Magnetic fingerprint of individual Fe4 molecular magnets under compression by a scanning tunnelling microscope

被引:54
作者
Burgess, Jacob A. J. [1 ,2 ]
Malavolti, Luigi [1 ,2 ,3 ,4 ]
Lanzilotto, Valeria [3 ,4 ]
Mannini, Matteo [3 ,4 ]
Yan, Shichao [1 ,2 ]
Ninova, Silviya [3 ,4 ]
Totti, Federico [3 ,4 ]
Rolf-Pissarczyk, Steffen [1 ,2 ]
Cornia, Andrea [5 ,6 ]
Sessoli, Roberta [3 ,4 ]
Loth, Sebastian [1 ,2 ]
机构
[1] Max Planck Inst Struct & Dynam Matter, D-22761 Hamburg, Germany
[2] Max Planck Inst Solid State Res, D-70569 Stuttgart, Germany
[3] Univ Florence, Dept Chem Ugo Schiff, I-50019 Sesto Fiorentino, Italy
[4] INSTM RU Florence, I-50019 Sesto Fiorentino, Italy
[5] Univ Modena & Reggio Emilia, Dept Chem & Geol Sci, I-41125 Modena, Italy
[6] INSTM RU Modena & Reggio Emilia, I-41125 Modena, Italy
基金
加拿大自然科学与工程研究理事会;
关键词
SPIN; HYSTERESIS; ANISOTROPY;
D O I
10.1038/ncomms9216
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Single-molecule magnets (SMMs) present a promising avenue to develop spintronic technologies. Addressing individual molecules with electrical leads in SMM-based spintronic devices remains a ubiquitous challenge: interactions with metallic electrodes can drastically modify the SMM's properties by charge transfer or through changes in the molecular structure. Here, we probe electrical transport through individual Fe-4 SMMs using a scanning tunnelling microscope at 0.5 K. Correlation of topographic and spectroscopic information permits identification of the spin excitation fingerprint of intact Fe-4 molecules. Building from this, we find that the exchange coupling strength within the molecule's magnetic core is significantly enhanced. First-principles calculations support the conclusion that this is the result of confinement of the molecule in the two-contact junction formed by the microscope tip and the sample surface.
引用
收藏
页数:7
相关论文
共 44 条
[1]   Tuning anisotropy barriers in a family of tetrairon(III) single-molecule magnets with an S=5 ground state [J].
Accorsi, S ;
Barra, AL ;
Caneschi, A ;
Chastanet, G ;
Cornia, A ;
Fabretti, AC ;
Gatteschi, D ;
Mortalò, C ;
Olivieri, E ;
Parenti, F ;
Rosa, P ;
Sessoli, R ;
Sorace, L ;
Wernsdorfer, W ;
Zobbi, L .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2006, 128 (14) :4742-4755
[2]   BAND THEORY AND MOTT INSULATORS - HUBBARD-U INSTEAD OF STONER-I [J].
ANISIMOV, VI ;
ZAANEN, J ;
ANDERSEN, OK .
PHYSICAL REVIEW B, 1991, 44 (03) :943-954
[3]   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)
[4]   A Few Comments on the Application of Density Functional Theory to the Calculation of the Magnetic Structure of Oligo-Nuclear Transition Metal Clusters [J].
Bencini, Alessandro ;
Totti, Federico .
JOURNAL OF CHEMICAL THEORY AND COMPUTATION, 2009, 5 (01) :144-154
[5]   Molecular spintronics using single-molecule magnets [J].
Bogani, Lapo ;
Wernsdorfer, Wolfgang .
NATURE MATERIALS, 2008, 7 (03) :179-186
[6]   Direct Observation of Magnetic Anisotropy in an Individual Fe4 Single-Molecule Magnet [J].
Burzuri, E. ;
Zyazin, A. S. ;
Cornia, A. ;
van der Zant, H. S. J. .
PHYSICAL REVIEW LETTERS, 2012, 109 (14)
[7]   Graphene Spintronic Devices with Molecular Nanomagnets [J].
Candini, Andrea ;
Klyatskaya, Svetlana ;
Ruben, Mario ;
Wernsdorfer, Wolfgang ;
Affronte, Marco .
NANO LETTERS, 2011, 11 (07) :2634-2639
[8]   Molecular magnets and surfaces: A promising marriage. A DFT insight [J].
Caneschi, Andrea ;
Gatteschi, Dante ;
Totti, Federico .
COORDINATION CHEMISTRY REVIEWS, 2015, 289 :357-378
[9]   Linear response approach to the calculation of the effective interaction parameters in the LDA+U method [J].
Cococcioni, M ;
de Gironcoli, S .
PHYSICAL REVIEW B, 2005, 71 (03)
[10]  
CP2K developers group, 2015, CP2K OP SOURC MOL DY