Materials Science and Engineering B-Advanced Functional Solid-State Materials
·
2025
·
IF 4.6
Yangyang Zhao,Haowei Li,Xiaoyu Wang,Tao Cong,Yijian Wang,Hesheng Zheng,Zhongyi Zhao,Xingchen Feng,Juntao Feng,Pei Wang,Kai Yang,Xifeng Ding
Solid oxide electrolysis cells (SOECs), featuring high current density and Faradaic efficiency, have been extensively recognized for CO 2 electrolysis abilities. However, it is a challenge to find high performance electrode materials with excellent catalytic activity and preferable stability. Herin, hetero-structured perovskite with exsolved Co-Fe nanoparticles is developed via in - situ reduction of the (Ba 0.9 K 0.1 ) 0.9 Co 0.5 Fe 0.4 Nb 0.1 O 3- δ ((BK) 0.9 CFNb). The corresponding SOEC R-(BK) 0.9 CFNb/LSGM/LSCF achieves excellent electrochemical performance with a current density of 0.813 A cm −2 at 1.5 V and 800 °C, which is 30 % higher than the counterpart with untreated (BK) 0.9 CFNb cathode. Its high catalytic activity is attributed to electron feeding effect of in situ exsolved Co-Fe nanoparticles and enhanced CO 2 adsorption with high concentration of oxygen vacancies in perovskite substrate surface. Moreover, the R-(BK) 0.9 CFNb-cell shows much better stability than parent (BK) 0.9 CFNb-cell, which is ascribed to the structural anchoring of the alloy nanoparticles. This study provide an attractive strategy for the future development of SOECs.
研究领域:
材料科学
·
能源化学
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产品关联
DOI
高影响因子
ENVIRONMENTAL RESEARCH
·
2021
·
IF 6.498
Zhendong Yu,Jiachen Ma,Jinlan Dai,Shiyu He,Xiaoyi Huang,Yuancai Lv,Yifan Liu,Chunxiang Lin,Junfeng Chen,Minghua Liu
In this study, a bimetallic composite catalyst (Co–Fe@C) was fabricated with calcination at high temperature (800 °C) by using Co-MIL-101 (Fe) as the precursor. The characterization results showed that the resulted Co–Fe@C composite mainly consisted of carbon, FeCo alloys, Fe 3 O 4 , Co 3 O 4 and FeO, and owned evident magnetism. In addition, the Co–Fe@C was employed to activate the peroxydisulfate (PDS) to degrade a representative organic pollutant ( p -arsanilic acid, p -ASA) and the main factors were optimized, which involved 0.2 g L −1 of catalyst dosage, 1.0 g L −1 of PDS dosage and 5.0 of initial pH. Under the optimal condition, Co–Fe@C/PDS system could completely degrade p -ASA (20 mg L −1 ) in 5 min. In the Co–Fe@C/PDS system, SO 4 − · , Fe(IV) and ·OH were the main species during p -ASA degradation. Under the attack of these species, p -ASA was first decomposed into phenols and then transformed into the organics acids and finally mineralized into CO 2 and H 2 O through a series of reactions like hydroxylation, dearsenification, deamination and benzene ring opening. Importantly, most of the released inorganic arsenic species (93.40%) could be efficiently adsorbed by the catalyst.
研究领域:
环境科学
·
化学工程
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产品关联
DOI
PubMed
高影响因子
Journal of Environmental Chemical Engineering
·
2021
·
IF 5.909
Peng Liu,Dengjie Zhong,Yunlan Xu,Nianbing Zhong,Guangjun He
Co/Fe co-doped porous graphite carbon (Co/Fe-PGC) nanocomposites were successfully prepared by one-step pyrolysis with CoFe-MOF, in which the Co/Fe nanoparticles were uniformly coated on porous graphite carbon derived from MOF. It was used to microelectrolysis-Fenton degrade rhodamine B through the main active substance ∙OH. The color and TOC removal rate of 100 mg/L rhodamine B reached 99.41% and 64.6%, respectively, for 30 min. Rhodamine B was degraded into small molecular organic acids, alcohols and lipids by N-demethylation and chromophore cleavage, until it was finally degraded into CO 2 and H 2 O, and no new colored organics were produced in the degradation process. The degradation process follows the first-order reaction kinetics, and its rate constant is much higher than that of the previous similar studies. The excellent catalytic performance of Co/Fe-PGC catalyst is attributed to the coupling effect of micro-electrolysis and Fenton reaction, and the acceleration of cobalt on electron transport and Fe 2+ reduction. Co 0 /Fe 0 undergoes galvanic corrosion to generate Co 2+ /Fe 2+ and H 2 O 2 , and then these products undergo Fenton reaction to generate Co 3+ /Fe 3+ and ∙OH, thus forming a circulating system of Co 3+ /Fe 3+ and Co 2+ /Fe 2+ , enhancing the activation of H 2 O 2 and ensuring the efficient degradation of RhB.
研究领域:
环境科学
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材料科学
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产品关联
DOI
高影响因子
APPLIED CATALYSIS B-ENVIRONMENTAL
·
2023
·
IF 22.1
Hexiang Wang,Chenliu Tang,Luwei Wang,Zhirong Sun,Xiang Hu
A MOF-derived carbon material containing CoFe alloy (Co/Fe@NPC-500) by calcining N-doped Co/Fe bimetallic MOF at a lower temperature was successfully synthesized as a cathode in electro-Fenton process for ceftazidime (CAZ) degradation. The presence of Co could accelerate the transfer of electrons from C atoms of carbon material to Fe, thus increasing the content of low-valent metals in the material, which had been demonstrated by characterizations and density functional theory (DFT) calculations. Thanks to the integrity of the MOF structure, the synergistic effect between Fe and Co, Co/Fe@NPC-500 cathode showed efficient removal efficiency for CAZ completely removed within 60 min and obtained a total organic carbon (TOC) removal rate of 52.1% at 90 min. Besides, based on the results of HPLC-MS and DFT calculations, the degradation pathway of CAZ was proposed. This study provides some useful information for the preparation of MOF-derived carbon materials containing low-valent metals for electro-Fenton process.
研究领域:
环境科学
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材料科学
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化学工程
✓ 已验证
产品关联
DOI
高影响因子
Journal of Environmental Chemical Engineering
·
2024
·
IF 7.4
Hui Li,Xinlei Ren,Wenxue Pan,Shiting Zhu,Jin Zhang,Zhiyuan Yang,Liu Qian,Yueying Wang,Yujing Huang,Lin Guo,Minghui Xiang
The reasonable control of the structure of metal–organic frameworks (MOFs) is a promising strategy for improving their peroxymonosulfate (PMS) activation activity. In this study, ZIF-67 @ZIF-8 was used as a template to prepare bimetallic core–shell Co-Fe@NC via Fe doping and high-temperature carbonization . Co-Fe@NC maintained the core–shell structure of the original MOF, in which cobalt was uniformly distributed in the nitrogen-doped graphite carbon skeleton and the surface of the graphite carbon skeleton was covered with iron. With the synergistic effect of the nitrogen-doped graphite carbon skeleton, iron, and cobalt, 100% of tetrabromobisphenol S (TBBPS) was removed in 60 min with k obs = 0.062 min −1 in Co-Fe@NC-0.2/PMS system. The addition of iron increased the graphitization degree with I D /I G value increased from 0.98 (Co@NC) to 1.034 (Co-Fe@NC-0.2) and electron transfer rate of the carbon skeleton. Besides, the Co leaching was effectively attenuated from 1.86 mg/L(Co@NC) to 0.78 mg/L (Co-Fe@NC-0.2) by the core-shell structure and bimetal strategy. Both O 2 · - and 1 O 2 contributed to the degradation of TBBPS according to quenching experiments. TBBPS was deeply degraded into small-molecule compounds through three degradation pathways by the Co-Fe@NC-0.2/PMS system. This study provides a new strategy for designing highly efficient bimetal–carbon composites for environmental remediation.
研究领域:
环境科学
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材料科学
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化学工程
✓ 已验证
产品关联
DOI
高影响因子
COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS
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2022
·
IF 5.518
Jun Liu,Hui Wang,Meng-Jie Chang,Wen-Juan Li,Wen-Yao Zhu,Ge Bai,Liu-Qing Yang,Hui-Ling Du,Zhen-Min Luo,Ting Shang
Metal ion doping is an efficient method to achieve high photocatalytic performance of semiconductors. However, the current synthetic methods by using inorganic salts as doped sources in the precursor reaction system might suffer from ion waste and second pollution. Herein, we developed a novel method by employing electrospun nanofibers as ion reservoir to release metal ions for the synthesis of ion-doped semiconductors with high photocatalytic activity . As demonstrated, Co/Fe co-doped BiOCl photocatalyst (Co/Fe-BOC) was facilely prepared in the presence of CoFe 2 O 4 nanofibers as Co and Fe ion reservoir via a simple solvothermal method . Compared with BiOCl, the resulted Co/Fe-BOC shows increased specific surface area, visible light response as well as separation and transportation efficiencies of photogenerated carriers. Thus, the Co/Fe-BOC exhibits significantly enhanced visible light photocatalytic activity to degrade 99.4% rhodamine B (RhB) within 4 min. This new doping approach not only avoids the ion waste and pollution during the reaction process but also facilitates the separation of the photocatalyst. Moreover, the CoFe 2 O 4 nanofibers could be repeatedly used as ion reservoir to prepare high-performance Co/Fe-BOC. This nanofiber-based ion doping approach provides a novel, universal and promising insight to obtain doped semiconductors with high photocatalytic activity.
研究领域:
材料科学
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环境科学
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化学
✓ 已验证
产品关联
DOI
高影响因子
JOURNAL OF COLLOID AND INTERFACE SCIENCE
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2020
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IF 7.489
Zhe Li,Shudi Mao,Ying Yang,Zhuo Sun,Ran Zhao
Capacitive deionization (CDI) is considered one of the most promising desalination technologies for obtaining fresh water from saline water. In this work, we synthesized a hollow core–shell Co-MOF@Fe/Co-LDH (Co-Fe-LDH) material by developing a strategy to simultaneously grow Co/Fe-LDH on the surface of a Co-MOF precursor in situ. Owing to the increase in the specific surface area of the hollow structure and the Faradaic process of a layered double hydroxide (LDH), the Co-Fe-LDH material exhibits high electrical double layer (EDL) capacitance and pseudocapacitance, which significantly improves the salt adsorption of the material during CDI (34.2 mg/g in a 600 mg/L NaCl solution at 1.2 V). The adsorption for NaCl in this work is approximately 2.5 times the maximum salt adsorption capacity (SAC) of LDH materials applied in nonmembrane CDI (NMCDI). This work may provide a promising model for the application of hollow LDH materials that exhibit pseudocapacitance in CDI.
研究领域:
材料科学
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环境工程
·
海水淡化技术
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产品关联
DOI
PubMed
高影响因子
Journal of Energy Chemistry
·
2022
·
IF 13.599
Weizhen Xie,Binglin Chen,Wenlong Jia,Huai Liu,Zheng Li,Shuliang Yang,Xing Tang,Xianhai Zeng,Yong Sun,Xixian Ke,Tianyuan Li,Huayu Fang,Lu Lin
Developing an efficient and easily available catalyst for the selective conversion of biomass-derived 5-hydroxymethylfurfural (HMF) into furan-2,5-dimethylcarboxylate (FDMC), a valuable biomass-based monomer, remains a high demand but formidable challenge. Herein, a facile strategy for the synthesis of N-doped carbon-supported Co/Fe bimetallic catalyst (CoFe-NC) was developed, which provided an outstanding FDMC yield of 93% in a batch reactor (base-free, 80 °C, 2 bar O 2 , 4 h). Interestingly, CoFe-NC also gave a high FDMC yield of 91% under continuous-flow conditions for 80 h (5 bar O 2 , 80 °C, GHSV 1320 h −1 , LHSV 0.6 h −1 , base-free). Notably, it is the first time that a non-noble catalyst gave such a high FDMC yield under continuous-flow conditions. The introduction of Fe could greatly improve both the electron intensity of Co-N x species and basicity of the catalyst, which endowed CoFe-NC with improved O 2 activation capacity and enhanced dehydrogenation activity for the oxidation-esterification of HMF. This work delineates the efficient strategy on the construction of N-doped carbon-supported non-noble catalyst, which might open a new avenue for developing highly efficient catalyst for FDMC production.
研究领域:
催化化学
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生物质转化
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材料科学
✓ 已验证
产品关联
DOI
高影响因子
Journal of Environmental Chemical Engineering
·
2021
·
IF 5.909
Ming-feng Sun,Ting Wang,Li-guang Wu,Yu-xing Wang
This study attempted to enhance the permeation and antifouling performance of polyvinylidene fluoride (PVDF) ultrafiltration membranes. Reverse microemulsion containing cobalt and iron (Co–Fe) bimetallic hydroxide nanoparticles was blended with the PVDF membranes to construct a novel PVDF hybrid membrane. The permeation performance, antifouling property, and long-term operational stability of the hybrid membranes were evaluated via ultrafiltration process of water flux and bovine serum albumin (BSA) rejection. Structural characterization showed that the protection endowed by reverse microemulsion made the hydroxide nanoparticles to distribute uniformly in the PVDF polymeric matrix. The introduction of well-distributed bimetallic hydroxide nanoparticles substantially improved the pore structures and hydrophilicity of the PVDF hybrid membranes, thereby enhancing their permeation performance and antifouling property. The optimal water flux of the PVDF hybrid membranes (MD-10) reached 328 L·m −2 ·h −1 and was 5.4-fold higher than that of neat PVDF. Moreover, the MD-10 membrane had a high a high BSA rejection rate (91.04%). After four cycles of successive fouling-cleaning processes, the water flux of the MD-10 membrane still exceeded 160 L·m −2 ·h −1 and was fourfold higher than that of neat PVDF. However, excessive amounts of the microemulsion could not be uniformly mixed with the PVDF membranes, thereby decreasing the permeation and antifouling performance of the PVDF hybrid membranes.
研究领域:
膜科学
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纳米技术
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材料科学
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环境工程
✓ 已验证
DOI
高影响因子
APPLIED CATALYSIS A-GENERAL
·
2022
·
IF 5.723
Xin Jin,Yajun Huang,Song He,Guanyu Chen,Xinyu Liu,Chunxiang He,Chunhua Du,Qilin Chen
Sulfate radical-based advanced oxidation processes (SR-AOPs) were frequently utilized for the degradation of various organic pollutants due to their efficient and clean advantages. In this work, Co-Fe based Prussian blue analogues (PBA) nanoparticles were firmly immobilized on nickel foam (NF) as a novel activator for peroxymonosulfate (PMS), and the complete degradation of tetracycline (TC) was achieved within 20 min under optimal conditions. The TC degradation efficiency of samples were investigated under various factors including Co loading, PMS dosage, initial TC concentration, pH, and inorganic anions. The mechanism for PMS activation indicated that reactive oxygen species including sulfate radicals, hydroxyl radicals, superoxide radicals and singlet oxygen contributed to TC degradation. The possible pathway of TC degradation was investigated by liquid chromatography-mass spectroscopy. This work presented a new combination of efficient and easily recoverable supported catalysts and provided useful information for the wastewater treatment .
研究领域:
环境科学
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化学工程
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材料科学
·
水处理
✓ 已验证
产品关联
DOI
高影响因子
CARBOHYDRATE POLYMERS
·
2020
·
IF 7.182
Chen Hou,Wenqiang Chen,Linhui Fu,Sufeng Zhang,Chen Liang,Yang Wang
In this study, a sulfate radical-advanced oxidation process (SR-AOP) was proposed by utilizing a bimetallic Co/Fe metal-organic frameworks/cellulose nanofiber membrane (Co/Fe bi-MOFs/CNF) as a catalyst for TBBPA degradation. Sulfate radicals (SO 4 –) and hydroxyl radicals (OH · ) were generated through the activation of peroxymonosulfate (PMS) by Co/Fe bi-MOFs/CNF. Co/Fe bi-MOFs/CNF was prepared by a facile solvothermal method and vacuum filtration. CNF acted as a natural substrates material to relieve the agglomeration of loaded MOFs . Additionally the composite membranes was easily separated from the reaction solution. The properties of the composite materials and the main factors that influenced TBBPA degradation were elucidated in detail, along with the TBBPA degradation intermediates, recyclability, and TBBPA degradation pathway. Almost 100 % of TBBPA was degraded within 30 min under optimal conditions, and the rate constant was determined to be 0.764 min −1 . Furthermore, the degradation rate of the composite membrane was 60 % after 4 cycles.
研究领域:
环境科学
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材料科学
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化学工程
·
废水处理
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产品关联
DOI
PubMed
高影响因子
ChemSusChem
·
2019
·Vol. 12
·期 21
·4791-4798
·
IF 7.804
Xiaohao Liu,Chenguang Wang,Ying Zhang,Yan Qiao,Yang Pan,Longlong Ma
Graphical Linked in to lignin : 4-Alkylphenol is produced selectively over a magnetic Co 1 –Fe 0.1 @NC catalyst from real lignin oil as feedstock, which is obtained by a “lignin-first” strategy from raw biomass. The incorporation of Fe attenuates the adsorption of 4-alkylphenol to the catalyst, which inhibits the further hydrogenation of 4-alkylphenol to 4-alkylcyclohexanol. Lignin valorization to produce high-value chemicals selectively is an enormous challenge in biorefinery. In this study, 4-alkylphenol, formed by breaking the robust C aryl −OCH 3 bonds solely with the retention of other structures in lignin-derived methoxylalkylphenols, was produced selectively over a Co 1 –Fe 0.1 @NC catalyst from real lignin oil as feedstock, which was obtained by a “lignin-first” strategy from either birch or cornstalk. A yield of 64.7 or 88.3 mol % of 4-propylphenol was obtained if birch lignin oil or eugenol was used as the substrate, respectively. The catalysts were characterized by using methods that include Brunauer–Emmett–Teller measurements, XRD, X-ray photoelectron spectroscopy, high-resolution transmission electron microscopy, high-angle annular dark-field scanning transmission electron microscopy, energy-dispersive X-ray spectroscopy, and temperature-programmed desorption with synchrotron vacuum ultraviolet photoionization mass spectrometry. The results of catalyst characterization and comparison experiments indicated that CoN x was the main active phase for demethoxylation and hydrogenation, and the incorporation of Fe weakens the adsorption of 4-propylphenol to the catalyst, which inhibits the excessive hydrogenation of 4-propylphenol. This work shows the potential to produce high-value-added 4-alkylphenol from renewable raw biomass.
研究领域:
化学工程
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催化
·
可再生能源
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绿色化学
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材料科学
✓ 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）