Heo Jaeyoung, Dumett Torres Daniel, Banerjee Progna, Jain Prashant K
Department of Materials Science & Engineering, University of Illinois at Urbana-Champaign, Urbana, IL, 61801, USA.
Department of Chemistry, University of Illinois at Urbana-Champaign, Urbana, IL, 61801, USA.
Nat Commun. 2019 Apr 3;10(1):1505. doi: 10.1038/s41467-019-09502-5.
Solid-solid phase transitions are processes ripe for the discovery of correlated atomic motion in crystals. Here, we monitor an order-disorder transition in real-time in nanoparticles of the super-ionic solid, CuSe. The use of in-situ high-resolution transmission electron microscopy allows the spatiotemporal evolution of the phase transition within a single nanoparticle to be monitored at the atomic level. The high spatial resolution reveals that cation disorder is nucleated at low co-ordination, high energy sites of the nanoparticle where cationic vacancy layers intersect with surface facets. Time-dependent evolution of the reciprocal lattice of individual nanoparticles shows that the initiation of cation disorder is accompanied by a ~3% compression of the anionic lattice, establishing a correlation between these two structural features of the lattice. The spatiotemporal insights gained here advance understanding of order-disorder transitions, ionic structure and transport, and the role of nanoparticle surfaces in phase transitions.
固-固相变是发现晶体中相关原子运动的成熟过程。在这里,我们实时监测了超离子固体CuSe纳米颗粒中的有序-无序转变。原位高分辨率透射电子显微镜的使用使得能够在原子水平上监测单个纳米颗粒内相变的时空演化。高空间分辨率表明,阳离子无序在纳米颗粒的低配位、高能位点处成核,在这些位点阳离子空位层与表面晶面相交。单个纳米颗粒倒易晶格的时间相关演化表明,阳离子无序的起始伴随着阴离子晶格约3%的压缩,从而在晶格的这两个结构特征之间建立了关联。这里获得的时空见解推动了对有序-无序转变、离子结构和传输以及纳米颗粒表面在相变中的作用的理解。