Magnetic behaviour of TbPc2 single-molecule magnets chemically grafted on silicon surface

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作者
Matteo Mannini
Federico Bertani
Cristina Tudisco
Luigi Malavolti
Lorenzo Poggini
Kasjan Misztal
Daniela Menozzi
Alessandro Motta
Edwige Otero
Philippe Ohresser
Philippe Sainctavit
Guglielmo G. Condorelli
Enrico Dalcanale
Roberta Sessoli
机构
[1] University of Firenze,Department of Chemistry ‘Ugo Schiff’ and INSTM RU
[2] via della Lastruccia 3-13,Department of Chemistry
[3] University of Parma and INSTM RU,Department of Chemical Science
[4] Parco Area delle Scienze 17/A,undefined
[5] University of Catania and INSTM RU,undefined
[6] Viale Andrea Doria,undefined
[7] 6,undefined
[8] Synchrotron SOLEIL,undefined
[9] L'Orme des Merisiers Saint-Aubin—BP 48,undefined
[10] IMPMC-CNRS,undefined
[11] Université Pierre et Marie Curie,undefined
[12] 4 place Jussieu 75252,undefined
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摘要
Single-molecule magnets (SMMs) are among the most promising molecular systems for the development of novel molecular electronics based on spin transport. Going beyond investigations focused on physisorbed SMMs, in this work the robust grafting of terbium(III) bis(phthalocyaninato) complexes to a silicon surface from a diluted solution is achieved by rational chemical design yielding the formation of a partially oriented monolayer on the conducting substrate. Here by exploiting the surface sensitivity of X-ray circular magnetic dichroism, we evidence an enhancement of the magnetic bistability of this SMM, in contrast to the dramatic reduction of the magnetic hysteresis that characterizes monolayer deposits evaporated on noble and ferromagnetic metals. Photoelectron spectroscopy investigations and density functional theory analysis suggest a non-innocent role played by the silicon substrate, evidencing the potentiality of this approach for robust integration of bistable magnetic molecules in electronic devices.
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