ESPOSITO, VINCENZODE, WEI N.MARANI, DEBORATEOCOLI, FRANCESCATHYDEN, KARL T.S.FLORIO, DANIEL Z. deFONSECA, FABIO C.2016-12-192016-12-192016ESPOSITO, VINCENZO; DE, WEI N.; MARANI, DEBORA; TEOCOLI, FRANCESCA; THYDEN, KARL T.S.; FLORIO, DANIEL Z. de; FONSECA, FABIO C. Accelerated ceria–zirconia solubilization by cationic diffusion inversion at low oxygen activity. <b>Journal of Materials Chemistry A</b>, v. 4, n. 43, p. 16871-16878, 2016. DOI: <a href="https://dx.doi.org/10.1039/c6ta06308j">10.1039/c6ta06308j</a>. Disponível em: http://repositorio.ipen.br/handle/123456789/26914.2050-7488http://repositorio.ipen.br/handle/123456789/26914Fast elemental diffusion at the Gd-doped ceria/Y-stabilized zirconia interface occurs under reducing conditions at low oxygen activity (pO2 < 10 12 atm) and high temperature (1400 C). This effect leads to formation of thick ceria–zirconia solid solution reaction layers in the micro-range vs. thin layers of few tens of nanometers under oxidative conditions (i.e. in synthetic air at pO2 ¼ 0.21 atm). The fast dissolution occurs by an inversion of the dominating limiting mechanism from the expected Zr4+ diffusion into the CGO lattice at high pO2 to an unexpected Ce3+ diffusion into the YSZ component under reducing conditions. The diffusion coefficient of 8-fold coordinated Ce3+ in YSZ at 1400 C and pO2 ¼ 10 13 atm is estimated to be around 10 11 cm2 s 1. This value is around 3 orders of magnitude higher than Zr4+ interdiffusion in CGO under oxidative conditions and about 8 orders of magnitude higher than Ce4+ self-diffusion in CGO in air at the same temperature.16871-16878closedAccessdiffusionoxygendissolutionmicrostructurecerium oxideszirconium oxidesArtigo de periódico43410.1039/c6ta06308jhttps://orcid.org/0000-0003-0708-202193.18