Water adsorption at zirconia: from the ZrO 2 (111)/Pt 3 Zr(0001) model system to powder samples

• Published in: Journal of materials chemistry. A, Materials for energy and sustainability Materials for energy and sustainability, 2018, Vol.6 (36), p.17587-17601
• Main Authors: Lackner, Peter, Hulva, Jan, Köck, Eva-Maria, Mayr-Schmölzer, Wernfried, Choi, Joong Il J., Penner, Simon, Diebold, Ulrike, Mittendorfer, Florian, Redinger, Josef, Klötzer, Bernhard, Parkinson, Gareth S., Schmid, Michael
• Format: Article
• Language: English
• ISSN: 2050-7488; 2050-7496
• DOI: 10.1039/C8TA04137G

We present a comprehensive study of water adsorption and desorption on an ultrathin trilayer zirconia film using temperature programmed desorption (TPD), X-ray photoelectron spectroscopy (XPS), as well as scanning tunneling microscopy (STM) at different temperatures. The saturation coverage is one H 2 O per surface Zr atom, with about 12% dissociation. The monolayer TPD peak (180 K, desorption barrier 0.57 ± 0.04 eV) has a tail towards higher temperatures, caused by recombinative desorption from defect sites with dissociated water. STM shows that the defects with the strongest H 2 O adsorption are found above subsurface dislocations. Additional defect sites are created by multiple water adsorption/desorption cycles; these water-induced changes were also probed by CO 2 TPD. Nevertheless, the defect density is much smaller than in previous studies of H 2 O/ZrO 2 . To validate our model system, transmission Fourier-transform infrared absorption spectroscopy (FTIR) studies at near-ambient pressures were carried out on monoclinic zirconia powder, showing comparable adsorption energies as TPD on the ultrathin film. The results are also compared with density functional theory (DFT) calculations, which suggest that sites with strong H 2 O adsorption contain twofold-coordinated oxygen.