxide structure as the mole fraction of +3 cations increases. The thermal conductivity of the prepared high-entropy ceramics with porosity of 49.8%–50.1% is very low ranging from 0.33 to 0.37 W·m −1 ·K −1 . Among them, the single-phase C-type rare earth sesquioxide with a higher oxygen vacancy concentration was employed as a catalyst in the CO 2 hydrogenation reaction, attaining a high CO 2 conversion rate of 82.0%. The obtained results have deepened understanding of the role of oxygen vacancies and have important guiding significance for the study of high-entropy oxides with fluorite derived structures.

研究领域: 材料科学 · 陶瓷 · 催化 · 能源材料 · 固态化学
✓ 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。