Lanthanide permanent magnets are widely used in applications ranging from nanotechnology to industrial engineering. However, limited access to the rare earths and rising costs associated with their extraction are spurring interest in the development of lanthanide‐free hard magnets. Zero‐ and one‐dimensional magnetic materials are intriguing alternatives due to their low densities, structural and chemical versatility, and the typically mild, bottom‐up nature of their synthesis. Here, we present two one‐dimensional cobalt(II) systems Co(hfac)2(R‐NapNIT) (R‐NapNIT=2‐(2′‐(R‐)naphthyl)‐4,4,5,5‐tetramethylimidazoline‐1‐oxyl‐3‐oxide, R=MeO or EtO) supported by air‐stable nitronyl nitroxide radicals. These compounds are single‐chain magnets and exhibit wide, square magnetic hysteresis below 14 K, with giant coercive fields up to 65 or 102 kOe measured using static or pulsed high magnetic fields, respectively. Magnetic, spectroscopic, and computational studies suggest that the record coercivities derive not from three‐dimensional ordering but from the interaction of adjacent chains that compose alternating magnetic sublattices generated by crystallographic symmetry.
Lanthanide permanent magnets are widely used in applications ranging from nanotechnology to industrial engineering. However, limited access to the rare earths and rising costs associated with their extraction are spurring interest in the development of lanthanide‐free hard magnets. Zero‐ and one‐dimensional magnetic materials are intriguing alternatives due to their low densities, structural and chemical versatility, and the typically mild, bottom‐up nature of their synthesis. Here, we present two one‐dimensional cobalt(II) systems Co(hfac)2(R‐NapNIT) (R‐NapNIT=2‐(2′‐(R‐)naphthyl)‐4,4,5,5‐tetramethylimidazoline‐1‐oxyl‐3‐oxide, R=MeO or EtO) supported by air‐stable nitronyl nitroxide radicals. These compounds are single‐chain magnets and exhibit wide, square magnetic hysteresis below 14 K, with giant coercive fields up to 65 or 102 kOe measured using static or pulsed high magnetic fields, respectively. Magnetic, spectroscopic, and computational studies suggest that the record coercivities derive not from three‐dimensional ordering but from the interaction of adjacent chains that compose alternating magnetic sublattices generated by crystallographic symmetry.
more » « less- Award ID(s):
- 1800252
- PAR ID:
- 10149509
- Publisher / Repository:
- Wiley Blackwell (John Wiley & Sons)
- Date Published:
- Journal Name:
- Angewandte Chemie International Edition
- Volume:
- 59
- Issue:
- 26
- ISSN:
- 1433-7851
- Page Range / eLocation ID:
- p. 10610-10618
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
More Like this
-
more » « less
Abstract -
more » « less
Abstract Tremendous progress in the development of single molecule magnets (SMMs) raises the question of their device integration. On this route, understanding the properties of low‐dimensional assemblies of SMMs, in particular in contact with electrodes, is a necessary but difficult step. Here, it is shown that fullerene SMM self‐assembled on metal substrate from solution retains magnetic hysteresis up to 10 K. Fullerene‐SMM DySc2N@C80and Dy2ScN@C80are derivatized to introduce a thioacetate group, which is used to graft SMMs on gold. Magnetic properties of grafted SMMs are studied by X‐ray magnetic circular dichroism and compared to the films of nonderivatized fullerenes prepared by sublimation. In self‐assembled films, the magnetic moments of the Dy ions are preferentially aligned parallel to the surface, which is different from the disordered orientation of endohedral clusters in nonfunctionalized fullerenes. Whereas chemical derivatization reduces the blocking temperature of magnetization and narrows the hysteresis of Dy2ScN@C80, for DySc2N@C80equally broad hysteresis is observed as in the fullerene multilayer. Magnetic bistability in the DySc2N@C80grafted on gold is sustained up to 10 K. This study demonstrates that self‐assembly of fullerene‐SMM derivatives offers a facile solution‐based procedure for the preparation of functional magnetic sub‐monolayers with excellent SMM performance.
-
more » « less
Abstract Chiral single photons are highly sought to enhance encoding capacities or enable propagation-dependent routing in nonreciprocal devices. Unfortunately, most semiconductor quantum emitters (QEs) produce only linear polarized photons unless external magnets are applied. Magnetic proximity coupling utilizing 2D ferromagnets promises to make bulky external fields obsolete. Here we directly grow Fe-doped MoS2(Fe:MoS2) via chemical vapor deposition that displays pronounced hard ferromagnetic properties even in monolayer form. This approach with monolayer ferromagnets enables full utilization of the strain from the pillar stressor to form QE in WSe2deterministically. The Fe:MoS2/WSe2heterostructures display strong hysteretic magneto-response and high-purity chiral single photons with a circular polarization degree of 92 ± 1% (74% average) without external magnetic fields. Furthermore, the chiral single photons are robust against uncontrolled twist-angle and external stray-fields. This ability to manipulate quantum states and transform linear polarized photons into high-purity chiral photons on-chip enables nonreciprocal device integration in quantum photonics.
-
more » « less
Abstract Noncollinear spin textures in low-dimensional magnetic systems have been studied for decades because of their extraordinary properties and promising applications derived from the chirality and topological nature. However, material realizations of topological spin states are still limited. Employing first-principles and Monte Carlo simulations, we propose that monolayer chromium trichloride (CrCl3) can be a promising candidate for observing the vortex/antivortex type of topological defects, so-called merons. The numbers of vortices and antivortices are found to be the same, maintaining an overall integer topological unit. By perturbing with external magnetic fields, we show the robustness of these meron pairs and reveal a rich phase space to tune the hybridization between the ferromagnetic order and meron-like defects. The signatures of topological excitations under external magnetic field also provide crucial information for experimental justifications. Our study predicts that two-dimensional magnets with weak spin-orbit coupling can be a promising family for realizing meron-like spin textures.
-
more » « less
Abstract Coherent control and manipulation of quantum degrees of freedom such as spins forms the basis of emerging quantum technologies. In this context, the robust valley degree of freedom and the associated valley pseudospin found in two‐dimensional transition metal dichalcogenides is a highly attractive platform. Valley polarization and coherent superposition of valley states have been observed in these systems even up to room temperature. Control of valley coherence is an important building block for the implementation of valley qubit. Large magnetic fields or high‐power lasers have been used in the past to demonstrate the control (initialization and rotation) of the valley coherent states. Here, the control of layer–valley coherence via strong coupling of valley excitons in bilayer WS2to microcavity photons is demonstrated by exploiting the pseudomagnetic field arising in optical cavities owing to the transverse electric–transverse magnetic (TE–TM)mode splitting. The use of photonic structures to generate pseudomagnetic fields which can be used to manipulate exciton‐polaritons presents an attractive approach to control optical responses without the need for large magnets or high‐intensity optical pump powers.
