Au Pd Bimetallic Catalysts Research Articles

Bimetallic PdAu catalysts for formic acid dehydrogenation

A series of monometallic and bimetallic palladium gold catalyst were prepared and studied for the formic acid dehydrogenation reaction. Different Pd/Au compositions were employed (PdxAu100-x, where x = 25; 50 and 75) and their impact on alloy structure, particle size and dispersion was evaluated. Active phase composition and reaction parameters such as temperature, formic acid concentration or formate/formic acid ratio were adjusted to obtain active and selective catalyst for hydrogen production. An important particle size effect was observed and related to Pd/Au composition for all bimetallic catalysts.

Pickering HIPEs derived hierarchical porous nitrogen-doped carbon supported bimetallic AuPd catalyst for base-free aerobic oxidation of HMF to FDCA in water

As an important renewable alternative to the production of petroleum-derived terephthalic acid, selective aerobic oxidation of biomass derivative 5-hydroxymethylfurfural (HMF) into high value-added 2,5-furandicarboxylic acid (FDCA) is attracting increasing attention. Herein, a novel hierarchical porous nitrogen-doped carbon (NC) supported bimetallic AuPd catalyst was synthesized by Pickering high internal phase emulsions (Pickering HIPEs) templating method, subsequent carbonization and the sol-curing technique. By varying Pickering HIPEs parameter, nitrogen-doped content and the loaded AuPd nanoparticles, AuxPdy/NC catalysts with adjustable porous structure and basicity were obtained. Benefiting from the synergistic effects of the high basicity of NC support and efficient bimetallic AuPd catalyst, tandem oxidation of HMF to FDCA reactions can be carried out under base-free condition in water, which makes the biomass transformation process environmental friendliness and economic. And the highest yield of FDCA at 96.7% was achieved under the optimal reaction conditions. Regeneration test revealed the obtained AuxPdy/NC catalyst was recovered and reused at least five times without significant loss of catalytic activity. The present work offers a versatile strategy for developing nitrogen-doped carbon supported highly efficient bimetallic catalysts with hierarchical porous structure and adjusting basicity for a wide range of base-free catalytic oxidation in water.

Complete Benzene Oxidation over Mono and Bimetallic Pd—Au Catalysts on Alumina-Supported Y-Doped Ceria

The protection of environment and human health stimulates intensive research for abatement of volatile organic compounds (VOCs) in the atmosphere. Complete catalytic oxidation is an efficient, environmentally friendly and economically feasible method for elimination of VOCs. This study aims to design high performing and cost-effective catalytic formulations by exploration of appropriate and economically viable supports. Alumina-supported ceria (30 wt.%) and Y2O3 (1 wt.%)-doped ceria were prepared by mechanical mixing and were used as support of mono Au (2 wt.%) and Pd (1 wt.%) and bimetallic Pd-Au catalysts. The characterization by textural measurements, X-ray powder diffraction (PXRD), X-ray photoelectron spectroscopy (XPS), EPR (electron paramagnetic resonance) and temperature-programmed reduction (TPR) was carried out in order to clarify the relationship between catalyst composition, textural, structural and surface properties, reducibility and catalytic performance for complete benzene oxidation. Among all studied catalysts, Pd-based catalysts exhibited the best combustion activity. In particular, monometallic Pd on alumina supported Y-doped ceria attained 100% of complete benzene conversion at 180 °C. These catalytic materials have potential to meet stringent emission regulations in an economical and effective way.

Continuous Flow Synthesis of Bimetallic AuPd Catalysts for the Selective Oxidation of 5‐Hydroxymethylfurfural to 2,5‐Furandicarboxylic Acid

AbstractThe production of 2,5‐furandicarboxylic acid (FDCA) from the selective oxidation of 5‐hydroxymethylfurfural (HMF) is a critical step in the production of biopolymers from biomass‐derived materials. In this study, we report the catalytic performance of monometallic Au and Pd, and bimetallic AuPd nanoparticles with different Au : Pd molar ratios synthesised under continuous flow conditions using a millifluidic set‐up and subsequently deposited onto titanium dioxide as the chosen support. This synthetic technique provided a better control over mean particle size and metal alloy composition, that resulted in higher FDCA yield when the catalysts were compared to similar batch‐synthesised materials. A 99% FDCA yield was obtained with the millifluidic‐prepared AuPd/TiO2 catalyst (Au : Pd molar composition of 75 : 25) after being calcined and reduced at 200 °C. The heat treatment caused a partial removal of the protective ligand (polyvinyl alcohol) encapsulating the nanoparticles and so induced stronger metal‐support interactions. The catalyst reusability was also tested, and showed limited particle sintering after five reaction cycles.

Pd–Au bimetallic catalysts supported on ZnO for selective 1,3-butadiene hydrogenation

The effect of the ZnO morphology on the properties of Pd–Au bimetallic catalysts has been discussed.

Selective oxidation using Au-Pd catalysts: Role of the support in the stabilization of colloidal Au-Pd NPs

• Properties and morphology of the support play a significant role in the final Au-Pd particle size. • Nanostructured ceria is most effective in stabilizing Au-Pd colloidal NPs. • Au-Pd particle size and Ce 3+ in ceria are correlated with activity. • Au-Pd supported on ceria displays higher selectivity to benzaldehyde. Bimetallic Au-Pd NPs with a mean particle size of ca. 1.7 nm were prepared by colloidal synthesis with PVA as a stabilizer and immobilized on various ceria and titania nanostructures. The catalysts were characterised by TEM, XRD, XPS, ICP-AES, and their catalytic performance assessed in the solvent-less selective oxidation of benzyl alcohol. It is shown that even with a technique such as sol-immobilization, the final particle size is sensitive to the physiochemical properties and morphology of the support. In particular, ceria nanostructures were found to be more effective at stabilizing colloidal Au-Pd NPs than titania. Among the ceria nanostructured supports investigated, Au-Pd/ceria nanorods exhibited the highest catalytic activity (TOF > 34,700 h −1 ) and highest benzaldehyde yield. The particle size of the supported Au-Pd was found to be correlated with the surface area and concentration of Ce 3+ and oxygen vacancies in the ceria nanostructures. Overall, the catalytic activity of supported bimetallic Au-Pd catalysts is likely to be governed by a complex interplay of contributions from the particle size, and support morphology, structure and properties.

Structural and electronic feature evolution of Au-Pd bimetallic catalysts supported on graphene and SiO2 in H2 and O2

The structure and electronic feature evolution of graphene (Gr)- and SiO2-supported Au-Pd bimetallic nanoparticles (NPs) in H2 and O2 at different temperatures were investigated with a series of techniques and DFT calculation method. It was found that a uniform Au-Pd alloy nanostructure was formed on Gr, while a Au@Pd core-shell structure was generated on SiO2. The formation of Au-Pd alloy nanostructure on Gr originates from a strong s-p-d hybridization among Au 5d6s, Pd 4d and Gr C 2p, which greatly facilitates the electron transfer among Au, Pd and Gr and enhances the reduction of palladium species. The higher stability of the geometric and electronic structures of Au-Pd NPs on Gr than on SiO2 in both H2 and O2 atmospheres below 100 °C results from the fact that Gr could timely supplement the electrons transferring to O2 from metallic species in O2-treatment process, but play a contrary role in H2-treatment process. Such unique geometric and electronic structures endow Au-Pd/Gr show higher catalytic activity than Au-Pd/SiO2 in selective oxidation of methanol to methyl formate. A further investigation of catalytic mechanism reveals that the activation of O2 is dominated by the methanol-assisted way on Au and Au-Pd alloy NPs, whereas the direct dissociation of O2 mainly occurs on Pd and Au@Pd NPs.

Ring-Opening Transformation of 5-Hydroxymethylfurfural Using a Golden Single-Atomic-Site Palladium Catalyst

The development of function-integrated catalysts to enable scalable and efficient biomass valorization is an important topic. Here, a stepwise methodology was developed to fabricate novel supported Au–Pd bimetallic catalysts featuring immobilized well-defined on-surface nanoarchitectures (Pd∧Au). This was achieved by an atomic decoration of a trace amount of Pd (Pd/Au molar ratio of 0.01–0.02) on the surface of 2 nm Au nanoparticle (NP, 0.86 wt %) preanchored to titania. Benefiting from their unique structural merits and the cooperative interplay among the selective hydrogenation activity furnished by the ultrasmall Pd∧Au NPs and prominent Lewis acidity endowed by TiO2, Pd0.02∧Au/TiO2 exhibits excellent activity with 100% conversion and over 90% selectivity and stability (turnover number up to 48 300) toward controlled ring-opening conversion of 5-hydroxymethylfurfural and related furanic compounds to the corresponding di- and triketone-type products under mild conditions (120 °C, 10 bar of H2). The resul...

Formation of PdO on Au–Pd bimetallic catalysts and the effect on benzyl alcohol oxidation

A series of catalysts consisting of gold–palladium bimetallic nanoparticles (Au–Pd NPs in the range of 1–6 nm) anchored on foamlike mesoporous silica were used for the aerobic oxidation of benzyl alcohol. A remarkable synergistic effect was observed on these Au–Pd NP catalysts prepared by a one-pot method. Both experimental and theoretical study revealed a close relationship between the surface PdO species on the catalysts and their catalytic performance; that is, higher surface PdO content leads to lower catalytic activity. The surface content of PdO species on the catalysts could be tuned by controlling the Au/Pd ratios, because the formation of Au–Pd alloy NPs and electron transfer between surface Au and Pd atoms prevented the oxidation of surface Pd and retarded the formation of PdO species. An optimal Au/Pd ratio of 1/4.5 on the foamlike mesoporous silica support was obtained, with nearly no surface PdO species formed, and resulted in the highest benzyl alcohol conversion of 96%. The bimetallic Au–Pd catalysts exhibited much higher catalytic activity for benzyl alcohol oxidation (TOF = 50,000–60,000 h−1) than the monometallic Pd catalyst (TOF = 12,500 h−1), on which surface Pd is easily oxidized to PdO. These results provide direct evidence for the synergistic effect of Au–Pd bimetallic catalysts in benzyl alcohol oxidation.

Size, nanostructure, and composition dependence of bimetallic Au–Pd supported on ceria–zirconia mixed oxide catalysts for selective oxidation of benzyl alcohol

A bimetallic Au–Pd catalyst supported on ceria–zirconia with Au:Pd molar ratio 0.8 has been synthesized using a simultaneous deposition–precipitation method and oxidized at 250, 450, and 700 °C in order to modify its particle size, nanostructure, and composition. Combined X-ray energy dispersive spectroscopy (XEDS) and X-ray photoelectron spectroscopy (XPS) analysis clearly evidence that the bimetallic Au–Pd catalyst oxidized at 250 °C is made up of a mixture of monometallic Au and Pd and bimetallic Au–Pd nanoparticles with Au:Pd ratios varying over a wide range. Increasing oxidation temperature leads to a stronger interaction between Au and Pd. Meanwhile, a slight increase of particle size and a narrowing of the Au:Pd ratio in the bimetallic nanoparticles take place. Compared with titania and activated carbon supports, the resistance against sintering at high temperatures of Au–Pd metal particles supported on ceria–zirconia is proven to be higher. A synergistic effect has been observed for selective oxidation of benzyl alcohol on these catalysts. The catalytic activity decreases only slightly after oxidation at 450 °C. However, oxidation at 700 °C results in much lower catalytic activity. Migration of Pd onto Au particles during oxidation of benzyl alcohol enhances the catalytic activity of a physical mixture of monometallic Au and Pd supported on ceria–zirconia catalysts. This fact, jointly with an analysis of the intrinsic activity, reveals the influence of the actual nature of Au–Pd interactions in the bimetallic particles, which points to higher activity of Au@Pd or AuPd@Pd nanostructures on ceria–zirconia supports.

Carbon monoxide and formic acid electrooxidation study on Au decorated Pd catalysts prepared via microwave assisted polyol method

In this study, carbon supported Pd monometallic and PdAu bimetallic catalysts are prepared by using microwave assisted polyol method to investigate their carbon monoxide and formic acid electrooxidation activities. These catalysts are characterized by using Scanning Electron Micrsocopy (SEM-EDX) and N2 adsorption desorption measurements. EDX measurements reveal that catalysts are prepared at desired ratios. The electrochemical characterization was performed via cyclic voltammetry and CO stripping voltammetry. Electrochemical surface area (ECSA) was calculated thanks to CO oxidation peaks. It was reported that CO tolerance and ECSA of the PdAu/C catalysts were higher than that of the Pd/C, attributed to sweeping effect of Au particles in terms of CO adsorption. Furthermore, formic acid electrooxidation activity of these catalysts are examined by using cyclic voltammetry (CV). PdAu/CNT catalyst at prepared at 90:10 Pd:Au ratio exhibited the highest formic acid electroxidation activity. It is clear that PdAu/CNT catalyst is a promising catalyst for CO and formic acid electrooxidation.

Selective hydrogenolysis of lignin and model compounds to monophenols over AuPd/CeO2

The mild depolymerization of lignin into aromatic monomer is a grand challenge owing to the various aryl ether C–O bonds, particularly for the most abundant β-O-4, α-O-4 and 4-O-5 linkages. Rod-shaped CeO2 supported AuPd bimetallic catalysts fabricated by sol-immobilization method presented robust alloy structure, as evidenced by TEM, XPS, UV–vis, and CO-DRIFTS. For the hydrogenolysis of CO bond model compound with formic acid, Au1Pd1/CeO2 showed about 23.5 and 6 folds increase in activity compared with its monometallic counterparts Au/CeO2 and Pd/CeO2, respectively. The outstanding performance was mainly ascribed to the increased adsorption ability of electron-deficient Pd for aromatic C–O bond. Additionally, formic acid-mediated Au1Pd1/CeO2 has efficiently performed hydrogenolysis of real lignin into a variety of valuable monophenols, achieving 44.1% yield at low temperature.

Selective Oxidation of Veratryl Alcohol over Au-Pd/Ce0.62Zr0.38O₂ Catalysts Synthesized by Sol-Immobilization: Effect of Au:Pd Molar Ratio.

The selective oxidation of veratryl alcohol (VA), a model compound of lignin, with oxygen molecules to produce veratraldehyde (VAld) was studied over monometallic Au, Pd, and bimetallic Au:Pd nanoparticles supported on a Ce0.62Zr0.38O2 mixed oxide for the first time. These bimetallic Au-Pd catalysts with Au:Pd molar ratios from 0.4 to 4.3 were synthesized by the sol-immobilization method. Furthermore, all the catalysts were characterized by inductively coupled plasma-atomic emission spectroscopy (ICP-AES), N2 physisorption, X-ray photoelectron spectroscopy (XPS), scanning transmission electron microscopy-high angle annular dark field (STEM-HAADF) imaging, energy dispersive X-ray spectroscopy (EDXS), and temperature programmed reduction (TPR) techniques. A synergistic effect between gold and palladium was observed over all the bimetallic catalysts in a wide range of studied Au:Pd ratios. Remarkably, the optimum Au:Pd ratio for this reaction was 1.4 with a turnover frequency of almost six times larger than for the monometallic gold and palladium catalysts. Selectivity to veratraldehyde was higher than 99% for the monometallic Au, Pd, and all the bimetallic Au-Pd catalysts, and stayed constant during the reaction time.

Effect of Y Modified Ceria Support in Mono and Bimetallic Pd–Au Catalysts for Complete Benzene Oxidation

Mono metallic and bimetallic Pd (1 wt. %)–Au (3 wt. %) catalysts were prepared using two ceria supports doped with 1 wt. % Y2O3. Yttrium was added by impregnation or co-precipitation. The catalyst synthesis was carried out by deposition–precipitation method, with sequential deposition–precipitation of palladium over previously loaded gold in the case of the bimetallic samples. The obtained materials, characterized by X-ray powder diffraction (XRD), High resolution transmission electron microscopy (HRTEM), X-ray photoelectron spectroscopy (XPS), and temperature programmed reduction (TPR) techniques, were tested in the complete benzene oxidation (CBO). The results of the characterization analyses and the catalytic performance pointed to a close relationship between structural, redox, and catalytic properties of mono and bimetallic catalysts. Among the monometallic systems, Pd catalysts were more active as compared to the corresponding Au catalysts. The bimetallic systems exhibited the best combustion activity. In particular, over Pd–Au supported on Y-impregnated ceria, 100% of benzene conversion towards total oxidation at the temperature of 150 °C was obtained. Comparison of surface sensitive XPS results of fresh and spent catalysts ascertained the redox character of the reaction.

Ti-Doped Pd-Au Catalysts for One-Pot Hydrogenation and Ring Opening of Furfural

Pd-Au bimetallic catalysts with different Pd/Au atomic ratios, supported on ordered structured silica (Hexagonal mesoporous silica—HMS, or Santa Barbara Amorphous-15—SBA-15) were evaluated for one-pot hydrogenation of furfural to 1,2-pentanediol. The surface and structural properties of the catalysts were deeply investigated by X-ray photoelectron spectroscopy (XPS), X-ray diffraction (XRD), N2 adsorption isotherms (BET), Infrared spectroscopy (IR), and acid capacity measurements. XPS studies revealed that Ti doped supports had higher dispersion of the active phase, particularly in the case of Pd-Au materials in which Ti played an important role in stabilizing the metallic species. Among the various process conditions studied, such as temperature (160 °C), catalyst amount (10% w/w), and reaction time (5 h), H2 pressure (500 psi) was found to improve the 1,2-pentanediol selectivity. The SBA silica bimetallic Ti-doped system showed the best performance in terms of stability and reusability, after multiple cycles. Under specific reaction conditions, the synergism between Pd-Au alloy and Ti doping of the support allowed the ring opening pathway towards the formation of 1,2-pentanediol in furfural hydrogenation.

Aerobic oxidation of 5-hydroxymethylfurfural to 2,5-difurancarboxylic acid over Pd-Au nanoparticles supported on Mg-Al hydrotalcite

A series of reconstructed hydrotalcite supported monometallic Au or Pd and bimetallic Pd-Au nanoparticles with various Pd/Au ratios were synthesized. The physicochemical properties of these catalysts were charaterized by X-ray diffraction (XRD), X-ray photoelectronic spectroscopy (XPS), Transimission electron microscopy, N2 adsorption, etc. The catalysts were used for the aerobic oxidaiton of 5-hydroxymethylfurfural(HMF) into 2,5-furandicarboxylic acid (FDCA) in an alkaline aqueous solution. The monometallic Pd or Au catalyst could not oxidize the intermediate product-5-hydroxymethyl-2-furanic acid (HMFCA), while bimetallic Pd-Au catalysts exhibited good performances for HMFCA oxidation. A high yield of FDCA up to 90% was achieved over the Pd-Au/HT catalyst with the Au/Pd ratio of 4 at 60 °C for 6 h. The enhanced oxidation activity of HMF for the bimetallic catalysts is attributed to the syneretic effect between Au and Pd nanoparticles and the formation of smaller particle size that facilicates the oxidation of HMF to FDCA. The Pd-Au/HT(1 :4) catalyst also exhibited a good stabiblity without significant loss in FDCA yield after five succesive cycles.

Interconversion between CO2 and HCOOH under Basic Conditions Catalyzed by PdAu Nanoparticles Supported by Amine-Functionalized Reduced Graphene Oxide as a Dual Catalyst

Recently, the utilization of formic acid (FA) or formate as promising hydrogen carriers through the interconversion between CO2 and HCOOH or HCO3– and HCOO–, respectively, has attracted increasing research interest. In this work, a PdAu bimetallic catalyst supported on phenylenediamine-alkalized reduced graphene oxide (Pd0.50Au0.50/PDA-rGO) was developed for catalyzing bicarbonate hydrogenation under basic conditions as well as FA/formate dehydrogenation under acidic and basic conditions. Without any additives, a very high yield (94%) of potassium formate (PF) can be achieved from the hydrogenation of potassium bicarbonate at 50 °C for 16 h. On the other hand, initial TOFs of 1.63 × 103 and 6.98 × 103 h–1 were accomplished in the dehydrogenations of 6 mol/L PF and 8 mol/L FA, respectively, at 80 °C. This work successfully demonstrates highly efficient CO2 hydrogenation and is the first report of a Pd-based heterogeneous catalyst for the additive-free dehydrogenation of concentrated (>6 mol/L) PF or FA sol...

Light-Driven Small Molecule Oxidation on Pd-Au Bimetallic Film-Coupled Electrodes

The ability to efficiently oxidize small molecules containing C-C bonds (e.g. ethanol and ethylene glycol) is challenging at low temperature (i.e., < 80°C). It was previously shown that bimetallic catalysts (e.g. Pd-Au systems) have enhanced electrocatalytic activities for various organic reactions.1 Moreover, an increased overall selectivity and turnover frequency for primary alcohol conversion to aldehydes has been reported after the addition of Au to Pd nanocrystals.2 However dissociation of the C-C bonds is often incomplete and only undergoes a partial oxidation to intermediate product(s). Therefore, a breakthrough technology is required to overcome this obstacle at low temperature. One strategy is to tailor bimetallic catalysts for photo-electrochemical oxidation reactions by engineering the plasmonic response. For example, bimetallic Pd-Au nanostructures have been tuned to the visible portion of the solar spectrum for use as plasmonic H2 sensors.3 We report the use of nanolithography patterned Pd-Au bimetallic catalysts for the photo-electrochemical oxidation of ethanol and ethylene glycol. We consider the effect of laser and solar-simulated excitations on nanostructured Pd-Au bimetallic electrodes fabricated on atomic layer deposited TiO2 films coupled to a back contact.4-5 The Pd-Au bimetallic electrodes with and without film-coupling are evaluated in parallel with discrete dipole approximation (DDA) modeling derived from doubly-periodic array simulations, which allows assessment of the absorption, scattering, and near-field enhancements. For select bimetallic configurations, we compare the selectivity and kinetics of the photo-electrochemical oxidation reactions and discuss the catalytic response driven by light excitation. Lu, C.L.; Prasad, K. S.; Wu, H.L.; Ho, J.A.; Huang, M.H. JACS 2010, 132 (41), 14546-14553.Enache, D. I.; Edwards, J. K.; Landon, P.; Solsona-Espriu, B.; Carley, A. F.; Herzing, A. A.; Watanabe, M.; Kiely, C. J.; Knight, D. W.; Hutchings, G. J. Science 2006, 311 (5759), 362-365.Nugroho, F. A.; Iandolo, B.; Wagner, J. B.; Langhammer, C. ACS Nano 2016, 10 (2), 2871-9.McClure, J. P.; Grew, K. N.; Das, N. C.; Chu, D.; Baker, D.; Strnad, N.; Gobrogge, E. MRS Advances 2017, 2 (55), 3397-3402.Ciracì, C.; Chen, X.; Mock, J. J.; McGuire, F.; Liu, X.; Oh, S.-H.; Smith, D. R. Applied Physics Letters 2014, 104 (2), 023109.

Porous Nanocrystalline Silicon Supported Bimetallic Pd-Au Catalysts: Preparation, Characterization, and Direct Hydrogen Peroxide Synthesis.

Bimetallic Pd-Au catalysts were prepared on the porous nanocrystalline silicon (PSi) for the first time. The catalysts were tested in the reaction of direct hydrogen peroxide synthesis and characterized by standard structural and chemical techniques. It was shown that the Pd-Au/PSi catalyst prepared from conventional H2[PdCl4] and H[AuCl4] precursors contains monometallic Pd and a range of different Pd-Au alloy nanoparticles over the oxidized PSi surface. The PdAu2/PSi catalyst prepared from the [Pd(NH3)4][AuCl4]2 double complex salt (DCS) single-source precursor predominantly contains bimetallic Pd-Au alloy nanoparticles. For both catalysts the surface of bimetallic nanoparticles is Pd-enriched and contains palladium in Pd0 and Pd2+ states. Among the catalysts studied, the PdAu2/PSi catalyst was the most active and selective in the direct H2O2 synthesis with H2O2 productivity of 0.5 at selectivity of 50% and H2O2 concentration of 0.023 M in 0.03 M H2SO4-methanol solution after 5 h on stream at −10°C and atmospheric pressure. This performance is due to high activity in the H2O2 synthesis reaction and low activities in the undesirable H2O2 decomposition and hydrogenation reactions. Good performance of the PdAu2/PSi catalyst was associated with the major part of Pd in the catalyst being in the form of the bimetallic Pd-Au nanoparticles. Porous silicon was concluded to be a promising catalytic support for direct hydrogen peroxide synthesis due to its inertness with respect to undesirable side reactions, high thermal stability, and conductivity, possibility of safe operation at high temperatures and pressures and a well-established manufacturing process.

TiO2 Supported gold–palladium catalyst for effective syngas production from methane partial oxidation

The CO and H2 (syngas) production from methane partial oxidation (MPO) using TiO2 supported Au-Pd bimetallic catalysts are discussed. The supported Au, Pd and Au-Pd bimetallic nanoparticles were prepared by an incipient wetness impregnation or co-impregnation method and were characterized. The supported Au-Pd catalyst was selective for reforming and was more active compared to bare TiO2, TiO2 supported Au only, or Pd only catalysts. The catalyst properties before and after MPO reaction were investigated, including the stability of the TiO2 support, and the stability of Au and Pd nanoparticles. The supported Au-Pd catalyst has the highest TON (TONH2 = 23 at 650 °C), compared to supported Au catalyst (TONH2 < 1) and supported Pd catalyst (TONH2 < 1). Based on the analysis of outlet gases from the MPO reaction in a flow reactor, synergetic effects between Au and Pd, where Pd activates CH bonds while gold modulates the behavior of oxygen at the catalyst surface, are shown to contribute to MPO. Additionally, the Au-Pd/TiO2 material shows long-term activity (>12 h) for the MPO reaction at 600 °C.