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Formation of Co–O bonds and reversal of thermal annealing effects induced by X-ray irradiation in (Y, Co)-codoped CeO(2) nanocrystals

We report an unconventional effect of synchrotron X-ray irradiation in which Co–O bonds in thermally annealed (Y, Co)-codoped CeO(2) nanocrystal samples were formed due to, instead of broken by, X-ray irradiation. Our experimental data indicate that escaping oxygen atoms from X-ray-broken Ce–O bonds...

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Detalles Bibliográficos
Autores principales: Wu, Tai-Sing, Chen, Sheng-Fu, Weng, Shih-Chang, Soo, Yun-Liang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8799635/
https://www.ncbi.nlm.nih.gov/pubmed/35091660
http://dx.doi.org/10.1038/s41598-022-05691-0
Descripción
Sumario:We report an unconventional effect of synchrotron X-ray irradiation in which Co–O bonds in thermally annealed (Y, Co)-codoped CeO(2) nanocrystal samples were formed due to, instead of broken by, X-ray irradiation. Our experimental data indicate that escaping oxygen atoms from X-ray-broken Ce–O bonds may be captured by Co dopant atoms to form additional Co–O bonds. Consequently, the Co dopant atoms were pumped by X-rays from the energetically-favored thermally-stable Co-O4 square-planar structure to the metastable octahedral Co-O6 environment, practically a reversal of thermal annealing effects in (Y, Co)-codoped CeO(2) nanocrystals. The band gap of doped CeO(2) with Co dopant in the Co-O6 structure was previously found to be 1.61 eV higher than that with Co in the Co-O4 environment. Therefore, X-ray irradiation can work with thermal annealing in opposing directions to fine tune and optimize the band gap of the material for specific technological applications.