A discovery of field-controlling selective adsorption for micro ZnO rods with unexpected piezoelectric catalytic performance

Abstract 3D metal-organic frameworks (MOFs) can be appropriate templates for the fabrication of nanomaterials due to they have active sites exposed on the channel or surface, which thus provide them with improved catalytic performance. In this study, a 3D cobalt-based MOF [Co(H2bpta)]n (Co-MOF), where H4bpta denotes 2,2′,4,4′-biphenyltetracarboxylic acid, has been constructed with the use of a ligand with a high carbon content. On this basis, a 2D magnetic carbon-coated cobalt nanoparticle composite (C@Co) was prepared by using the title MOF. Magnetic C@Co can readily absorb dye from the solution and can thus act as an inexpensive and fast-acting adsorbent. Moreover, we have explored the adsorption isotherms, kinetics and thermodynamics of the anion dyes in detail. The adsorption capacity of the C@Co for investigated methyl orange (MO) and congo red (CR) dyes were 773.48 and 495.66 mg g− 1, respectively. It is noteworthy that MO adsorption is higher in existing materials. Thermodynamic studies suggest that the adsorption processes are spontaneous and exothermic. This study opens a new insight into the synthesis and application of carbon-based materials that enable the selective removal of organic dyes.

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Porous Al-doped ZnO rods with selective adsorption properties

Applied Surface Science ◽

10.1016/j.apsusc.2017.03.018 ◽

2017 ◽

Vol 409 ◽

pp. 102-110 ◽

Cited By ~ 29

Author(s):

Bilel Chouchene ◽

Tahar Ben Chaabane ◽

Kevin Mozet ◽

Emilien Girot ◽

Serge Corbel ◽

...

Keyword(s):

Selective Adsorption ◽

Adsorption Properties ◽

Doped Zno ◽

Zno Rods

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Atom-probe analysis of the solid-liquid interface

Proceedings, annual meeting, Electron Microscopy Society of America ◽

10.1017/s0424820100139755 ◽

1995 ◽

Vol 53 ◽

pp. 676-677

Author(s):

J.A. Panitz

Keyword(s):

Molecular Level ◽

Selective Adsorption ◽

Electronic Devices ◽

Atom Probe ◽

Chemical Agent ◽

Hostile Environment ◽

Solid Interface ◽

Solid Liquid Interface ◽

Solid Liquid ◽

Chemically Selective

The first few atomic layers of a solid can form a barrier between its interior and an often hostile environment. Although adsorption at the vacuum-solid interface has been studied in great detail, little is known about adsorption at the liquid-solid interface. Adsorption at a liquid-solid interface is of intrinsic interest, and is of technological importance because it provides a way to coat a surface with monolayer or multilayer structures. A pinhole free monolayer (with a reasonable dielectric constant) could lead to the development of nanoscale capacitors with unique characteristics and lithographic resists that surpass the resolution of their conventional counterparts. Chemically selective adsorption is of particular interest because it can be used to passivate a surface from external modification or change the wear and the lubrication properties of a surface to reflect new and useful properties. Immunochemical adsorption could be used to fabricate novel molecular electronic devices or to construct small, “smart”, unobtrusive sensors with the potential to detect a wide variety of preselected species at the molecular level. These might include a particular carcinogen in the environment, a specific type of explosive, a chemical agent, a virus, or even a tumor in the human body.

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The design and catalytic performance of molybdenum active sites on an MCM-41 framework for the aerobic oxidation of 5-hydroxymethylfurfural to 2,5-diformylfuran

Catalysis Science & Technology ◽

10.1039/c8cy02291g ◽

2019 ◽

Vol 9 (3) ◽

pp. 811-821 ◽

Cited By ~ 7

Author(s):

Zhao-Meng Wang ◽

Li-Juan Liu ◽

Bo Xiang ◽

Yue Wang ◽

Ya-Jing Lyu ◽

...

Keyword(s):

Catalytic Activity ◽

Active Sites ◽

Aerobic Oxidation ◽

Catalytic Performance ◽

Mcm 41

The catalytic activity decreases as –(SiO)3Mo(OH)(O) > –(SiO)2Mo(O)2 > –(O)4–MoO.

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Optimizing electron density of nickel sulfide electrocatalysts through sulfur vacancy engineering for alkaline hydrogen evolution

Journal of Materials Chemistry A ◽

10.1039/d0ta05594h ◽

2020 ◽

Vol 8 (35) ◽

pp. 18207-18214

Author(s):

Dongbo Jia ◽

Lili Han ◽

Ying Li ◽

Wenjun He ◽

Caichi Liu ◽

...

Keyword(s):

Hydrogen Evolution ◽

Electron Density ◽

Rational Design ◽

Nickel Sulfide ◽

Catalytic Performance ◽

Sulfide Catalysts ◽

Sulfur Vacancy

A novel, rational design for porous S-vacancy nickel sulfide catalysts with remarkable catalytic performance for alkaline HER.

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Catalytic Resonance Theory: Parallel Reaction Pathway Control

10.26434/chemrxiv.10271090 ◽

2019 ◽

Author(s):

M. Alexander Ardagh ◽

Manish Shetty ◽

Anatoliy Kuznetsov ◽

Qi Zhang ◽

Phillip Christopher ◽

...

Keyword(s):

Chemical Reactions ◽

Active Site ◽

Active Sites ◽

Reaction Pathway ◽

Control Strategies ◽

Oscillation Amplitude ◽

Catalytic Performance ◽

Parallel Reaction ◽

Resonance Theory ◽

Static Conditions

Catalytic enhancement of chemical reactions via heterogeneous materials occurs through stabilization of transition states at designed active sites, but dramatically greater rate acceleration on that same active site is achieved when the surface intermediates oscillate in binding energy. The applied oscillation amplitude and frequency can accelerate reactions orders of magnitude above the catalytic rates of static systems, provided the active site dynamics are tuned to the natural frequencies of the surface chemistry. In this work, differences in the characteristics of parallel reactions are exploited via selective application of active site dynamics (0 < ΔU < 1.0 eV amplitude, 10<sup>-6</sup> < f < 10<sup>4</sup> Hz frequency) to control the extent of competing reactions occurring on the shared catalytic surface. Simulation of multiple parallel reaction systems with broad range of variation in chemical parameters revealed that parallel chemistries are highly tunable in selectivity between either pure product, even when specific products are not selectively produced under static conditions. Two mechanisms leading to dynamic selectivity control were identified: (i) surface thermodynamic control of one product species under strong binding conditions, or (ii) catalytic resonance of the kinetics of one reaction over the other. These dynamic parallel pathway control strategies applied to a host of chemical conditions indicate significant potential for improving the catalytic performance of many important industrial chemical reactions beyond their existing static performance.

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