期刊
ADVANCED FUNCTIONAL MATERIALS
卷 28, 期 3, 页码 -出版社
WILEY-V C H VERLAG GMBH
DOI: 10.1002/adfm.201703266
关键词
aqueous Na-ion storage; biphase cobalt-manganese oxide; capacitive and diffusion-limited redox capacities; in situ X-ray diffraction; pair distribution function
类别
资金
- US Department of Energy (DOE), Office of Science, Basic Energy Sciences [DE-SC0010286]
- DOE Office of Science [DE-AC02-06CH11357]
- Scientific User Facilities Division, Office of Basic Energy Sciences, U.S. Department of Energy [DE-AC05-00OR22725]
- Oak Ridge National Laboratory
- U.S. Department of Energy, Office of Basic Energy Sciences [DE-SC-00112704]
Manganese-based metal oxide electrode materials are of great importance in electrochemical energy storage for their favorable redox behavior, low cost, and environmental friendliness. However, their storage capacity and cycle life in aqueous Na-ion electrolytes is not satisfactory. Herein, the development of a biphase cobalt-manganese oxide (Co-Mn-O) nanostructured electrode material is reported, comprised of a layered MnO2 center dot H2O birnessite phase and a (Co(0.83)Mn(0.13)Va(0.04))(tetra)(Co0.38Mn1.62)(octa)O-3.72 (Va: vacancy; tetra: tetrahedral sites; octa: octahedral sites) spinel phase, verified by neutron total scattering and pair distribution function analyses. The biphase Co-Mn-O material demonstrates an excellent storage capacity toward Na-ions in an aqueous electrolyte (121 mA h g(-1) at a scan rate of 1 mV s(-1) in the half-cell and 81 mA h g(-1) at a current density of 2 A g(-1) after 5000 cycles in full-cells), as well as high rate performance (57 mA h g(-1) a rate of 360 C). Electrokinetic analysis and in situ X-ray diffraction measurements further confirm that the synergistic interaction between the spinel and layered phases, as well as the vacancy of the tetrahedral sites of spinel phase, contribute to the improved capacity and rate performance of the Co-Mn-O material by facilitating both diffusion-limited redox and capacitive charge storage processes.
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