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Highly Efficient Polydopamine-coated Poly(methyl methacrylate) Nanofiber Supported Platinum⁻nickel Bimetallic Catalyst for Formaldehyde Oxidation at Room Temperature.

ABSTRACT: We fabricated one fibrous-membrane type of flexible and lightweight supported catalyst via loading platinum-nickel nanoparticles (PtNi NPs) directly on the polydopamine-coated polymethylmethacrylate electrospun-fibers (PMMA@PDA). The polymer support with the PDA layer provided numerous active sites, leading to well-monodispersed and sized PtNi NPs on the nanofibers. Through the rational design of PtNi NPs, the resultant catalyst system exhibited 90% conversion for decomposing HCHO (10 ppm) at room temperature with only a low dosage (0.02 g), retaining the high activity for 100 hours. This superior catalytic performance stems from the formate oxidation, which was the key intermediate during HCHO decomposition, and was promoted by the existence of a sufficient Pt-OH-Ni interface in the PtNi NPs with an appropriate Pt/Ni ratio of 1:5. Such tailored Pt-based nanoparticles ideally work together with the polymer nanofibers as a support for catalytic reaction. Compared with classical catalysts, our system can handle a comparable efficiency with much lower air resistance and remarkably lower dosage. Furthermore, the membrane-like morphology provides easy handling and minimizes the leaching of catalyst nanoparticles.

SUBMITTER: He FG

PROVIDER: S-EPMC6523936 | biostudies-literature |

REPOSITORIES: biostudies-literature

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An earth-abundant bimetallic catalyst coated metallic nanowire grown electrode with platinum-like pH-universal hydrogen evolution activity at high current density.

Project description:A self-supported and flexible current collector solely made of earth-abundant elements, NiCo layered double hydroxide (LDH) wrapped around Cu nanowires (Cu-Ws) grown on top of commercially available Cu mesh (Cu-m), outperforms the benchmark 40 wt% Pt/C in catalyzing the electrochemical hydrogen evolution reaction (HER). The Cu-m/Cu-W/NiCo-LDH cathode operates both in acidic and alkaline media exhibiting high turnover frequencies (TOF) at 30 mV (0.3 H2 s-1 in 1 M KOH and 0.32 H2 s-1 in 0.5 M H2SO4, respectively) and minimal overpotentials of 15 ± 6 mV in 1 M KOH and 27 ± 2 mV in 0.5 M H2SO4 at -10 mA cm-2. Cu-m/Cu-W/NiCo-LDH outperforms the activity of 40 wt% Pt/C that needs overpotentials of 22 and 18 mV in 1 M KOH and 0.5 M H2SO4, respectively. With a tremendous advantage over Pt/C in triggering proton reduction with fast kinetics, similar mass activity and pH-universality, the current collector demonstrates outstanding operational durability even at above -1 A cm-2. The high density of electronic states near the Fermi energy level of Cu-Ws is found to be a pivotal factor for efficient electron transfer to the NiCo-LDH catalyst. This class of self-supported electrodes is expected to trigger rapid progress in developing high performance energy conversion and storage devices.

| S-EPMC8152688 | biostudies-literature

Supported Bimetallic AuPd Nanoparticles as a Catalyst for the Selective Hydrogenation of Nitroarenes.

Project description:The solvent-free selective hydrogenation of nitrobenzene was carried out using a supported AuPd nanoparticles catalyst, prepared by the modified impregnation method (MIm), as efficient catalyst >99% yield of aniline (AN) was obtained after 15 h at 90 °C, 3 bar H? that can be used without any further purification or separation, therefore reducing cost and energy input. Supported AuPd nanoparticles catalyst, prepared by MIm, was found to be active and stable even after four recycle experiments, whereas the same catalyst prepared by SIm was deactivated during the recycle experiments. The most effective catalyst was tested for the chemoselective hydrogenation of 4-chloronitrobenzene (CNB) to 4-chloroaniline (CAN). The activation energy of CNB to CAN was found to be 25 kJ mol-1, while that of CNB to AN was found to be 31 kJ mol-1. Based on this, the yield of CAN was maximized (92%) by the lowering the reaction temperature to 25 °C.

| S-EPMC6165381 | biostudies-literature

High-Power Abiotic Direct Glucose Fuel Cell Using a Gold-Platinum Bimetallic Anode Catalyst.

Project description:We developed a high-power abiotic direct glucose fuel cell system using a Au-Pt bimetallic anode catalyst. The high power generation (95.7 mW cm-2) was attained by optimizing operating conditions such as the composition of a bimetallic anode catalyst, loading amount of the metal catalyst on a carbon support, ionomer/carbon weight ratio when the catalyst was applied to the anode, glucose and KOH concentrations in the fuel solution, and operating temperature and flow rate of the fuel solution. It was found that poly(N-vinyl-2-pyrrolidone)-stabilized Au80Pt20 nanoparticles (mean diameter 1.5 nm) on a carbon (Ketjen Black 600) support function as a highly active anode catalyst for the glucose electrooxidation. The ionomer/carbon weight ratio also greatly affects the cell properties, which was found to be optimal at 0.2. As for the glucose concentration, a maximum cell power was derived at 0.4-0.6 mol dm-3. A high KOH concentration (4.0 mol dm-3) was preferable for deriving the maximum power. The cell power increased with the increasing flow rate of the glucose solution up to 50 cm3 min-1 and leveled off thereafter. At the optimal condition, the maximum power density and corresponding cell voltage of 58.2 mW cm-2 (0.36 V) and 95.7 mW cm-2 (0.34 V) were recorded at 298 and 328 K, respectively.

| S-EPMC6643607 | biostudies-literature

Printed Circuit Board-Derived Glass Fiber-Epoxy Resin-Supported Mo-Cu Bimetallic Catalyst for Glucose Synthesis.

Project description:A glass fiber-epoxy resin (GFER) framework derived from mixed waste printed circuit boards (MWPCBs) was utilized to prepare a cost-effective, reusable Mo-Cu bimetallic Bronsted-Lewis solid acid catalyst through wet-impregnation under near-infrared radiation (NIRR) activation. The efficacy of the novel Mo-Cu catalyst was assessed in the synthesis of glucose through hydrolysis of jute (Corchorus olitorius) fiber, and the process parameters were optimized (Mo precursor loading: 1.0 wt %, catalyst concentration: 5 wt %, hydrolysis temperature: 80 °C, and hydrolysis time: 10 min) through Taguchi orthogonal design. The GFER support and the prepared catalysts were characterized through thermogravimetric, X-ray diffraction (XRD), Fourier-transform infrared (FTIR), Brunauer-Emmett-Teller (BET)-density functional theory, and TPD analyses. The optimal Mo-Cu catalyst and the GFER support possessed 45.377 and 7.049 m2/g BET area, 0.04408 and 0.02317 cc/g pore volume, 1.9334 and 0.7482 nm modal pore size, and surface acidity of 0.48 and 0.40 mmol NH3/g catalyst, respectively. X-ray photoelectron spectroscopy bands confirmed the coexistence of Mo6+ and Cu2+ species; XRD and FTIR analyses indicated the presence of MoO3 and CuO crystalline phases in all prepared catalysts. The optimal catalyst prepared through NIRR (wavelength 0.75-1.4 ?m)-activated hydrothermal treatment resulted in a significantly greater glucose yield (75.84 mol %) than that achieved (53.64 mol %) using a conventionally prepared catalyst. Thus, an energy-efficient application of NIRR (100 W) could significantly improve catalytic properties over conventional hydrothermal treatment (500 W). The present investigation provides an innovative application of MWPCB-derived GFER as a promising cost-effective support for the preparation of highly efficient inexpensive solid catalysts for sustainable synthesis of glucose from low-cost waste jute fiber.

| S-EPMC6643727 | biostudies-literature

Controlled Nutrient Delivery to Pancreatic Islets Using Polydopamine-Coated Mesoporous Silica Nanoparticles

Project description:In the present study, we designed a nanoscale platform for the sustained and controlled delivery of nutrients to pancreatic islets-upon transplantation. Our platform consists of a mesoporous silica nanoparticle (MSNP), loaded with glutamine (G), an essential amino acid required for islet survival and function, and capped with polydopamine (PD). To control the release of glutamine, various concentrations (0.5 - 2 mg/mL) of PD and incubation times (0.5 – 2 h) with MSNPs were investigated in terms of pharmacological properties and biological functions. After extensive testing, PD-G-MSNPs made using PD coating of 0.5 mg/mL incubated for 0.5 h resulted in the optimal platform to maintain the islet viability and functionality in vitro. Following syngeneic renal sub-capsule islet transplantation in STZ-diabetic mice, PD-G-MSNPs improved the engraftment of pancreatic islets as well as their function, resulting in re-establishment of glycemic control. Collectively, our data shows that PD-G-MSNPs can support transplanted islets by providing them with a controlled and sustained supply of nutrients.

2023-12-04 | GSE247020 | GEO

Overcoming immiscibility toward bimetallic catalyst library.

Project description:Bimetallics are emerging as important materials that often exhibit distinct chemical properties from monometallics. However, there is limited access to homogeneously alloyed bimetallics because of the thermodynamic immiscibility of the constituent elements. Overcoming the inherent immiscibility in bimetallic systems would create a bimetallic library with unique properties. Here, we present a nonequilibrium synthesis strategy to address the immiscibility challenge in bimetallics. As a proof of concept, we synthesize a broad range of homogeneously alloyed Cu-based bimetallic nanoparticles regardless of the thermodynamic immiscibility. The nonequilibrated bimetallic nanoparticles are further investigated as electrocatalysts for carbon monoxide reduction at commercially relevant current densities (>100 mA cm-2), in which Cu0.9Ni0.1 shows the highest multicarbon product Faradaic efficiency of ~76% with a current density of ~93 mA cm-2. The ability to overcome thermodynamic immiscibility in multimetallic synthesis offers freedom to design and synthesize new functional nanomaterials with desired chemical compositions and catalytic properties.

| S-EPMC7182425 | biostudies-literature

Enhanced Formaldehyde Oxidation Performance of the Mesoporous TiO<sub>2</sub>(B)-Supported Pt Catalyst: The Role of Hydroxyls.

Project description:As one of the crystal phases of titania, TiO2(B) was first utilized as a catalyst carrier for the oxidation of formaldehyde (HCHO). The mesoporous TiO2(B) loaded with Pt nanoparticles enhanced the HCHO oxidation reaction whose reaction rate was 4.5-8.4 times those of other crystalline TiO2-supported Pt catalysts. Simultaneously, Pt/TiO2(B) exhibited long-term stable HCHO oxidation performance. The structural characterization results showed that in comparison with Pt/anatase, Pt/TiO2(B) had more abundant hydroxyls, facilitating increasing the content of oxygen species. Studies on the role of hydroxyls in HCHO oxidation of Pt/TiO2(B) illustrated that synergistic involvement of terminally bound hydroxyls and bridging hydroxyls in HCHO oxidation accelerated the transformation from HCHO to formate via dioxymethylene. Moreover, hydroxyls could avoid the accumulation of excessive formate on Pt/TiO2(B) and promote the rapid oxidation of CO. Accordingly, the hydroxyl groups could accelerate each substep of formaldehyde oxidation, which enabled Pt/TiO2(B) to exhibit excellent formaldehyde oxidation performance.

| S-EPMC9330097 | biostudies-literature

Microwave-Induced Chemotoxicity of Polydopamine-Coated Magnetic Nanocubes.

Project description:Polydopamine-coated FeCo nanocubes (PDFCs) were successfully synthesized and tested under microwave irradiation of 2.45 GHz frequency and 0.86 W/cm(2) power. These particles were found to be non-toxic in the absence of irradiation, but gained significant toxicity upon irradiation. Interestingly, no increase in relative heating rate was observed when the PDFCs were irradiated in solution, eliminating nanoparticle (NP)-induced thermal ablation as the source of toxicity. Based on these studies, we propose that microwave-induced redox processes generate the observed toxicity.

| S-EPMC4581245 | biostudies-literature

Cellulose Nanofiber Composite with Bimetallic Zeolite Imidazole Framework for Electrochemical Supercapacitors.

Project description:Cellulose nanofiber (CNF) and hybrid zeolite imidazole framework (HZ) are an emerging biomaterial and a porous carbonous material, respectively. The composite of these two materials could have versatile physiochemical characteristics. A cellulose nanofiber and cobalt-containing zeolite framework-based composite was prepared using an in-situ and eco-friendly chemical method followed by pyrolysis. The composite was comprised of cobalt nanoparticles decorated on highly graphitized N-doped nanoporous carbons (NPC) wrapped with carbon nanotubes (CNTs) produced from the direct carbonization of HZ. By varying the ratio of CNF in the composite, we determined the optimal concentration and characterized the derived samples using sophisticated techniques. Scanning electron microscopy (SEM), X-ray diffraction analysis (XRD), and X-ray photoelectron spectroscopy (XPS) confirmed the functionalization of CNF in the metallic cobalt-covered N-doped NPC wrapped with CNTs. The CNF-HZNPC composite electrodes show superior electrochemical performance, which is suitable for supercapacitor applications; its specific capacitance is 146 F/g at 1 A/g. Furthermore, the composite electrodes retain a cycling stability of about 90% over 2000 charge-discharge cycles at 10 A/g. The superior electrochemical properties of the cellulose make it a promising candidate for developing electrodes for energy storage applications.

| S-EPMC7913791 | biostudies-literature

Synthesis and catalytic performance of polydopamine supported metal nanoparticles.

Project description:Polydopamine (PDA) is an emerging nature-inspired biopolymer material that possesses many interesting properties including self-assembly and universal adhesion. PDA is also able to form coordination bonds with various metal ions, which can be reduced to metal nanoparticles (NPs) as a result of thermal annealing under protective environment. In this study, PDA has been utilized as a support material to synthesize Pt NPs in an aqueous solution at room temperature. The catalytic performance of the resulting PDA-Pt nanocomposite was evaluated using an electrochemical workstation which showed comparable activity to Pt/C material for hydrogen evolution reaction (HER). Furthermore, Cu, Ni, and Cu-Ni NPs supported on PDA were also obtained using this strategy with assistance of subsequent thermal annealing. The phase evolution of the NPs was studied by in-situ X-ray diffraction while the morphology of the nanoparticles was investigated using electron microscopic techniques. Preliminary results showed the NPs supported on PDA also possessed HER activity. This work demonstrates that PDA can be utilized as a potential support for synthesis of metal NPs that can be exploited in engineering applications such as catalysts.

| S-EPMC7319955 | biostudies-literature

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