Space-confined synthesis of sinter-resistant high-entropy nanoparticle library

S Shaoqing Chen (Department of Energy and Chemical Engineering/Center for Dimension-Controllable Organic Frameworks) X Xia Li Z Ziqiang Qu X Xiang Li Y Yuanzhu Gao P Peng-Fei Liu (Institute of High Energy Physics, Chinese Academy of Sciences) Z Zhi-Qiang Dong P Peng Yu (Eastern Institute for Advanced Study) Q Qiming Sun (Innovation Center for Chemical Science, College of Chemistry, Chemical Engineering and Materials Science, Jiangsu Key Laboratory of Advanced Negative Carbon Technologies) S Shixue Dou Z Zhongfan Liu (Center for Nanochemistry, Beijing Science and Engineering Center for Nanocarbons, Beijing National Laboratory for Molecular Sciences, College of Chemistry and Molecular Engineering) J Jingyu Sun (Bio-X Institutes, Key Laboratory for the Genetics of Development and Neuropsychiatric Disorders (Ministry of Education), Center for Brain Health and Brain Technology, Global Institute of Future Technology, Institute of Psychology and Behavioral Science, Shanghai Jiao Tong University)

Abstract

Abstract The tailorable confinement of high-entropy nanoparticles (HE-NPs) within molecular sieves (HE-NPs@MSs), synergizing merits of cocktail effects and geometric polymorphs, holds potential for advancing heterogeneous catalysis. However, effective and universal synthesis affording size homogeneity and production scalability remains elusive. In this contribution, we present a versatile strategy for encapsulating ultrafine HE-NPs within diverse mesoporous/microporous MSs to enable the rational construction of HE-NPs@MS library. By utilizing the approach of quenching space-confined liquid metal droplets, the resulting HE-NPs@MSs comprise anti-sintered HE-NPs (1 to 5 nm in diameter) with narrow size distributions. As a proof-of-concept demonstration, a HE-NPs@MS prototype catalyst containing trace amounts of Pt is employed in the propane dehydrogenation reaction, achieving a propylene formation rate of up to 44.2 mol gPt⁻¹ h⁻¹, which is 31.6 times greater than that of the monometallic Pt@MS counterpart. Our strategy facilitates high-throughput synthesis and large-scale production, opening tantalizing opportunities in the utilization of high-entropy nanomaterials for various applications.

Article Details

Volume / Issue Vol. 16, Issue 1
Published August 11, 2025
ISSN 2041-1723
Publisher Nature Portfolio

Journal Info

Nature Communications

Nature Portfolio

ISSN: 2041-1723 Open Access Life Sciences

Authors (12)

S

Shaoqing Chen

Department of Energy and Chemical Engineering/Center for Dimension-Controllable Organic Frameworks

X

Xia Li

Z

Ziqiang Qu

X

Xiang Li

Y

Yuanzhu Gao

P

Peng-Fei Liu

Institute of High Energy Physics, Chinese Academy of Sciences

Z

Zhi-Qiang Dong

P

Peng Yu

Eastern Institute for Advanced Study

Q

Qiming Sun

Innovation Center for Chemical Science, College of Chemistry, Chemical Engineering and Materials Science, Jiangsu Key Laboratory of Advanced Negative Carbon Technologies

S

Shixue Dou

Z

Zhongfan Liu

Center for Nanochemistry, Beijing Science and Engineering Center for Nanocarbons, Beijing National Laboratory for Molecular Sciences, College of Chemistry and Molecular Engineering

J

Jingyu Sun

Bio-X Institutes, Key Laboratory for the Genetics of Development and Neuropsychiatric Disorders (Ministry of Education), Center for Brain Health and Brain Technology, Global Institute of Future Technology, Institute of Psychology and Behavioral Science, Shanghai Jiao Tong University