Facile synthesis of hierarchical porous Co3O4 nanoboxes as efficient cathode catalysts for Li-O2 batteriesElectronic supplementary information (ESI) available. See DOI: 10.1039/c6ta01995a

Rechargeable Li-O 2 batteries with remarkably high theoretical energy densities have attracted extensive attention. However, to enable Li-O 2 batteries for practical applications, numerous challenges need to be overcome, e.g. high overpotential, low rate capability, and poor cycling stability. The k...

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Main Authors Zhang, Jian, Lyu, Zhiyang, Zhang, Feng, Wang, Liangjun, Xiao, Peng, Yuan, Kaidi, Lai, Min, Chen, Wei
Format Journal Article
Published 26.04.2016
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Abstract Rechargeable Li-O 2 batteries with remarkably high theoretical energy densities have attracted extensive attention. However, to enable Li-O 2 batteries for practical applications, numerous challenges need to be overcome, e.g. high overpotential, low rate capability, and poor cycling stability. The key factor to tackle these issues is to develop highly-efficient cathode catalysts. Moreover, cathode catalysts with a porous structure and large surface area are favorable in Li-O 2 batteries. In this paper, hierarchical porous Co 3 O 4 nanoboxes with well-defined interior voids, functional shells and a large surface area have been facilely synthesized via an ion exchange reaction between Prussian blue analogue nanocubic precursors and OH − at a low temperature (60 °C). The obtained products possess hierarchical pore sizes and an extremely large surface area (272.5 m 2 g −1 ), which provide more catalytically active sites to promote the oxygen reduction reaction (ORR) and oxygen evolution reaction (OER) as a Li-O 2 battery cathode, as well as facilitating the diffusion of oxygen and the electrolyte. The hierarchical porous Co 3 O 4 nanobox cathode shows enhanced discharge capacity, reduced overpotential, improved rate performance and cycle stability, in comparison with the EC-300J carbon cathode. The superb performance of the hierarchical porous Co 3 O 4 nanoboxes, together with the facile fabrication approach, presents an alternative method to develop advanced cathode catalysts for Li-O 2 batteries. A hierarchical porous Co 3 O 4 nanobox catalyst with an extremely large surface area is developed via an ion-exchange process and used as efficient cathode catalyst for Li-O 2 batteries.
AbstractList Rechargeable Li-O 2 batteries with remarkably high theoretical energy densities have attracted extensive attention. However, to enable Li-O 2 batteries for practical applications, numerous challenges need to be overcome, e.g. high overpotential, low rate capability, and poor cycling stability. The key factor to tackle these issues is to develop highly-efficient cathode catalysts. Moreover, cathode catalysts with a porous structure and large surface area are favorable in Li-O 2 batteries. In this paper, hierarchical porous Co 3 O 4 nanoboxes with well-defined interior voids, functional shells and a large surface area have been facilely synthesized via an ion exchange reaction between Prussian blue analogue nanocubic precursors and OH − at a low temperature (60 °C). The obtained products possess hierarchical pore sizes and an extremely large surface area (272.5 m 2 g −1 ), which provide more catalytically active sites to promote the oxygen reduction reaction (ORR) and oxygen evolution reaction (OER) as a Li-O 2 battery cathode, as well as facilitating the diffusion of oxygen and the electrolyte. The hierarchical porous Co 3 O 4 nanobox cathode shows enhanced discharge capacity, reduced overpotential, improved rate performance and cycle stability, in comparison with the EC-300J carbon cathode. The superb performance of the hierarchical porous Co 3 O 4 nanoboxes, together with the facile fabrication approach, presents an alternative method to develop advanced cathode catalysts for Li-O 2 batteries. A hierarchical porous Co 3 O 4 nanobox catalyst with an extremely large surface area is developed via an ion-exchange process and used as efficient cathode catalyst for Li-O 2 batteries.
Author Chen, Wei
Lai, Min
Zhang, Jian
Xiao, Peng
Yuan, Kaidi
Lyu, Zhiyang
Wang, Liangjun
Zhang, Feng
AuthorAffiliation Department of Chemistry
National University of Singapore
National University of Singapore (Suzhou) Research Institute
School of Physics and Optoelectronic Engineering
Nanjing University
Nanjing University of Information Science & Technology
School of Chemistry and Chemical Engineering
Department of Physics
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