The role of M@Ni6 superstructure units in honeycomb-ordered layered oxides for Li/Na ion batteries. (May 2021)

• Record Type: Journal Article
• Authors: Hu, Zongxiang; Weng, Mouyi; Chen, Zhefeng; Tan, Wenchang; Li, Shunning; Pan, Feng
• Is Part Of: Nano energy. Volume 83(2021)
• Publication Date: 2021-05
• Subjects: Li/Na ion batteries -- Honeycomb-ordered -- Electronic structure -- Superstructure unit; Nanoscience -- Periodicals; Nanotechnology -- Periodicals; Nanostructured materials -- Periodicals; Power resources -- Technological innovations -- Periodicals; Nanoscience; Nanostructured materials; Nanotechnology; Power resources -- Technological innovations; Periodicals; 621.042
• DOI: 10.1016/j.nanoen.2021.105834
• Languages: English
• ISSNs: 2211-2855

Abstract

Abstract: Honeycomb-ordered layered transition metal (TM) oxides, which are characteristic of a honeycomb network, have recently emerged as a novel class of cathode materials with high voltage and superior long-term cycling stability. Here, we provide a systematic first-principles study of the structural and electrochemical properties of honeycomb-ordered ANi2/3 M1/3 O2 (A = Li and Na; M = As, Sb and Bi) aimed at disentangling the role of the M 5+ species. Our results show that M endorses strong bonding with O and can give rise to superior thermodynamic stability of the compound as compared to ANiO2 counterparts. Upon alkali deintercalation of ANi2/3 M1/3 O2, there is a driving force for disproportionation of Ni 3+ ions, which originates from the high-symmetric MO6 octahedron and leads to the activation of both Ni 2+ /Ni 3+ and Ni 3+ /Ni 4+ redox couples. The distortion of NiO6 octahedron can be modulated by the size of M, and a clear correlation is revealed between the distortion from octahedral symmetry and the electronic structures of the compounds, including the energy position of e g orbitals and the temporary stabilization of Ni 3+ ions. Both properties are linked to the voltage and polarization of the cathodes. This work provides a basis for further development of cathode materials based on honeycomb-ordered superstructure. Graphical Abstract: We have systematically investigated the structural and electrochemical properties of honeycomb-ordered ANi2/3 M1/3 O2 (A = Li and Na; M = As, Sb and Bi) with M@Ni6 superstructure units using first principles calculations. We show that the thermodynamic stability of the compounds and the propensity for disproportionation of Ni 3+ ions upon alkali deintercalation are significantly related to the M 5+ species. The size of M determines the degree of distortion of NiO6 octahedron and influences both the energy position of e g orbitals and the temporary stabilization of Ni 3+ ions, which are linked to the voltage and polarization of the cathodes. ga1 Highlights: Pentavalent main-group elements contribute to the high thermodynamic stability of honeycomb-ordered layered oxides. Disproportionation of Ni 3+ ions leads to the activation of both Ni 2+ /Ni 3+ and Ni 3+ /Ni 4+ redox couples. The size of main group elements influences the voltage and polarization of the cathodes by distorting NiO6 octahedron.