Issue 4, 2013

Rapid room-temperature synthesis of nanosheet-assembled ZnO mesocrystals with excellent photocatalytic activity

Abstract

We have investigated the growth of ZnO in a simple alkaline solution by chemical precipitation. ZnO nano(micro)structures with well-defined morphologies have been realized by tuning the Zn2+ : OH ratio and the amount of the complexing agent NH4F. Importantly, we have demonstrated a fast spontaneous room-temperature formation of ZnO mesocrystals constructed with nanosheet subunits. The growth of ZnO involves the phase transformation from two intermediate compounds ZnF(OH) and Zn(OH)2. The nanosheets are observed to be ZnO (10[1 with combining macron]0) facets from the side- and top-view high-resolution TEM measurements. By comparing the arrangement of the (10[1 with combining macron]0) nanosheets in the mesocrystal with the organization of the {10[1 with combining macron]0} planes in the wurtzite crystal structure of ZnO, we identify for the first time the assembly of 2D nanosheets into 3D architectures by epitaxy. This unique self-assembly by epitaxy effectively separates the nanosheets in an ordered manner, producing a robust, geometrically ideal photocatalyst that is easily separable and recyclable. Being constructed of reactive (10[1 with combining macron]0) facets, the microstructured ZnO exhibits much higher photocatalytic efficiency than its nanoparticle counterpart. The defective nature of the (10[1 with combining macron]0) facets confirmed by the photoluminescence study explains the visible photocatalysis of the nanosheet assemblies.

Graphical abstract: Rapid room-temperature synthesis of nanosheet-assembled ZnO mesocrystals with excellent photocatalytic activity

Supplementary files

Article information

Article type
Paper
Submitted
11 Oct 2012
Accepted
07 Nov 2012
First published
29 Nov 2012

CrystEngComm, 2013,15, 754-763

Rapid room-temperature synthesis of nanosheet-assembled ZnO mesocrystals with excellent photocatalytic activity

M. Wang, Y. Zhang, Y. Zhou, F. Yang, E. J. Kim, S. H. Hahn and S. G. Seong, CrystEngComm, 2013, 15, 754 DOI: 10.1039/C2CE26660A

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