TY - JOUR
T1 - Achieving ultra-long cycling life for MnO2 cathode
T2 - Modulating Mn3+ spin state to suppress Jahn–Teller distortion and manganese dissolution
AU - Zhang, Ziyi
AU - Zheng, Jie
AU - Chen, Xinya
AU - Yu, Xinyu
AU - Li, Lijie
AU - Bao, Lixia
AU - Peng, Jiong
AU - Li, Xin
N1 - Publisher Copyright:
© 2025 Elsevier B.V.
PY - 2025/3
Y1 - 2025/3
N2 - MnO2 is emerging as an electrode material for sodium-ion capacitors due to its high specific capacity and low cost. However, Jahn-teller distortion and manganese dissolution pose a formidable challenge in practical applications. Herein, the Mn3+ spin state, causing J-T distortion, is modulated to address these issues, which is achieved through strategically incorporating Co into the MnO2 lattice to increase electron occupancy in the t2g orbital. The transition from a high-spin Mn3+ to a low-spin state leads to electron movement from the dx2-y2 orbitals to the dxy orbitals, which effectively lowers the energy level of the eg orbitals, reduces orbital degeneracy, and enhances the stability of the Mn-O bond. DFT calculations, In situ Raman and inductively coupled plasma optical emission spectroscopy (ICP-OES) demonstrate that the distortion of [MnO6] and Mn dissolution of Co-MnO2 are reduced by 69 % and 80 % respectively compared with MnO2 during the charge-discharge cycle. Consequently, Co-MnO2 exhibits approximately 98 % capacity retention after 40,000 cycles at 10 A/g, achieving exceptional long-term stability. This study provides new insights into the relationships among J-T distortion, manganese dissolution and spin state, provides a novel approach to enhance the stability of MnO2 for electrochemistry applications.
AB - MnO2 is emerging as an electrode material for sodium-ion capacitors due to its high specific capacity and low cost. However, Jahn-teller distortion and manganese dissolution pose a formidable challenge in practical applications. Herein, the Mn3+ spin state, causing J-T distortion, is modulated to address these issues, which is achieved through strategically incorporating Co into the MnO2 lattice to increase electron occupancy in the t2g orbital. The transition from a high-spin Mn3+ to a low-spin state leads to electron movement from the dx2-y2 orbitals to the dxy orbitals, which effectively lowers the energy level of the eg orbitals, reduces orbital degeneracy, and enhances the stability of the Mn-O bond. DFT calculations, In situ Raman and inductively coupled plasma optical emission spectroscopy (ICP-OES) demonstrate that the distortion of [MnO6] and Mn dissolution of Co-MnO2 are reduced by 69 % and 80 % respectively compared with MnO2 during the charge-discharge cycle. Consequently, Co-MnO2 exhibits approximately 98 % capacity retention after 40,000 cycles at 10 A/g, achieving exceptional long-term stability. This study provides new insights into the relationships among J-T distortion, manganese dissolution and spin state, provides a novel approach to enhance the stability of MnO2 for electrochemistry applications.
KW - Jahn-Teller distortion
KW - Manganese dissolution
KW - Mn3+ spin state
KW - Modulate
UR - http://www.scopus.com/inward/record.url?scp=85218421940&partnerID=8YFLogxK
U2 - 10.1016/j.ensm.2025.104128
DO - 10.1016/j.ensm.2025.104128
M3 - Article
AN - SCOPUS:85218421940
SN - 2405-8297
VL - 76
JO - Energy Storage Materials
JF - Energy Storage Materials
M1 - 104128
ER -