Coupling single-molecule magnets to quantum circuits

被引:82
作者
Jenkins, Mark [1 ,2 ]
Huemmer, Thomas [3 ,4 ]
Jose Martinez-Perez, Maria [1 ,2 ]
Garcia-Ripoll, Juanjo [5 ]
Zueco, David [1 ,2 ,6 ]
Luis, Fernando [1 ,2 ]
机构
[1] Univ Zaragoza, CSIC, Inst Ciencia Mat Aragon, E-50009 Zaragoza, Spain
[2] Univ Zaragoza, Dept Fis Mat Condensada, E-50009 Zaragoza, Spain
[3] Univ Munich, D-80799 Munich, Germany
[4] Max Planck Inst Quantum Opt, D-85748 Garching, Germany
[5] IFF CSIC, Inst Fis Fundamental, E-28006 Madrid, Spain
[6] Fdn ARAID, E-50004 Zaragoza, Spain
关键词
MAGNETIZATION; PHOTON; QUBITS; TM; TB; HO; DY; ER;
D O I
10.1088/1367-2630/15/9/095007
中图分类号
O4 [物理学];
学科分类号
0702 ;
摘要
In this work we study theoretically the coupling of single-molecule magnets (SMMs) to a variety of quantum circuits, including microwave resonators with and without constrictions and flux qubits. The main result of this study is that it is possible to achieve strong and ultrastrong coupling regimes between SMM crystals and the superconducting circuit, with strong hints that such a coupling could also be reached for individual molecules close to constrictions. Building on the resulting coupling strengths and the typical coherence times of these molecules (similar to mu s), we conclude that SMMs can be used for coherent storage and manipulation of quantum information, either in the context of quantum computing or in quantum simulations. Throughout the work we also discuss in detail the family of molecules that are most suitable for such operations, based not only on the coupling strength, but also on the typical energy gaps and the simplicity with which they can be tuned and oriented. Finally, we also discuss practical advantages of SMMs, such as the possibility to fabricate the SMMs ensembles on the chip through the deposition of small droplets.
引用
收藏
页数:22
相关论文
共 65 条
[1]   Electron spin ensemble strongly coupled to a three-dimensional microwave cavity [J].
Abe, Eisuke ;
Wu, Hua ;
Ardavan, Arzhang ;
Morton, John J. L. .
APPLIED PHYSICS LETTERS, 2011, 98 (25)
[2]   Molecular nanomagnets for information technologies [J].
Affronte, Marco .
JOURNAL OF MATERIALS CHEMISTRY, 2009, 19 (12) :1731-1737
[3]   Mononuclear lanthanide single-molecule magnets based on polyoxometalates [J].
AlDamen, Murad A. ;
Clemente-Juan, Juan M. ;
Coronado, Eugenio ;
Marti-Gastaldo, Carlos ;
Gaita-Arino, Alejandro .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2008, 130 (28) :8874-+
[4]   Mononuclear Lanthanide Single Molecule Magnets Based on the Polyoxometalates [Ln(W5O18)2]9- and [Ln(β2-SiW11O39)2]13- (LnIII = Tb, Dy, Ho, Er, Tm, and Yb) [J].
AlDamen, Murad A. ;
Cardona-Serra, Salvador ;
Clemente-Juan, Juan M. ;
Coronado, Eugenio ;
Gaita-Arino, Alejandro ;
Marti-Gastaldo, Carlos ;
Luis, Fernando ;
Montero, Oscar .
INORGANIC CHEMISTRY, 2009, 48 (08) :3467-3479
[5]   Cavity QED with Magnetically Coupled Collective Spin States [J].
Amsuess, R. ;
Koller, Ch. ;
Noebauer, T. ;
Putz, S. ;
Rotter, S. ;
Sandner, K. ;
Schneider, S. ;
Schramboeck, M. ;
Steinhauser, G. ;
Ritsch, H. ;
Schmiedmayer, J. ;
Majer, J. .
PHYSICAL REVIEW LETTERS, 2011, 107 (06)
[6]   Storing quantum information in chemically engineered nanoscale magnets [J].
Ardavan, A. ;
Blundell, S. J. .
JOURNAL OF MATERIALS CHEMISTRY, 2009, 19 (12) :1754-1760
[7]   Will spin-relaxation times in molecular magnets permit quantum information processing? [J].
Ardavan, Arzhang ;
Rival, Olivier ;
Morton, John J. L. ;
Blundell, Stephen J. ;
Tyryshkin, Alexei M. ;
Timco, Grigore A. ;
Winpenny, Richard E. P. .
PHYSICAL REVIEW LETTERS, 2007, 98 (05)
[8]   Design of magnetic coordination complexes for quantum computing [J].
Aromi, Guillem ;
Aguila, David ;
Gamez, Patrick ;
Luis, Fernando ;
Roubeau, Olivier .
CHEMICAL SOCIETY REVIEWS, 2012, 41 (02) :537-546
[9]   Quantum Spintronics: Engineering and Manipulating Atom-Like Spins in Semiconductors [J].
Awschalom, David D. ;
Bassett, Lee C. ;
Dzurak, Andrew S. ;
Hu, Evelyn L. ;
Petta, Jason R. .
SCIENCE, 2013, 339 (6124) :1174-1179
[10]  
Balasubramanian G, 2009, NAT MATER, V8, P383, DOI [10.1038/nmat2420, 10.1038/NMAT2420]