TY - JOUR
T1 - Oxygen-Deficient P2-Na0.7Mn0.75Ni0.25O2- xCathode by a Reductive NH4HF2Treatment for Highly Reversible Na-Ion Storage
AU - Amedzo-Adore, Mawuse
AU - Yang, Junghoon
AU - Han, Dongwook
AU - Chen, Mingzhe
AU - Agyeman, Daniel Adjei
AU - Zhang, Jiliang
AU - Zhao, Ruirui
AU - Kang, Yong Mook
N1 - Publisher Copyright:
©
PY - 2021/8/23
Y1 - 2021/8/23
N2 - Oxygen-deficient P2-Na0.7Mn0.75Ni0.25O2-x (OD-NMNO) for sodium-ion batteries is prepared by a modified high-temperature solid-state reaction using NH4HF2 to induce oxygen vacancies inside. OD-NMNO has a reduced lattice parameter along the c-axis and thereby a reduced unit cell volume compared with that of pristine P2-Na0.7Mn0.75Ni0.25O2 (P-NMNO) owing to the presence of oxygen vacancies (leading to the highly ionic character of Mn, as well as shorter transition metal-oxygen (TM-O) bonds) in the layered crystal structure of P-NMNO. The resultant OD-NMNO demonstrates a higher initial discharge capacity (>150 mA h g-1 at 10 mA g-1), superior rate capability, and improved cycling performance (69.4% after 100 cycles at 50 mA g-1) in comparison with P-NMNO because of the optimum oxygen vacancies in its whole lattice. These oxygen vacancies reinforce the TM-O bonds in OD-NMNO, preventing irreversible phase transitions during cycling, as well as facilitating Na+-ion diffusion from the surface to the bulk. These results break up the conventional preconception that defects generally deteriorate the layered structure of sodium transition metal oxides due to the induced structural instability.
AB - Oxygen-deficient P2-Na0.7Mn0.75Ni0.25O2-x (OD-NMNO) for sodium-ion batteries is prepared by a modified high-temperature solid-state reaction using NH4HF2 to induce oxygen vacancies inside. OD-NMNO has a reduced lattice parameter along the c-axis and thereby a reduced unit cell volume compared with that of pristine P2-Na0.7Mn0.75Ni0.25O2 (P-NMNO) owing to the presence of oxygen vacancies (leading to the highly ionic character of Mn, as well as shorter transition metal-oxygen (TM-O) bonds) in the layered crystal structure of P-NMNO. The resultant OD-NMNO demonstrates a higher initial discharge capacity (>150 mA h g-1 at 10 mA g-1), superior rate capability, and improved cycling performance (69.4% after 100 cycles at 50 mA g-1) in comparison with P-NMNO because of the optimum oxygen vacancies in its whole lattice. These oxygen vacancies reinforce the TM-O bonds in OD-NMNO, preventing irreversible phase transitions during cycling, as well as facilitating Na+-ion diffusion from the surface to the bulk. These results break up the conventional preconception that defects generally deteriorate the layered structure of sodium transition metal oxides due to the induced structural instability.
KW - bond length
KW - electrochemical performance
KW - oxygen vacancy
KW - sodium-ion batteries
KW - transition metal oxide
UR - http://www.scopus.com/inward/record.url?scp=85112583070&partnerID=8YFLogxK
U2 - 10.1021/acsaem.1c01334
DO - 10.1021/acsaem.1c01334
M3 - Article
AN - SCOPUS:85112583070
SN - 2574-0962
VL - 4
SP - 8036
EP - 8044
JO - ACS Applied Energy Materials
JF - ACS Applied Energy Materials
IS - 8
ER -