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| Main Authors: | , , , , , , , , , , , , , , , , , , , , |
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| Format: | Preprint |
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2026
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| Online Access: | https://arxiv.org/abs/2603.25234 |
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| _version_ | 1866908915551174656 |
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| author | Paul, Pralay Abeywickrama, Kusal M. Geng, Nisha Parashar, Mritunjaya Brown, Levi Sharma, Mohin Saini, Darshpreet Kaur Artola, Melissa Ayala Byers, Todd A. Rout, Bibhudutta Ju, Yiwei Pan, Xiaoqing Goswami, Sumit Purayil, Sreehari Puthan Kerr, Casey Biswas, Dhiman Summers, Ben Wang, Bin Hahn, Horst Javadi, Alisa Venkatesan, T. |
| author_facet | Paul, Pralay Abeywickrama, Kusal M. Geng, Nisha Parashar, Mritunjaya Brown, Levi Sharma, Mohin Saini, Darshpreet Kaur Artola, Melissa Ayala Byers, Todd A. Rout, Bibhudutta Ju, Yiwei Pan, Xiaoqing Goswami, Sumit Purayil, Sreehari Puthan Kerr, Casey Biswas, Dhiman Summers, Ben Wang, Bin Hahn, Horst Javadi, Alisa Venkatesan, T. |
| contents | In highly purified host, the coherence of quantum emitters is ultimately limited by hyperfine interactions between the emitter and lattice nuclei possessing non-zero nuclear magnetic moments. This limitation can only be mitigated through isotopic purification. In this work, we investigate CeO2 as a host composed entirely of nuclei with zero nuclear moment. High-quality CeO2 thin films were grown by PLD and doped with Tm and Er ions. Structural characterization using X-ray diffraction, atomic force microscopy, and ion channeling confirms single-crystalline, atomically smooth films with dopants substitutionally incorporated at Ce lattice sites. Photoluminescence lifetime measurements show significantly longer lifetimes for Er-doped CeO2 (2.9 - 5.3 ms) compared with Tm-doped films (14 - 68 μs). Moreover, the Er-doped PLD films exhibit longer lifetimes at ~1% dopant concentration than previously reported for MBE-grown films. Density functional theory calculations reveal a substantial overlap between unoccupied O 2p and Tm 4f states near the valence band maximum, whereas Er 4f states remain well isolated. This electronic interaction likely introduces non-radiative recombination pathways in Tm-doped CeO2, explaining the reduced lifetimes. These findings highlight the importance of selecting appropriate dopant-host combinations and optimized growth conditions to minimize non-radiative channels for quantum applications. |
| format | Preprint |
| id |
arxiv_https___arxiv_org_abs_2603_25234 |
| institution | arXiv |
| publishDate | 2026 |
| record_format | arxiv |
| spellingShingle | Epitaxial CeO2 Films as a Host for Quantum Applications Paul, Pralay Abeywickrama, Kusal M. Geng, Nisha Parashar, Mritunjaya Brown, Levi Sharma, Mohin Saini, Darshpreet Kaur Artola, Melissa Ayala Byers, Todd A. Rout, Bibhudutta Ju, Yiwei Pan, Xiaoqing Goswami, Sumit Purayil, Sreehari Puthan Kerr, Casey Biswas, Dhiman Summers, Ben Wang, Bin Hahn, Horst Javadi, Alisa Venkatesan, T. Quantum Physics Materials Science In highly purified host, the coherence of quantum emitters is ultimately limited by hyperfine interactions between the emitter and lattice nuclei possessing non-zero nuclear magnetic moments. This limitation can only be mitigated through isotopic purification. In this work, we investigate CeO2 as a host composed entirely of nuclei with zero nuclear moment. High-quality CeO2 thin films were grown by PLD and doped with Tm and Er ions. Structural characterization using X-ray diffraction, atomic force microscopy, and ion channeling confirms single-crystalline, atomically smooth films with dopants substitutionally incorporated at Ce lattice sites. Photoluminescence lifetime measurements show significantly longer lifetimes for Er-doped CeO2 (2.9 - 5.3 ms) compared with Tm-doped films (14 - 68 μs). Moreover, the Er-doped PLD films exhibit longer lifetimes at ~1% dopant concentration than previously reported for MBE-grown films. Density functional theory calculations reveal a substantial overlap between unoccupied O 2p and Tm 4f states near the valence band maximum, whereas Er 4f states remain well isolated. This electronic interaction likely introduces non-radiative recombination pathways in Tm-doped CeO2, explaining the reduced lifetimes. These findings highlight the importance of selecting appropriate dopant-host combinations and optimized growth conditions to minimize non-radiative channels for quantum applications. |
| title | Epitaxial CeO2 Films as a Host for Quantum Applications |
| topic | Quantum Physics Materials Science |
| url | https://arxiv.org/abs/2603.25234 |