<HashMap><database>biostudies-literature</database><scores><citationCount>0</citationCount><reanalysisCount>0</reanalysisCount><viewCount>49</viewCount><searchCount>0</searchCount></scores><additional><omics_type>Unknown</omics_type><volume>9(1)</volume><submitter>Wu L</submitter><pubmed_abstract>Charged colloids at interfaces hold such a simple configuration that their interactions are supposed to be fully elucidated in the framework of classical electrostatics, yet the mysterious existence of attractive forces between these like-charged particles has puzzled the scientific community for decades. Here, we perform the in situ grazing-incidence small-angle X-ray scattering study of the dynamic self-assembling process of two-dimensional interfacial colloids. This approach allows simultaneous monitoring of the in-plane structure and ordering and the out-of-plane immersion depth variation. Upon compression, the system undergoes multiple metastable intermediate states before the stable hexagonal close-packed monolayer forms under van der Waals attraction. Remarkably, the immersion depth of colloidal particles is found to increase as the interparticle distance decreases. Numerical simulations demonstrate the interface around a colloid is deformed by the electrostatic force from its neighboring particles, which induces the long-range capillary attraction.</pubmed_abstract><journal>Nature communications</journal><pagination>1335</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5889402</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>In situ X-ray scattering observation of two-dimensional interfacial colloidal crystallization.</pubmed_title><pmcid>PMC5889402</pmcid><pubmed_authors>Wu L</pubmed_authors><pubmed_authors>Chen G</pubmed_authors><pubmed_authors>Wang G</pubmed_authors><pubmed_authors>Wang X</pubmed_authors><view_count>49</view_count></additional><is_claimable>false</is_claimable><name>In situ X-ray scattering observation of two-dimensional interfacial colloidal crystallization.</name><description>Charged colloids at interfaces hold such a simple configuration that their interactions are supposed to be fully elucidated in the framework of classical electrostatics, yet the mysterious existence of attractive forces between these like-charged particles has puzzled the scientific community for decades. Here, we perform the in situ grazing-incidence small-angle X-ray scattering study of the dynamic self-assembling process of two-dimensional interfacial colloids. This approach allows simultaneous monitoring of the in-plane structure and ordering and the out-of-plane immersion depth variation. Upon compression, the system undergoes multiple metastable intermediate states before the stable hexagonal close-packed monolayer forms under van der Waals attraction. Remarkably, the immersion depth of colloidal particles is found to increase as the interparticle distance decreases. Numerical simulations demonstrate the interface around a colloid is deformed by the electrostatic force from its neighboring particles, which induces the long-range capillary attraction.</description><dates><release>2018-01-01T00:00:00Z</release><publication>2018 Apr</publication><modification>2021-02-21T03:54:52Z</modification><creation>2019-03-26T23:28:02Z</creation></dates><accession>S-EPMC5889402</accession><cross_references><pubmed>29626195</pubmed><doi>10.1038/s41467-018-03767-y</doi></cross_references></HashMap>