期刊
INORGANIC CHEMISTRY FRONTIERS
卷 6, 期 3, 页码 715-722出版社
ROYAL SOC CHEMISTRY
DOI: 10.1039/c8qi01279b
关键词
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资金
- Nature Science Foundation of China [51572075]
- Open Foundation of the State Key Laboratory of Silicate Materials for Architectures at WUT [SYSJJ2018-05]
- Analytic Testing Center of HUST
The thermolysis of metal-organic frameworks (MOFs) opens a new window for the fabrication of oxide semiconductors due to its simplicity, low cost and large-area uniformity of the resulting material. However, this approach usually requires high annealing temperatures over 350 degrees C. In this work, sub-micro hierarchical porous Co3O4 dodecahedra were synthesized by the thermolysis of zeolitic imidazolate frameworks 67 (ZIF-67) at a low temperature of 268 degrees C assisted by ammonium perchlorate (AP), in which ZIF-67 was employed as a metal source and a sacrificial template. The formation mechanism was probably attributable to the generation of Co-O bonds between the Co atom of ZIF-67 and the O atom of AP at lower temperatures which can accelerate the weakening of Co-N bonds of ZIF-67 and thus lead to an abrupt decomposition of ZIF-67 at 268 degrees C. More importantly, the generation of the Co-O bond and the weakening of the Co-N bond were identified using the FTIR, Raman and XPS results. As confirmed by DFT results, ZIF-67 can be decomposed into Co3O4 at lower temperatures assisted by AP than that in air. In addition, the obtained sub-micro hierarchical porous Co3O4 dodecahedra showed a very large specific surface area of 106.11 m(2) g(-1), much larger than that in previous reports. Therefore, this work can provide a novel atomic insight into the formation mechanism of Co3O4 hierarchical porous structures derived from ZIF-67 with AP at lower temperatures and also an energy-efficient method to synthesize porous metal oxide structures.
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