Anisotropic surface potentials induced by competitive ion adsorption enable the synthesis of branched cubic Pt mesocrystals

Creation of complex nanostructured materials through oriented attachment (OA) requires the manipulation of interparticle forces, including electrostatic repulsion, which depends strongly on surface potentials and can be modified through the effect of solution environment on interfacial chemistry. Here we show that time-dependent anisotropies in surface potential driven by competitive ion adsorption can alter facet-selectivity during OA. This phenomenon enables the synthesis of branched cubic Pt mesocrystals. Initially, Pt nanoparticles attach preferentially at their {100} facets to form a well-defined cubic core. Over time, changes in ion adsorption shift the attachment preference to the {111} facets, promoting branch formation. In both stages, anisotropic surface potentials generate electrostatic torques that align the particles prior to attachment. These findings demonstrate a generalizable strategy for directing the architecture of nanomaterials through time-resolved control of interfacial chemistry during OA, offering new pathways for the design of complex mesoscale structures.

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Publication Details

Journal
Nature Communications
Published
2025-11-05
DOI
https://doi.org/10.1038/s41467-025-64494-9
Primary Topic
Pickering emulsions and particle stabilization
Type
article
Field-Weighted Citation Impact
0.00

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article

Anisotropic surface potentials induced by competitive ion adsorption enable the synthesis of branched cubic Pt mesocrystals

Yun Kyung Shin, Hanlei Zhang, Zihua Zhu, Hua Zhou et al.
Nature Communications
Pickering emulsions and particle stabilization
article

Anisotropic surface potentials induced by competitive ion adsorption enable the synthesis of branched cubic Pt mesocrystals

Yun Kyung Shin, Hanlei Zhang, Zihua Zhu, Hua Zhou, Eric Jensen, James J. De Yoreo, Kristian Mølhave, Jaehun Chun, Trevor Moser, Jaeyoung Heo, Kristen A. Fichthorn, James Evans, Yuna Bae, Dongsheng Li, Eun Mi Kim
article en

Abstract

Creation of complex nanostructured materials through oriented attachment (OA) requires the manipulation of interparticle forces, including electrostatic repulsion, which depends strongly on surface potentials and can be modified through the effect of solution environment on interfacial chemistry. Here we show that time-dependent anisotropies in surface potential driven by competitive ion adsorption can alter facet-selectivity during OA. This phenomenon enables the synthesis of branched cubic Pt mesocrystals. Initially, Pt nanoparticles attach preferentially at their {100} facets to form a well-defined cubic core. Over time, changes in ion adsorption shift the attachment preference to the {111} facets, promoting branch formation. In both stages, anisotropic surface potentials generate electrostatic torques that align the particles prior to attachment. These findings demonstrate a generalizable strategy for directing the architecture of nanomaterials through time-resolved control of interfacial chemistry during OA, offering new pathways for the design of complex mesoscale structures.

Nature CommunicationsVol. 16(1)
Argonne National Laboratory (US), Pennsylvania State University (US), Pacific Northwest National Laboratory (US), University of Washington (US), Environmental Molecular Sciences Laboratory (US), Technical University of Denmark (DK)
National Science Foundation, U.S. Department of Energy, Battelle, Office of Science, Society for Personality and Social Psychology, Division of Materials Research, Office of Advanced Cyberinfrastructure, Basic Energy Sciences, Biological and Environmental Research, Pacific Northwest National Laboratory
Openalex Percentile: Top 74%
Pickering emulsions and particle stabilization
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