Colossal Magnetoresistance without Mixed Valence in a Layered Phosphide Crystal
Source abstract
Abstract
Abstract Materials with strong magnetoresistive responses are the backbone of spintronic technology, magnetic sensors, and hard drives. Among them, manganese oxides with a mixed valence and a cubic perovskite structure stand out due to their colossal magnetoresistance (CMR). A double exchange interaction underlies the CMR in manganates, whereby charge transport is enhanced when the spins on neighboring Mn3+ and Mn4+ ions are parallel. Prior efforts to find different materials or mechanisms for CMR resulted in a much smaller effect. Here an enormous CMR at low temperatures in EuCd2P2 without manganese, oxygen, mixed valence, or cubic perovskite structure is shown. EuCd2P2 has a layered trigonal lattice and exhibits antiferromagnetic ordering at 11 K. The magnitude of CMR (104%) in as‐grown crystals of EuCd2P2 rivals the magnitude in optimized thin films of manganates. The magnetization, transport, and synchrotron X‐ray data suggest that strong magnetic fluctuations are responsible for this phenomenon. The realization of CMR at low temperatures without heterovalency leads to a new regime for materials and technologies related to antiferromagnetic spintronics.
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Research context
OpenAlex topics: Magnetic and transport properties of perovskites and related materials · Advanced Condensed Matter Physics · Electronic and Structural Properties of Oxides
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Departments of Physics Boston College 140 Commonwealth Avenue Chestnut Hill MA 02467 USA
Physics Department University of Connecticut Storrs CT 06269 USA
Institute of Material Science University of Connecticut Storrs CT 06269 USA
Advanced Photon Source Argonne National Laboratory Argonne IL 60439 USA
School of Physical Sciences Dublin City University Dublin 9 D09 V209 Ireland
Funding
National Science Foundation · U.S. Department of Energy · Office of Science · Basic Energy Sciences
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