APPLIED CATALYSIS B-ENVIRONMENTAL
·
2025
·
IF 21.1
Jie Liu,Xinru Wei,Shan Lu,Ningyuan Song,Yanru Liu,Shu Yang,Fangxu Dai,Yunmei Du,Lei Wang
How to skillfully enhance the OH - binding energy of the hydrophilic site to accelerate water decomposition and avoid OH - poisoning is a huge challenge for achieving efficient alkaline HER kinetics. Therefore, the Ru-Fe 2 P/Re 3 P 4 model was designed from the perspective of coordinating the binding energy and spillover path of OH - . Density functional theory (DFT) disclosed that Re and Ru atoms act as hydrophilic sites and hydrogen evolution sites, respectively, to synergistically promote alkaline HER. In addition, the Ru dopant reduced the water dissociation energy barrier by enhancing the OH - binding energy of the Re hydrophilic sites. Meanwhile, Fe atoms with stronger OH - binding energy exhibited the OH - detoxification effect by promoting the OH - dynamic spillover from the Re sites. Given these, a unique Ru-ReFeP/IF-Q electrode was prepared by the ‘vapor phase phosphorization-quenching Ru doping’ strategy. As anticipated, the Ru-ReFeP/IF-Q electrode, driven by the Re-Ru-Fe alkaline hydrogen evolution reaction (HER) mechanism, only requires an overpotential of 172 mV at the industrial-level current density of 1 A cm −2 . The reinforced signal peaks attributed to Ru-H and Fe-OH species in the in-situ Raman spectra confirmed the detoxifying effect of Fe sites in avoiding OH - poisoning at hydrophilic active sites. In summary, this work provides a novel design idea for accelerating alkaline HER kinetics from the perspective of synergistically optimizing the binding energy and spillover path of OH - byproducts.
研究领域:
电催化
·
材料化学
·
物理化学
·
能源科学
·
纳米催化
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表面科学
✓ 已验证
产品关联
DOI
高影响因子
FIBERS AND POLYMERS
·
2021
·Vol. 22
·期 2
·345-353
·
IF 2.153
Liu Jun,Sun Meng,Chang Meng-Jie,Fan Si-Meng,Hui Qian,Ni Fu-Rong,Yuan Bin
Novel CoFe 2 O 4 /MIL-100(Fe) (CFO/MIL-100(Fe)) core/shell nanofibers were prepared by successive ionic layer adsorption and reaction (SILAR) assembly of MIL-100(Fe) on electrospun CoFe 2 O 4 nanofibers. The MIL-100(Fe) shells were constructed on the dispersed CoFe 2 O 4 fiber surface with high uniformity, homogeneous thickness and high stability. Due to the inherent porosity of MIL-100(Fe), a higher specific surface area of 225.77 m 2 /g is achieved for the CFO/MIL-100(Fe)-10 sample. The formed CFO/MIL-100(Fe) catalysts exhibit high catalytic activity towards degradation of rhodamine B (RhB) under visible light irradiation. The photocatalytic activity remains above 77 % within 60 min illumination after four cycles. Due to the simple synthetic method, highly uniform structure, strong magnetic recoverable, as well as good photocatalytic performance, the obtained CFO/MIL-100(Fe) core/shell nanofibers could be promising photocatalysts for practical application.
研究领域:
材料科学
·
环境科学
✓ 已验证
DOI
高影响因子
APPLIED SURFACE SCIENCE
·
2025
·
IF 6.9
Di Wang,Jing Wang,Yiqiang Wu,Delin Sun,Wenlei Wang
Transition metal ions and non-metal co-doped carbon-based materials have attracted extensive attention due to their unique properties and excellent catalytic effect. Fe 2 O 3 /TiO 2 @Fe/Ti-N-C multifunctional photocatalyst with Fe-Ti alloy and abundant nitrogen defects was reported. The photocatalytic results showed that the removal rates of Cr (VI), Congo red (CR) and levofloxacin (LFX) in water by Fe 2 O 3 /TiO 2 @Fe/Ti-N-C were 88.46, 96.71 and 99.06 %, respectively. The photoelectric test results show that bimetallic conjugated structure of Fe and Ti can effectively increase the light absorption range and accelerate the carrier separation. N-defects can significantly increase the lifetime and concentration of photogenerated holes, thereby improving the catalytic efficiency of the photocatalyst. The single factor experiments proved that the optimal pH for the degradation of Cr(VI), CR and LFX by Fe 2 O 3 /TiO 2 @Fe/Ti-N-C was 1, 11 and 9, respectively. In addition, Ca 2+ and Mg 2+ promoted the degradation of Cr(VI) and inhibited the degradation of CR and LFX. SO 4 2- inhibited the degradation of Cr(VI) and promoted the degradation of CR and LFX. Cl - inhibited the degradation of Cr(VI), CR and LFX. This study elucidates the mechanism of N-defects and bimetallic sites in photocatalytic reactions, and provides theoretical support for efficient removal of heavy metals and organic pollutants in water.
研究领域:
环境科学
·
材料科学
✓ 已验证
产品关联
DOI
高影响因子
INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH
·
2020
·
IF 3.573
Yanshu Luo,Bingqiong Tan,Xianghui Liang,Shuangfeng Wang,Xuenong Gao,Zhengguo Zhang,Yutang Fang
MIL-100(Fe) has been proven to have good hydrothermal stability and high vapor uptake and is considered as a promising dehumidification material. However, reduction of the production cost and assembly of the adsorbent and glass fiber paper substrate into the MIL-100(Fe) monolith are challenging. This work presented a dry gel conversion strategy for the rapid synthesis of the MIL-100(Fe) monolith at low temperatures. The porosity and crystalline phase of the products obtained under different crystallization temperatures and times were carefully studied. XRD and SEM characterization indicated that the MIL-100(Fe) crystal could be conveniently synthesized on the substrate at a low temperature of 50–70 °C and in a short time of 2–6 h. The spherical particles assembled from crystals dispersed evenly and tightly on the glass fiber paper. The synthesized MIL-100(Fe) monolith had a thickness of about 270 μm and a MIL-100(Fe) loading of 77.7%. Dynamic and static water vapor adsorption tests revealed that the monolithic adsorbent obtained at 50 °C for 6 h had the largest vapor saturation adsorption capacity (0.581 g/g) and the fastest adsorption rate. Moreover, the monolith owned a low regeneration temperature (below 80 °C) and a satisfactory cycle stability. Convenient equipment, mild synthetic conditions, low renewable energy consumption, and good performance will promote its application in the rotary dehumidification system.
研究领域:
材料科学
·
化学工程
✓ 已验证
DOI
高影响因子
JOURNAL OF THE ELECTROCHEMICAL SOCIETY
·
2021
·Vol. 168
·期 9
·090512
·
IF 4.316
Yuebing Wang,Dunpeng Yang,Aling Chen,Qingfeng Yi
The development of an efficient, stable and low-cost cathode catalyst is necessary for the practical application of Zn-air batteries. In this paper, Fe3+/Co2+ ions were in situ incorporated into polydopamine during the polymerization of dopamine on the surface of the SiO2 spheres. After subsequent pyrolysis and leaching SiO2, the products loaded with different metals (NHCS-Fe, NHCS-Co, NHCS-Fe1Co0.6, NHCS-Fe1Co4, NHCS-Fe1Co10) were obtained. The samples possess a typical hollow carbon sphere (HCS) structure and show efficient oxygen reduction reaction (ORR) performance under neutral and alkaline conditions. Especially in the neutral electrolyte, the NHCS-Fe exhibits the comparable electrochemical catalytic activity to the commercial Pt/C. For NHCS-Fe, its ORR half-wave potential in neutral and alkaline media is 0.78 V and 0.83 V respectively. Corresponding neutral Zn-air battery reveals a maximum power density of 118.8 mW·cm−2, while they are respective 0.82 V and 46.99 mW·cm−2 for Pt/C. Alkaline Zn-air battery with NHCS-Fe releases a maximum power density of 262.4 mW·cm−2, displaying superior performance to Pt/C. Our work is instructive for the synthesis of novel ORR catalysts with outstanding activity by a versatile synthesis strategy.
研究领域:
材料科学
·
电化学
✓ 已验证
DOI
高影响因子
CHEMICAL ENGINEERING JOURNAL
·
2015
·
IF 4.321
Xiaori Fu,Xiaogang Gu,Shuguang Lu,Minhui Xu,Zhouwei Miao,Xiang Zhang,Yacong Zhang,Yunfei Xue,Zhaofu Qiu,Qian Sui
In this study, the application of sodium percarbonate (SPC) catalyzed by various chelated-Fe(II) to stimulate the degradation of benzene in groundwater remediation was investigated. Effective oxidation of benzene was achieved in CIT/SPC/Fe(II) and OA/SPC/Fe(II) systems. The reaction mechanism for benzene degradation in CIT/SPC/Fe(II) and OA/SPC/Fe(II) systems was elucidated by free radical probe compound tests, free radical scavenger tests and electron paramagnetic resonance (EPR) analysis. And hydroxyl radical (HO ) and superoxide anion radical ( O 2 - ) were confirmed as the predominant species responsible for benzene degradation. Besides, the effects of various factors, such as the solution characteristics including the presence of anions (Cl − , HCO 3 − , SO 4 2− and NO 3 − ), natural organic materials (NOM), and the initial solution pH on benzene degradation were also evaluated. The influences caused by SO 4 2− , NO 3 − , Cl − and NOM were negligible, but HCO 3 − anion had a slightly inhibitive effect in low concentration (1 mM) and an apparently inhibitive effect in high concentration (10–100 mM). However, the additions of CIT and OA eliminated the adverse influence of HCO 3 − and ensured a high benzene degradation efficiency at wider pH range. Finally, results obtained in actual groundwater test strongly demonstrated that Fe(II)-CIT and Fe(II)-OA catalyzed SPC systems are applicable for the remediation of benzene-contaminated groundwater in practice.
研究领域:
环境科学
·
化学
✓ 已验证
产品关联
DOI
高影响因子
APPLIED CATALYSIS B-ENVIRONMENTAL
·
2014
·
IF 6.007
Qi Huang,Menghua Cao,Zhihui Ai,Lizhi Zhang
In this study, an environmentally benign polyaminocarboxylic ligand diethylenetriamine pentacetate (DTPA) was first used to promote the aerobic 4-chlorophenol (4-CP) degradation with Fe@Fe 2 O 3 core–shell nanowires, and then compared with the most used counterpart ethylenediamine tetraacetate (EDTA) of poor biodegradability. Although the 4-CP removal rate in the Fe@Fe 2 O 3 /DTPA/Air system was slower owing to the preferential degradation of DTPA, the total organic carbon removal rate in the Fe@Fe 2 O 3 /DTPA/4-CP/Air system was much faster than that in the Fe@Fe 2 O 3 /EDTA/4-CP/Air system. We interestingly found that hydroxyl radicals could more easily react with DTPA to produce DTPA radicals than with EDTA to produce EDTA radicals. Ligands (DTPA or EDTA) could significantly accelerate the hydroxyl radicals production with Fe@Fe 2 O 3 , while more hydroxyl radicals were generated in the Fe@Fe 2 O 3 /DTPA/Air system. We also employed gas chromatography-mass spectrometry and ion chromatography to detect organic intermediates and chloride ions to probe the 4-chlorophenol degradation pathways, and found its degradation pathways were dependent on the reactive oxygen species generated in the different systems. This study can clarify the roles of polyaminocarboxylic ligands on the molecular oxygen activation with nanoscale zero-valent iron, and also provide a green chlorophenols removal method.
研究领域:
环境科学
·
化学
✓ 已验证
产品关联
DOI
高影响因子
JOURNAL OF COLLOID AND INTERFACE SCIENCE
·
2021
·
IF 8.128
Hongda Li,Honggao Deng,Shaonan Gu,Chenpu Li,Boran Tao,Shumin Chen,Xiong He,Guofu Wang,Wenfeng Zhang,Haixin Chang
The “FeMo cofactors” in biological nitrogenase play a decisive role in nitrogen reduction. Herein, a novel bionic Fe/Mo bimetallene was applied in photocatalytic nitrogen reduction. The surface coating Fe/Mo bimetallene of Bi 2 Mo 0.3 W 0.7 O 6 (BMWO) nanocrystals could effectively promote the separation and transportation of photogenerated carriers by multi–electron redox reactions and deliver 2.8 times longer photo–carrier lifetime. Consequently, the nitrogen fixation activity of Fe/Mo bimetallene–coated BMWO nanocrystal photocatalyst was obviously enhanced (218.93 μmol g –1 h −1 ), which was about 4.8 times that of unmodified BMWO nanocrystals. This work provides a novel approach to design bionic Fe/Mo bimetallene–modified inorganic semiconductor photocatalysts for nitrogen reduction.
研究领域:
材料科学
·
催化化学
·
环境科学
✓ 已验证
DOI
高影响因子
JOURNAL OF COLLOID AND INTERFACE SCIENCE
·
2025
·
IF 9.7
Mengyue Qi,Huamei Tong,Gaojie Li,Xinyu Zheng,Yu Liu,Cheng Ye,Zaoxue Yan,Deli Jiang
Designing and development of electrocatalysts with high catalytic capacity and stability for oxygen evolution reaction (OER) is significant for sustainable water splitting. In this study, we rationally designed Fe-doped Co 2 RuO 4 /RuO 2 heterostructure electrocatalysts on nickel foam (NF) through mixture hydrothermal, ion exchanging, and calcining methods. The synergistic effect between the Fe-Co 2 RuO 4 /RuO 2 heterogeneous interfaces can result in superior inherent activity. Meanwhile, the unique nanosheet on nanosheet structure delivers abundant exposed active sites, leading to improved catalytic activity. The resultant Fe-Co 2 RuO 4 /RuO 2 heterostructured catalysts possessed superior OER property, attaining a current density of 50 mA cm −2 with only 253 mV overpotential in 1.0 M KOH alkaline solution, and demonstrating good durability with continuous operation for up to 50 h. This research provides robust support for the research and development of RuO 2 -based electrocatalysts through effective interface engineering and doping strategies, and opens up new avenues for the industrial application of water splitting technology.
研究领域:
材料科学
·
能源化学
✓ 已验证
产品关联
DOI
PubMed
高影响因子
JOURNAL OF ELECTROANALYTICAL CHEMISTRY
·
2021
·
IF 4.464
Fuad Abduro Bushira,Shimeles Addisu Kitte,Haijuan Li,Lirong Zheng,Ping Wang,Yongdong Jin
Simultaneous highly sensitive and accurate detection of dopamine (DA) and uric acid (UA) is of great importance since they are important biomolecules that are commonly coexisted in the human body and play a crucial role in numerous physiological and pathological features. In this work, Fe-N 5 single atom catalyst (SAC) supported on graphene was firstly employed for simultaneous electrochemical detection DA and UA. Owing to its unique electronic structure and abundant active sites, under optimal conditions, the enzyme-like Fe-N 5 SAC constructed electrochemical (bio)sensor exhibits excellent linear characteristic responses in the range of 0.005–500 and 0.01–480 µM, as well as the low limit of detection of 0.007 and 0.027 nM for DA and UA, respectively. More critically, the developed electrochemical system shows promising merits of exceptional stability, good repeatability, and, consequently, it was successfully applied for simultaneous sensitive detection of DA and UA in human serum samples.
研究领域:
生物医学工程
·
分析化学
✓ 已验证
DOI
高影响因子
APPLIED ORGANOMETALLIC CHEMISTRY
·
2024
·
IF 3.7
Yi Jing Jia,Jin Quan Tao,Hao Ran Liu,Wen Bin Huang,Rongpeng Yao,Miaomiao Niu,Rongrong Li,Qiang Wei,Ya Song Zhou
To enhance the CO 2 hydrogenation activity and low-carbon olefin selectivity of Fe-based catalysts, a strategy involving the use of metal promoters to modulate the structure of active metal centers in catalyst preparation was proposed. The incipient wetness impregnation method was used to introduce modifying agents K and/or Co into the Fe/Al 2 O 3 catalyst. Characterization techniques such as XRD, BET, SEM, HRTEM, H 2 -TPR, XPS, CO 2 -TPD, NH 3 -TPD, and TG were employed to investigate the effects of the modifying agents on the dispersion, reducibility, electronic properties, and acid–base properties of active metal species. Furthermore, the influence of K and Co modification on the CO 2 hydrogenation activity and low-carbon olefin selectivity of Fe/Al 2 O 3 catalysts was explored. The results revealed that the introduction of K generated more basic sites and electron-rich active metal centers in the catalyst, facilitating the adsorption and activation of CO 2 , while suppressing the hydrogenation of olefins and the formation of methane, thus improving the selectivity towards low-carbon olefins. Co promoter facilitated the dispersion of Fe species, exposing more active sites and enhancing the FTS reaction activity, leading to more CO being converted into C 2+ hydrocarbon products. Under the synergistic effect of K and Co, the CO 2 conversion activity of the Fe-based catalyst significantly increased, achieving a CO 2 conversion rate of 37%, while the selectivity towards C 2 -C 4= increased to 31.9%.
研究领域:
催化化学
·
材料科学
✓ 已验证
产品关联
DOI
高影响因子
Journal of Functional Biomaterials
·
2024
·Vol. 15
·期 7
·185
·
IF 5
Yu Wu,Sen Xu,Fengjuan Ding,Weibing Zhang,Haiyan Liu
In this work, a new type of FE-1 COF material is prepared by a reversible imine condensation reaction with diaminoferrocene and diaminodiformaldehyde as materials. The material is connected by imine bonds to form a COF skeleton, and the presence of plenty of nitrogen-containing groups gives the material good hydrophilicity; the presence of metal Fe ions provides the material application potential in the enrichment of phosphopeptides. According to the different binding abilities of N-glycopeptide and phosphopeptide on FE-1 COF, it can simultaneously enrich N-glycopeptide and phosphopeptide through different elution conditions to realize its controllable and selective enrichment. Using the above characteristics, 18 phosphopeptides were detected from α-casein hydrolysate, 8 phosphopeptides were detected from β-casein hydrolysate and 21 glycopeptides were detected from IgG hydrolysate. Finally, the gradual elution strategy was used; 16 phosphopeptides and 19 glycopeptides were detected from the α-casein hydrolysate and IgG hydrolysate. The corresponding glycopeptides and phosphopeptides were identified from the human serum. It proves that the FE-1 COF material has a good enrichment effect on phosphopeptides and glycopeptides.
研究领域:
分析化学
·
蛋白质组学
·
生物化学
✓ 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）