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。

347,358+ SCI 论文 与阿拉丁产品引用相关
2,303,472.95 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。

产品列表

视图 列表 网格

显示第49至60个,产品总数155个

设置提升方向
MnO₂
METALLURGICAL AND MATERIALS TRANSACTIONS B-PROCESS METALLURGY AND MATERIALS PROCESSING SCIENCE · 2020 ·Vol. 52 ·期 1 ·314-321 · IF 2.035

The Distribution of Cobalt Between Co-Cu Alloys and Alumina-Saturated MnO-SiO2-Al2O3 Slags

Ren Guoxing,Xiao Songwen,Xia Longgong,Liao Caibin,Liu Zhihong

To obtain fundamental information on the dissolution of cobalt into alumina-saturated MnO-SiO 2 -Al 2 O 3 slags in the smelting reduction of spent lithium-ion batteries, the equilibrium distribution of cobalt between Co-Cu alloys and alumina-saturated MnO-SiO 2 -Al 2 O 3 slags was measured at 1573 K and 1623 K under a controlled CO-CO 2 atmosphere. The results show that (i) the solubility of cobalt in the slag increased with increasing concentration of cobalt in the alloy and increasing oxygen partial pressure in the atmosphere at a fixed concentration of cobalt in the alloy, and (ii) the activity coefficient of CoO in the slag increased with increasing cobalt oxide in the slag. The activity coefficient of CoO in the slag, γ CoO, referred to as solid CoO, can be described as a function of the concentration of CoO in slag as follows: γ CoO  = 11.2957(wt pct CoO in slag) + 12.0944 (1573 K, (wt pct MnO)/(wt pct SiO 2 )= 0.76–0.83); γ CoO  = 2.2286(wt pct CoO in slag) + 4.5232 (1623 K, (wt pct MnO)/(wt pct SiO 2 )= 0.78–0.85).

✓ 已验证 产品关联 DOI 高影响因子
查看原文 查看 PubMed
CERAMICS INTERNATIONAL · 2016 · IF 2.758

Fabrication of MnO@C-CNTs composite by CVD for enhanced performance of lithium ion batteries

Chunlong Dai,Minqiang Wang,Jingang Yang,Linyu Hu,Maowen Xu

A novel MnO@Amorphous C-Carbon nanotubes (MnO@C-CNTs) composite is prepared by chemical vapor deposition (CVD). When used as an anode material for Li-ion batteries, the MnO@C-CNTs composite exhibits an initial discharge capacity of 1164   mA   h   g −1 at 100   mA   g −1 and the discharge capacity gradually increased from 571.7   mA   h   g −1 to 654   mA   h   g −1 after 100 cycles at 1   A   g −1 , which shows an increase of the capacity rather than attenuation. Furthermore, the MnO@C-CNTs electrode can deliver a capacity of up to 228   mA   h   g −1 at 5   A   g −1 . These results indicate that the three-dimensional conductive network of the MnO@C-CNTs composite could prevent the aggregation of MnO particles, and its open structure allows electrolyte penetration, and reduces the diffusion path of the lithium ions , hence maximizes utilization of the electrochemically active MnO particles, while enhances the conductivity of electrode material and Li + transport. This work offers a universal approach to design various metal oxides@C-CNTs composite.

CAS / MDL: 1344-43-0
✓ 已验证 产品关联 DOI 高影响因子
查看原文 查看 PubMed
Journal of Energy Storage · 2024 · IF 8.9

Enhanced cyclability of O3-NaNi0.33Fe0.31Mn0.36O2 by Mg and Cu synergistic doping with strengthened MnO bonds

Yuxuan Wu,Yinda Li,Yunhao Lu,Jicheng Jiang,Aijun Zhou,Bo Xu,Xiongwen Xu,Jian Tu,Bin Pan,Xinbing Zhao,Jian Xie

Among some practical O3-type layered oxide cathodes, NaNi 1/3 Fe 1/3 Mn 1/3 O 2 (NFM) features a high specific capacity and moderate cyclability. However, sluggish Na + transfer kinetics, low structural stability, and rapid capacity loss during long-term cycling, are still posing a challenge to commercial applications of this material. In this work, we propose a Mg and Cu co-doped O3-type NaMg 0.02 Cu 0.02 Ni 0.33 Fe 0.27 Mn 0.36 O 2 (MC-NFM) with a stable structure and good cycling stability. It was found that the Mn O bonds in MC-NFM are obviously reinforced by synergistic doping with small amounts of Mg and Cu, leading to enhanced structural robustness, decreased Na + migration barrier, and delayed O3-P3 phase transition. As a result, longer cycle life and enhanced rate performance are achieved. MC-NFM can yield a specific capacity of 142.1 mAh g −1 at 0.1C and 116.0 mAh g −1 at 5C, and maintain 83.6 % of its initial capacity after 400 cycles at 1C. This work provides a promising design of O3-type cathode for sodium-ion batteries.

✓ 已验证 DOI 高影响因子
查看原文 查看 PubMed
INTERNATIONAL JOURNAL OF HYDROGEN ENERGY · 2023 · IF 7.2

Ni-based catalyst assisted by MnO to boost the hydrogen storage performance of magnesium hydride

Chengwang Yin,Shujun Qiu,Yongpeng Xia,Fen Xu,Lixian Sun,Hailiang Chu

Magnesium hydride (MgH 2 ) stands out as a promising solid-state material for high-density hydrogen storage , offering enormous potential for applications in hydrogen transportation and storage. However, the stable thermodynamics and sluggish kinetics of dehydrogenation/hydrogenation of MgH 2 impede its practical use in on-board hydrogen storage. In this study, the nanocomposite of nickel/manganese oxide (Ni/MnO) was successfully synthesized through the hydrogenation of nickel-manganese two-dimensional layered double hydroxide (NiMn-LDH) and then introduced into MgH 2 by ball milling to form BM-MgH 2 -Ni/MnO composite. Notably, BM-MgH 2 -Ni/MnO-10 displayed excellent hydrogen absorption/dehydrogenation properties. For example, its onset hydrogen release temperature was remarkably reduced to 175.6 °C, 84 °C lower than that of BM-MgH 2 . At a temperature of 250 °C, it could desorb about 6.2 wt% of H 2 within 60 min. The fully dehydrogenated product could absorb 5.5 wt% of H 2 within 10 min at 150 °C. Moreover, BM-MgH 2 -Ni/MnO-10 exhibited excellent cycling performance. Throughout the cycling process, the in-situ formation of Mg 2 Ni/Mg 2 NiH 4 and metal Mn was detected, leading to a synergistic effect that significantly enhanced the hydrogen storage capability of MgH 2 . This study presents innovative concepts for designing active catalysts to enhance the kinetics of de-/hydrogenation reactions of MgH 2 .

✓ 已验证 DOI 高影响因子
查看原文 查看 PubMed
JOURNAL OF ELECTROANALYTICAL CHEMISTRY · 2019 · IF 3.218

Polypyrrole-derived nitrogen-doped carbon coated hierarchical MnO porous microspheres for highly reversible lithium storage

Peilin Zhang,Jinzhe Liu,Chencheng Zhou,Shouzhi Guo,Shuo Li,Yun Yang,Jing Wu,Di Yu,Hanfei Chen,Ming Zhao,Luyang Chen

Manganese monoxide (MnO) has emerged as a promising anode material in lithium-ion batteries (LIBs) due to its large lithiation capacity, low voltage hysteresis and environmental friendliness. In this work, we have developed the nitrogen-doped carbon coated MnO porous microspheres (MnO@NC), which consist of small nanocrystals with interparticle mesopores via a self-templated solvothermal synthesis and subsequent in-situ pyrolysis of polypyrrole precursors. By virtue of the conductive outer layer of nitrogen-doped carbon (NC) and the abundant inner mesopores, the hierarchical MnO@NC porous microspheres manifest the superior lithium storage properties as anode for LIBs. In detail, the optimized MnO@NC electrode delivers a high initial discharge capacity of 1037 mAh g − 1 at 0.2 A g − 1 , remains the discharge capacity of 890 mAh g −1 at 1A g − 1 after 500 cycles, indicates the outstanding rate capability with a specific capacity of 450 mAh g − 1 at 5A g − 1 .

✓ 已验证 DOI 高影响因子
查看原文 查看 PubMed
INTERNATIONAL JOURNAL OF HYDROGEN ENERGY · 2023 · IF 7.2

Controllable synthesis of Co/MnO heterointerfaces embedded in graphitic carbon for rechargeable Zn–air battery

Xiaowei Guo,Yang Yuan,Shanshan Li,Jingwen Wang,Zhengyu Bai,Lin Yang

Owing to the unique geometric and electronic structure, design and synthesis of electrocatalysts with well defined heterointerfaces are essential for clean energy technologies, for instance water-splitting and Zn-air batteries. Herein, a bifunctional electrocatalyst assembled by Co/MnO nanoparticles and nitrogen doping double-sphere carbon (denoted as Co/MnO@N-DSC), was fabricated via a solvothermal and pyrolysis strategy. The Co/MnO@N-DSC catalysts exhibit an enhanced bifunctional oxygen electrocatalytic performance for Oxygen reduction reaction (ORR) (E 1/2 , 0.84 V vs . RHE) and oxygen evolution reaction (OER) (E onset , 1.54 V vs . RHE). As an air cathode catalyst, the Co/MnO@N-DSC-based Zn-air battery can afford prime performance, over the commercial noble-metal-based Zn-air battery. Theoretical calculation results indicate that the synergism of Co (111)/MnO (200) heterointerfaces can enhance charge transfer and provide extra electrons for the reaction processes. This work provides a promising manoeuvre to uplift bifunctional catalytic activity by increasing the synergy from heterointerfaces of transition-metal/metal oxide in oxygen electrocatalysis .

✓ 已验证 DOI 高影响因子
查看原文 查看 PubMed
CERAMICS INTERNATIONAL · 2018 · IF 3.057

Electrospun carbon nanofibers decorated with MnO nanoparticles as a sulfur-absorbent for lithium-sulfur batteries

Jinghui Zhu,Rosaiah Pitcheri,Tuo Kang,Ya Guo,Jing Li,Yejun Qiu

Shuttle effect of the dissolved polysulfide is a main disadvantage for Li-S batteries, which has been explored by several polar materials to absorb lithium polysulfide with physical and chemical effect. Herein, for the first time, a composite of carbon nanofibers decorated with MnO nanoparticles (CNF-MnO) has been prepared by the facile electrospinning method followed by thermal treatment. SEM and TEM characterization delivered that the MnO NPs on CNF did not change the morphology but decrease the electronic conductivity of CNF-MnO composite. The CNF-MnO composite exhibited excellent electrochemical cyclic stability because of its strong chemical absorption for polysulfide. Interestingly, CNF-MnO composite served as both cathode as well interlayer for Li-S batteries. The CNF-MnO-S as cathode material showed an initial discharge capacity of 683.2 mAh g -1 at 1.0 C and remained 592.0 mAh g -1 even after 250 cycles with the capacity decay of 0.053% per cycle. As well, CNF-MnO as interlayer delivered superior cycling stability even at high current density of 3.0 C, where the capacity still maintained 542.2 mAh g -1 over 200 cycles.

✓ 已验证 DOI 高影响因子
查看原文 查看 PubMed
Materials Chemistry Frontiers · 2021 ·Vol. 6 ·期 4 ·491-502 · IF 6.482

In situ formation of MnO@N-doped carbon for asymmetric supercapacitor with enhanced cycling performance

Maiyong Zhu,Chengyu Tu,Xuan Li,Qiao Luo,Songjun Li

Searching electrodes with high specific capacitance, rate capability, long cycling life and economic efficiency is central for next-generation supercapacitors. In this work, a hybrid electrode consisting of MnO and N-doped carbon (MnO–NC) was constructed using KMnO4 and carboxymethyl chitosan as manganese sources and carbon sources respectively. The effect of the ratio of KMnO4 to carboxymethyl chitosan on the structure and electrochemical performance of MnO–NC was investigated in detail. At the optimized condition, a high specific capacitance of 326.36 F g−1 was obtained with satisfied cyclic stability. Moreover, an asymmetric supercapacitor (ASC) device (MnO–NC//AC), consisting of MnO–NC as the positive electrode and activated carbon (AC) as the negative electrode was assemble, which exhibited a specific energy density was 9.35 W h kg−1 at a power density of 374.83 W kg−1. Owing to the long activation process, the capacitance of the ASC device remains 172% after 10 000 cycles. These results indicate that the prepared MnO–NC has great prospects for the application of high-performance supercapacitors.

✓ 已验证 DOI 高影响因子
查看原文 查看 PubMed
COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS · 2025 · IF 5.4

Carbon-encapsulated MnO composites derived from Mn-hexamine coordination frameworks as high-performance supercapacitor electrodes

Shurui Xu,Jiaer Li,Bingyu Zhu,Xin Tang,Yujian Li,Linjia Wang,Wenbo Liao,Xiaobo Fu,Hang Chen,Junling Tu,Kailai Zhang,Baizeng Fang,Guoyu Zhong

Investigating renewable, eco-friendly, carbon-based materials with superior electrochemical performance is pivotal for advancing the practical implementation of supercapacitors, yet it presents challenges. In this study, a novel MnO@C-HMT-T composite, consisting of porous carbon-encapsulated MnO, was synthesized from a Mn-hexamine coordinated precursor via an in-situ pyrolysis approach. Among the different materials prepared, the MnO@C-HMT-800 stood out. It displayed a mesoporous architecture with a high specific surface area of 1353.1 m 2 g −1 , which facilitates ion transport and energy storage. Additionally, the MnO encapsulated in the carbon layer enables the generation of pesudocapacitance via the redox reaction of Mn 2+ and Mn 3+ . The interaction between the double-layer capacitance of the porous carbon and the pseudocapacitance of the manganese oxides endows the MnO@C-HMT-T composite with superior electrochemical performance. Consequently, the MnO@C-HMT-800 electrode exhibits an impressive specific capacitance of 575.2 F/g at a current density of 1 A/g, demonstrating exceptional stability at 95.6 % after 10,000 cycles. This surpasses the performance of most reported Mn-based materials in the literature. This work presents an innovative and straightforward process for fabricating carbon-encapsulated transition oxides that could be highly valuable in energy storage systems.

✓ 已验证 产品关联 DOI 高影响因子
查看原文 查看 PubMed
Journal of Water Process Engineering · 2025 · IF 6.7

Architecture-engineered Fe₃O₄-MnO₂ composite for peroxydisulfate activation: Visible light-enhanced redox cycling mechanism

Yongzhi Tu,Ziming Zhang,Peien Huang,Jiale Zou,Zhi Xiong,Meiting Zheng,Zhifei Ma,Jianxin Chen

Unlike conventional Fe₃O₄-MnO₂ composites, an architecture-engineered Fe₃O₄-MnO₂ (FM-21) heterostructure was constructed by anchoring Fe₃O₄ nanoparticles onto α-MnO₂ nanorods. Under visible light irradiation, the FM-21/PDS system achieves 96.5 % Orange II degradation within 60 min with a kinetic rate constant of 0.0596 min −1 , significantly outperforming its individual components and dark condition controls. Multiple characterization techniques confirm that the unique interfacial configuration establishes a direct Z-scheme charge transfer pathway, substantially enhancing charge carrier separation efficiency. XPS analysis provides direct evidence that visible light accelerates the co-cycling of Fe 3+ /Fe 2+ and Mn 4+ /Mn 3+ redox pairs, thereby maintaining highly efficient PDS activation. Quenching experiments and EPR analysis further reveal that the synergistic effect between radical and non-radical pathways, which is dominated by singlet oxygen ( 1 O₂) and holes (h + ), drives the degradation process. This mechanism enables the degradation of various pollutants with minimal dependence on their charge characteristics, demonstrating the catalyst's broad applicability. The catalyst also exhibits practical advantages including magnetic separability and stable performance over five consecutive cycles. This study demonstrates that the synthesized FM-21 exhibits significant potential for visible light-enhanced PDS activation in eliminating recalcitrant organic pollutants.

CAS / MDL: 1317-61-9 64-75-5
✓ 已验证 产品关联 DOI 高影响因子
查看原文 查看 PubMed
COLLOIDS AND SURFACES B-BIOINTERFACES · 2015 · IF 4.152

Fabrication and evaluation of tumor-targeted positive MRI contrast agent based on ultrasmall MnO nanoparticles

Haitao Huang,Tao Yue,Ke Xu,Jafar Golzarian,Jiahui Yu,Jin Huang

Gd(III) chelate is currently used as positive magnetic resonance imaging (MRI) contrast agent in clinical diagnosis, but generally induces the risk of nephrogenic systemic fibrosis (NSF) due to the dissociated Gd 3+ from Gd(III) chelates. To develop a novel positive MRI contrast agent with low toxicity and high sensitivity, ultrasmall MnO nanoparticles were PEGylated via catechol-Mn chelation and conjugated with cRGD as active targeting function to tumor. Particularly, the MnO nanoparticles with a size of ca. 5   nm were modified by α,β-poly(aspartic acid)-based graft polymer containing PEG and DOPA moieties and, meanwhile, conjugated with cRGD to produce the contrast agent with a size of ca. 100   nm and a longitudinal relaxivity ( r 1 ) of 10.2   mM −1   S −1 . Such nanoscaled contrast agent integrated passive- and active-targeting function to tumor, and its efficient accumulation behavior in tumor was verified by in vivo distribution study. At the same time, the PEG moiety played a role of hydrophilic coating to improve the biocompatibility and stability under storing and physiological conditions, and especially might guarantee enough circulation time in blood. Moreover, in vivo MRI revealed a good and long-term effect of enhancing MRI signal for as-fabricated contrast agent while cell viability assay proved its acceptable cytotoxicity for MRI application. On the whole, the as-fabricated PEGylated and cRGD-functionalized contrast agent based on ultrasmall MnO nanoparticles showed a great potential to the T 1 -weighted MRI diagnosis of tumor.

✓ 已验证 DOI PubMed 高影响因子
查看原文 查看 PubMed
CHEMICAL ENGINEERING JOURNAL · 2017 · IF 6.216

Formation of multiporous MnO/N-doped carbon configuration via carbonthermal reduction for superior electrochemical properties

Qianxu Ye,Juanjian Ru,Jinhui Peng,Guo Chen,Ding Wang

Herein, the multiporous MnO/N-doped carbon (MnO/NC) composite based on the abundant and inexpensive electrolytic manganese dioxide were fabricated through a facile microwave-assisted carbonthermal reduction, combined with a subsequent in-situ polymerization of polydopamine onto MnO along with thermal treatment. As an anode material, it retains a reversible capacity of 770.5   mAh   g −1 at 300   mA   g −1 and high Coulombic efficiency of 99% over 500 cycles, superior than those values of the pure multiporous MnO alone. The impressive performance is attributed to the splendid structure stability contributed by well-connected three-dimensional porous configuration and the enhanced reaction kinetics as well as electrical conductivity incurred by N-doped carbon layer with multiple type nitrogen.

✓ 已验证 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。