The encapsulation of active metals in microcapsules would be highly advantageous in maintaining or improving the reaction performance of an array of widely used chemical reactions. However, conventional methods suffer from low uniformity, complicated fabrication steps, sintering, leaching, decline of catalytic activity, and/or poor reusability. Here, we report an efficient microfluidic approach to encapsulate Pt nanoparticle stabilized by polyvinylpyrrolidone (PVP) in photocurable double-emulsion droplets with semipermeable thin shells. The encapsulated catalysts are prepared by the in situ photopolymerization of a double emulsion. The rapid and exquisite microfluidics-based fabrication process successfully generates monodisperse microcapsules without loss of the PVP-Pt nanoparticles, which is the first demonstration of the microfluidic encapsulation of active metal with promising catalytic activity. Specifically, compared to quasi-homogeneous catalysis of PVP-Pt nanoparticles for 4-nitrophenol hydrogenation, the encapsulated PVP-Pt nanoparticles demonstrate excellent catalytic activity, a leaching-proof nature, and high reusability under the same reaction conditions. We envision that the approach described here may be an example of elegant catalyst design to efficiently overcome difficult problems in active-metal encapsulation and to dramatically enhance catalytic activity by taking advantage of the unique aspects of microfluidic methods.
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http://dx.doi.org/10.1016/j.jcis.2015.11.037 | DOI Listing |
Nanoscale Adv
June 2024
Advanced Ceramics Research Center, Nagoa Institute of Technolgy Gokiso-cho, Showa-ku Nagoya Aichi 466-8555 Japan
In this work, platinum (Pt) nanoparticles (NPs) were prepared the reduction of Pt salts in an ethylene glycol induced polyol process with an altered polyvinylpyrrolidone (PVP)/Pt molar ratio. With the systematic elucidation of the hydrodynamic size in a liquid; the solid-state size and morphology, crystal structure, surface chemical state and thermal decomposition behavior of the synthesized Pt NPs; as well as the reducing dynamic of Pt cations, the role of PVP in the polyol synthesis of Pt NPs is clarified for the first time. It was found that the amount of PVP does not affect the reducing dynamic of Pt cations, but the chemical state of PVP capped on Pt NPs and the resultant particle size significantly depend on the initial PVP/Pt molar ratio in the precursor solution.
View Article and Find Full Text PDFRSC Adv
May 2023
College of Chemical Engineering, Beijing University of Chemical Technology Beijing 100029 China.
In order to solve the problem that UO in direct ethanol fuel cell anode catalysts is easily lost in acidic solution, resulting in the degradation of catalytic performance, this paper prepared a C/UO/PVP/Pt catalyst in three steps by adding polyvinylpyrrolidone (PVP). The test results by XRD, XPS, TEM and ICP-MS showed that PVP had a good encapsulation effect on UO, and the actual loading rates of Pt and UO were similar to the theoretical values. When 10% PVP was added, the dispersion of Pt nanoparticles was significantly improved, which reduced the particle size of Pt nanoparticles and provided more ethanol electrocatalytic oxidation reaction sites.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
July 2021
Hefei National Laboratory for Physical Sciences at the Microscale, CAS Key Laboratory of Soft Matter Chemistry, Department of Chemistry, University of Science and Technology of China, Hefei, Anhui, 230026, P. R. China.
Interfacial electron transfer between cocatalyst and photosensitizer is key in heterogeneous photocatalysis, yet the underlying mechanism remains subtle and unclear. Surfactant coated on the metal cocatalysts, greatly modulating the microenvironment of catalytic sites, is largely ignored. Herein, a series of Pt co-catalysts with modulated microenvironments, including polyvinylpyrrolidone (PVP) capped Pt nanoparticles (denoted as Pt ), Pt with partially removed PVP (Pt ), and clean Pt without PVP (Pt), were encapsulated into a metal-organic framework (MOF), UiO-66-NH , to afford Pt @UiO-66-NH , Pt @UiO-66-NH , and Pt@UiO-66-NH , respectively, for photocatalytic hydrogen production.
View Article and Find Full Text PDFHum Cell
October 2020
Prefectural University of Hiroshima, Nanatsuka 5562, Shobara, Hiroshima, 727-0023, Japan.
Carcinostatic effects of combined use of hydrogen nano-bubbles (nano-H) and platinum-povidone (PVP--Pt) were examined. Hydrogen-dissolved medium was prepared by hydrogen-gas bubbling with a microporous gas-emittance-terminal into a medium in the absence or presence of PVP-Pt (nano-H, nano-H/PVP-Pt). Human esophagus-derived carcinoma cells KYSE70 were repressed for cell proliferation with nano-H/PVP-Pt more markedly than with nano-H, indicating the hydrogen-intensification for PVP-Pt-alone-carcinostasis.
View Article and Find Full Text PDFJ Mater Chem B
April 2018
School of Chemical Engineering, University of Queensland, St. Lucia, Queensland 4072, Australia.
Metal microcapsules have recently received attention and are being developed as improved carrier materials when compared to polymer microcapsules. In this work we have developed a novel, simplified method by which polymeric microcapsules can be synthesised using a combination of poly(vinyl pyrrolidone)-stabilised platinum nanoparticles (PVP-Pt) and poly(vinyl pyrrolidone) (PVP) as stabilisers, to allow for a secondary metal shell to be grown. We investigate the relationship between the molar ratio of reducing agent to platinum salt and the size of the resulting NPs and seek to develop further fundamental understanding of the factors governing the secondary metal shell thickness and quality, to allow production of cost-effective metal microcapsules without sacrificing core retention efficiency.
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