Modification of graphene photodetector by TiO2 prepared by oxygen plasma
Single-layer graphene has been proved to be an ideal material for broadband high-speed photodetector. However, the pure graphene photodetector photoresponsivity is limited to tens of mA/W by the low optical absorption and short exciton life of graphene. When higher responsivity is needed, the graphe...
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Veröffentlicht in: | Journal of materials science 2021-06, Vol.56 (18), p.10938-10946 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Single-layer graphene has been proved to be an ideal material for broadband high-speed photodetector. However, the pure graphene photodetector photoresponsivity is limited to tens of mA/W by the low optical absorption and short exciton life of graphene. When higher responsivity is needed, the graphene layer needs to be coupled with other materials, e.g., Titanium Dioxide (TiO
2
). Conventional TiO
2
recipes require either solution or high temperature which tends to destruct the graphene layer. In this work, TiO
2
is synthesized by oxygen plasma treating Ti film. This novel synthesis route of TiO
2
avoids defects introduced by the conventional recipes. The hybrid device shows a high photoresponsivity of ~ 179 A/W, a fast response time of ~ 20 ms and a specific detectivity of ~ 9.12 × 10
9
Jones with the incident light intensity of sub-microwatt. Under the illumination, the photon absorption in graphene creates electron–hole pairs, which were separated at TiO
2
/graphene interface by an internal electric field and corresponding electrons transfer from the graphene to TiO
2
layer. The high photoresponsivity is attributed to the long lifetime of the photoexcited charge carriers caused by a built-in field at the interface of TiO
2
/graphene. Our research provides an effective method to improve the photoresponse of the graphene-based photodetector. In addition, our TiO
2
recipe could be applied in the fabrication of other electronic devices where solution or high temperature processes are difficult. |
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ISSN: | 0022-2461 1573-4803 |
DOI: | 10.1007/s10853-021-05971-6 |