Template-free generation and integration of functional 1D magnetic nanostructures

• Published in: Nanoscale Vol. 15; no. 45; pp. 185 - 1851
• Main Authors: Sedrpooshan, Mehran, Bulbucan, Claudiu, Ternero, Pau, Maltoni, Pierfrancesco, Preger, Calle, Finizio, Simone, Watts, Benjamin, Peddis, Davide, Burke, Adam M, Messing, Maria E, Westerström, Rasmus
• Format: Journal Article
• Language: English
• Published: Cambridge Royal Society of Chemistry 23.11.2023
• Subjects: Aerosols; Anisotropy; Coercivity; Condensed Matter Physics; Den kondenserade materiens fysik; Electronic circuits; Engineering and Technology; functional materials; Fysik; gas-phase synthesis; Magnetic measurement; magnetic nanostructures; Magnetic properties; Magnetic storage; Magnetization reversal; Magneto-transport; Magnetoresistance; Magnetoresistivity; Micromagnetic simulation; Nano Technology; nanomagnetism; nanoparticle deposition; Nanoparticles; Nanostructure; Nanoteknik; Nanowires; Natural Sciences; Naturvetenskap; Physical Sciences; self-assembled; Self-assembly; spark ablation; STXM-XMCD; Substrates; Teknik; X ray microscopy
• ISSN: 2040-3364; 2040-3372; 2040-3372
• DOI: 10.1039/d3nr03878e

The direct integration of 1D magnetic nanostructures into electronic circuits is crucial for realizing their great potential as components in magnetic storage, logical devices, and spintronic applications. Here, we present a novel template-free technique for producing magnetic nanochains and nanowires using directed self-assembly of gas-phase-generated metallic nanoparticles. The 1D nanostructures can be self-assembled along most substrate surfaces and can be freely suspended over micrometer distances, allowing for direct incorporation into different device architectures. The latter is demonstrated by a one-step integration of nanochains onto a pre-patterned Si chip and the fabrication of devices exhibiting magnetoresistance. Moreover, fusing the nanochains into nanowires by post-annealing significantly enhances the magnetic properties, with a 35% increase in the coercivity. Using magnetometry, X-ray microscopy, and micromagnetic simulations, we demonstrate how variations in the orientation of the magnetocrystalline anisotropy and the presence of larger multi-domain particles along the nanochains play a key role in the domain formation and magnetization reversal. Furthermore, it is shown that the increased coercivity in the nanowires can be attributed to the formation of a uniform magnetocrystalline anisotropy along the wires and the onset of exchange interactions. This work reports on a novel template-free technique for producing isolated 1D magnetic nanochains and nanowires directly onto substrates and device architectures by directed self-assembly of gas-phase-generated nanoparticles.