Realization of magnetostructural coupling by modifying structural transitions in MnNiSi-CoNiGe system with a wide Curie-temperature window.

Sci Rep

Jiangsu Key Laboratory of Advanced Micro&Nano Materials and Technology, School of Materials Science and Engineering, Nanjing University of Science and Technology, Nanjing 210094, China.

Published: March 2016

The magnetostructural coupling between structural and magnetic transitions leads to magneto-multifunctionalities of phase-transition alloys. Due to the increasing demands of multifunctional applications, to search for the new materials with tunable magnetostructural transformations in a large operating temperature range is important. In this work, we demonstrate that by chemically alloying MnNiSi with CoNiGe, the structural transformation temperature of MnNiSi (1200 K) is remarkably decreased by almost 1000 K. A tunable magnetostructural transformation between the paramagnetic hexagonal and ferromagnetic orthorhombic phase over a wide temperature window from 425 to 125 K is realized in (MnNiSi)1-x(CoNiGe)x system. The magnetic-field-induced magnetostructural transformation is accompanied by the high-performance magnetocaloric effect, proving that MnNiSi-CoNiGe system is a promising candidate for magnetic cooling refrigerant.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4793218PMC
http://dx.doi.org/10.1038/srep23386DOI Listing

Publication Analysis

Top Keywords

magnetostructural coupling
8
mnnisi-conige system
8
tunable magnetostructural
8
magnetostructural transformation
8
realization magnetostructural
4
coupling modifying
4
modifying structural
4
structural transitions
4
transitions mnnisi-conige
4
system wide
4

Similar Publications

Semiquantitative studies on the correlations between the electrostatic potential of a single Dy ion and its energy barrier in the containing-Dy single molecule magnets.

Dalton Trans

February 2025

School of Chemistry and Environmental Engineering, Wuhan Institute of Technology, Key Laboratory of Novel Reactor and Green Chemical Technology of Hubei Province, Key Laboratory for Green Chemical Process of Ministry of Education, Wuhan 430074, P. R. China.

Although the design of containing-Dy single molecule magnets (SMMs) based on electrostatic potential has been employed for several years, rational studies on the correlations between the electrostatic potential of a single Dy ion and its energy barriers have not been reported previously. In this work, a novel "Y"-shaped MnIII5DyIII3 complex, [MnIII5DyIII3(NO)(OCH)(L)(L')(tea)(teaH)]OH·3CHOH·2HO (1, HL = 2-methoxy-6-[()-(1-1,2,4-triazol-3-ylimino)methyl]phenol, Htea = triethanolamine and HL' = 2-hydroxy-3-methoxybenzaldehyde), was obtained through the reaction of the HL ligand, teaH, Dy(NO)·6HO and MnCl·4HO in CHOH and DMF. Structural analysis revealed that the coordination geometry of Dy1 in 1 is muffin-like (MFF-9, ), while the geometries of Dy2 and Dy3 fall among spherical capped square antiprism-like (CSAPR-9, ), spherical tricapped trigonal prism-like (TCTPR-9, ) and muffin-like (MFF-9, ).

View Article and Find Full Text PDF

We report the preparation of three neutral linear trinuclear Ni(II) complexes [Ni(LX)] (1-3) by self-assembly of Ni(II) ions and NO-tripodal Schiff base ligands, LX, which were obtained by condensation between the triamine tris(methylhydrazine)phosphorylsulfide and salicylaldehyde derivatives with substituents X=H (L1) (1), Br (L2) (2) and NO (L3) (3) in para position to the phenoxo group. Experimental magneto-structural studies carried out on these complexes indicate that the magnetic exchange interactions between the neighboring Ni(II) ions are ferromagnetic in nature, moderate in magnitude and clearly dependent of the electronic properties of the substituent in para position. Thus, the electron-withdrawing NO group decreases the ferromagnetic coupling, whereas the Br substituent, with small electronic effects, does not significantly vary the exchange coupling observed for the unsubstituted complex.

View Article and Find Full Text PDF

Type-II multiferroicity from non-collinear spin order is recently explored in the van der Waals material NiI. Despite the importance for improper ferroelectricity, the microscopic mechanism of the helimagnetic order remains poorly understood. Here, the magneto-structural phases of NiI are investigated using resonant magnetic X-ray scattering (RXS) and X-ray diffraction.

View Article and Find Full Text PDF

Growth and properties of hybrid Au-CoNinanowires embedded in SrTiO/SrTiO(001).

Nanotechnology

December 2024

Sorbonne Université, CNRS, Institut des NanoSciences de Paris, INSP, UMR7588, F-75005 Paris, France.

We present a sequential growth scheme based on pulsed laser deposition, which yields dense arrays of ultrathin, match-shaped Au/CoNi nanopillars, vertically embedded in SrTiOthin films. Analysis of the magnetic properties of these nanocomposites reveals a pronounced out-of-plane anisotropy. We show that the latter not only results from the peculiar nanoarchitecture of the hybrid films but is further enhanced by strong magneto-structural coupling of the wires to the surrounding matrix.

View Article and Find Full Text PDF

Interlayer Ions Control Spin Canting in Low-Dimensional Manganese Trimers in 12R-BaMnO ( = Ce, Pr) Layered Perovskites.

Inorg Chem

December 2024

Materials, Chemical, and Computational Sciences Directorate, National Renewable Energy Laboratory, Golden, Colorado 80401, United States.

To synthetically target a specific material with select performance, the underlying relationship between structure and function must be understood. For targeting magnetic properties, such understanding is underdeveloped for a relatively new class of layered hexagonal perovskites, the 12R-BaMnO family. Here, we perform a detailed magnetostructural study of the layered hexagonal perovskite materials 12R-BaMnO, where = diamagnetic Ce or paramagnetic ≈ 1/2 Pr.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!