Nature of the "Z"-phase in layered Na-ion battery cathodes. Issue 7 (17th May 2019)

• Record Type: Journal Article
• Authors: Somerville, James W.; Sobkowiak, Adam; Tapia-Ruiz, Nuria; Billaud, Juliette; Lozano, Juan G.; House, Robert A.; Gallington, Leighanne C.; Ericsson, Tore; Häggström, Lennart; Roberts, Matthew R.; Maitra, Urmimala; Bruce, Peter G.
• Is Part Of: Energy & environmental science. Volume 12:Issue 7(2019)
• Page Start: 2223
• Page End: 2232
• Publication Date: 2019-05-17
• Subjects: Energy conversion -- Periodicals; Fuel switching -- Periodicals; Environmental sciences -- Periodicals; Environmental chemistry -- Periodicals; 333.79
• DOI: 10.1039/c8ee02991a
• Languages: English
• ISSNs: 1754-5692

Abstract

Abstract : In this article, the nature of the "Z"-phase, which forms on charging many P2-type compounds to high voltages, is probed. Abstract : Layered sodium transition metal oxides with the P2 structure, e.g. Na2/3 [Ni1/3 Mn2/3 ]O2, are regarded as candidates for Na-ion battery cathodes. On charging, extraction of Na destabilizes the P2 phase (ABBA oxide ion stacking) in which Na + is in trigonal prismatic coordination, resulting in layer gliding and formation of an O2 phase (ABAC stacking) with octahedral coordination. However, many related compounds do not exhibit such a simple P2 to O2 transition but rather form a so called "Z"-phase. Substituting Ni by Fe in Na2/3 [Ni1/3 Mn2/3 ]O2 is attractive as it reduces cost. The Fe containing compounds, such as Na2/3 [Ni1/6 Mn1/2 Fe1/3 ]O2, form a "Z"-phase when charged above 4.1 V vs. Na + /Na. By combining ex situ and operando X-ray diffraction with scanning transmission electron microscopy and simulated diffraction patterns, we demonstrate that the "Z"-phase is most accurately described as a continuously changing intergrowth structure which evolves from P2 to O2 through the OP4 structure as an intermediate. On charging, Na + removal results in O-type stacking faults within the P2 structure which increase in proportion. At 50% O-type stacking faults, the ordered OP4 phase forms and on further charging more O-type stacking faults are formed progressing towards a pure O2 structure. This gives the superficial appearance of a solid solution. Furthermore, in contrast to some previous studies, we did not detect Fe migration at any state-of-charge using 57 Fe-Mössbauer spectroscopy. It was, however, found that the Fe-substitution serves to disrupt cation ordering in the material.