Quantifying Adsorption of Organic Molecules on Platinum in Aqueous Phase by Hydrogen Site Blocking and in Situ X-ray Absorption Spectroscopy
- Univ. of Washington, Seattle, WA (United States); Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Univ. of Michigan, Ann Arbor, MI (United States)
- Pacific Northwest National Lab. (PNNL), Richland, WA (United States)
- Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Technische Univ. München, Garching (Germany)
- Univ. of Washington, Seattle, WA (United States)
The adsorption equilibrium constants of phenol, benzaldehyde, cyclohexanol, and benzyl alcohol on Pt in aqueous phase have been determined via cyclic voltammetry (CV) measuring the capacity to adsorb hydrogen in the presence of organic molecules. The enthalpies of adsorbed phenol on Pt in aqueous phase estimated by this technique were approximately –41 and –21 kJ/mol relative to aqueous phenol for sites on (110)/(100)-like sites and (111) facets, respectively. The enthalpy of phenol aqueous adsorption on (111) (–21 kJ/mol) can be compared to the gas phase enthalpy of adsorption of phenol on single crystal Pt(111) from previous work (–200 kJ/mol), to understand the individual factors influencing adsorption in liquid phase. The results show that adsorbates with very strong intrinsic bonding at a gas / solid interface have markedly reduced adsorption enthalpy due to strong solvation of both the Pt surface and the organic. Using the CV method, the decrease of the heat of adsorption in the sequence benzaldehyde > benzyl alcohol > phenol > cyclohexanol points to a strong interaction of the aromatic ring with the metal surface. Combining CV and X-ray absorption spectroscopy, we show that the inhibition of hydrogen adsorption by organic molecules is a suitable method of determining the coverage of organic reactants and that these molecules have defined Pt-C bonds in adsorbed state. N.S. was funded by the WRF Innovation Fellowship in Clean Energy Institute. The research described in this paper is part of the Chemical Transformation Initiative at Pacific Northwest National Laboratory (PNNL), conducted under the Laboratory Directed Research and Development Program at PNNL, a multiprogram national laboratory operated by Battelle for the U.S. Department of Energy. C.T.C. also acknowledges the U.S. Department of Energy, Office of Science, Office of Basic Energy Sciences, Chemical Sciences Division Grant No. DE-FG02-96ER14630 for support of this work. This research used resources of the Advanced Photon Source Sector 20, a U.S. Department of Energy (DOE) Office of Science User Facility operated for the DOE Office of Science by Argonne National Laboratory under Contract No. DE-AC02-06CH11357, and the Canadian Light Source and its funding partners. We thank and acknowledge Mahalingam Balasubramanian for his help.
- Research Organization:
- Pacific Northwest National Laboratory (PNNL), Richland, WA (United States); Univ. of Washington, Seattle, WA (United States)
- Sponsoring Organization:
- USDOE Office of Science (SC), Basic Energy Sciences (BES). Chemical Sciences, Geosciences, and Biosciences Division
- Grant/Contract Number:
- AC05-76RL01830; FG02-96ER14630; AC02-06CH11357
- OSTI ID:
- 1572282
- Alternate ID(s):
- OSTI ID: 1557217
- Report Number(s):
- PNNL-SA-144087
- Journal Information:
- ACS Catalysis, Vol. 9, Issue 8; ISSN 2155-5435
- Publisher:
- American Chemical Society (ACS)Copyright Statement
- Country of Publication:
- United States
- Language:
- English
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