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。

346,438+ SCI 论文 与阿拉丁产品引用相关
2,295,919.25 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409至420个,产品总数931个

设置提升方向
Fe2O3
JOURNAL OF ALLOYS AND COMPOUNDS · 2026 · IF 6.7

Ru-doped CoFe MOF-derived Co3O4-Fe2O3 heterostructure via mild pyrolysis for efficient oxygen evolution

Man Wang,Shichao Chen,Kang Wang,Song Song,Xitao Wang

A Ru-doped CoFe MOF-derived Co 3 O 4 -Fe 2 O 3 heterostructure was fabricated via mild pyrolysis. • The low-temperature strategy preserves the 2D MOF nanosheet scaffold. • Ru incorporation modulates Co/Fe electronic states and suppresses structural aggregation during mild pyrolysis. • Ru 0.024 CoFe MOF-250 requires only 227 mV at 20 mA cm −2 with a Tafel slope of 33.67 mV dec −1 . • Excellent durability is demonstrated by only 8.3 mV potential increase after 100 h at 20 mA cm −2 . Metal-organic frameworks (MOFs) are promising for the oxygen evolution reaction (OER), yet they suffer from framework collapse and active-site aggregation during high-temperature pyrolysis. Herein, a Ru-doped CoFe MOF is grown in situ on nickel foam (NF) and subsequently annealed at 250 °C, forming a Co 3 O 4 -Fe 2 O 3 @Ru 0.024 CoFe MOF heterostructure. The incorporation of Ru modulates the local electronic structure of the Co/Fe centers, while mild annealing at 250 °C generates Co 3 O 4 -Fe 2 O 3 nanophases within the partially preserved MOF nanosheet scaffold. This creates intimate heterointerfaces that facilitate rapid charge transfer. In 1.0 M KOH, the optimized electrode delivers a current density of 20 mA cm -2 at an overpotential of only 227 mV, exhibits a low Tafel slope of 33.67 mV dec −1 , and achieves an electrochemical surface area (ECSA) of 133.5 cm 2 . After 100 h of operation at 20 mA cm −2 , the potential increases by merely 8.3 mV. This work presents an effective strategy that combines Ru doping with mild pyrolysis to construct efficient and stable MOF-based OER electrocatalysts.

CAS / MDL: 100-21-0
✓ 已验证 产品关联 DOI 高影响因子
查看原文 查看 PubMed
Environmental Science-Nano · 2023 · IF 7.3

Nitrate formation and iron dissolution in the heterogeneous reactions of NH3 on nano α-Fe2O3

Ruixue Wang,Kun Li,Narcisse Tsona Tchinda,Wenxing Wang,Lin Du

Ammonia (NH3), the most common alkaline gas in the atmosphere, participates in heterogeneous reactions on the surface of aerosols and produces ammonium (NH4+). While most previous studies have focused on the effect of NH3 on the heterogeneous reactions of other gases on mineral dust aerosols, little research has been done on the heterogeneous reactions of NH3 influenced by acidic gases. Here, the effects of sulfur dioxide (SO2), formic acid, acetic acid and acrylic acid on the heterogeneous reaction of NH3 on the surface of nano α-Fe2O3 particles were investigated. We found that NH3 can promote the dissolution of α-Fe2O3 through NH3–Fe complexation and be oxidized to NO3−, while the addition of acidic gas inhibits the NH3–Fe complex formation and converts it into physical adsorption. SO2 promoted the conversion of NH3 to NH4+, while weakly inhibiting the oxidation of NH3 to NO3− by competing for oxidation sites under light conditions. Organic acids, on the other hand, inhibited the heterogeneous conversion of NH3, and strongly competed for oxidation sites under light conditions, significantly reducing NO3− production. This study reveals the various influences of acidic gases on NH3 heterogeneous reactions on α-Fe2O3 particles, which helps to improve the understanding of atmospheric processes involving NH3, acidic gases, and mineral dust aerosols.

CAS / MDL: 1309-37-1
✓ 已验证 产品关联 DOI 高影响因子
查看原文 查看 PubMed
Nanomaterials · 2023 ·Vol. 13 ·期 18 ·2579 · IF 5.3

Interface Engineering of CoFe-LDH Modified Ti: α-Fe2O3 Photoanode for Enhanced Photoelectrochemical Water Oxidation

Yue Chang,Minmin Han,Yehui Ding,Huiyun Wei,Dawei Zhang,Hong Luo,Xiaogang Li,Xiongbo Yan

Effectively regulating and promoting the charge separation and transfer of photoanodes is a key and challenging aspect of photoelectrochemical (PEC) water oxidation. Herein, a Ti-doped hematite photoanode with a CoFe-LDH cocatalyst loaded on the surface was prepared through a series of processes, including hydrothermal treatment, annealing and electrodeposition. The prepared CoFe-LDH/Ti:α-Fe2O3photoanode exhibited an outstanding photocurrent density of 3.06 mA/cm2at 1.23 VRHE, which is five times higher than that of α-Fe2O3alone. CoFe-LDH modification and Ti doping on hematite can boost the surface charge transfer efficiency, which is mainly attributed to the interface interaction between CoFe-LDH and Ti:α-Fe2O3. Furthermore, we investigated the role of Ti doping in enhancing the PEC performance of CoFe-LDH/Ti:α-Fe2O3. A series of characterizations and theoretical calculations revealed that, in addition to improving the electronic conductivity of the bulk material, Ti doping also further enhances the interface coupling of CoFe-LDH/α-Fe2O3and finely regulates the interfacial electronic structure. These changes promote the rapid extraction of holes from hematite and facilitate charge separation and transfer. The informative findings presented in this work provide valuable insights for the design and construction of hematite photoanodes, offering guidance for achieving excellent performance in photoelectrochemical (PEC) water oxidation.

✓ 已验证 产品关联 DOI PubMed 高影响因子
查看原文 查看 PubMed
CHEMICAL ENGINEERING JOURNAL · 2023 · IF 15.1

Efficient activation of peroxymonosulfate by amorphous MnO2/α-Fe2O3 for the degradation of organic pollutants

Ronghao Wu,Xin Hu,Yihui Li,Yongfu Li,Yanjiang Cai,Peikun Jiang,Bing Yu

Constructing bimetallic nanostructures with specific crystalline phases provides an attractive strategy to develop highly efficient catalysts and explore structure-dependent catalytic properties. Herein, a new iron-based bimetallic catalyst consisting of amorphous MnO 2 and crystalline α-Fe 2 O 3 was synthesized for peroxymonosulfate (PMS) activation, named as a-MnO 2 /α-Fe 2 O 3 . The results show that the removal efficiency of sulfamethoxazole is over 90% within 120 min by the a-MnO 2 /α-Fe 2 O 3 in the presence of PMS at broad pH conditions ranging from 3 to 9. Furthermore, a complete degradation of bisphenol A (BPA) is achieved within 2 min in the a-MnO 2 /α-Fe 2 O 3 /PMS system under optimum conditions, and the BPA degradation rate constant of 1.67 min −1 outperforms most reported Fe- and Mn- based catalysts. The results of electron paramagnetic resonance analysis, quenching tests and Raman spectroscopy analysis show that the mechanism for the a-MnO 2 /α-Fe 2 O 3 -based PMS activation is dominated by the formation of activated surface-PMS complexes. ≡Mn(Ⅳ)–OH and ≡Fe(III)–OH of a-MnO 2 /α-Fe 2 O 3 are active sites for PMS adsorption to form inner-sphere complexes (≡Mn(Ⅳ)-OOSO 3 - ) through the replacement of surface hydroxyl groups. Finally, the a-MnO 2 /α-Fe 2 O 3 exhibits a remarkable removal efficiency of over 99% for BPA in column-bed tests conducted over 600 cycles, demonstrating its immense potential for practical applications.

CAS / MDL: 80-05-7
✓ 已验证 产品关联 DOI 高影响因子
查看原文 查看 PubMed
Crystals · 2023 ·Vol. 13 ·期 5 ·810 · IF 2.7

Novel Mixed-Phase α/γ-Fe2O3 Micro-Flower Assembled with Nanosheets for Enhancing Acetone Detection

Ruonan Tian,Huai Tan,Gang Chen,Hongtao Guan,Chengjun Dong,Zongyou Yin

Although individual γ-Fe2O3and α-Fe2O3have been widely fabricated for gas sensors, their mixed phase of α/γ-Fe2O3might deliver excellent sensing properties. In this study, a facile solvothermal method was used to fabricate Fe-alkoxide. After thermal treatment, it was converted into γ-Fe2O3, α-Fe2O3and their mixed-phase α/γ-Fe2O3with a nanosheets-assembled flower-like structure. We studied the influence of calcination temperature on the phase and sensing properties on acetone detection. The α/γ-Fe2O3which annealed at 400 °C included 18% α-Fe2O3and it exhibited excellent sensing performance towards acetone compared to that of γ-Fe2O3and α-Fe2O3. It showed a response of 353 to acetone with a concentration of 200 ppm, and a low limit of detection of 0.5 ppm at 160 °C. In addition, the change in responses with acetone concentration from 50 to 200 ppm shows a good linear relationship. Moreover, this material has good reproducibility and selectivity as well as a fast response time of 22 s and recovery time of 14 s to 200 ppm. Therefore, our mixed phase of α/γ-Fe2O3possesses great prospects for acetone detection.Keywords:Fe2O3;phase;gas sensor;acetone;sensing performance

✓ 已验证 产品关联 DOI 高影响因子
查看原文 查看 PubMed
ACS Applied Nano Materials · 2023 · IF 5.9

Double-Loss Co-Ti3C2Tx/Fe2O3/PAN Hollow Fiber Composite Material for High-Efficiency Electromagnetic Absorption

Ning Chen,Shaohua Wei,Yongjun Feng,Shui Hu,Ying Tang,Wenqiang He,Yabin Zhang,Ding Cao,Zhifeng Fu

Electromagnetic absorbing materials (EMAs) are materials that irreversibly convert electromagnetic waves into another type of energy. With the development of communication technology, electromagnetic absorption materials have broad prospects in smart phones, wearable devices, and aerospace. MXenes have excellent dielectric loss properties, and the synthesis and application of MXene functional materials with magnetic properties will be one of the hotspots and focuses of future research. In this study, magnetic Co-Ti3C2Tx MXenes were prepared by molten salt etching, and Co-Ti3C2Tx/Fe2O3/polyacrylonitrile (PAN) hollow fiber composites with double-loss capability were prepared by coaxial electrospinning technology. The maximum reflection loss of the Co-Ti3C2Tx/Fe2O3/PAN hollow fiber can reach −54.62 dB at 9.86 GHz, and the effective absorption bandwidth is 6.39 GHz. The Co-Ti3C2Tx/Fe2O3/PAN hollow fibers with excellent electromagnetic absorption capability exhibit potential for efficient EMA materials due to their synergistic effect of impedance matching and magnetic/dielectric loss.

CAS / MDL: 196506-01-1
✓ 已验证 产品关联 DOI 高影响因子
查看原文 查看 PubMed
MICROCHIMICA ACTA · 2023 ·Vol. 190 ·期 5 ·1-10 · IF 5.7

Electrochemical peptide nucleic acid functionalized α-Fe2O3/Fe3O4 nanosheets for detection of CYP2C19*2 gene

Ni Yun,Chen Xiu,Ling Chen,Zhu Ziye,Yue Yao,Wang Jie,He Aolin,Liu Ruijiang

The CYP2C19*2 gene carriers and non-carriers are closely related to the dosage of clopidogrel. To correctly guide the use of clopidogrel and promote individualized therapy, an ultra-sensitive electrochemical biosensor was developed for the detection of CYP2C19*2 gene. The heterogeneous α-Fe 2 O 3 /Fe 3 O 4 nanosheets were prepared via the hydrothermal-calcination process, and the preparation parameters were optimized. The average diameter and thickness of the nanosheets were approximately 150 nm and 53 nm, respectively; and the saturation magnetization was 80.2 emu/g. The α-Fe 2 O 3 /Fe 3 O 4 @Au nanosheets were prepared by sodium borohydride reduction method, and self-assembled to the electrode surface with magnetic field. Ultra-sensitive detection of CYP2C19*2 gene was realized through the recognition ability of strong single base mismatching of peptide nucleic acid and signal amplification effect of magnetic α-Fe 2 O 3 /Fe 3 O 4 @Au nanosheets. Under optimal detection conditions, the current had a good linear correlation with the negative logarithm of CYP2C19*2 gene concentration in the range 1 pM—1 nM, and the detection limit was 0.64 pM (S/N = 3). Meanwhile, the electrochemical signals of target DNA and incomplete complementary DNA were detected. The constructed biosensor exhibited good selectivity, reproducibility, and stability, providing a promising strategy for the detection of other gene mutations by electrochemical biosensors. Graphical Abstract

CAS / MDL: 9002-98-6 51805-45-9
✓ 已验证 产品关联 DOI PubMed 高影响因子
查看原文 查看 PubMed
ELECTROCHIMICA ACTA · 2023 · IF 6.6

Upgraded lithium storage performance of defect-rich Si@C anode assisted by Fe2O3-induced pseudocapacitance

Yunfei Yao,Zhiying He,Xiangyang Xu,Yuanlin Tong,Dongsheng Chen,Chenyu Huang,Hongye Zhao

Following a flowsheet comprised of a hydrothermal reaction and a dehydration/carbonization, Si-xFe/O@C anodes featured with Fe-doping and carbon encapsulation were assembled. Comparing with pure Si, Si disseminated with in situ generated nano-scaled ferric oxide (Fe 2 O 3 ) particulates displays remarkably improved cyclic performance. Fe 2 O 3 may induce amorphization and optimize electrical conductivity, by enhancing the formation of Fe and Li 2 O amidst charging-discharging cycles. The as-derived Fe phase benefits the transport and storage of lithium-ion and electrons. Meanwhile, numerous tiny interfaces can be constructed between Fe granules and adjacent Li x Si or Li 2 O, and generate pseudocapacitance. After the carbonization of resorcinol-formaldehyde resin encapsulated on Si granules, core-shell structured Si- x Fe/O@C particulates can be assembled. Owing to the synergism of defect-rich structure, carbon layer well-wrapped thereon and interfacial pseudocapacitance, these nanocomposite anode materials exhibit long cyclic and upgraded rate performance. After 200 cycles, Si-0.42Fe/O@C anode retains a capacity of 929 mAh·g −1 at 1 A·g −1 and 735 mAh·g −1 at 2 A·g −1 . In the rate performance test operated at 5 A·g −1 , a high current density, 844 mAh·g −1 could be released. Si-0.42Fe/O@C can be charged with a specific capacity exceeding 250 mAh·g −1 over the potential range of 0.75-3 V at various current densities, demonstrating the contribution of nano-Fe pseudocapacitance effect to the energy storage of Si anodes.

CAS / MDL: 68-12-2
✓ 已验证 产品关联 DOI 高影响因子
查看原文 查看 PubMed
CHEMOSPHERE · 2023 · IF 8.8

3D porous carbon-embedded nZVI@Fe2O3 nanoarchitectures enable prominent performance and recyclability in antibiotic removal

Jianzheng Yang,Hua Tian,Jianrong Guo,Junhui He

Overcoming the instability and poor recyclability during the practical applications of contaminant scavengers is a challenging topic. Herein, a three-dimensional (3D) interconnected carbon aerogel (nZVI@Fe 2 O 3 /PC) embedding a core-shell nanostructure of nZVI@Fe 2 O 3 was elaborately designed and fabricated via an in-situ self-assembly process. The porous carbon with 3D network architecture exhibits strong adsorption towards various antibiotic contaminants in water, where the stably embedded nZVI@Fe 2 O 3 nanoparticles not only serve as magnetic seeds for recycling, but also avoid the shedding and oxidation of nZVI in the adsorption process. As a result, nZVI@Fe 2 O 3 /PC efficiently captures sulfamethoxazole (SMX), sulfamethazine (SMZ), ciprofloxacin (CIP), tetracycline (TC) and other antibiotics in water. In particular, an excellent adsorptive removal capacity of 329 mg g −1 and a rapid capture kinetics (99% of removal efficiency in 10 min) under a wide pH adaptability (2–8) are achieved using nZVI@Fe 2 O 3 /PC as an SMX scavenger. nZVI@Fe 2 O 3 /PC displays exceptional long-term stability given that it shows excellent magnetic property after it is stored in water solution for 60 d, making it an ideal stable scavenger for contaminants in an etching-resistant and efficient manner. This work would also provide a general strategy to develop other stable iron-based functional architectures for efficient catalytic degradation, energy conversion and biomedicine.

✓ 已验证 产品关联 DOI PubMed 高影响因子
查看原文 查看 PubMed
JOURNAL OF ALLOYS AND COMPOUNDS · 2019 · IF 4.175

Synthesis and electrochemical properties of α-Fe2O3 porous microrods as anode for lithium-ion batteries

Shaowei Yao,Zhiqiang Shi,Xingxiang Zhang

A new α-Fe 2 O 3 porous microrods using as an anode for lithium-ion batteries (LIBs) were prepared by a facile hydrothermal reaction and heat treatment at different temperature. The effect of calcination temperature on the structure, morphology and electrochemical performance of α-Fe 2 O 3 microrods anode materials has been systematically investigated. The results demonstrate that the calcination temperature can affect mesoporous distribution and the primary particle size of α-Fe 2 O 3 microrods and then affect the electrochemical performance. The α-Fe 2 O 3 microrods calcined at 700 °C (F700) outperformed other samples in terms of reversible capacity, cyclability, and rate capability. F700 exhibits excellent reversible capacity of 1083 mAh g −1 in the first cycle and 733 mAh g −1 after 100 cycles at 100 mA g −1 in the range of 0.01–2.5 V. Therefore, α-Fe 2 O 3 microrods can be one promising anode materials for LIBs.

✓ 已验证 产品关联 DOI 高影响因子
查看原文 查看 PubMed
JOURNAL OF MATERIALS SCIENCE · 2019 ·Vol. 54 ·期 11 ·8236-8246 · IF 3.442

Synergetic effect of Fe2O3 and BiVO4 as photocatalyst nanocomposites for improved photo-Fenton catalytic activity

Wen Yun,Zhao Yue,Guo Mingzhen,Xu Yan

Photo-Fenton reactions and the related functional nanomaterials have been widely studied for applications in wastewater treatment industry. Herein, visible-light-responsive Fe 2 O 3 nanoparticle-decorated BiVO 4 nanoplates were designed and successfully prepared through a one-pot hydrothermal route. The as-prepared Fe 2 O 3 /BiVO 4 nanocomposites exhibit excellent photo-Fenton catalytic activity toward the discoloration of methylene blue (MB) and Rhodamine B (RhB) dye molecules in the presence of H 2 O 2 . The experimental results indicate that nearly 100% of MB (100 mL, 10 mg L −1 ) and RhB (100 mL, 5 mg L −1 ) dye molecules are degraded in the presence of 1 g L −1 Fe 2 O 3 /BiVO 4 -1 (FB-1) photo-Fenton catalyst and 0.5 mL of H 2 O 2 within 20 min. The Fe 2 O 3 /BiVO 4 Fenton photocatalyst also demonstrates high reusability under visible light irradiation with λ ≥ 420 nm. The photoinduced electrons on the conduction band of BiVO 4 nanoplates can move toward the surface of Fe 2 O 3 /BiVO 4 to accelerate the reduction of Fe 3+ ; then, the as-formed Fe 2+ ions on the surface of the catalyst greatly enhance the decomposition of H 2 O 2 to form reactive · OH species for the use in photodegradation of MB and RhB dye molecules. The synergetic effect of Fe 2 O 3 and BiVO 4 reported in this work might provide more opportunity to fabricate other novel semiconductor-based Fenton nanocomposites for contamination treatments in wastewater.

CAS / MDL: 7803-55-6
✓ 已验证 产品关联 DOI 高影响因子
查看原文 查看 PubMed
Russian Journal of Physical Chemistry A · 2019 ·Vol. 93 ·期 7 ·1343-1348 · IF 0.581

Magnetically Separable and Recyclable γ-Fe2O3/HAp/Ag3PO4 Composite Microsheets: Fabrication, Characterization, and Photocatalytic Performance

Liang An,Zhao Xiaolian,Xu Chengkang,Yan Zhaoxiong,Yang Zhihua,Xu Zhihua

Abstract In this work, magnetically separable and recyclable γ-Fe 2 O 3 /HAp/Ag 3 PO 4 composite microsheets were prepared by hydrothermal and in-situ ion-exchange methods, in which photoactive Ag 3 PO 4 nanoparticles and magnetic γ-Fe 2 O 3 nanoparticles are distributed on the hydroxyapatite (HAp) microsheets. Characterization of the samples was performed by XRD, FE-SEM, EDS, FT-IR, and VSM. The photocatalytic performance of the samples was checked by investigating the degradation process of four different organic dyes under visible-light irradiation. Photocatalytic experiments reveal that all γ-Fe 2 O 3 /HAp/Ag 3 PO 4 samples show certain photocatalytic activities for the degradation of OII, and the degradation rate is different when diverse γ-Fe 2 O 3 /HAp/Ag 3 PO 4 samples are added into the OII solution. FHA-4 exhibits the highest degradation rate, and it could degrade different organic dyes, which means it has the potential to be applied into the treatment of complex wastewater containing different organic dyes. In addition, FHA-4 exhibits ferromagnetic feature, and can be easily separated from water by an external magnetic field.

CAS / MDL: 1309-37-1
✓ 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。