Growth of Size‐Tunable Ag2O Polyhedra and Revelation of Their Bulk and Surface Lattices

Abstract By primarily adjusting the reagent amounts, particularly the volume of AgNO 3 solution introduced, Ag 2 O cubes with decreasing sizes from 440 to 79 nm, octahedra from 714 to 106 nm, and rhombic dodecahedra from 644 to 168 nm are synthesized. 733 nm cuboctahedra are also prepared for structural analysis. With in‐house X‐ray diffraction (XRD) peak calibration, shape‐related peak shifts are recognizable. Synchrotron XRD measurements at 100 K reveal the presence of bulk and surface layer lattices. Bulk cell constants also deviate slightly. They show a negative thermal expansion behavior with shrinking cell constants at higher temperatures. The Ag 2 O crystals exhibit size‐ and facet‐dependent optical properties. Bandgaps red‐shift continuously with increasing particle sizes. Optical facet effect is also observable. Moreover, synchrotron XRD peaks of a mixture of Cu 2 O rhombicuboctahedra and edge‐ and corner‐truncated cubes exposing all three crystal faces can be deconvoluted into three components with the bulk and the 111 microstrain phase as the major component. Interestingly, while the unheated Cu 2 O sample shows clear diffraction peak asymmetry, annealing the sample to 450 K yields nearly symmetric peaks even when returning the sample to room temperature, meaning even moderately high temperatures can permanently change the crystal lattice.