8 research outputs found
Orthoborates LiCdRE<sub>5</sub>(BO<sub>3</sub>)<sub>6</sub> (RE = Sm–Lu and Y) with Rare-Earth Ions on a Triangular Lattice: Synthesis, Crystal Structure, and Optical and Magnetic Properties
Single crystals of LiCdY<sub>5</sub>(BO<sub>3</sub>)<sub>6</sub> were successfully grown from a Li<sub>2</sub>O–B<sub>2</sub>O<sub>3</sub> flux, and its lanthanide
homotypic compounds, LiCdRE<sub>5</sub>(BO<sub>3</sub>)<sub>6</sub> (RE = Sm–Lu), have been prepared by solid-state reaction.
They crystallize in the noncentrosymmetric space group <i>P</i>6<sub>5</sub>22 with cell parameters in the ranges of <i>a</i> = 7.0989(2)–6.9337(1) Å and <i>c</i> = 25.9375(1)–24.8960(6)
Ã…. As a representative example, LiCdY<sub>5</sub>(BO<sub>3</sub>)<sub>6</sub> features a triangular lattice in the <i>ab</i> plane composed of three distinct crystallographic Y sites. The triangular
lattices spaced with the same distance of 16<i>c</i> are further
stacked to build three-dimensional frameworks by reinforcement of
the isolated planar BO<sub>3</sub> groups and distorted LiO<sub>4</sub> tetrahedra. Magnetic measurements show that Eu and Sm compounds
exhibit typical Van Vleck-type paramagnetism and other rare-earth
borates show weak antiferromagnetic behavior. In addition, UV–vis–near-IR
diffuse-reflectance and photoluminescence spectra were performed to
understand the transition energy levels of active rare-earth ions
and their relationships to magnetism
Observation of Resonant Quantum Magnetoelectric Effect in a Multiferroic Metal–Organic Framework
A resonant quantum magnetoelectric
coupling effect has been demonstrated
in the multiferroic metal–organic framework of [(CH<sub>3</sub>)<sub>2</sub>NH<sub>2</sub>]ÂFeÂ(HCOO)<sub>3</sub>. This material shows
a coexistence of a spin-canted antiferromagnetic order and ferroelectricity
as well as clear magnetoelectric coupling below <i>T</i><sub>N</sub> ≈ 19 K. In addition, a component of single-ion
quantum magnets develops below ∼8 K because of an intrinsic
magnetic phase separation. The stair-shaped magnetic hysteresis loop
at 2 K signals resonant quantum tunneling of magnetization. Meanwhile,
the magnetic field dependence of dielectric permittivity exhibits
sharp peaks just at the critical tunneling fields, evidencing the
occurrence of resonant quantum magnetoelectric coupling effect. This
resonant effect enables a simple electrical detection of quantum tunneling
of magnetization
Observation of Resonant Quantum Magnetoelectric Effect in a Multiferroic Metal–Organic Framework
A resonant quantum magnetoelectric
coupling effect has been demonstrated
in the multiferroic metal–organic framework of [(CH<sub>3</sub>)<sub>2</sub>NH<sub>2</sub>]ÂFeÂ(HCOO)<sub>3</sub>. This material shows
a coexistence of a spin-canted antiferromagnetic order and ferroelectricity
as well as clear magnetoelectric coupling below <i>T</i><sub>N</sub> ≈ 19 K. In addition, a component of single-ion
quantum magnets develops below ∼8 K because of an intrinsic
magnetic phase separation. The stair-shaped magnetic hysteresis loop
at 2 K signals resonant quantum tunneling of magnetization. Meanwhile,
the magnetic field dependence of dielectric permittivity exhibits
sharp peaks just at the critical tunneling fields, evidencing the
occurrence of resonant quantum magnetoelectric coupling effect. This
resonant effect enables a simple electrical detection of quantum tunneling
of magnetization
Observation of Magnetodielectric Effect in a Dysprosium-Based Single-Molecule Magnet
Materials that possess
coupled magnetic and electric properties
are of significant interest because of their potential use in next-generation
magnetoelectric devices such as digital information storage. To date,
the magnetoelectric materials that have been studied in-depth have
been limited mainly to inorganic oxides such as perovskite oxides.
Molecular materials are a promising alternative because their magnetic
and electric elements can be combined together at the molecular level
via relatively simple molecular designs. Here, we report the coupling
of magnetic and electric properties through a magnetodielectric (MD)
effect in a single-crystal sample, which is constructed from dysprosiumÂ(III)
single-molecule magnets (SMMs). The MD effect originates from intrinsic
spin–lattice coupling of the dysprosiumÂ(III) ion within the
sample. This is the first observation of the MD effect in a SMM-based
material, which could pave the way toward the synthesis of advanced
materials that combine distinct magnetic and electric properties using
molecular chemistry for use in molecular devices with nanoscale size
Observation of Magnetodielectric Effect in a Dysprosium-Based Single-Molecule Magnet
Materials that possess
coupled magnetic and electric properties
are of significant interest because of their potential use in next-generation
magnetoelectric devices such as digital information storage. To date,
the magnetoelectric materials that have been studied in-depth have
been limited mainly to inorganic oxides such as perovskite oxides.
Molecular materials are a promising alternative because their magnetic
and electric elements can be combined together at the molecular level
via relatively simple molecular designs. Here, we report the coupling
of magnetic and electric properties through a magnetodielectric (MD)
effect in a single-crystal sample, which is constructed from dysprosiumÂ(III)
single-molecule magnets (SMMs). The MD effect originates from intrinsic
spin–lattice coupling of the dysprosiumÂ(III) ion within the
sample. This is the first observation of the MD effect in a SMM-based
material, which could pave the way toward the synthesis of advanced
materials that combine distinct magnetic and electric properties using
molecular chemistry for use in molecular devices with nanoscale size
Enhanced Catalytic Activities of NiPt Truncated Octahedral Nanoparticles toward Ethylene Glycol Oxidation and Oxygen Reduction in Alkaline Electrolyte
The
high cost and poor durability of Pt nanoparticles (NPs) are great
limits for the proton exchange membrane fuel cells (PEMFCs) from being
scaled-up for commercial applications. Pt-based bimetallic NPs together
with a uniform distribution can effectively reduce the usage of expensive
Pt while increasing poison resistance of intermediates. In this work,
a simple one-pot method was used to successfully synthesize ultrafine
(about 7.5 nm) uniform NiPt truncated octahedral nanoparticles (TONPs)
in dimethylformamid (DMF) without any seeds or templates. The as-prepared
NiPt TONPs with Pt-rich surfaces exhibit greatly improved catalytic
activities together with good tolerance and better stability for ethylene
glycol oxidation reaction (EGOR) and oxygen reduction reaction (ORR)
in comparison with NiPt NPs and commercial Pt/C catalysts in alkaline
electrolyte. For example, the value of mass and specific activities
for EGOR are 23.2 and 17.6 times higher comparing with those of commercial
Pt/C, respectively. Our results demonstrate that the dramatic enhancement
is mainly attributed to Pt-rich surface, larger specific surface area,
together with coupling between Ni and Pt atoms. This developed method
provides a promising pathway for simple preparation of highly efficient
electrocatalysts for PEMFCs in the near future
Strain-Mediated Coexistence of Volatile and Nonvolatile Converse Magnetoelectric Effects in Fe/Pb(Mg<sub>1/3</sub>Nb<sub>2/3</sub>)<sub>0.7</sub>Ti<sub>0.3</sub>O<sub>3</sub> Heterostructure
Strain-mediated
ferromagnetic/ferroelectric (FE) heterostructures have played an important
role in multiferroic materials to investigate the electric-field control
of magnetism in the past decade, due to their excellent performances,
such as room-temperature operation and large magnetoelectric (ME)
coupling effect. Because of the different FE-switching-originated
strain behaviors and varied interfacial coupling effect, both loop-like
(nonvolatile) and butterfly-like (volatile) converse ME effects have
been reported. Here, we investigate the electric-field control of
magnetism in a multiferroic heterostructure composed of a polycrystalline
Fe thin film and a PbÂ(Mg<sub>1/3</sub>Nb<sub>2/3</sub>)<sub>0.7</sub>Ti<sub>0.3</sub>O<sub>3</sub> single crystal, and the experimental
results exhibit complex behaviors, suggesting the coexistence of volatile
and nonvolatile converse ME effects. By separating the symmetrical
and antisymmetrical parts of the electrical modulation of magnetization,
we distinguished the loop-like hysteresis and butterfly-like magnetization
changes tuned by electric fields, corresponding to the strain effects
related to the FE 109° switching and 71/180° switching,
respectively. Further magnetic-field-dependent as well as angular-dependent
investigation of the converse ME effect confirmed the strain-mediated
magnetism involving competition among the Zeeman energy, magnetocrystalline
anisotropy energy, and strain-generated magnetoelastic energy. This
study is helpful for understanding the electric-field control of magnetism
in multiferroic heterostructures as well as its relevant applications
Real-Space Observation of Nonvolatile Zero-Field Biskyrmion Lattice Generation in MnNiGa Magnet
Magnetic
skyrmions, particular those without the support of external
magnetic fields over a wide temperature region, are promising as alternative
spintronic units to overcome the fundamental size limitation of conventional
magnetic bits. In this study, we use in situ Lorentz microscope to
directly demonstrate the generation and sustainability of robust biskyrmion
lattice at zero magnetic field over a wide temperature range of 16–338
K in MnNiGa alloy. This procedure includes a simple field-cooling
manipulation from 360 K (higher than Curie temperature <i>T</i><sub>C</sub> ∼ 350 K), where topological transition easily
occurs by adapting the short-range magnetic clusters under a certain
magnetic field. The biskyrmion phase is favored upon cooling below <i>T</i><sub>C</sub>. Once they are generated, the robust high-density
biskyrmions persist even after removing the external magnetic field
due to the topological protection and the increased energy barrier