Gold nanoparticles decorated rGO-encapsulated metal-organic frameworks composite sensor for the detection of dopamine

Author(s):  
Shaoming Yang ◽  
Jian Zhang ◽  
Chaopeng Bai ◽  
Kaiqiang Deng

In this study by way of encapsulation of reduced graphene oxide (rGO) into Ni-based metal-organic framework (Ni-MOFs) structure, the composite rGO@Ni-MOFs was first prepared. Then gold nanoparticles (AuNPs) decorated rGO@Ni-MOFs (rGO@Ni-MOFs/AuNPs) was obtained through the electrodeposition. The morphology and structure of rGO@Ni-MOFs/AuNPs were characterized by SEM, FTIR and XRD. The rGO@Ni-MOFs/AuNPs modified electrode was used for the detection of dopamine (DA). The combining the catalysis from Ni-MOFs and AuNPs with the conductivity of rGO endowed rGO@Ni-MOFs/AuNPs with synergetic high catalytic activity to the electrochemical oxidation of DA. The developed modified electrode had a good linear relationship with DA in the concentration range of 0.5 μM~120 μM, and the detection limit was 0.33 μM (S/N=3). Additionally, the potential interferents, electrode stability, reproducibility and practical applications were also studied and satisfactory results were obtained.

Nanoscale ◽  
2022 ◽  
Author(s):  
Rijia Lin ◽  
Yuqi Yao ◽  
Muhammad Yazid Bin Zulkifli ◽  
Xuemei Li ◽  
Shuai Gao ◽  
...  

The practical applications of metal-organic frameworks (MOFs) usually require their assembly into mechanically robust structures, usually achieved via coating onto various types of substrates. This paper describes a simple, scalable,...


2021 ◽  
Author(s):  
Hyunyong Kim ◽  
Hyunseok Kim ◽  
Kimoon Kim ◽  
Eunsung Lee

We report a bottom-up approach to immobilize catalysts into MOFs, including copper halides and gold chloride in a predictable manner. Interestingly, the structures of MOFs bearing NHC metal complexes maintained a similar 4-fold interpenetrated cube. They exhibited exceptionally high porosity despite the interpenetrated structure and showed good stability in various solvents. Moreover, these MOFs possess high size activity depending on the size of the substrates in various reactions, compared to homogeneous catalysis. Also, the high catalytic activity of MOFs can be preserved 4 times without significant loss of crystallinity. Incorporation of the various metal complexes into MOFs allows for the preparation of functional MOFs for practical applications.


2019 ◽  
Vol 55 (18) ◽  
pp. 2692-2695 ◽  
Author(s):  
Xinyan Jiao ◽  
Qingli Hao ◽  
Xifeng Xia ◽  
Zongdeng Wu ◽  
Wu Lei

For the first time, M-Nb2O5@C/rGO composites are fabricated by annealing the precursor of GO supported Nb-metal organic frameworks.


Catalysts ◽  
2018 ◽  
Vol 8 (9) ◽  
pp. 394 ◽  
Author(s):  
Tian Zhao ◽  
Ming Dong ◽  
Ling Yang ◽  
Yuejun Liu

Nowadays, the controllable synthesis of stable hierarchical metal–organic frameworks (MOFs) is very important for practical applications, especially in catalysis. Herein, a well-known chromium–benzenedicarboxylate metal–organic framework, MIL-101(Cr), with a stable hierarchical structure, was produced by using phenylphosphonic acid (PPOA) as a modulator via the hydrothermal method. The presence of phenylphosphonic acid could create structural defects and generate larger mesopores. The synthesized hierarchical MIL-101(Cr) possesses relatively good porosity, and the larger mesopores had widths of 4–10 nm. The hierarchical MIL-101(Cr) showed significant improvement for catalytic activity in the oxidation of indene. Further, the presence of a hierarchical structure could largely enhance large dye molecule uptake properties by impregnating.


2014 ◽  
Vol 2 (15) ◽  
pp. 5323-5329 ◽  
Author(s):  
Min Jiang ◽  
Liangjun Li ◽  
Dandan Zhu ◽  
Hongyu Zhang ◽  
Xuebo Zhao

A stable highly porous metal–organic framework (MOF) layer on reduced graphene oxide immobilized glassy carbon electrode shows good electrocatalytic activity for oxygen reduction reaction.


Author(s):  
Yan-Yuan Jia ◽  
Xiao-Ting Liu ◽  
Wen-He Wang ◽  
Li-Zhu Zhang ◽  
Ying-Hui Zhang ◽  
...  

Metal–organic frameworks (MOFs) are typically built by assembly of metal centres and organic linkers, and have emerged as promising crystalline materials in a variety of fields. However, the stability of MOFs is a key limitation for their practical applications. Herein, we report a novel Sr 2+ -MOF [Sr 4 (Tdada) 2 (H 2 O) 3 (DMF) 2 ] (denoted as NKU- 105 , NKU = Nankai University; H 4 Tdada = 5,5'-((thiophene-2,5-dicar bonyl)bis(azanediyl))diisophthalic acid; DMF =  N,N -dimethylformamide) featuring an open square channel of about 6 Å along the c -axis. Notably, NKU- 105 exhibits much outstanding chemical stability against common organic solvents, boiling water, acids and bases, relative to most MOF materials. Furthermore, NKU- 105 is an environment-friendly luminescent material with a bright cyan emission. This article is part of the themed issue ‘Coordination polymers and metal–organic frameworks: materials by design’.


2021 ◽  
Author(s):  
Hyunyong Kim ◽  
Hyunseok Kim ◽  
Kimoon Kim ◽  
Eunsung Lee

We report a bottom-up approach to immobilize catalysts into MOFs, including copper halides and gold chloride in a predictable manner. Interestingly, the structures of MOFs bearing NHC metal complexes maintained a similar 4-fold interpenetrated cube. They exhibited exceptionally high porosity despite the interpenetrated structure and showed good stability in various solvents. Moreover, these MOFs possess high size activity depending on the size of the substrates in various reactions, compared to homogeneous catalysis. Also, the high catalytic activity of MOFs can be preserved 4 times without significant loss of crystallinity. Incorporation of the various metal complexes into MOFs allows for the preparation of functional MOFs for practical applications.


RSC Advances ◽  
2021 ◽  
Vol 11 (1) ◽  
pp. 501-509
Author(s):  
Shan Huang ◽  
Ming Lu ◽  
Lei Wang

Based on cytochrome c-multiwalled carbon nanotubes (Cyt c-MWCNTs) and cobalt metal organic frameworks/gold nanoparticles (Co-MOFs/AuNPs), an electrochemical biosensor was proposed for the detection of nitrite.


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