TY - JOUR
T1 - High-performance Na ion cathodes based on the ubiquitous and reversible O redox reaction
AU - Assadi, M. Hussein N.
AU - Fronzi, Marco
AU - Ford, Mike
AU - Shigeta, Yasuteru
N1 - Funding Information:
This work was supported in part by MEXT as a social and scientic priority issue: the creation of new functional devices and high-performance materials to support next-generation industries, to be tackled by using a post-K computer. Computational resources were provided by Kyushu University’s high performance computing center and the supercomputers at the Institute for Solid State Physics at the University of Tokyo and the Center for Computational Sciences at the University of Tsukuba.
Publisher Copyright:
© 2018 The Royal Society of Chemistry.
PY - 2018
Y1 - 2018
N2 - Utilising reversible oxygen redox in Na and transition metal oxides offers unprecedented opportunities for the design of high voltage, high capacity and affordable cathodes for application in rechargeable Na-ion batteries. Through a judicious materials search and theoretical investigations, we identified new compounds with excellent energy storage properties that rely on oxygen states for charge compensation during the redox reaction. According to our predictions, Na2-xMoO4 demonstrates a voltage of 4.743 V and an energy density of ∼617.3 W h kg-1. These values exceed the performance of most commercialised Na-ion cathode materials. Furthermore, both Na4-xZr5O12, demonstrating a voltage of 3.583 V, and Na1-xPd2PO3, demonstrating a voltage of 2.630 V, exhibit a meagre absolute volume change of ∼1% during the sodiation/desodiation process. Because of this minor volume change, these compounds are suitable for all-solid-state battery applications. An examination of the electronic structures of these compounds reveals that O states are always present at the top of the valence band regardless of the presence of 4d transition metal species or their oxidation states. This feature is attributed to the exceedingly substantial 4d-2p hybridisation over the entire valence band which also prevents the bonding of oxidised O ions in the desodiated compounds, thus preventing irreversible oxygen loss.
AB - Utilising reversible oxygen redox in Na and transition metal oxides offers unprecedented opportunities for the design of high voltage, high capacity and affordable cathodes for application in rechargeable Na-ion batteries. Through a judicious materials search and theoretical investigations, we identified new compounds with excellent energy storage properties that rely on oxygen states for charge compensation during the redox reaction. According to our predictions, Na2-xMoO4 demonstrates a voltage of 4.743 V and an energy density of ∼617.3 W h kg-1. These values exceed the performance of most commercialised Na-ion cathode materials. Furthermore, both Na4-xZr5O12, demonstrating a voltage of 3.583 V, and Na1-xPd2PO3, demonstrating a voltage of 2.630 V, exhibit a meagre absolute volume change of ∼1% during the sodiation/desodiation process. Because of this minor volume change, these compounds are suitable for all-solid-state battery applications. An examination of the electronic structures of these compounds reveals that O states are always present at the top of the valence band regardless of the presence of 4d transition metal species or their oxidation states. This feature is attributed to the exceedingly substantial 4d-2p hybridisation over the entire valence band which also prevents the bonding of oxidised O ions in the desodiated compounds, thus preventing irreversible oxygen loss.
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U2 - 10.1039/c8ta05961f
DO - 10.1039/c8ta05961f
M3 - Article
AN - SCOPUS:85058155489
SN - 2050-7488
VL - 6
SP - 24120
EP - 24127
JO - Journal of Materials Chemistry A
JF - Journal of Materials Chemistry A
IS - 47
ER -