Spin coherence and magnetization dynamics of TMA2[KCo1−xFex(CN)6] toward coordination-framework spin qubits

Metal compounds with S = 1/2 coordination-frameworks have been emerging as new powerful qubit candidates. In this study, we have reported the CN-based coordination framework TMA2[KCo1−xFex(CN)6] to be a qubit. We explored the magnetization dynamics and spin coherence of the magnetic dilution of the...

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Veröffentlicht in:Physical chemistry chemical physics : PCCP 2024-10, Vol.26 (38), p.24924-24930
Hauptverfasser: Gupta, Shraddha, Wakizaka, Masanori, Yamane, Takeshi, Sato, Kazunobu, Ishikawa, Ryuta, Nobuto Funakoshi, Yamashita, Masahiro
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Sprache:eng
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Zusammenfassung:Metal compounds with S = 1/2 coordination-frameworks have been emerging as new powerful qubit candidates. In this study, we have reported the CN-based coordination framework TMA2[KCo1−xFex(CN)6] to be a qubit. We explored the magnetization dynamics and spin coherence of the magnetic dilution of the S = 1/2 Fe(iii) complex TMA2[KFe(CN)6] (TMA = tetramethylammonium) in its Co(iii)-based diamagnetic analogue TMA2[KCo(CN)6]. Alternating-current (AC) susceptibility data illustrate a slow magnetic relaxation upon applying a field of 0.1 T, which follows the phonon-bottleneck relaxation mechanism along with the Raman process. A magnetic relaxation time (τ) of 0.3 s (2% Fe) was realized at 1.8 K. Moreover, pulsed EPR data reveal a coherence duration of 1 μs (0.1% Fe) at 4 K with successful observation of Rabi oscillation at 4 K and 13 K (2% Fe) using MW pulses with variable irradiation-field strengths. The overall results indicate that TMA2[KCo1−xFex(CN)6] represents a promising qubit candidate, as it is capable of being placed in any superposition of the two distinct Ms states (Ms = +1/2 and Ms = −1/2).
ISSN:1463-9076
1463-9084
DOI:10.1039/d4cp02263g