Effect of alkali-metal cation on oxygen adsorption at Pt single-crystal electrodes in non-aqueous electrolytes.

The effect of Group 1 alkali-metal cations (Na+, K+, and Cs+) on the oxygen reduction and evolution reactions (ORR and OER) using dimethyl sulfoxide (DMSO)-based electrolytes was investigated. Cyclic voltammetry (CV) utilising different Pt-electrode surfaces (polycrystalline Pt, Pt(111) and Pt(100)) was undertaken to investigate the influence of surface structure upon the ORR and OER. For K+ and Cs+, negligible variation in the CV response (in contrast to Na+) was observed using Pt(111), Pt(100) and Pt(poly) electrodes, consistent with a weak surface-metal/superoxide complex interaction. Indeed, changes in the half-wave potentials (E1/2) and relative intensities of the redox peaks corresponding to superoxy (O2-) and peroxy (O22-) ion formation were consistent with a solution-mediated mechanism for larger cations, such as Cs+. Support for this finding was obtained via in situ shell-isolated nanoparticle-enhanced Raman spectroscopy (SHINERS). During the ORR and in the presence of Cs+, O2- and weakly adsorbed caesium superoxide (CsO2) species were detected. Because DMSO was found to strongly interact with the surface at potentials associated with the ORR, CsO2 was readily displaced at more negative potentials via increased solvent adsorption at the surface. This finding highlights the important impact of the solvent during ORR/OER reactions.

Investigating the presence of adsorbed species on Pt steps at low potentials.

The study of the OH adsorption process on Pt single crystals is of paramount importance since this adsorbed species is considered the main intermediate in many electrochemical reactions of interest, in particular, those oxidation reactions that require a source of oxygen. So far, it is frequently assumed that the OH adsorption on Pt only takes place at potentials higher than 0.55 V (versus the reversible hydrogen electrode), regardless of the Pt surface structure. However, by CO displacement experiments, alternating current voltammetry, and Raman spectroscopy, we demonstrate here that OH is adsorbed at more negative potentials on the low coordinated Pt atoms, the Pt steps. This finding opens a new door in the mechanistic study of many relevant electrochemical reactions, leading to a better understanding that, ultimately, can be essential to reach the final goal of obtaining improved catalysts for electrochemical applications of technological interest.

Observation of Substituent Effects in the Electrochemical Adsorption and Hydrogenation of Alkynes on Pt{hkl} Using SHINERS.

By combining cyclic voltammetry (CV) and shell-isolated nanoparticle-enhanced Raman spectroscopy (SHINERS), the adsorption behavior of two alkynes, propargyl alcohol (PA) and 2-methyl-3-butyn-2-ol (MeByOH), undergoing hydrogenation on Pt basal plane single-crystal electrodes is investigated. It is found that PA and MeByOH give rise to strong surface sensitivities in relation to both hydrogenation activity and molecular fragmentation into adsorbed species such as CO. For PA, irreversible adsorption is strongly favored for Pt{100} and Pt{110} but is weak in the case of Pt{111}. It is suggested that the presence of the primary alcohol substituent is key to this behavior, with the order of surface reactivity being Pt{100} > Pt{110} > Pt{111}. In contrast, for MeByOH, strong irreversible adsorption is observed on all three basal plane Pt surfaces and we propose that this reflects the enhanced activity of the alkyne moiety arising from the inductive effect of the two methyl groups, coupled with the decreased activity of the tertiary alcohol substituent toward fragmentation. Pt{111} also exhibits singular behavior in relation to MeByOH hydrogenation in that a sharp Raman band at 1590 cm-1 is observed corresponding to the formation of a di-σ/π-bonded surface complex as the alkyne adsorbs. This band frequency is some 20 cm-1 higher than the analogous broadband observed for PA and MeByOH adsorbed on all other basal plane Pt surfaces and may be viewed as a fingerprint of Pt{111} terraces being present at a catalyst surface undergoing hydrogenation. Insights into the hydrogenation activity of different Pt{hkl} surfaces are obtained using quantitative comparisons between Raman bands at hydrogenation potentials and at 0.4 V vs Pd/H, the beginning of the double-layer potential region, and it is asserted (with support from CV) that Pt{110} is the most active plane for hydrogenation due to the presence of surface defects generated via the lifting of the (1 × 2) to (1 × 1) clean surface reconstruction following flame annealing and hydrogen cooling. Our findings are also consistent with the hypothesis that Pt{111} planes are most likely to provide semihydrogenation selectivity of alkynes to alkenes, as reported previously.

Metastable ionic diodes derived from an amine-based polymer of intrinsic microporosity.

A highly rigid amine-based polymer of intrinsic microporosity (PIM), prepared by a polymerization reaction involving the formation of Tröger's base, is demonstrated to act as an ionic diode with electrolyte-dependent bistable switchable states.

Oxygen reduction reaction activity on Pt{111} surface alloys.

PtM overlayers (where M=Fe, Co or Ni) supported on Pt{111} are prepared via thermal annealing in either a nitrogen/water or hydrogen ambient of dilute aqueous droplets containing M(Z+) cations directly attached to the electrode. Two different PtM phases are detected depending on the nature of the post-annealing cooling environment. The first of these consists of small (<20 nm), closely packed microcrystals comprised of a central metallic core and a shell (several monolayers thick) of mixed metal oxides/hydroxides. The second type of PtM phase is prepared by cooling in a stream of hydrogen gas. Although this second phase also consists of numerous microcrystals covering the Pt{111} electrode surface, these are both flatter than before and moreover are entirely metallic in character. A positive shift in the onset of PtM oxide formation correlates with increased activity towards the oxygen reduction reaction (ORR), which we ascribe to the greater availability of platinum metallic sites under ORR conditions.

Specific adsorption of perchlorate anions on Pt{hkl} single crystal electrodes.

The voltammetry of Pt{111}, Pt{100}, Pt{110} and Pt{311} single crystal electrodes as a function of perchloric acid concentration (0.05-2.00 M) has been studied in order to test the assertion made in recent reports by Watanabe et al. that perchlorate anions specifically adsorb on polycrystalline platinum. Such an assertion would have significant ramifications for our understanding of electrocatalytic processes at platinum surfaces since perchlorate anions at low pH have classically been assumed not to specifically adsorb. For Pt{111}, it is found that OHad and electrochemical oxide states are both perturbed significantly as perchloric acid concentration is increased. We suggest that this is due to specific adsorption of perchlorate anions competing with OHad for adsorption sites. The hydrogen underpotential deposition (H UPD) region of Pt{111} however remains unchanged although evidence for perchlorate anion decomposition to chloride on Pt{111} is reported. In contrast, for Pt{100} no variation in the onset of electrochemical oxide formation is found nor any shift in the potential of the OHad state which normally results from the action of specifically adsorbing anions. This suggests that perchlorate anions are non-specifically adsorbed on this plane although strong changes in all H UPD states are observed as perchloric acid concentration is increased. This manifests itself as a redistribution of charge from the H UPD state situated at more positive potential to the one at more negative potential. For Pt{110} and Pt{311}, marginal changes in the onset of electrochemical oxide formation are recorded, associated with specific adsorption of perchlorate. Specific adsorption of perchlorate anions on Pt{111} is deleterious to electrocatalytic activity in relation to the oxygen reduction reaction (ORR) as measured using a rotating disc electrode (RDE) in a hanging meniscus configuration. This study supports previous work suggesting that a large component of the ORR activity on platinum is governed by simple site blocking by specifically adsorbed anions and/or electrosorbed oxide.

Microbial synthesis of core/shell gold/palladium nanoparticles for applications in green chemistry.

We report a novel biochemical method based on the sacrificial hydrogen strategy to synthesize bimetallic gold (Au)-palladium (Pd) nanoparticles (NPs) with a core/shell configuration. The ability of Escherichia coli cells supplied with H(2) as electron donor to rapidly precipitate Pd(II) ions from solution is used to promote the reduction of soluble Au(III). Pre-coating cells with Pd(0) (bioPd) dramatically accelerated Au(III) reduction, with the Au(III) reduction rate being dependent upon the initial Pd loading by mass on the cells. Following Au(III) addition, the bioPd-Au(III) mixture rapidly turned purple, indicating the formation of colloidal gold. Mapping of bio-NPs by energy dispersive X-ray microanalysis suggested Au-dense core regions and peripheral Pd but only Au was detected by X-ray diffraction (XRD) analysis. However, surface analysis of cleaned NPs by cyclic voltammetry revealed large Pd surface sites, suggesting, since XRD shows no crystalline Pd component, that layers of Pd atoms surround Au NPs. Characterization of the bimetallic particles using X-ray absorption spectroscopy confirmed the existence of Au-rich core and Pd-rich shell type bimetallic biogenic NPs. These showed comparable catalytic activity to chemical counterparts with respect to the oxidation of benzyl alcohol, in air, and at a low temperature (90°C).

Tunable gold catalysts for selective hydrocarbon oxidation under mild conditions.

Oxidation is an important method for the synthesis of chemical intermediates in the manufacture of high-tonnage commodities, high-value fine chemicals, agrochemicals and pharmaceuticals: but oxidations are often inefficient. The introduction of catalytic systems using oxygen from air is preferred for 'green' processing. Gold catalysis is now showing potential in selective redox processes, particularly for alcohol oxidation and the direct synthesis of hydrogen peroxide. However, a major challenge that persists is the synthesis of an epoxide by the direct electrophilic addition of oxygen to an alkene. Although ethene is epoxidized efficiently using molecular oxygen with silver catalysts in a large-scale industrial process, this is unique because higher alkenes can only be effectively epoxidized using hydrogen peroxide, hydroperoxides or stoichiometric oxygen donors. Here we show that nanocrystalline gold catalysts can provide tunable active catalysts for the oxidation of alkenes using air, with exceptionally high selectivity to partial oxidation products ( approximately 98%) and significant conversions. Our finding significantly extends the discovery by Haruta that nanocrystalline gold can epoxidize alkenes when hydrogen is used to activate the molecular oxygen; in our case, no sacrificial reductant is needed. We anticipate that our finding will initiate attempts to understand more fully the mechanism of oxygen activation at gold surfaces, which might lead to commercial exploitation of the high redox activity of gold nanocrystals.

The characterisation of supported platinum nanoparticles on carbon used for enantioselective hydrogenation: a combined electrochemical-STM approach.

The action of chiral modifiers like cinchonine and cinchonidine in facilitating enationselectivity in heterogeneous catalysis is investigated using a combination of electrochemical and scanning probe methods. The surface chirality of corner kink sites is suggested as being crucial for chirality recognition at supported catalyst nanoparticles. Other aspects of chirality in relation to one, two, three and four dimensions are also discussed.

The influence of anions and kink structure on the enantioselective electro-oxidation of glucose.

The electro-oxidation of glucose in sulfuric acid using well-defined chiral platinum single crystal electrodes has been demonstrated previously to be an enantioselective reaction with the degree of enantioselectivity being dependent on the surface density of kink sites. The chirality of the surface originates from the microstructure of the kink site whereby the sequence of the three fundamental adsorption sites [111], [100] and [110] constituting the kink may be viewed from the electrolyte phase either in a clockwise (R-enantiomer) or anti-clockwise (S-enantiomer) fashion. In the present study, this work is extended to examine the role of both kink structure and specifically adsorbed anions on the mechanism of chiral discrimination. Kinked surfaces based on [111] terraces (Pt[976],Pt[643] and Pt[531]),[100] terraces (Pt[721]) and [110] terraces (Pt[11,7,1] and Pt[841]) have been investigated and both the magnitude and potential dependence of the enantioselective electro-oxidation of glucose characterised. Additionally, the changes engendered by interchanging the character of the two steps whose confluence form the kink whilst maintaining the symmetry of the terrace has also been examined via a comparison of Pt[643] and Pt[431]. Low energy electron diffraction (LEED) was used to confirm that all surfaces when clean and thermally annealed were in their (1 x 1) state. Cyclic voltammetry (CV) confirmed this finding for flame-annealed electrodes after cooling in hydrogen. Three general points emerge from the electro-oxidation studies: (i) The highest degree of enantioselectivity is exhibited by kink sites adjacent to [111] and [110] terraces in sulfuric acid. (ii) The adsorption of specifically adsorbed anions like bisulfate/sulfate influences strongly the chiral discriminatory behaviour of all surfaces. (iii) No electro-oxidation takes place at [110] sites, as evidenced by complete overlap of the [110] step hydrogen underpotential deposition (UPD) charge in glucose and glucose-free solutions. Nonetheless it is deduced that [110] sites must play some part in the initial orienting of the glucose molecule prior to reaction. Ideas based on these findings are developed in order to rationalise in particular the influence of anion adsorption on the initial enantioselective interaction of the glucose molecule with the chiral surface.