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CHINESE JOURNAL OF CHEMICAL ENGINEERING · 2021 · IF 3.171

Catalytic hydrogenation performance of ZIF-8 carbide for electrochemical reduction of carbon dioxide

Shuai Fan,Huiyuan Cheng,Manman Feng,Xuemei Wu,Zihao Fan,Dongwei Pan,Gaohong He

The conversion of CO 2 electrocatalytic hydrogenation into energy-rich fuel is considered to be the most effective way to carbon recycle. Nitrogen-doping carbonized ZIF-8 is proposed as carrier of the earth-rich Sn catalyst to overcome the limit of electron transfer and CO 2 adsorption capacity of Sn. Hierarchically porous structure of Sn doped carbonized ZIF-8 is controlled by hydrothermal and carbonization conditions, which induces much higher specific surface area than that of the commercial Sn nanoparticle (1003.174 vs. 7.410 m 2 ·g −1 ). The shift of nitrogen peaks in X-ray Photoelectron Spectroscopy spectra indicates interaction between ZIF-8 and Sn, which induces the shift of electron cloud from Sn to the chemical nitrogen to enhance conductivity and regulate electron transfer from catalyst to CO 2 . Lower mass transfer resistance and Warburg resistance are investigated through EIS, which significantly improves the catalytic activity for CO 2 reduction reaction (CO 2 RR). Onset potential of the reaction is reduced from −0.74 V to less than −0.54 V vs. RHE. The total Faraday efficiency of HCOOH and CO reaches 68.9% at −1.14 V vs. RHE, which is much higher than that of the commercial Sn (45.0%) and some other Sn-based catalyst reported in the literature.

CAS / MDL: 693-98-1 10196-18-6
研究领域: 材料科学 · 环境科学 · 化学工程
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CHINESE JOURNAL OF CHEMICAL ENGINEERING · 2021 · IF 3.171

Enhancing laccase stability and activity for dyes decolorization using ZIF-8@MWCNT nanocomposite

Pascal Habimana,Yanjun Jiang,Jing Gao,Jean Bernard Ndayambaje,Osama M. Darwesh,Jean Pierre Mwizerwa,Xiaobing Zheng,Li Ma

The continuous use of chemical dyes in various industries, and their discharge into industrial effluents, results in severe problems to human life and water pollution. Laccases have the ability to decolorize dyes and toxic chemicals in industrial effluents as green biocatalysts. Their possible industrial applications have been limited by poor reusability, low stability, and loss of free laccase action. In this research, laccase was immobilized on zeolitic imidazolate framework coated multi-walled carbon nanotubes (Laccase@ZIF-8@MWCNTs) via metal affinity adsorption to develop an easy separable and stable enzyme. The optimum reaction conditions for immobilized laccase are at a pH of 3.0 and a temperature of 60 °C. The immobilized laccase was enhanced in storage and thermal stability. The results indicated that Laccase@ZIF-8@MWCNTs still maintained 68% of its original activity after 10 times of repeated use. Most importantly, the biocatalytic system was applied for decolorization of different dyes (20 mg·L −1 ) without a mediator, and up to 97.4% for Eriochrome black T and 95.6% Acid red 88 was achieved in 25 min. Biocatalysts with these properties may be used in a variety of environmental and industrial applications.

研究领域: 环境科学 · 生物技术 · 材料科学
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JOURNAL OF SOLID STATE CHEMISTRY · 2022 · IF 3.656

ZIF – 67 derived hybrid CuCo2S4@MoS2 catalyst for efficient electrocatalytic hydrogen evolution reaction

Li-hu Qian,Wei-wei Dong,Min-da Xu,Yan-Bo Cao,Xuan Wu,Xiao-jie Song,Yi Ding,Xi Wang

Developing hybrid metal sulfide electrocatalyst with excellent hydrogen evolution reaction (HER) catalytic performance and stability is vital to its commercial applications. Herein, hybrid CuCo 2 S 4 @ MoS 2 catalysts were designed with CuCo 2 S 4 synthesized by using ZIF-67 as a template and externally decorated with MoS 2 . The hybrid catalysts (denoted as C@M-0.5, C@M ​− ​1, C@M ​− ​2) show improved catalytic activity than those of MoS 2 and CuCo 2 S 4 due to large surface area and the interface between nanoflower-like MoS 2 and three-dimensional interconnected lamellar stacked CuCo 2 S 4 , which boost charge transport capability and improve the HER kinetic process. The influences of different ratio of CuCo 2 S 4 to MoS 2 on the electrocatalytic activity are investigated in detail. Specifically, C@M ​− ​1 exhibit the best HER performance with an overpotential of 143 ​mV@ 10 ​mA/cm 2 , a Tafel slope of 45.2 mV/dec and satisfactory long-time stability. This work rationally designs hybrid CuCo 2 S 4 @MoS 2 catalyst to preserve the merits of using the ZIF-67 as a template and make use of the synergistic coupling effects between CuCo 2 S 4 and MoS 2 , which can be extended to synthesize other catalysts in different energy conversion fields.

CAS / MDL: 10026-22-9 693-98-1
研究领域: 材料科学 · 能源化学
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JOURNAL OF SOLID STATE CHEMISTRY · 2023 · IF 3.3

Facile synthesis of AgBr@ZIF-8 hybrid photocatalysts for degradation of Rhodamine B

Yongmin Chen,Shulan Pu,Dongying Wang,Yongchao Zhang,Guojiang Wan,Qiang Zhao,Yan Sun

Zeolitic imidazolate framework-8 (ZIF-8) was coupled with AgBr using a facile deposition–precipitation method to synthesize AgBr@ZIF-8 composites. The photocatalytic activity of prepared photocatalysts was evaluated by the degradation of Rhodamine B (RhB). As expected, the photocatalytic activity of the AgBr@ZIF-8 photocatalysts was superior to that of ZIF-8 and AgBr. Among the AgBr@ZIF-8 photocatalysts, AgBr@ZIF-8 with a ZIF-8 loading of 5 ​wt% exhibited the highest photocatalytic efficiency of 99.5 % within 15 ​min. The remarkable photocatalytic activity of the AgBr@ZIF-8 composites was attributed to the heterojunction between ZIF-8 and AgBr, which reduced the recombination rate of electron-hole pairs, thereby enhancing the photocatalytic efficiency of the catalysts. According to the trapping experiment, superoxide radicals (•O 2 - ) and holes (h + ) were certified as the main species in the efficient removal of RhB.

CAS / MDL: 693-98-1
研究领域: 材料科学 · 环境科学
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APPLIED SURFACE SCIENCE · 2022 · IF 7.392

Efficient adsorption of La(III) by magnetic carbon nitride based ZIF-8 nanocomposites

Jiaming Wang,Minxin Shi,Yuanyuan Qin,Yuhua Huang,Xiancai Li,Xiaohua Cao

The enrichment and recovery of low concentration rare earth ions from wastewater resources has become an important research direction to achieve high quality utilization of rare earth resources. In this experiment, graphitic carbon nitride was used as the substrate, which was firstly compounded with Fe 3 O 4 to become magnetic graphitic carbon nitride material by alcohol heat method, and then in situ compounded with ZIF-8 in aqueous phase at room temperature to form the composite g-C 3 N 4 /Fe 3 O 4 @ZIF-8. Finally, the composite was characterized. The adsorption performance of g-C 3 N 4 /Fe 3 O 4 @ZIF-8 and the control g-C 3 N 4 /Fe 3 O 4 and ZIF-8 for La(III) under various conditions was investigated by adsorption experiment. In addition, the types and mechanism of La(III) adsorption were discussed by kinetic, isothermal adsorption line and thermodynamic modeling studies. Finally, the stability performance and reusability of the composite were evaluated by regeneration experiments. The result show that g-C 3 N 4 /Fe 3 O 4 @ZIF-8 has good adsorption performance on lanthanide ions. g-C 3 N 4 /Fe 3 O 4 @ZIF-8 reached adsorption equilibrium at about 20 min. When pH is 6 and the solid–liquid ratio of adsorbent is 0.25 g/L, the adsorption amount was 176.68 mg/g. g-C 3 N 4 /Fe 3 O 4 @ZIF-8 had good selectivity for lanthanum(III), and it retains 81 % of initial adsorption performance after five times of reuse.

CAS / MDL: 57-13-6
研究领域: 环境科学 · 材料科学
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2D Materials · 2019 ·Vol. 7 ·期 1 ·015001 · IF 7.343

Pd-ZIF-L-GO ternary nanolaminates for enhanced heterogeneous catalysis

Hong Jiang,Na Zhou,Ze-Xian Low,Yefei Liu,Weihong Xing,Huanting Wang,Rizhi Chen

A novel sheet-on-sheet Pd-ZIF/GO (Pd/ZG) catalyst is synthesized by constructing ZIF-L with GO and PVP-Pd nanoparticles (NPs) via a facile in situ method. The in situ introduction of GO promotes the formation of ZIF-L, leading to a higher yield of Pd/ZG, about three times higher than Pd/ZIF-L. We ascribe this to the possible interaction of the oxygen-containing groups on the GO surface with the Zn2+ cations in ZIF nodes and the PVP wrapped on the Pd surface, resulting in the formation of sheet-on-sheet Pd-ZIF/GO with good Pd dispersion. The Pd/ZG shows superior catalytic performance in the reduction of nitroarenes, and its turnover frequency (TOF) value is five times higher than Pd/ZIF-L. The superior catalytic activity can be ascribed to the uniformly dispersed tiny Pd NPs between ZIF-L and GO nanosheets, fast mass transfer in porous structure, and excellent electron conductivity due to strong interactions among ZIF-L, GO and PVP-Pd. These findings provide new opportunities for rational design of catalysts and their applications in the reduction of nitroarenes, important processes for industrial synthesis of pesticides, dyes, medicines, etc.

研究领域: 材料科学 · 催化化学 · 工业化学
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ANALYST · 2019 ·Vol. 144 ·期 12 ·3892-3897 · IF 4.019

R-phycoerythrin proteins@ZIF-8 composite thin films for mercury ion detection

Xiaobin Wang,Zhishan Fang,Zhuoyi Li,Wen Ying,Danke Chen,Haiping He,Xinsheng Peng

Mercury, as one of the most prevalent toxic metals released by various natural and anthropogenic processes, causes severe pollution of soil and groundwater. In this work, R-phycoerythrin (R-PE) proteins encapsulated into ZIF-8 composite thin films were prepared via a solid-confinement conversion process and applied as fluorescent sensors for mercury ion detection. The R-PE proteins encapsulated into ZIF-8 exhibit dual color emissions including green (518 nm) and red (602, 650 nm) fluorescence, while the original orange emission (578 nm) of pure R-PE is significantly suppressed. R-PE@ZIF-8 presents excellent selectivity and sensitivity for mercury detection in a large pH range without buffer solution. Under the optimal conditions, there is a good linear relationship between the fluorescence quenching efficiencies of R-PE@ZIF-8 and logarithmic concentrations of mercury ions in the range of 0.001–50 μM with the detection limit (LOD) of 6.7 nM much lower than the guideline value given by the World Health Organization. Furthermore, multi-peak detection of R-PE@ZIF-8 improves the detection accuracy of Hg2+ concentration.

研究领域: 环境科学 · 生物化学
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JOURNAL OF MOLECULAR LIQUIDS · 2024 · IF 5.3

Green synthesis of ZIF-67 nanoparticles via microfluidics: Towards sustainable nanomaterial production

Mina Naderi,Ataallah Soltani Goharrizi,HongKai Wu,Mahmood Barani,Ataallah Kamyabi

This study explored the synthesis of zeolitic imidazolate framework-67 (ZIF-67) nanoparticles using a microfluidic reactor, focusing on the effects of reactant concentration, temperature, and flow rate on the material’s properties. Design Expert software was utilized to optimize these variables to enhance the synthesis process while preventing reactor clogging due to precipitate formation. The experiments varied concentrations of cobalt (II) nitrate hexahydrate and 2-methylimidazole, along with temperature and flow rates. After synthesis, the samples underwent extensive characterization, including FTIR, NMR, TEM, SAED, and XRD analyses. FTIR results confirmed the successful formation of ZIF-67, with varying conditions leading to shifts in peak positions and intensities, indicating changes in bonding and molecular structure. NMR spectra provided insights into the hydrogen environments within the nanoparticles. TEM and SAED analyses revealed that the nanoparticles predominantly exhibited a uniform rhombic dodecahedral morphology with diameters ranging from 5 to 10 nm. XRD patterns were consistent with simulated data, showing variations in peak positions and crystallinity with changes in synthesis conditions. The study highlighted that increasing reactant concentrations, temperature, and flow rate generally enhanced the production rate and crystallinity of ZIF-67, with 2-methylimidazole concentration having the most significant impact. The findings contributed to optimizing ZIF-67 synthesis, demonstrating the feasibility of using microfluidic reactors and green solvents for producing high-quality nanoparticles with controlled properties.

CAS / MDL: 10026-22-9
研究领域: 材料科学 · 化学工程 · 环境科学
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ENVIRONMENTAL SCIENCE AND POLLUTION RESEARCH · 2020 ·Vol. 27 ·期 22 ·28396-28407 · IF 3.056

Removal of boron from water by GO/ZIF-67 hybrid material adsorption

Hu Guangzhuang,Zhang Wei,Chen Yuantao,Xu Cheng,Liu Rong,Han Zhen

With the development of the boron industry, boron pollution is getting more and more serious, and excessive boron will harm human health. In this paper, graphene oxide was used as a template to prepare ZIF-67, and GO/ZIF-67 was successfully prepared. GO/ZIF-67 was used for the first time to remove boron from water. SEM, XRD, and other characterization methods were used to confirm the structure. The adsorption kinetics, adsorption isotherm, adsorption thermodynamics, and adsorption mechanism of boron by GO/ZIF-67 were studied in this paper. The adsorption capacity of GO/ZIF-67 for boron is up to 66.65 mg·g −1 at 25 °C, and adsorption process reaches equilibrium in 400 min. Adsorption kinetics indicates that the adsorption process conforms to the pseudo-first-order kinetic model, and adsorption thermodynamics indicates that the adsorption process is a spontaneous endothermic process controlled by entropy change. The adsorption capacity of boron by GO/ZIF-67 does not decrease significantly after four cycles. The adsorption of boron by GO/ZIF-67 has both chemical and physical adsorption. From Zeta potential and adsorption kinetics, it can be seen that there is physical adsorption during the adsorption process and boron mainly has positive charge on the surface of GO/ZIF-67 and graphene oxide hydroxyl bonding. Based on the adsorption thermodynamics and XPS, it is known that there is chemisorption during the adsorption process, and mainly the combination of boron and cobalt sites.

CAS / MDL: 7782-42-5
研究领域: 环境科学 · 材料科学
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Polymers · 2018 ·Vol. 11 ·期 1 ·27 · IF 2.935

Enzymes@ZIF-8 Nanocomposites with Protection Nanocoating: Stability and Acid-Resistant Evaluation

Yuxiao Feng,Le Zhong,Muhammad Bilal,Zhilei Tan,Ying Hou,Shiru Jia,Jiandong Cui

Zeolitic imidazole framework-8 (ZIF-8) with tunable pore sizes and high surface areas have recently emerged as a promising support for immobilizing enzymes. However, the instability in the aqueous acidic environment and difficulty of recovery has limited their practical applications in some cases. In this study, catalase/ZIF-8 composites with a protective nanocoating were prepared by the controlled self-assembly of silanes or coordination complexes (tannic acid (TA) and Fe3+). The properties of the catalase (CAT)/ZIF-8 composites with a protective nanocoating were also determined. The recovered activity of CAT/ZIF-8 and CAT/ZIF-8 with protective nanocoating was 70% and 65%, respectively. Compared with the conventional CAT/ZIF-8 composites, CAT/ZIF-8 with protective nanocoating exhibited excellent acid resistance. For example, after treatment for 60 min in phosphate buffer solution (pH 3.0), CAT/ZIF-8 composites only maintained 20% of their initial activity (about 12 U/mg). However, CAT/ZIF-8 with a protective nanocoating could still retain about 50% of its initial activity (about 10 U/mg). Meanwhile, the thermostability and storage stability of the CAT/ZIF-8 composites was enhanced significantly due to the presence of nanocoating compared with conventional CAT/ZIF-8. More importantly, the CAT/ZIF-8 with a protective nanocoating retained 40% of its initial activity after 7 cycles, whereas CAT/ZIF-8 only retained 8% of the initial activity. The approach in this study could be an efficient strategy to prepare enzyme/ZIF-8 composites with both high acid resistance and excellent recyclability.Keywords:enzyme/ZIF-8 nanocomposites;nanocoating;stability;acid resistance

研究领域: 生物化学 · 材料科学
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JOURNAL OF ALLOYS AND COMPOUNDS · 2023 · IF 6.2

ZIF-90 derived carbon-coated kerf-loss silicon for enhanced lithium storage

Yahong Yuan,Jiale Wan,Zhuqing Zhao,Xiang Chen,Shuaibo Gao,Hongwei Xie,Huayi Yin

The utilization of kerf-loss silicon (KL-Si) waste as anode materials in lithium-ion batteries (LIBs) faces limitations of the rapid structural degradation during repeated charging/discharging. To overcome this limitation, 3D carbon-coated Si is constructed to buffer the Si volume expansion caused by the lithiation, while simultaneously forming a robust conductive network. Meanwhile, the well-dispersed porous carbon (C) shell, doped with suitable heteroatoms, plays a pivotal role in facilitating rapid ion transfer rates. In addition, a cobalt (Co) and nitrogen (N)-doped C shell is employed to encapsulate KL-Si, aimed at enhancing its lithium (Li) storage performances. The electrochemical performance of KL-Si@C-ZIF/N/Co composites, synthesized through the encapsulation of KL-Si with a metal-organic framework (MOF) structure (ZIF-90) followed by heat treatment. The resulting composites exhibit an outstanding reversible capacity of 981 mAh g −1 and an impressive capacity retention of 81.9% at 2 A g −1 even after 350 cycles. This paper presents a promising method for maximizing the value-added utilization of KL-Si and reveals the advantages of MOF-derived porous C shell in accommodating the inherent volume expansion of Si-based anodes.

研究领域: 材料科学 · 能源存储技术
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RSC Advances · 2022 ·Vol. 12 ·期 20 ·12702-12709 · IF 4.036

Bimetallic CoCu-ZIF material for efficient visible light photocatalytic fuel denitrification

Yi Lu,Haibo Pan,Jiafeng Lai,Yuzhou Xia,Lu Chen,Ruowen Liang,Guiyang Yan,Renkung Huang

Effective design of photocatalysts is an effective method to improve the separation of photogenerated carriers, which improves the photocatalytic performance of photocatalysts. In this work, CoCu-ZIF materials with bimetallic structure were synthesized at room temperature for efficient photocatalytic fuel denitrification. The properties and structures of CoCu-ZIF photocatalysts can be effectively controlled by adjusting the molar ratio of cobalt to copper. The as-prepared CoCu-ZIF photocatalysts were characterized by XRD, FT-IR, SEM, TEM, UV-vis, Raman, BET and other techniques. The photoactivity of CoCu-ZIF for the denitrogenation of NCCs has been evaluated using visible light (λ ≥ 420 nm). The results indicate that Co8Cu2-ZIF photocatalysts exhibit excellent photocatalytic properties, in which the denitrification rate almost reached 80% after 4 hours under visible light irradiation, which is higher than the degradation ability of ZIF-67 (38%). Transient photoelectrochemical experiments and EIS Nyquist plots indicate that Co8Cu2-ZIF with unique structure efficiently improves the separation and transfer of photogenerated electron–hole pairs. Moreover, a possible reaction mechanism was proposed by LC-MS analysis.

研究领域: 材料科学 · 环境科学
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