JOURNAL OF HAZARDOUS MATERIALS
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2020
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IF 9.038
Qi Yang,Dan Chen,Libing Chu,Jianlong Wang
In present work, we studied a novel Fe/C nanomaterial fabricated using Fe-based metal organic frameworks (MOFs) as precursors through thermal pyrolysis to catalyze gamma irradiation-induced degradation of antibiotics, cephalosporin C (CEP-C) and sulfamethazine (SMT) in aqueous solution. The MOFs-derived Fe/C nanomaterials (DMOFs) had the regular octahedrons structure of MOFs and contained element C, Fe and O, while Fe° with a fraction of Fe 3 O 4 and Fe 2 O 3 were identified. Results showed that DMOFs addition could accelerate the generation of OH during gamma irradiation, while the intermediates of bonds cleavages of antibiotic molecules and OH addition were identified. DMOFs were more effective to improve the decomposition of antibiotic having the higher adsorption capacity like SMT. The degradation rate of CEP-C and SMT increased by 1.3 times and 1.8 times, and TOC reduction at 1.0 kGy reached 42 % and 51 %, respectively by gamma/DMOFs treatment, while only 20.2 % (CEP-C) and 4.5 % (SMT) of TOC reduction were obtained by γ-irradiation alone. The crystal structure, functional groups and magnetism of DMOFs changed slightly after gamma irradiation, which made it possible to be reused. DMOFs were promising to enhance the degradation of antibiotics during gamma irradiation.
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
PubMed
高影响因子
CHEMICAL ENGINEERING JOURNAL
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2022
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IF 16.744
Xiuting Wu,Caishuo Yin,Mengfan Zhang,Yaqian Xie,Jingjing Hu,Ruilai Long,Xianming Wu,Xianwen Wu
The materials driven by metal-organic frameworks (abbreviated MOFs) and their derivatives can prevent self-aggregation and inherit their original morphology. The adjustable porosity features of pristine MOFs can achieve an outstanding electrochemical performance. Herein, we report a novel cathode material of V 2 O 3 /V 3 O 5 /Zn 2 VO 4 @NC composite (abbreviated ZnVO-800) with hierarchical structure and heterojunction derived from zeolitic imidazolate framework-8 (abbreviated ZIF-8) by self-sacrificed route. The ZnVO-800 cathode undergoes two- step reactions in relation with H + and Zn 2+ synergistic insertion/extraction and exhibits rapid Zn 2+ diffusion kinetics and high electrochemical activity after activation. Specifically, the reversible capacity of the activated electrode reaches up to 314.0 mAh·g −1 at the initial discharge of 0.5A·g −1 as it applies to aqueous zinc ion batteries (abbreviated AZIBs). Remarkably, it exhibits a high reversible capacity of 100.1 mAh·g −1 and an excellent cycleability with a capacity retention of 90.8 % even after 3000 cycles. The electrochemical mechanism reveals that the ZnVO-800 with poor electrochemical characteristics is transformed into Zn x V 2 O 5 ·nH 2 O with high electrochemical activity by in-situ electrochemical activation process. Subsequently, Zn 2+ /H + is reversibly inserted/extracted in the cathode material. The heterojunction with hierarchical structure can not only increase the contact interface between electrolyte and cathode materials, but also shorten the ions diffusion path, which is conducive to rapid dynamics and long-term cycleability.
研究领域:
材料科学
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电化学
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能源存储
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产品关联
DOI
高影响因子
CATALYSIS LETTERS
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2019
·Vol. 150
·期 3
·815-825
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IF 2.372
Huang Yan-Feng,Zhang Lu,Ma Li,Li Ying,Zhong Chongli
Abstract Fe 3 O 4 @Cu/C and Fe 3 O 4 @CuO composites were achieved using nanoparticle-encapsulated MOFs Fe 3 O 4 @HKUST-1 as both a precursor and a self-sacrificing template. Fe 3 O 4 @HKUST-1 was thermally converted into magnetic Fe 3 O 4 @Cu/C and Fe 3 O 4 @CuO composites in different atmosphere (N 2 and air). The resulting composites not only kept superparamagnetic characteristics, but also exhibited improved peroxidase-like catalytic activity and high stability when compared to the precursor Fe 3 O 4 @HKUST-1. The morphology, crystal structure, magnetic and porous properties of Fe 3 O 4 @Cu/C and Fe 3 O 4 @CuO composites were characterized, and the kinetics parameters and the influence factors on the peroxidase-mimicking activity such as temperature, pH and H 2 O 2 concentration were evaluated. On account of the excellent peroxidase-like activity, the as-prepared Fe 3 O 4 @Cu/C and Fe 3 O 4 @CuO composites were successfully used for the catalytic removal of methylene blue (MB) dye with H 2 O 2 oxidant. This work provides an effective way to fabricate highly reactive MOFs-derived biomimetic catalysts, which have potential applications in bioassays and pollutant degradation. Graphic Abstract Fe 3 O 4 @Cu/C and Fe 3 O 4 @CuO composites were achieved using Fe 3 O 4 nanoparticle-encapsulated HKUST-1 as self-sacrificial templates and demonstrated excellent peroxidase-like activity.
研究领域:
材料科学
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催化化学
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环境科学
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DOI
高影响因子
CARBON
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2021
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IF 9.594
Zhen Xiang,Xiang Zhang,Yuyang Shi,Lei Cai,Jie Cheng,Haojie Jiang,Xiaojie Zhu,Yanyan Dong,Wei Lu
Developing high-efficiency electromagnetic wave absorption materials with versatility has been a hotspot and it remains a huge challenge. Here, we reported versatile laminated Ni nanoparticles @ porous carbon (Ni@C) nanocomposites synthesized by a facile carbonization of Ni-based metal-organic frameworks (MOFs) precursor. It was found that the phase components (Ni and C phases) and nano/microstructure (laminated and porous characterizations) were well-modified by controlling the calcination temperature, which led to the variation of the degree of graphitization , magnetic properties , and electromagnetic performances. It showed that the laminated porous Ni@C nanocomposites achieved enhanced microwave absorption performances with a thin thickness of 1.5 mm, a strong reflection loss of −59.8 dB and an effective absorption bandwidth of 4.5 GHz. The underlying microwave absorption mechanism was owing to the improved synergistic effects of polarization relaxation, electron transport , ferromagnetic resonance, as well as multiple reflections and scattering in the laminated porous Ni@C nanocomposites. Furthermore, the multicomponent and laminated porous architecture endowed nanocomposites with favorable waterproof, heat isolation and infrared shielding versatility. Therefore, this work demonstrated a facile approach to develop MOFs-derived versatile laminated porous nanocomposites with efficient microwave absorbing performances.
研究领域:
材料科学
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电磁学
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产品关联
DOI
高影响因子
COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS
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2023
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IF 5.2
Aotian Gu,Chunhui Gong,Manli He,Kaiwei Chen,Xinyu Zhou,Peng Wang,Kai Chen,Yan Jiao,Yi Yang
Advanced oxidation processes activated by transition metal have attracted much attention for their excellent performance in the removal of organic pollutants , but the development of efficient and environmentally benign catalysts is still a significant challenge. In this work, carbon shell encapsulating Co/Fe sulfide nanoparticles (Co/Fe@SC X ) were synthesized by pyrolysis of the resorcinol-formaldehyde (RF) coated MIL-101 @ZIF-67 bimetal Metal-organic frameworks (MOFs). In the degradation of TCP , Co/Fe@SC 600 exhibited the highest TCP removal rate (97.33%) and reaction rate constant (k obs ) (0.169 min −1 ), as well as the mineralization rate of up to 60.19%. Compared to other prepared catalysts, Co/Fe@SC 600 not only possessed excellent catalytic activity, but also exhibited the lowest Co ion leaching concentration, good stability and high resistance to environmental factors. Further studies showed that the non-radical pathway dominated by 1 O 2 contributed most to the TCP degradation, and the radicals also played the indispensable role. The potential TCP degradation pathways in the reaction system was also investigated by analyzing the intermediate products during the degradation process. Overall, this study may provide some interesting insights into the design of advanced catalysts.
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
CHEMICAL ENGINEERING JOURNAL
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2021
·
IF 13.273
Cong Geng,Peng Wei,Huamei Chen,Haichao Liu,Shenshen Zheng,Haobin Wang,Yahong Xie
Carbon-based perovskite solar cells (C-PSCs) facilitate modularization and commercialization due to their excellent thermal stability and low cost. However, C-PSCs show the poor performance that charge carrier extraction by the carbon electrode alone is not as efficient as in the case of conventional hole transport materials (HTMs) based PSCs. In this work, an inorganic hole buffer layer of nitrogen-doped carbon/Co 3 O 4 (Co 3 O 4 @NC) nanoparticles derived from MOFs is introduced to adjust energy alignment and passivate perovskite (PSK) grain boundaries (GBs). Moreover, a simple processing method on the Co 3 O 4 @NC nanoparticles manipulated by controllable ultraviolet/ozone (UVO) treatment is employed, to further improve the interfacial performance of MAPbI 3 /Co 3 O 4 @NC and reduce the hysteresis. Through interface engineering, it is found that Co 3 O 4 @NC inorganic hole buffer layer effectively promotes photo‐generated charge separation and extraction, and suppresses charge recombination at the MAPbI 3 /Carbon electrode (CE) interface, resulting in improved photovoltaic performance. Consequently, the optimal C-PSCs without encapsulation achieved a maximum PCE of 14.63%, which is 22.3% more efficient than the pristine device (11.96%), and exhibited outstanding long-term stability.
研究领域:
材料科学
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能源技术
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光电转换
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DOI
高影响因子
ELECTROCHIMICA ACTA
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2024
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IF 5.5
Zhenwu Zhong,Xiaoyu Yang,Zhaoxiang Qi,Ke Zhao,Salman Riaz,Ying Qi,Peng Wei,Min Jae Ko,Jian Cheng,Yahong Xie
Carbon-based MAPbI 3 perovskite solar cells (C-PSCs) have attracted significant attention due to their low cost and stable performance. However, due to inherent structural defects and an energy level mismatch between the perovskite layer and the carbon electrode, C-PSCs still show a poorer power conversion efficiency (PCE) than traditional perovskite solar cells (PSCs). In this study, LaFeO 3 @C nanocomposite particles were successfully synthesized via pyrolysis of La-containing MIL-100(Fe) MOF gel. By introducing these pre-synthesized LaFeO 3 @C bimetallic composite oxide nanoparticles into the carbon electrode, the device featuring a FTO/SnO 2 /CH 3 NH 3 PbI 3 /LaFeO 3 @C/C architecture achieved an impressive maximum PCE of 16.35%, surpassing that of the pristine device by 9.36%. The enhanced optoelectronic performance can be primarily attributed to enhanced interfacial contacts, superior interfacial charge extraction ability, and better electrical conductivity . The LaFeO 3 @C-based device maintained more than 90% of the initial PCE after being stored for 31 days at room temperature and ambient humidity. This study provides a novel strategy for the preparation of efficient and stable C-PSCs from the perspective of spatial structure regulation of bimetallic MOF-based composites.
研究领域:
材料科学
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能源科学
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产品关联
DOI
高影响因子
JOURNAL OF COLLOID AND INTERFACE SCIENCE
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2021
·
IF 8.128
Zhenlin Ma,Rong Zheng,Yu Liu,Yulong Ying,Weidong Shi
Recently, carbon nanotubes (CNT)-based interconnected architectures exhibit promising prospects in supercapacitors due to their flexibility and high electrical conductivity. Herein, a three-dimensional (3D) interconnected network structure combined with conductive carbon nanotubes interpenetrating MOFs-derived Co-Ni-S composite spheres (Co-Ni-S/CNTs) was synthesized. Such 3D interconnected architecture significantly leads to a favorable electronic structure, fast charge-transfer capacity, and more pseudocapacitive. The Co-Ni-S/CNTs-based hybrid electrode exhibits an extraordinary specific capacitance of 540.6C g −1 at 1 A g −1 and competitive rate performance (capacity retention rate of 69.9% when the current density increases to 10 times). Subsequently, a hybrid supercapacitor is assembled using Co-Ni-S/CNTs as the positive electrode and commercial activated carbon as negative electrode. The device delivers a high energy density of 63.5 W h kg −1 at 800 W kg −1 and keeps 83.0% initial capacitance retention after 10,000 cycles. The encouraging performances demonstrate the significant contribution of the 3D interconnected architecture for the future energy storage.
研究领域:
材料科学
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能源存储
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产品关联
DOI
PubMed
高影响因子
CARBON
·
2023
·
IF 10.9
Mushan Yuan,Haoruo Zhang,Yang Fei,Junyu Lu,Junliang He,Baowei Qiu,Zhong Zeng,Hui Liu,Wenbin Chen,Mei Liang,Yang Chen,Huawei Zou
Developing an efficient EM wave absorbing material that can broadband absorb EM waves in a wide thickness range is a significant challenge. Herein, we report a multi-scale heterogeneous Co/C composite foam with a three-dimensional (3D) lamellar network to address this challenge. The internal structure of melamine foam (MF) is engineered via carboxymethyl cellulose (CMC) in-situ lamella formation to guarantee excellent impedance matching. Meanwhile, the CMC lamellar network extends the EM wave transmission path. The MOF-derived particles grow uniformly in the lamellar network, covering channels of EM wave transmission, which significantly enriches the EM wave loss mechanism and enhances attenuation capability. Benefiting from the synergistic effect of the 3D lamellar network and multi-scale heterogeneous carbon source, an EM absorber strikes a balance between impedance matching and absorption efficiency. As a result, Co/C@MC delivers an effective absorption bandwidth (EAB) that is more than 8 GHz in the whole range of thicknesses from 3.5 to 8 mm, Ni/C@MC exhibits an EAB of 8.5 GHz at 3.3 mm and Fe/C@MC shows the optimal reflection loss of −76.9 dB at 2.5 mm. This work provides a lamellar network/regional enhancement unit strategy for preparing ultra-efficient broadband EM wave absorbing materials.
研究领域:
材料科学
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电磁学
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产品关联
DOI
高影响因子
JOURNAL OF ELECTROANALYTICAL CHEMISTRY
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2024
·
IF 4.1
Yongming Zhu,Hong Sun,Tianyu Zhang,Qiang Li,Zhichao Xue,Mingfu Yu,Jie Li,Xue Wang
Rechargeable lithium-oxygen batteries (LOBs) are acknowledged as potential candidates for advanced energy storage devices as a result of their considerable theoretical energy densities . Nevertheless, they encounter significant challenges throughout discharging and recharging phases, including the difficult decomposition of Li 2 O 2 products, sluggish reaction kinetics, and limited cycle stability. In this study, an efficient catalyst was synthesized by in situ growth of metal–organic frameworks (MOFs)-derived cobalt manganese layered double hydroxide (CoMn-LDH) array on Ti 3 C 2 T x MXene nanosheets (CoMn-LDH@Ti 3 C 2 T x ). The LOBs with CoMn-LDH@Ti 3 C 2 T x cathode demonstrated high discharge specific capacity of 27.61 Ah g −1 at 100 mA g −1 and an extended cycle stability of over 224 cycles at 500 mA g −1 . Density functional theory (DFT) computations showed that CoMn-LDH@Ti 3 C 2 T x facilitates electron redistribution, optimising the adsorption energy of intermediates, thereby lowering the energy barriers for oxygen reduction reactions (ORR) and oxygen evolution reactions (OER). Consequently, this work presents a multi-level nanostructured catalyst preparation strategy derived from MOFs, offering new insights for the fabrication of efficient electrocatalytic materials.
研究领域:
材料科学
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能源存储与转换
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电化学
✓ 已验证
产品关联
DOI
高影响因子
APPLIED SURFACE SCIENCE
·
2020
·
IF 6.182
Yuehong Xie,Chao Feng,Yuan Guo,Shiang Li,Cheng Guo,Yi Zhang,Jide Wang
This paper introduces a facile strategy to fabricate trifunctional electocatalysts through one pool treatment on MOFs to obtain carbon nanotube coated ultrafine CoNi alloy (CoNi@NCNTs) nanocomposites with N-doped rich-defect and abundant cavity structure. During the pyrolysis process, volatile CNx species from dicyandiamide were trapped by ZIF-67@Ni-ZIF nanosheets, simultaneously introducing nitrogen atom into carbon matrix to achieve the rich-defect porous nanotubes and abundant cavity structure. The as-prepared nanomaterials can simultaneously boost the ORR, OER and HER catalytic activity with strong durability. Significantly, the CoNi@NCNTs-700 exhibits excellent electrocatalytic activity including half-wave potential (E ORR, 1/2 ) of 0.80 V, lower operating voltage (E OER, 10 ) of 1.60 V at 10 mA cm −2 and potential difference (ΔE) of 0.80 V between E OER, 10 to E ORR, 1/2 in 0.1 M KOH, and low overpotential (E HER, 10 ) of −0.130 V reaching 10 mA cm −2 in acidic medium. The remarkable activity is ascribed to defect-rich porous carbon nanotubes structure and the synergistic effect between CoNi alloy nanoparticles, N-dope carbon and CoNi-Nx. And hollow structure facilitates to improve conductivity and stability. This work offers a useful archetypical template to design and construct efficient and stable trifunctional electrocatalysts, illustrating its viability for practical applications of energy conversion and storage devices.
研究领域:
材料科学
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电化学
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能源转换与存储
✓ 已验证
DOI
高影响因子