Evidence map›Paper›PMID 40118859›Full record

ArticleNature communications2025

Dynamic and asymmetric colloidal molecules.

Huang Fang, Qiong Gao, Yujie Rong, Yanshuang Chen, Jiping Huang, Hua Tong, Zhihong Nie, Hajime Tanaka, Wei Li, Peng Tan

Abstract read
In one paragraph

Article in Nature communications, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Huang Fang *Department of Physics and State Key Laboratory of Surface Physics, Fudan University, Shanghai, 200438, P. R. China.ORCID http://orcid.org/0000-0001-5802-9330
Qiong Gao *Department of Physics and State Key Laboratory of Surface Physics, Fudan University, Shanghai, 200438, P. R. China.ORCID http://orcid.org/0009-0001-3498-5616
Yujie Rong *Department of Physics and State Key Laboratory of Surface Physics, Fudan University, Shanghai, 200438, P. R. China.
Yanshuang ChenDepartment of Physics and State Key Laboratory of Surface Physics, Fudan University, Shanghai, 200438, P. R. China.
Jiping HuangDepartment of Physics and State Key Laboratory of Surface Physics, Fudan University, Shanghai, 200438, P. R. China.ORCID http://orcid.org/0000-0002-3617-3275
Hua TongDepartment of Physics, University of Science and Technology of China, Hefei, 230026, P. R. China.ORCID http://orcid.org/0000-0001-9201-7237
Zhihong NieDepartment of Macromolecular Science, Fudan University, Shanghai, 200438, P. R. China. znie@fudan.edu.cn.ORCID http://orcid.org/0000-0001-9639-905X
Hajime TanakaResearch Center for Advanced Science and Technology, University of Tokyo, 4-6-1 Komaba, Meguro-ku, Tokyo, 153-8904, Japan. tanaka@iis.u-tokyo.ac.jp.ORCID http://orcid.org/0000-0002-4444-1890
Wei LiState Key Laboratory of Molecular Engineering of Polymers, Fudan University, Shanghai, 200438, P. R. China. weilichem@fudan.edu.cn.ORCID http://orcid.org/0000-0002-4641-620X
Peng TanDepartment of Physics and State Key Laboratory of Surface Physics, Fudan University, Shanghai, 200438, P. R. China. tanpeng@fudan.edu.cn.ORCID http://orcid.org/0000-0002-9163-8100

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

"Colloidal molecules" represent artificial colloidal clusters replicating the geometries of molecules and exhibiting flexibility and fluctuations similar to macromolecules and proteins. Their dynamic and anisotropic characters make them unique and indispensable building blocks for creating hierarchically organized superstructures. Despite the progress in synthesizing and assembling colloidal molecules, unveiling their dynamic characters is challenging in experiments. Here, we employ real-time three-dimensional imaging and simulations to reveal dynamic colloidal molecule structures in micrometre-sized colloidal-emulsion models with tunable electrostatic interactions. Our findings reveal that colloidal molecules' dynamic structures are inherently asymmetric, with angular symmetry emerging through continuous ordering from a liquid-like configuration. We further develop an effective method to guide the ordering of colloidal molecules towards a desired structure by dynamically adjusting the ionic strength in the solvent during the ordering process. We validate this method using molecular dynamics simulations and propose a practical protocol for its experimental implementation. Our research contributes to a clearer physical understanding of dynamic colloidal molecules and offers potential solutions to the complexities inherent in their formation process.

Identifiers

PMID40118859
PMCPMC11928658

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.