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Research Article | Open Access

Surface entropy-engineering: Towards general synthesis of high entropy subnano-oxides

Siyang Nie1Qingda Liu1 ( )Liang Wu2 ( )Xun Wang1 ( )
Engineering Research Center of Advanced Rare Earth Materials, Department of Chemistry, Tsinghua University, Beijing 100084, China
School of Chemistry and Chemical Engineering, Shanghai Jiao Tong University, Shanghai 200240, China
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Abstract

High entropy oxides (HEOs), composed of at least five nearly equimolar principal atoms occupying a similar sublattice, demonstrate promising catalytic potential but limited activity. Low-dimensional HEOs, serving as the metastable phase, possess distinctive electronic structures and fully exposed active sites, which anticipate showcasing appealing performance; however, their synthesis remains challenging. Herein, through the incorporation of clusters for kinetic control, a library of single-phase high entropy oxides (HEOs) with single-unit-cell thickness was synthesized under mild conditions (373 K). By modulating the surface entropies, including vibrational, translational, and rotational entropy, the synthesized high entropy subnano-oxides can exhibit structures, such as subnano-wires, subnano-sheets, and spiral coils. Contributed by the fully exposed active sites and electron delocalization among two-dimensional (2D) layer, HEOs presented as subnano-sheets display enhanced catalytic activity for photocatalytic reduction of CO2 to CH4, achieving a yield (5777 ± 230.21 μmol·g−1·h−1), which is 41 times higher than that of bulk HEO obtained from the high-temperature calcination synthetic route.

Graphical Abstract

High-entropy oxides with controlled morphologies are synthesized by modulating the surface entropy of subnano-materials.

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Nano Research
Article number: 94908030

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Cite this article:
Nie S, Liu Q, Wu L, et al. Surface entropy-engineering: Towards general synthesis of high entropy subnano-oxides. Nano Research, 2026, 19(4): 94908030. https://doi.org/10.26599/NR.2025.94908030
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Received: 15 August 2025
Revised: 01 September 2025
Accepted: 01 September 2025
Published: 06 January 2026
© The Author(s) 2026. Published by Tsinghua University Press.

This is an open access article under the terms of the Creative Commons Attribution 4.0 International License (CC BY 4.0, https://creativecommons.org/licenses/by/4.0/).