Exchange coupling in a frustrated trimetric molecular magnet reversed by a 1D nano-confinement

Kód výsledku v IS VaVaI

<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61388955%3A_____%2F19%3A00517214" target="_blank" >RIV/61388955:_____/19:00517214 - isvavai.cz</a>

Výsledek na webu

<a href="http://hdl.handle.net/11104/0302495" target="_blank" >http://hdl.handle.net/11104/0302495</a>

DOI - Digital Object Identifier

<a href="http://dx.doi.org/10.1039/c9nr00796b" target="_blank" >10.1039/c9nr00796b</a>

Jazyk výsledku

angličtina

Název v původním jazyce

Exchange coupling in a frustrated trimetric molecular magnet reversed by a 1D nano-confinement

Popis výsledku v původním jazyce

Single-molecule magnets exhibit magnetic ordering due to exchange coupling between localized spin components that makes them primary candidates as nanometric spintronic elements. Here we manipulate exchange interactions within a single-molecule magnet by nanometric structural confinement, exemplified with single-wall carbon nanotubes that encapsulate trimetric nickel(II) acetylacetonate hosting three frustrated spins. It is revealed from bulk and Ni 3d orbital magnetic susceptibility measurements that the carbon tubular confinement allows a unique one-dimensional arrangement of the trimer in which the nearest-neighbour exchange is reversed from ferromagnetic to antiferromagnetic, resulting in quenched frustration as well as the Pauli paramagnetism is enhanced. The exchange reversal and enhanced spin delocalisation demonstrate the means of mechanically and electrically manipulating molecular magnetism at the nanoscale for nano-mechatronics and spintronics.

Název v anglickém jazyce

Exchange coupling in a frustrated trimetric molecular magnet reversed by a 1D nano-confinement

Popis výsledku anglicky

Single-molecule magnets exhibit magnetic ordering due to exchange coupling between localized spin components that makes them primary candidates as nanometric spintronic elements. Here we manipulate exchange interactions within a single-molecule magnet by nanometric structural confinement, exemplified with single-wall carbon nanotubes that encapsulate trimetric nickel(II) acetylacetonate hosting three frustrated spins. It is revealed from bulk and Ni 3d orbital magnetic susceptibility measurements that the carbon tubular confinement allows a unique one-dimensional arrangement of the trimer in which the nearest-neighbour exchange is reversed from ferromagnetic to antiferromagnetic, resulting in quenched frustration as well as the Pauli paramagnetism is enhanced. The exchange reversal and enhanced spin delocalisation demonstrate the means of mechanically and electrically manipulating molecular magnetism at the nanoscale for nano-mechatronics and spintronics.

Druh

J_imp - Článek v periodiku v databázi Web of Science

CEP obor

—

OECD FORD obor

10403 - Physical chemistry

Projekt

Výsledek vznikl pri realizaci vícero projektů. Více informací v záložce Projekty.

Návaznosti

P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Rok uplatnění

2019

Kód důvěrnosti údajů

S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Název periodika

Nanoscale

ISSN

2040-3364

e-ISSN

—

Svazek periodika

11

Číslo periodika v rámci svazku

22

Stát vydavatele periodika

GB - Spojené království Velké Británie a Severního Irska

Počet stran výsledku

7

Strana od-do

10615-10621

Kód UT WoS článku

000470756000006

EID výsledku v databázi Scopus

2-s2.0-85067014352