How Crystal Size and Number Steer Asymmetric Crystallization

Chiral amplification processes during crystallization can hinge on subtle asymmetries in crystal populations, yet the underlying kinetic drivers remain elusive. Here we experimentally investigate how size and mass imbalances between two enantiomeric crystal populations translate to asymmetric growth rates that determine asymmetric crystal growth. We find that the interplay between imbalances in size and mass can yield positive, linear or even negative nonlinear chiral amplification. Consequently, though small crystals have a thermodynamically higher solubility than large ones, a minority population of small crystals can collectively outgrow and ultimately dominate a majority of larger crystals. This amplification due to size effects can be further enhanced or dampened by controlling growth rates. Our findings uncover an intricate kinetic selection mechanism driven by population-level growth rates and governed by fundamental crystallization dynamics. Together, these results provide new insights into the origin of nonlinear amplification phenomena and offer practical guidance for competitive asymmetric crystallization and self-assembly processes.

Authors

Institutions

Publication Details

Journal
The Journal of Physical Chemistry Letters
Published
2026-01-16
DOI
https://doi.org/10.1021/acs.jpclett.5c03059
Citations
1
Primary Topic
Origins and Evolution of Life
Type
article
Field-Weighted Citation Impact
23.83
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

How Crystal Size and Number Steer Asymmetric Crystallization

Sjoerd W. van Dongen, Willem L. Noorduin, Bernard Kaptein, Karin G.P. Dautzenberg et al.
1 citations
The Journal of Physical Chemistry Letters
Origins and Evolution of Life
23.83
article

How Crystal Size and Number Steer Asymmetric Crystallization

Sjoerd W. van Dongen, Willem L. Noorduin, Bernard Kaptein, Karin G.P. Dautzenberg, Pepijn J. Rang
article en
1 citations

Abstract

Chiral amplification processes during crystallization can hinge on subtle asymmetries in crystal populations, yet the underlying kinetic drivers remain elusive. Here we experimentally investigate how size and mass imbalances between two enantiomeric crystal populations translate to asymmetric growth rates that determine asymmetric crystal growth. We find that the interplay between imbalances in size and mass can yield positive, linear or even negative nonlinear chiral amplification. Consequently, though small crystals have a thermodynamically higher solubility than large ones, a minority population of small crystals can collectively outgrow and ultimately dominate a majority of larger crystals. This amplification due to size effects can be further enhanced or dampened by controlling growth rates. Our findings uncover an intricate kinetic selection mechanism driven by population-level growth rates and governed by fundamental crystallization dynamics. Together, these results provide new insights into the origin of nonlinear amplification phenomena and offer practical guidance for competitive asymmetric crystallization and self-assembly processes.

The Journal of Physical Chemistry LettersVol. 17(4)
Institute for Atomic and Molecular Physics (NL), Geosyntec Consultants (United States) (US), University of Amsterdam (NL)
Openalex Percentile: Top 2%
Origins and Evolution of Life
23.83
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.

How Crystal Size and Number Steer Asymmetric Crystallization — Sjoerd W. van Dongen, Willem L. Noorduin, et al. · The Journal of Physical Chemistry Letters (2026) | TGRS Research Map | TGRS