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Updated: Jun 12, 2025

Author Spotlight: Magnetometric Characterization of Intermediates in the Solid-State Electrochemistry of Redox-Active Metal-Organic Frameworks
Published on: June 9, 2023
Spin coherence and magnetization dynamics of TMA2[KCo1-Fe(CN)6] toward coordination-framework spin qubits
Shraddha Gupta1,2, Masanori Wakizaka3, Takeshi Yamane4
1School of Chemical Science and Engineering, Tongji University, Siping Road 1239, Shanghai 200092, P. R. China. shraddha.gupta.q7@alumni.tohoku.ac.jp.
Metal compounds with S = 1/2 coordination-frameworks are promising qubit candidates. This study reports TMA2[KCo1-Fe(CN)6] as a qubit, demonstrating long magnetic relaxation times and spin coherence.
Area of Science:
- Quantum computing materials science
- Molecular magnetism
- Coordination chemistry
Background:
- S = 1/2 coordination-frameworks are emerging as potent qubit candidates.
- Understanding magnetization dynamics and spin coherence is crucial for qubit development.
Purpose of the Study:
- To investigate the qubit potential of the CN-based coordination framework TMA2[KCo1-Fe(CN)6].
- To explore the magnetic dilution effects of Fe(III) in a Co(III)-based diamagnetic analogue.
Main Methods:
- Alternating-current (AC) susceptibility measurements to study magnetic relaxation.
- Pulsed Electron Paramagnetic Resonance (EPR) to assess spin coherence.
- Magnetic dilution of Fe(III) in TMA2[KCo(CN)6] framework.
Main Results:
- Slow magnetic relaxation observed, following phonon-bottleneck and Raman processes.
- A magnetic relaxation time (τ) of 0.3 s at 1.8 K (2% Fe).
- A coherence duration of 1 μs at 4 K (0.1% Fe) and observed Rabi oscillations.
Conclusions:
- TMA2[KCo1-Fe(CN)6] demonstrates significant potential as a qubit.
- The material can be placed in superpositions of distinct Ms states, essential for qubit operation.
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