Evidence map›Paper›PMID 41363006›Full record

ArticleACS nano2025

Stationary Atoms in Liquid Metals and Their Role in Solidification Mechanisms.

Christopher Leist, Sadegh Ghaderzadeh, Emerson C Kohlrausch, Johannes Biskupek, Luke T Norman, Ilya Popov, Jesum Alves Fernandes, Ute Kaiser, Elena Besley, Andrei N Khlobystov

Abstract read
In one paragraph

Article in ACS nano, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Review
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.

Christopher LeistCentral Facility Materials Science Electron Microscopy, Ulm University, Ulm 89081, Germany.
Sadegh GhaderzadehSchool of Chemistry, University of Nottingham, Nottingham NG7 2RD, United Kingdom.
Emerson C KohlrauschSchool of Chemistry, University of Nottingham, Nottingham NG7 2RD, United Kingdom.
Johannes BiskupekCentral Facility Materials Science Electron Microscopy, Ulm University, Ulm 89081, Germany.
Luke T NormanSchool of Chemistry, University of Nottingham, Nottingham NG7 2RD, United Kingdom.
Ilya PopovSchool of Chemistry, University of Nottingham, Nottingham NG7 2RD, United Kingdom.
Jesum Alves FernandesSchool of Chemistry, University of Nottingham, Nottingham NG7 2RD, United Kingdom.
Ute KaiserCentral Facility Materials Science Electron Microscopy, Ulm University, Ulm 89081, Germany.
Elena BesleySchool of Chemistry, University of Nottingham, Nottingham NG7 2RD, United Kingdom.ORCID 0000-0002-9910-7603
Andrei N KhlobystovSchool of Chemistry, University of Nottingham, Nottingham NG7 2RD, United Kingdom.ORCID 0000-0001-7738-4098

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

According to common understanding, the primary difference between a liquid and a solid metal lies in atomic motion─atoms move rapidly in liquids, while they remain stationary in a solid lattice. The solidification process involves a transition from random atomic motion to an ordered crystalline structure, with nucleation playing a crucial role. However, our research indicates that the boundary between these two phases is not as distinct as previously believed: liquid metal nanoparticles can contain stationary atoms, and the number and positions of these atoms influence the solidification pathway upon cooling. Using spherical and chromatic aberration-corrected high-resolution transmission electron microscopy (HRTEM) at low accelerating voltages, we studied the solidification of platinum, palladium, and gold. We have developed a methodology that enables imaging of metal particles over a wide temperature range, from 20 to 800 °C, without compromising atomic resolution. When a nanoparticle melts, the contrast contribution of the fast-moving atoms vanishes in the HRTEM images, allowing stationary atoms to be visualized through the liquid layer as distinct atomic points of contrast that remain fixed in position on the imaging time scale (1 s or longer). These atoms are pinned at vacancy defect sites on graphene. By conducting HRTEM image contrast analysis during time-series imaging of individual 3-6 nm particles while changing the temperature from 800 to 20 °C, we uncover the mechanisms behind classical crystal nucleation, amorphous solidification, and the formation of supercooled liquid platinum. If the number of stationary platinum atoms is small (approximately fewer than 10) and positioned randomly, liquid-to-crystal nucleation can occur. However, if the number is higher, these stationary atoms can disrupt the crystallization process, particularly if they align along the perimeter of the liquid nanoparticle. We found that liquid nanodroplets, corralled by stationary atoms, remain liquid down to 200-300 °C, which is several hundred degrees below the bulk metal crystallization temperature. In these cases, supercooled liquid metal transforms into a metastable amorphous solid instead of crystallizing. Our results highlight the significance of stationary atoms in liquids, influenced by the local environment, which may hold significant implications for the use of metal nanoparticles on carbon in heterogeneous catalysis and other thermally activated processes.

Indexed as

crystal nucleationgraphenemeltingnanoparticlephase transition

Identifiers

PMID41363006
PMCPMC12752686

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.