TY - JOUR
T1 - Structural Insight into Layer Gliding and Lattice Distortion in Layered Manganese Oxide Electrodes for Potassium-Ion Batteries
AU - Zhang, Qing
AU - Didier, Christophe
AU - Pang, Wei Kong
AU - Liu, Yajie
AU - Wang, Zhijie
AU - Li, Sean
AU - Peterson, Vanessa K.
AU - Mao, Jianfeng
AU - Guo, Zaiping
PY - 2019/8/14
Y1 - 2019/8/14
N2 - Potassium-ion batteries (PIBs) are an emerging, affordable, and environmentally friendly alternative to lithium-ion batteries, with their further development driven by the need for suitably performing electrode materials capable of reversibly accommodating the relatively large K+. Layer-structured manganese oxides are attractive as electrodes for PIBs, but suffer from structural instability and sluggish kinetics of K+ insertion/extraction, leading to poor rate capability. Herein, cobalt is successfully introduced at the manganese site in the KxMnO2 layered oxide electrode material and it is shown that with only 5% Co, the reversible capacity increases by 30% at 22 mA g-1 and by 92% at 440 mA g-1. In operando synchrotron X-ray diffraction reveals that Co suppresses Jahn–Teller distortion, leading to more isotropic migration pathways for K+ in the interlayer, thus enhancing the ionic diffusion and consequently, rate capability. The detailed analysis reveals that additional phase transitions and larger volume change occur in the Co-doped material as a result of layer gliding, with these associated with faster capacity decay, despite the overall capacity remaining higher than the pristine material, even after 500 cycles. These results assert the importance of understanding the detailed structural evolution that underpins performance that will inform the strategic design of electrode materials for high-performance PIBs. © 2019 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
AB - Potassium-ion batteries (PIBs) are an emerging, affordable, and environmentally friendly alternative to lithium-ion batteries, with their further development driven by the need for suitably performing electrode materials capable of reversibly accommodating the relatively large K+. Layer-structured manganese oxides are attractive as electrodes for PIBs, but suffer from structural instability and sluggish kinetics of K+ insertion/extraction, leading to poor rate capability. Herein, cobalt is successfully introduced at the manganese site in the KxMnO2 layered oxide electrode material and it is shown that with only 5% Co, the reversible capacity increases by 30% at 22 mA g-1 and by 92% at 440 mA g-1. In operando synchrotron X-ray diffraction reveals that Co suppresses Jahn–Teller distortion, leading to more isotropic migration pathways for K+ in the interlayer, thus enhancing the ionic diffusion and consequently, rate capability. The detailed analysis reveals that additional phase transitions and larger volume change occur in the Co-doped material as a result of layer gliding, with these associated with faster capacity decay, despite the overall capacity remaining higher than the pristine material, even after 500 cycles. These results assert the importance of understanding the detailed structural evolution that underpins performance that will inform the strategic design of electrode materials for high-performance PIBs. © 2019 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
KW - cobalt doping
KW - cooperative Jahn–Teller distortions
KW - potassium-ion batteries
KW - rate capability
UR - http://www.scopus.com/inward/record.url?scp=85068193072&partnerID=8YFLogxK
UR - https://www.scopus.com/record/pubmetrics.uri?eid=2-s2.0-85068193072&origin=recordpage
U2 - 10.1002/aenm.201900568
DO - 10.1002/aenm.201900568
M3 - RGC 21 - Publication in refereed journal
SN - 1614-6832
VL - 9
JO - Advanced Energy Materials
JF - Advanced Energy Materials
IS - 30
M1 - 1900568
ER -