Abstract
In this work, we report the simple solid-state formation of mesoporous Co3O4 nano-needles with a 3D single-crystalline framework. The synthesis is based on controlled thermal oxidative decomposition and re-crystallization of precursor β-Co(OH)2 nano-needles. Importantly, after thermal treatment, the needle-like morphology can be completely preserved, despite the fact that there is a large volume contraction accompanying the process: β-Co(OH)2 → Co3O 4. Because of the intrinsic crystal contraction, a highly mesoporous structure with high specific surface area has been simultaneously created. The textual properties can be easily tailored by varying the annealing temperature between 200-400 °C. Interestingly, thermal re-crystallization at higher temperatures leads to the formation of a perfect 3D single-crystalline framework. Thus derived mesoporous Co3O4 nano-needles serve as a good model system for the study of lithium storage properties. The optimized sample manifests very low initial irreversible loss (21%), ultrahigh capacity, and excellent cycling performance. For example, a reversible capacity of 1079 mA h g-1 can be maintained after 50 cycles. The superior electrochemical performance and ease of synthesis may suggest their practical use in lithium-ion batteries. © The Royal Society of Chemistry 2008.
Original language | English (US) |
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Pages (from-to) | 4397 |
Journal | Journal of Materials Chemistry |
Volume | 18 |
Issue number | 37 |
DOIs | |
State | Published - 2008 |
Externally published | Yes |
Bibliographical note
KAUST Repository Item: Exported on 2020-10-01Acknowledgements: The authors are grateful to the National Science Foundation (DMR 0404278) and to the KAUST-Cornell (KAUST-CU) Center for Energy and Sustainability for supporting this study. Facilities available through the Cornell Center for Materials Research (CCMR), and Cornell Integrated Microscopy Center (CIMC) were used for this study.
This publication acknowledges KAUST support, but has no KAUST affiliated authors.