RSC Advances
·
2016
·Vol. 6
·期 81
·77358-77365
·
IF 3.289
Ting-Ting Li,Jinjie Qian,Yue-Qing Zheng
Metal–organic frameworks (MOFs) have been demonstrated as suitable metal sources and sacrificial templates for the preparation of porous transition-metal oxide nanomaterials. Herein, porous CuO micro-polyhedra assembled from numerous nanoparticles are synthesized simply by employing a Cu-based MOF as a precursor via a one-step calcination process under an air atmosphere. Benefitting from their high porosity and large specific surface area, porous CuO materials exhibit excellent electrocatalytic performances toward water oxidation in pH 9.2 KBi solution. A low catalytic onset potential at 1.05 V vs. NHE (NHE = normal hydrogen electrode) is obtained based on electrochemical measurements. A faradaic efficiency of nearly 98% and a stable catalytic current density of 2.2 mA cm−2 are achieved under an applied potential of 1.30 V vs. NHE over an electrolysis period of 10 h. In addition, based on the Tafel plot, the required overpotentials are only ∼410 mV and ∼510 mV for achieving the catalytic current densities of 0.1 mA cm−2 and 1.0 mA cm−2, respectively. The excellent performances make it an appealing candidate as a potential catalyst for green energy applications.
研究领域:
材料化学
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电化学
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纳米材料
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能源催化
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无机功能材料
✓ 已验证
DOI
高影响因子
CHEMICAL COMMUNICATIONS
·
2016
·Vol. 52
·期 64
·9969-9971
·
IF 6.567
Yan Zhang,Yubin Niu,Min-Qiang Wang,Jingang Yang,Shiyu Lu,Jin Han,Shu-Juan Bao,Maowen Xu
In this communication, we designed and synthesized a novel calcium–organic framework and presented it as an anode material for sodium-ion batteries. The results show that it delivers a reversible capacity of higher than 140 mA h g−1 even after 300 cycles. The remarkable performance is attributed to the high structural stability and extremely low solubility of the calcium–organic framework in electrolytes.
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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无机化学
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功能材料
✓ 已验证
DOI
高影响因子
JOURNAL OF SOLID STATE CHEMISTRY
·
2019
·
IF 2.291
Zhuo Dai Li,Huai Qiang Zhang,Xiao Hong Xiong,Feng Luo
Covalent organic frameworks (COFs) represent an exciting new type of porous organic materials, which are constructed with organic building units via strong covalent bonds . Here in, the COF-2,4,6-Triformylphloroglucinol p-Phenylenediamine (COF-TpPa-1) was synthesized by solvothermal method for the removal of U(VI) from aqueous solution. Effects of pH, adsorption dose, contact time, uranium solution concentration, temperature and adsorption and desorption cycle on the efficiency of COF-TpPa-1 removal of U(VI) are investigated. SEM, XRD , TGA and FT-IR were employed to characterize the samples and analyze adsorption mechanism. The results manifested COF-TpPa-1 has the high adsorption capacity ( q m = 152 mg/g), quick adsorption kinetic , high selectivity , outstanding recycle performance and good resistance to acids, bases and high temperature.
研究领域:
环境化学
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材料科学
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核化学
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污染治理
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吸附科学
✓ 已验证
DOI
高影响因子
Nano Energy
·
2016
·
IF 11.553
Zhaoqiang Li,Caixia Li,Xiaoli Ge,Jingyun Ma,Zhiwei Zhang,Qun Li,Chengxiang Wang,Longwei Yin
Reduced graphene oxide (RGO) wrapped metal-organic frameworks (MOFs) derived cobalt doped porous carbon polyhedrons synthesized via a carbonization process, are for the first time used for sulfur immobilizers (RGO/C–Co-S) as cathodes for high performance lithium-sulfur (Li–S) batteries. The RGO/C–Co–S cathode exhibits greatly improved electrochemical performance, showing excellent specific capacity of 949 mAh g −1 at 300th cycle at a current density 0.3 A g −1 , displaying enhanced rate capability with specific capacity of 772, 704 and 606 mAh g −1 at current density of 0.5, 1 and 2 A g −1 , respectively. The synergetic effect of MOFs-derived porous carbon, homogeneously distributed Co nanoparticles and RGO nanosheets simultaneously contributes to the confinement of sulfur species. The presence of abundant mesopores and micropores is conducive to immobilize large amounts of S species. The homogenously inlaid ultrafine Co nanoparticles can further immobilize sulfur by chemical interactions between Co and S/polysulfides. The RGO nanosheets tightly wrapped on carbon hosts act as barrier layers to prevent polysulfides from diffusing out of the matrix, further suppressing shuttle effect. The porous structure and the RGO can effectively alleviate the volume changes resulted from charge–discharge process. This design strategy can be inspiring for MOF-derived materials in energy storage applications .
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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纳米材料
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电池技术
✓ 已验证
DOI
高影响因子
JOURNAL OF SOLID STATE CHEMISTRY
·
2021
·
IF 3.498
Sai-Li Zheng,Yonghe He,Xiao-Kang Qiu,Yuan-Hui Zhong,Lai-Hon Chung,Wei-Ming Liao,Jun He
A novel metal-organic framework [CuCN(TMBP)·H 2 O] n ( TCuCN ) has been synthesized by the reaction of 3,3′,5,5′-tetramethyl-4,4′-bipyrazole (TMBP) and CuCN. Its structure was determined by single-crystal X-ray diffraction (SCXRD) analysis and further characterized by power X-ray diffraction (PXRD) analysis, FT-IR spectroscopy and thermogravimetric (TG) analysis. Previously reported structurally analogous TCuCl , TCuBr , TCuI have also been synthesized for Br 2 adsorption comparison. All of these four MOFs exhibited reversible uptake of Br 2 vapor judging by the unchanged PXRD patterns . Among four MOFs, Br 2 -loaded TCuI showed the most uptake amount of Br 2 (15.7 wt%), providing the formula to be TCuI ·0.33Br 2 . The different uptake amount of Br 2 for TCuX (X = CN, Cl, Br, I) should be mainly ascribed to the intermolecular interaction between CuX and Br 2 .
研究领域:
无机化学
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材料化学
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配位化学
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多孔材料
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气体吸附
✓ 已验证
DOI
高影响因子
Journal of the Taiwan Institute of Chemical Engineers
·
2019
·
IF 3.834
Yunlei Zhang,Bing Li,Yanan Wei,Changhao Yan,Minjia Meng,Yongsheng Yan
Developing a green and economically viable approach for the direct synthesis of metal-organic frameworks (MOFs) catalysts with multifunctional active sites remains the key step for their applications in heterogeneous catalysis field. Herein, we report a green (aqueous solutions), mild (90 °C, atmospheric pressure), and modulated hydrothermal (MHT) approach to synthesize UiO-66-type MOFs catalysts with acid–base bi-functional sites, which were obtained via the coordination of monosodium 2-sulfoterephthalate and 2-aminoterephthalic with zirconium (Zr) ions. More importantly, a series of acid, base and acid–base catalysts with varied acid–base strengths can be readily prepared, by simply varying the ratio of organic ligands for preparing MOFs. The synthesized catalysts were characterized and their performances in glucose dehydration to produce 5-hydroxymethylfurfural (5-HMF) have been evaluated. The developed approach in this work has clearly depicted a roadmap for the facile synthesis of MOFs catalysts to facilitate their potential use in acid–base catalysis.
研究领域:
化学工程
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催化科学
✓ 已验证
产品关联
DOI
高影响因子
ANALYTICA CHIMICA ACTA
·
2019
·
IF 5.256
Xiaoxiao Wei,Yuzhi Wang,Jing Chen,Panli Xu,Wei Xu,Rui Ni,Jiaojiao Meng,Yigang Zhou
Novel polymeric deep eutectic solvents (PDES) based on 3-acrylamidopropyl trimethylammonium chloride/D-sorbitol functionalized amino-magnetic (Fe 3 O 4 NH 2 ) metal-organic framework (HKUST-1-MOF) composites (Fe 3 O 4 NH 2 @HKUST-1@PDES) were synthesized and characterized by field emission transmission electron microscope (FE-SEM), transmission electron microscope (TEM), X-ray diffraction (XRD), fourier transform infrared spectrometry (FT-IR), thermal gravimetric analysis (TGA), vibrating sample magnetometer (VSM) and zeta potentials . Then the composites were firstly utilized to selectively separate malachite green (MG) and crystal violet (CV) coupled with magnetic solid-phase extraction (MSPE). A response surface methodology (RSM) based on Latin hypercube sampling (LHS) was selected to analytically optimize the extraction parameters including initial concentration of dyes, extraction time, pH value and extraction temperature. The maximum extraction amount and optimal extraction conditions predicted by the RSM model matched well with the actual experimental results, and the extraction amount was 966.93 mg g −1 for MG and 788.90 mg g −1 for CV,respectively. The results indicated that the model possessed higher calculation accuracy through analyzing fewer sample points, thereby achieving theoretical prediction of extraction amount and conditions and being a prefect supplementary to actual experiments. The electrostatic interaction between the composites and cationic dyes played the main roll in the extraction process. The proposed extraction method exhibited lower limit of detection (98.19 ng mL −1 for MG and 23.97 ng mL −1 for CV) and preeminent precision (RSD ˂ 0.4%). Spiked recoveries of fish samples at three spiking levers ranged from 89.43% to 100.65% for MG and 95.29%–98.03% for CV. All results highlighted the excellent potential of Fe 3 O 4 NH 2 @HKUST-1@PDES-MSPE strategy in selective separation of cationic dyes in complex medium.
研究领域:
分析化学
·
材料科学
✓ 已验证
产品关联
DOI
PubMed
高影响因子
JOURNAL OF ELECTROANALYTICAL CHEMISTRY
·
2019
·
IF 3.218
Zhiwei Qiu,Tao Yang,Rui Gao,Guifen Jie,Wanguo Hou
In this study, a novel Cu-based metal−organic frameworks (Cu-MOFs) composite material was prepared, and used to develop a sensitive and efficient electrochemical ratiometric sensor for dopamine detection. Gold nanoparticles (NPs) and the conductive poly(xanthurenic acid) p(XA) were assembled on the Cu-tetrakis (4-carboxyphenyl) porphyrin (TCPP) surface by electrodeposition and cyclic voltammetry (CV) method, which greatly improved the electrocatalytic performance of the Cu-MOF modified electrode . Two substances (dopamine/DA, paracetamol/PA) with different electrochemical peaks were added to the electrolyte solutions , where DA was the analyte and PA was as a reference. The ratiometric value of differential pulse voltammetry (DPV) oxidation current (I DA /I PA ) linearly increased with the increasing concentration of DA with low detection limit. This electrochemical ratiometric approach based on the metal−organic framework composites is expected to be a valuable strategy for detection of other analytes.
研究领域:
分析化学
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生物传感器
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神经化学
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电分析化学
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纳米材料
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药物分析
✓ 已验证
DOI
高影响因子
Journal of Materials Chemistry A
·
2024
·Vol. 12
·期 31
·19968-19978
·
IF 10.7
Zicheng Huang,Wenjie Shao,Yijuan Zheng,Junyu Wang,Mao Wang,Shuang Li,Xiaohui Xu,Chong Cheng,Changsheng Zhao
Transition metal oxide-based catalysts are known as the most active oxygen evolution reaction (OER) catalysts due to their intrinsic electronic structures and binding strength of oxygenated intermediates. However, even the most active transition metal oxide-based OER catalysts have a turnover frequency far lower than that of the oxygen-evolving complexes in biological systems for intermolecular site aggregation. Herein, we implement the hybridization of a metal–organic framework and tungstic acid (WO3·xH2O-in-MIL-88) to achieve ordered FeNi site isolation at the molecular level and avoid intermolecular decomposition during the catalysis process. The optimized hybrid with 15% tungstic acid (15%-WO3·xH2O-in-MIL-88) achieves a much-enhanced OER activity and stability in terms of a low overpotential of 263 mV to reach a current density of 10 mA cm−2, a low Tafel slope of 39 mV dec−1, and long-term stability, which is much superior to that of the commercial RuO2 catalyst.
研究领域:
材料化学
·
电化学
·
催化化学
·
能源科学
·
无机化学
✓ 已验证
DOI
高影响因子
RSC Advances
·
2015
·Vol. 5
·期 123
·101982-101988
·
IF 3.84
Chang Liu,Bing Yan
Heterostructured chemosensors have excellent chemical stability, low contamination and excellent recyclability, and are regarded as a promising new generation of sensors with critical properties related to their sensing sensitivity and selectivity. Our preparation strategy for a heterostructured sensor is to construct it using a luminescent lanthanide complex and metal organic framework (MOF). A heterogeneous sensor is systematically produced using EuTTA and ZIF-8 to cover silica, and thin particles are obtained with small size and uniform morphology. Then, the particles were used as a highly selective and sensitive sensor to detect Cu2+ in aqueous solution. Eventually, we find that the well-structured silica@EuTTA@ZIF-8 microspheres have a good fluorescence stability, low detection limit and broad linear range in aqueous environments. These excellent properties make it a potential chemosensor for sensing of Cu2+ in environmental or biological solution systems.
研究领域:
分析化学
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环境监测
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生物传感
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材料科学
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无机化学
·
纳米技术
✓ 已验证
DOI
高影响因子
CHEMICAL ENGINEERING JOURNAL
·
2018
·
IF 6.735
Wei Teng,Nan Bai,Zehan Chen,Junming Shi,Jianwei Fan,Wei-xian Zhang
Porous carbon is the most important and most common adsorbent for the separation and treatment of organic pollutants. Characteristics such as accessible and large surface area, physical and chemical stability, and low-cost manufacturing method are desired for any adsorbent. Herein, a hierarchically porous carbon (HPC) was prepared by pyrolysis and graphitization of crystalline metal–organic frameworks (MOF-5) for enhanced adsorption of aromatic contaminants. The material treated at high temperature (950 °C) possesses large surface area (1512 m 2 /g), high porosity (0.94 cm 3 /g), and hierarchically porous structures. The generated mesopores around 4 nm improve the interconnectivity of micro- and macropores to make the porous material ideal for sorption of organic pollutants such as aromatic hydrocarbons. Effects of adsorbent dose, pH, ionic strength, contact time, and initial concentration on the adsorption of p -nitrophenol (PNP, as a model) were investigated. Adsorption isotherms and kinetics suggest that the adsorption is a spontaneous and endothermic physisorption process with monolayer surface coverage. The surface sites are electron-rich due to the graphitic layer, which has high affinity toward π electrons of the aromatic ring. The adsorption capacity of the hierarchically porous carbon (HPC) is nearly over 100% higher that of conventional activated carbon.
研究领域:
环境科学
·
材料科学
·
物理化学
·
吸附分离
·
污染治理
✓ 已验证
DOI
高影响因子
FUEL
·
2024
·
IF 6.7
Xingyan Liu,Tianrong Xiong,Yonggang Xu,Kunhe Yang,Youzhou He,Haifeng Yang,Hong Wu,Jiajia Jing,Siqi Li,Siping Wei
Defect engineering for MOFs is a promising approach to accelerate the charge transfer to further enhance the photocatalytic performance. Up to now, the current defect engineering strategy for MOFs mainly focuses on a single adjustment mode with the apparent ceiling effect, whether the further break out of the ceiling effect could be achieved through the combination of two or more adjustment modes is still in its infancy. In this work, the original NH 2 -MIL-125 was firstly adjusted by a single adjustment mode in ethanol solvothermal method to obtain partially linker defective NM-125-X (where X signifies the distinct temperatures used in the solvothermal treatment, with optimal results observed at X = 120). Subsequently, the NM-125-120 was further re-regulated by adjusting the ligand defects through another adjustment mode in water heating agitation, resulting in the ultimate defective NM-125-120-65. The NM-125-120-65 obtained through double defect engineering avenue showed superior photocatalytic performance with the hydrogen production rate of 11585.23 μmol·g −1 , which was 1.23 and 14.05 times as those of partially defective NM-125-120 (9427.65 μmol·g −1 ) and original NH 2 -MIL-125 (824.85 μmol·g −1 ), respectively. In addition, the NO removal rate of NM-125-120-65 was 64.8 % also higher than that of NM-125-120 (37.8 %) and NH 2 -MIL-125 (23.6 %). Through a series of comparative experiments, especially TGA and XPS, it was noted that the ligand defective NH 2 -MIL-125 can be formed by ethanol solvothermal method, and it was also confirmed that through further re-regulating the ligand defects in water heating agitation, the linker defects could also be further expanded. The PL emission spectra, IT diagrams, and EIS measurements displayed that the NM-125-120-65 had outstanding conductivity and excellent electron mobility compared to NM-125-120 and NH 2 -MIL-125. This work provided a novel approach for the subsequent defect engineering by another adjustment mode based on the existing defective MOFs via double linker defect engineering adjustment modes, so as to further obtain better photocatalytic performance for solving the environmental and energy crisis.
研究领域:
材料科学
·
环境化学
·
能源化学
·
光催化
·
纳米材料
·
物理化学
✓ 已验证
DOI
高影响因子
危险品化学品经营许可证（带存储）