# Mechanistic Transformation of CuI Nanoparticles Into Oxidation‐Resistant 2D Copper Nanoplates

**Authors:** Hyeuk Jin Han, Moon Young Yang, Changsoo Lee, Gangtae Jin, James L Hart, Rabecca Mutheu, Hyung il Lee, Seo Hyun Kim, Hanhwi Jang, Minjoon Kim, Yeon Sik Jung, William A. Goddard, Judy J. Cha, Chungseok Choi

PMC · DOI: 10.1002/smll.202508098 · Small (Weinheim an Der Bergstrasse, Germany) · 2025-11-18

## TL;DR

This study shows how copper(I) iodide nanoparticles can transform into stable, oxidation-resistant copper nanoplates through a unique defect-mediated process.

## Contribution

The paper reveals a defect-mediated uphill phase transformation mechanism for creating oxidation-resistant 2D copper nanostructures.

## Key findings

- Hexadecylamine and chloride ions induce iodine vacancies, enabling the transformation of CuI NPs into Cu{111} nanoplates.
- The resulting Cu nanoplates have ultrathin thicknesses and high aspect ratios, showing exceptional oxidation resistance for over 100 days.
- The {111} facets of the nanoplates suppress chemical oxidation, offering long-term structural stability under ambient conditions.

## Abstract

Unconventional phase transformations reveal new crystallization mechanisms, yet direct observation of such pathways during nanoscale solution‐phase synthesis remains challenging. This study uncovers an atypical growth process in which thermodynamically stable CuI nanoparticles (NPs) transform into high‐energy 2D Cu plates. Using a combination of in situ transmission electron microscopy, ex situ structural analysis, and density functional theory calculations shows that the formation of structural defects induced by hexadecylamine and chloride ions facilitates the transformation by promoting surface iodine vacancies. The resulting Cu{111} nanoplates, with ultrathin thicknesses (≈4 nm) and exceptionally high aspect ratios (≈450), display enhanced oxidation resistance and long‐term stability under ambient conditions. This resistance is attributed to the close‐packed {111} facets, which suppress chemical oxidation even after extended exposure to air over 100 days. These findings provide new insights into non‐classical crystallization pathways in metal nanomaterials and suggest a versatile approach for preparing oxidation‐resistant, structurally defined Cu nanostructures.

Thermodynamically stable CuI nanoparticles transform into less stable 2D Cu plates through a defect‐mediated uphill phase transformation. In situ TEM and DFT analyses reveal that Cl− and hexadecylamine promote iodine vacancies, enabling Cu aggregation and facet‐selective {111} growth. The resulting ultrathin Cu plates exhibit remarkable oxidation resistance and long‐term structural stability under ambient conditions.

## Linked entities

- **Chemicals:** CuI (PubChem CID 104815), hexadecylamine (PubChem CID 8926), Cl− (PubChem CID 312)

## Full-text entities

- **Chemicals:** metal (MESH:D008670), chloride (MESH:D002712), Copper (MESH:D003300), hexadecylamine (MESH:C013553), CuI (MESH:C073870), iodine (MESH:D007455), Cu{111 (-)

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12757985/full.md

## References

28 references — full list in the complete paper: https://tomesphere.com/paper/PMC12757985/full.md

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Source: https://tomesphere.com/paper/PMC12757985