Photoinduced Structural Instability Toward the Superionic Phase Transition in Cu <sub>2</sub> S

Copper(I) sulfide (Cu 2 S) undergoes a semiconductor-to-superionic phase transition associated with the destabilization of the ordered Cu sublattice. Herein, we investigated the structural dynamics of photoexcited Cu 2 S using time-resolved electron diffraction from picoseconds to milliseconds. The measurements reveal a rapid suppression (80%–90%) of semiconducting phase superlattice reflections in ∼10 ps, indicating prompt destabilization of Cu ordering. This process is accompanied by a slower lattice expansion of approximately 100 ps, observed as a shift of Bragg diffraction peaks corresponding to a lattice strain of ∼0.7%. The suppression of the superlattice reflections exhibits a fluence threshold, indicating a critical excitation density for destabilizing the ordered Cu sublattice. Density functional theory calculations show that photoexcitation populates antibonding states, weakening Cu–S bonds, and driving the observed structural destabilization. These findings reveal the ultrafast microscopic pathway toward the superionic phase in Cu 2 S and provide insights into photoinduced structural dynamics in superionic materials.

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Publication Details

Journal
The Journal of Physical Chemistry Letters
Published
2026-06-26
DOI
https://doi.org/10.1021/acs.jpclett.6c01164
Primary Topic
Copper-based nanomaterials and applications
Type
article
Field-Weighted Citation Impact
0.00

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article

Photoinduced Structural Instability Toward the Superionic Phase Transition in Cu 2 S

Keito Sano, Satoshi Ohmura, Masanori Sakamoto, Masaki Hada et al.
The Journal of Physical Chemistry Letters
Copper-based nanomaterials and applications
article

Photoinduced Structural Instability Toward the Superionic Phase Transition in Cu 2 S

Keito Sano, Satoshi Ohmura, Masanori Sakamoto, Masaki Hada, Arnaud Arbouet, Gaël Privault, Kaito En-ya
article en

Abstract

Copper(I) sulfide (Cu 2 S) undergoes a semiconductor-to-superionic phase transition associated with the destabilization of the ordered Cu sublattice. Herein, we investigated the structural dynamics of photoexcited Cu 2 S using time-resolved electron diffraction from picoseconds to milliseconds. The measurements reveal a rapid suppression (80%–90%) of semiconducting phase superlattice reflections in ∼10 ps, indicating prompt destabilization of Cu ordering. This process is accompanied by a slower lattice expansion of approximately 100 ps, observed as a shift of Bragg diffraction peaks corresponding to a lattice strain of ∼0.7%. The suppression of the superlattice reflections exhibits a fluence threshold, indicating a critical excitation density for destabilizing the ordered Cu sublattice. Density functional theory calculations show that photoexcitation populates antibonding states, weakening Cu–S bonds, and driving the observed structural destabilization. These findings reveal the ultrafast microscopic pathway toward the superionic phase in Cu 2 S and provide insights into photoinduced structural dynamics in superionic materials.

The Journal of Physical Chemistry Letters
Centre National de la Recherche Scientifique (FR), University of Tsukuba (JP), EarthTech International (United States) (US), International Union for Pure and Applied Biophysics (SE), Dynamic Systems (United States) (US), Ehime University (JP), The University of Tokyo (JP)
Japan Society for the Promotion of Science, Fusion Oriented REsearch for disruptive Science and Technology
Climate action
Openalex Percentile: Top 14%
Copper-based nanomaterials and applications
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