Project description:Nitrogen-doped graphene-supported single atoms convert CO2 to CO, but fail to provide further hydrogenation to methane - a finding attributable to the weak adsorption of CO intermediates. To regulate the adsorption energy, here we investigate the metal-supported single atoms to enable CO2 hydrogenation. We find a copper-supported iron-single-atom catalyst producing a high-rate methane. Density functional theory calculations and in-situ Raman spectroscopy show that the iron atoms attract surrounding intermediates and carry out hydrogenation to generate methane. The catalyst is realized by assembling iron phthalocyanine on the copper surface, followed by in-situ formation of single iron atoms during electrocatalysis, identified using operando X-ray absorption spectroscopy. The copper-supported iron-single-atom catalyst exhibits a CO2-to-methane Faradaic efficiency of 64% and a partial current density of 128 mA cm-2, while the nitrogen-doped graphene-supported one produces only CO. The activity is 32 times higher than a pristine copper under the same conditions of electrolyte and bias.
Project description:Gold and silver are miscible over the entire composition range, and form an attractive combination for fundamental studies on bimetallic catalysts. Au-Ag catalysts have shown synergistic effects for different oxidation and liquid-phase hydrogenation reactions, but have rarely been studied for gas-phase hydrogenation. In this study 3?nm particles of Au, Ag and Au-Ag supported on silica (SBA-15) were investigated as catalysts for selective hydrogenation of butadiene in an excess of propene. The Au catalyst was over an order of magnitude more active than the Ag catalyst at 120?°C. The initial activity of the Au-Ag catalysts scaled linearly with the Au-content, suggesting a direct correlation between the surface and overall compositions of the nanoparticles and the absence of synergistic effects. All Au-containing catalysts were highly selective to butenes (>99.9?%). The Au catalysts were stable, whereas the Au-Ag catalysts lost about half of their activity during 20?h run time at 200?°C, but the initial activity was restored by a consecutive oxidation-reduction treatment. Near ambient pressure x-ray photoelectron spectroscopy showed that exposure to H2 at elevated temperatures led to a gradual enrichment of the surface of the Au-Ag nanoparticles by Ag. These observations highlight the importance of considering progressive atomic rearrangements in bimetallic nanocatalysts under reaction conditions.
Project description:We report stable ultrathin Au nanowires supported on reduced graphene oxide with outstanding electrocatalytic activity for borohydride oxidation. Electrochemical impedance spectroscopy measurements showed abnormal inductive behavior, indicative of surface reactivation. DFT calculations indicate that the origin of the high activity stems from the position of the Au d-band center.
Project description:We have investigated the synthesis and application of Au-Cu/CeO₂ (Cu: Au = 2) in the continuous gas phase (P = 1 atm; T = 498 K) coupled hydrogenation of 5-hydroxymethyl-2-furaldehyde (HMF) with 2-butanol dehydrogenation. STEM-EDX analysis revealed a close surface proximity of both metals in Au-Cu/CeO₂ post-TPR. XPS measurements suggest (support → metal) charge transfer to form Auδ- and strong metal-support interactions to generate Cu⁰ and Cu⁺. Au-Cu/CeO₂ promoted the sole formation of 2,5-dihydroxymethylfuran (DHMF) and 2-butanone in the HMF/2-butanol coupling with full hydrogen utilisation. Under the same reaction conditions, Au/CeO₂ was fully selective to DHMF in standard HMF hydrogenation (using an external hydrogen supply), but delivered a lower production rate and utilised less than 0.2% of the hydrogen supplied. Exclusive -C=O hydrogenation and -OH dehydrogenation is also demonstrated for the coupling of a series of m-substituted (-CH₃, -CH₂CH₃, -CH₂OH, -CF₃, -N(CH₃)₂, -H) furaldehydes with alcohol (1-propanol, 1-butanol, 2-propanol, 2-butanol, cyclohexanol) dehydrogenation over Au-Cu/CeO₂, consistent with a nucleophilic mechanism. In each case, we observed a greater hydrogenation rate and hydrogen utilisation efficiency with a 3⁻15 times lower E-factor in the coupling process relative to standard hydrogenation. Our results demonstrate the feasibility of using hydrogen generated in situ through alcohol dehydrogenation for the selective hydrogenation of m-furaldehydes with important industrial applications.
Project description:Atomic catalysts are promising alternatives to bulk catalysts for the hydrogen evolution reaction (HER), because of their high atomic efficiencies, catalytic activities, and selectivities. Here, we report the ultrathin nanosheet of graphdiyne (GDY)-supported zero-valent palladium atoms and its direct application as a three-dimensional flexible hydrogen-evolving cathode. Our theoretical and experimental findings verified the successful anchoring of Pd0 to GDY and the excellent catalytic performance of Pd0/GDY. At a very low mass loading (0.2%: 1/100 of the 20 wt % Pt/C), Pd0/GDY required only 55 mV to reach 10 mA cm-2 (smaller than 20 wt % Pt/C); it showed larger mass activity (61.5 A mgmetal-1) and turnover frequency (16.7 s-1) than 20 wt % Pt/C and long-term stability during 72 hr of continuous electrolysis. The unusual electrocatalytic properties of Pd0/GDY originate from its unique and precise structure and valence state, resulting in reliable performance as an HER catalyst.
Project description:A sharp increase in the rate of hydrogen isotope scrambling was identified during the hydrogenation of olefins with H2 + D2 mixtures on Pt(111) catalysts, which spectroscopic data suggest is due to a sudden increase in atomic hydrogen surface mobility because of a decrease in the size of the islands of the adsorbed hydrocarbons.
Project description:We have studied the dissociative adsorption of hydrogen under high coverage conditions of adsorbed hydrogen on Pd and Pt nanoislands supported on Au(111) using Density Functional Theory calculations. The results reveal that for Pd/Au(111), the free energy of hydrogen adsorption ΔG is close to 0 kJ/mol when the coverage of adsorbed hydrogen is near 1 ML, where the available catalytic sites are located at the edges of the Pd nanoislands. In the case of Pt/Au(111), ΔG ≈ 0 kJ/mol under a broad range of hydrogen coverage conditions, from 1 ML to 3 ML, depending on the size of the Pt nanoislands. This is the case because the available catalytic sites are located at both the steps and terraces of Pt nanoislands. These findings indicate that Au surfaces with Pd or Pt nanoislands offer catalytic sites with ΔG ≈ 0 for hydrogen reactions, one key factor for an ideal electrocatalyst for hydrogen reactions.
Project description:Solar energy can be converted into chemical energy by photocatalytic water splitting to produce molecular hydrogen. Details of the photo-induced reaction mechanism occurring on the surface of a semiconductor are not fully understood, however. Herein, we employ a model photocatalytic system consisting of single atoms deposited on quantum dots that are anchored on to a primary photocatalyst to explore fundamental aspects of photolytic hydrogen generation. Single platinum atoms (Pt1) are anchored onto carbon nitride quantum dots (CNQDs), which are loaded onto graphitic carbon nitride nanosheets (CNS), forming a Pt1@CNQDs/CNS composite. Pt1@CNQDs/CNS provides a well-defined photocatalytic system in which the electron and proton transfer processes that lead to the formation of hydrogen gas can be investigated. Results suggest that hydrogen bonding between hydrophilic surface groups of the CNQDs and interfacial water molecules facilitates both proton-assisted electron transfer and sorption/desorption pathways. Surface bound hydrogen atoms appear to diffuse from CNQDs surface sites to the deposited Pt1 catalytic sites leading to higher hydrogen-atom fugacity surrounding each isolated Pt1 site. We identify a pathway that allows for hydrogen-atom recombination into molecular hydrogen and eventually to hydrogen bubble evolution.
Project description:To detect hydrogen gas leakage rapidly, many types of hydrogen sensors containing palladium alloy film have been proposed and fabricated to date. However, the mechanisms and factors that determine the response rate of such hydrogen sensor have not been established theoretically. The manners in which response time is forecasted and sensitive film is designed are key issues in developing hydrogen sensors with nanometer film. In this paper, a unilateral diffusion model of hydrogen atoms in Pd alloy based on Fick's second law is proposed to describe the Pd-H reaction process. Model simulation shows that the hydrogen sensor response time with Pd alloy film is dominated by two factors (film thickness and hydrogen diffusion coefficient). Finally, a series of response rate experiments with varying thicknesses of Pd-Y (yttrium) alloy film are implemented to verify model validity. Our proposed model can help researchers in the precise optimization of film thickness to realize a simultaneously speedy and sensitive hydrogen sensor. This study also aids in evaluating the influence of manufacturing errors on performances and comparing the performances of sensors with different thicknesses.