Spin relaxation in a single-electron graphene quantum dot

The relaxation time of a single-electron spin is an important parameter for solid-state spin qubits, as it directly limits the lifetime of the encoded information. Thanks to the low spin-orbit interaction and low hyperfine coupling, graphene and bilayer graphene (BLG) have long been considered promi...

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Veröffentlicht in:Nature communications 2022-06, Vol.13 (1), p.3637-3637, Article 3637
Hauptverfasser: Banszerus, L., Hecker, K., Möller, S., Icking, E., Watanabe, K., Taniguchi, T., Volk, C., Stampfer, C.
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Sprache:eng
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Zusammenfassung:The relaxation time of a single-electron spin is an important parameter for solid-state spin qubits, as it directly limits the lifetime of the encoded information. Thanks to the low spin-orbit interaction and low hyperfine coupling, graphene and bilayer graphene (BLG) have long been considered promising platforms for spin qubits. Only recently, it has become possible to control single-electrons in BLG quantum dots (QDs) and to understand their spin-valley texture, while the relaxation dynamics have remained mostly unexplored. Here, we report spin relaxation times ( T 1 ) of single-electron states in BLG QDs. Using pulsed-gate spectroscopy, we extract relaxation times exceeding 200 μ s at a magnetic field of 1.9 T. The T 1 values show a strong dependence on the spin splitting, promising even longer T 1 at lower magnetic fields, where our measurements are limited by the signal-to-noise ratio. The relaxation times are more than two orders of magnitude larger than those previously reported for carbon-based QDs, suggesting that graphene is a potentially promising host material for scalable spin qubits. Graphene has long been considered to be a promising host for spin qubits, however a demonstration of long spin relaxation times for a potential qubit has been lacking. Here, the authors report the electrical measurement of the single-electron spin relaxation time exceeding 200  μ s in a bilayer graphene quantum dot.
ISSN:2041-1723
2041-1723
DOI:10.1038/s41467-022-31231-5