Self-similar mesocrystals form via interface-driven nucleation and assembly

Guomin Zhu1,2, Maria L Sushko1, John S Loring1, Benjamin A Legg1,2, Miao Song1, Jennifer A Soltis1, Xiaopeng Huang1, Kevin M Rosso1, James J De Yoreo3,4

  1. Physical Sciences Division, Pacific Northwest National Laboratory, Richland, WA, USA.
  2. Department of Materials Science and Engineering, University of Washington, Seattle, WA, USA.
  3. Physical Sciences Division, Pacific Northwest National Laboratory, Richland, WA, USA. james.deyoreo@pnnl.gov.
  4. Department of Materials Science and Engineering, University of Washington, Seattle, WA, USA. james.deyoreo@pnnl.gov.

Abstract

Crystallization by particle attachment (CPA) is a frequently occurring mechanism of colloidal crystallization that results in hierarchical morphologies1-4. CPA has been exploited to create nanomaterials with unusual properties4-6 and is implicated in the development of complex mineral textures1,7. Oriented attachment7,8-a form of CPA in which particles align along specific crystallographic directions-produces mesocrystals that diffract as single crystals do, although the constituent particles are still discernible2,9. The conventional view of CPA is that nucleation provides a supply of particles that aggregate via Brownian motion biased by attractive interparticle potentials1,9-12. However, mesocrystals often exhibit regular morphologies and uniform sizes. Although many crystal systems form mesocrystals1-9 and individual attachment events have been directly visualized10, how random attachment events lead to well defined, self-similar morphologies remains unknown, as does the role of surface-bound ligands, which are ubiquitous in nanoparticle systems3,9,11. Attempts to understand mesocrystal formation are further complicated in many systems by the presence of precursor nanoparticles with a phase distinct from that of the bulk1,13,14. Some studies propose that such particles convert before attachment15, whereas others attribute conversion to the attachment process itself16 and yet others conclude that transformation occurs after the mesocrystals exceed a characteristic size14,17. Here we investigate mesocrystal formation by iron oxides, which are important colloidal phases in natural environments18,19 and classic examples of systems forming ubiquitous precursor phases and undergoing CPA accompanied by phase transformations15,19-21. Combining in situ transmission electron microscopy (TEM) at 80 degrees Celsius with 'freeze-and-look' TEM, we tracked the formation of haematite (Hm) mesocrystals in the presence of oxalate (Ox), which is abundant in soils, where iron oxides are common. We find that isolated Hm particles rarely appear, but once formed, interfacial gradients at the Ox-covered surfaces drive Hm particles to nucleate repeatedly about two nanometres from the surfaces, to which they then attach, thereby generating mesocrystals. Comparison to natural and synthetic systems suggests that interface-driven pathways are widespread.

Presented By Guomin Zhu

Physical SciencesNicholas Liao2021-02 (Feb)