The reviewed record of science sign in
Pith

arxiv: 2308.07800 · v3 · pith:5XRD4PGW · submitted 2023-08-15 · cond-mat.mtrl-sci · cond-mat.supr-con

Phases and magnetism at the microscale in compounds containing nominal Pb10-xCux(PO4)6O

Reviewed by Pith T0 review T1 audit T2 compute T3 formal T4 kernel pith:5XRD4PGWrecord.jsonopen to challenge →

classification cond-mat.mtrl-sci cond-mat.supr-con
keywords pb10-xcuxelectricalmagneticmicroscalechemicalcompoundscontainingcu2s
0
0 comments X
read the original abstract

Achieving superconductivity at room temperature could lead to substantial advancements in industry and technology. Recently, a compound known as Cu-doped lead-apatite, Pb10-xCux(PO4)6O (0.9 < x < 1.1), referred to as "LK-99", has been reported to exhibit unusual electrical and magnetic behaviors that appear to resemble a superconducting transition above room temperature. In this work we collected multiphase samples containing the nominal Pb10-xCux(PO4)6O phase (no superconductivity observed in our measured samples), synthesized by three independent groups, and studied their chemical, magnetic, and electrical properties at the microscale to overcome difficulties in bulk measurements. Through the utilization of optical, scanning electron, atomic force, and scanning diamond nitrogen-vacancy microscopy techniques, we are able to establish a link between local magnetic properties and specific microscale chemical phases. Our findings indicate that while the Pb10-xCux(PO4)6O phase seems to have a mixed magnetism contribution, a significant fraction of the diamagnetic response can be attributed to Cu-rich regions (e.g., Cu2S derived from a reagent used in the synthesis). Additionally, our electrical measurements reveal the phenomenon of current path switch and a change in resistance states of Cu2S. This provides a potential explanation for the electrical behavior observed in compounds related to Pb10-xCux(PO4)6O.

This paper has not been read by Pith yet.

discussion (0)

Sign in with ORCID, Apple, or X to comment. Anyone can read and Pith papers without signing in.