Gold, water adsorption

The sensor is based on high affinity of gold to mercury and on chemo-resistive properties of ultrathin gold layers adsorption of mercury leads to increase in the surface resistance [1,2]. However, this effect is not selective similar changes are caused by adsorption of water vapor and sulfuric compounds. The use of monomolecular layer of alkylthiols as a filter excludes this interference completely [3]. Sensor calibration is performed by thermoinjection of nanogram-amount of mercury quantitatively deposited by electrochemical reduction [4],... 

Isotherm I is typical of adsorption in micropores, which occurs, for instance, in zeolites and in activated carbons. Isotherm II represents multilayer physisorption on a flat surface (valid for many nonporous substances). Type HI and V isotherms are characteristics of weak gas-solid interactions (water adsorption on gold and bromine adsorption on silica are good examples). The type IV isotherm is frequently found in the study of heterogeneous catalysts its shape is characteristics... 

M. Luna, J. Colchero, A. Gil, J. Gomez-Herrero, and A. M. Baro, Application of non-contact scanning force microscopy to the study of water adsorption on graphite, gold and mica, Appi Surf.ScL, 157, 393 (2000). 

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Adsorption processes diagrammed, 266 Adsorption spectra of electrochromic polypyrrole, 363 Affinity for metal-water, 177 Air-solution interface, Nikitas on the potential of zero charge at, 30 Albury and Mount, interpretation of the semi-circle, 584 Alloys, potential of zero charge gold and silver, 142 tin and lead, 142 Kukk and Puttsepp on, 145 metals alloys, 141... 

Gibbs energy for the adsorption of water and the interfacial parameter, 187 Gokstein and the piezo electric method for the determination of the potential of zero charge, 42 Gold... 

H2O adsorbs strongly on both Au and Ti02. However, the influence of water on the catalyst or reaction is negligible [2]. PO is known to strongly interact with Ti02, and adsorption, desorption, and decomposition of PO are independent on the presence of gold [3]. 

This increase of the mass was ascribed earlier to the adsorption of perchlorate ions, °° a conclusion that found no confirmation in work published later. It turns out that other weakly adsorbing anions of different masses (NOJ, CFySOf) give the same values of frequency decrease as was observed for C104. Ultimately, the increase of the electrode mass in the preoxide region was explained in terms of the three-dimensional hydration of AuOH, which is present in small amounts at the gold surface. The mass increase was consistent with the surface hydration for a cluster of about 32 water molecules per one AuOH site. ... 

In a recent review, Haruta has reassessed the mechanism of CO oxidation on the basis of the Bond and Thompson and Kung models, i.e. that the CO is activated by adsorption on Au° on the surface of the gold nanoparticles and that dioxygen is activated by the atoms at the periphery between the support and the gold nanocrystals (Fig. 4.7). The atoms at the periphery are proposed by Haruta to be cationic in nature, possibly Au(OH)s or Au(OH) formed by the presence of water vapor that is essential for the observed high activity catalysts. It is clear that the debate will continue for the immediate future. There are two reasons why finding an answer to the key question of the nature of the active site in gold catalysts for CO oxidation. The first is purely scientific... 

In general, the contact adsorption of deh3drated anions changes the interfacial lattice structure of adsorbed water molecules, thereby changing the interfadal property. For example, the clean surfaces of metallic gold and silver, which are hydrophobic, become hydrophilic with the contact adsorption of dehydrated halogen anions. 

Such anion adsorption can be prevented by chemisorbing a mono-layer of a strongly adherent thiol molecule to the Au surfaces [97,98]. 1-Propanethiol (PT) was used here because the gold nanotubules can still be wetted with water after chemisorption of the PT monolayer [97].t The Em versus applied potential curves for an untreated and PT-treated gold nanotubule membrane, with KBr solutions present on either side of the membrane, are shown in Fig. 13. The untreated membrane shows only cation permselectivity, but the permselectivity of the PT-treated membrane can be switched, exactly as was the case with the nonadsorbing electrolyte (Fig. 12). 

Some attention has also been paid to the simultaneous adsorption of sulfate anions and organic compounds. Futamata [44] has detected coadsorption of water molecules and sulfate species with uracil on polycrystalline gold electrode, applying attenuated total reflection-infrared spectroscopy. The adsorbed sulfate species appeared either as S04 or HS04, depending on the pH of the electrolyte solution. Skoluda... 

On a pc-Au electrode in 1 M NaF vertically oriented pyridine molecules have been observed at 0.7 V (versus Ag/AgCl), applying in situ IR. In contrast, they have not been detected at this potential in electrochemical method [240]. Considering the fact that adsorption of pyridine on gold electrodes is a replacement reaction and taking into account the results obtained from quartz crystal microbalance experiments, the conclusion has been made that adsorption of one pyridine molecule is accompanied by the removal of 10-12 water molecules [241]. 

Pb UPD on polycrystalline An electrode in 0.1 M perchloric acid solution has been studied by Henderson et al. [484]. In this study, CV, electrochemical quartz crystal microbalance (EQCM), and probe beam deflection methods have been used. It has been found that Pb UPD proceeds in three steps. The first step comprised water ejection from the gold surface. This step was followed by metal UPD accompanied by the removal of the adsorbed OH. Also, Zeng and Bruckenstein have studied UPD and adsorption of Pb on pc-Au electrodes, applying XPS and TOF-SIMS method in case of 0.1 M NaCl electrolyte [485], and EQCM in case of 0.1 M NaCl04 and 0.1 M NaCl electrolytes [486]. In the presence of chloride anions, the adsorption of Pb—Cl complex has been found. 

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