Loading…
Tuning the magnetic properties of NiPS through organic-ion intercalation
Atomically thin van der Waals magnetic crystals are characterized by tunable magnetic properties related to their low dimensionality. While electrostatic gating has been used to tailor their magnetic response, chemical approaches like intercalation remain largely unexplored. Here, we demonstrate the...
Saved in:
Published in: | Nanoscale 2022-01, Vol.14 (4), p.1165-1173 |
---|---|
Main Authors: | , , , , , , , , , , |
Format: | Article |
Language: | |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Summary: | Atomically thin van der Waals magnetic crystals are characterized by tunable magnetic properties related to their low dimensionality. While electrostatic gating has been used to tailor their magnetic response, chemical approaches like intercalation remain largely unexplored. Here, we demonstrate the manipulation of the magnetism in the van der Waals antiferromagnet NiPS
3
through the intercalation of different organic cations, inserted using an engineered two-step process. First, the electrochemical intercalation of tetrabutylammonium cations (TBA
+
) results in a ferrimagnetic hybrid compound displaying a transition temperature of 78 K, and characterized by a hysteretic behavior with finite remanence and coercivity. Then, TBA
+
cations are replaced by cobaltocenium
via
an ion-exchange process, yielding a ferrimagnetic phase with higher transition temperature (98 K) and higher remanent magnetization. Importantly, we demonstrate that the intercalation and cation exchange processes can be carried out in bulk crystals and few-layer flakes, opening the way to the integration of intercalated magnetic materials in devices.
The intercalation of different organic cations in the layered antiferromagnet NiPS
3
yields ferrimagnetic ordering with a molecule-dependent transition temperature. A successful intercalation is demonstrated for bulk crystals and exfoliated flakes. |
---|---|
ISSN: | 2040-3364 2040-3372 |
DOI: | 10.1039/d1nr07281a |