TY - JOUR
T1 - High-capacity, fast-charging and long-life magnesium/black phosphorous composite negative electrode for non-aqueous magnesium battery
AU - Zhao, Qiannan
AU - Zhao, Kaiqi
AU - Han, Gao Feng
AU - Huang, Ming
AU - Wang, Ronghua
AU - Wang, Zhiqiao
AU - Zhou, Wang
AU - Ma, Yue
AU - Liu, Jilei
AU - Wang, Zhongting
AU - Xu, Chaohe
AU - Huang, Guangsheng
AU - Wang, Jingfeng
AU - Pan, Fusheng
AU - Baek, Jong Beom
N1 - Publisher Copyright:
© The Author(s) 2024.
PY - 2024/12
Y1 - 2024/12
N2 - Secondary non-aqueous magnesium-based batteries are a promising candidate for post-lithium-ion battery technologies. However, the uneven Mg plating behavior at the negative electrode leads to high overpotential and short cycle life. Here, to circumvent these issues, we report the preparation of a magnesium/black phosphorus (Mg@BP) composite and its use as a negative electrode for non-aqueous magnesium-based batteries. Via in situ and ex situ physicochemical measurements, we demonstrate that Mg ions are initially intercalated in black phosphorus two-dimensional structures, forming chemically stable MgxP intermediates. After the formation of the intermediates, Mg electrodeposition reaction became the predominant. When tested in the asymmetric coin cell configuration, the Mg@BP composite electrode allowed stable stripping/plating performances for 1600 h (800 cycles), a cumulative capacity of 3200 mAh cm−2, and a Coulombic efficiency of 99.98%. Assembly and testing of the Mg@BP | |nano-CuS coin cell enabled a discharge capacity of 398 mAh g−1 and an average cell discharge potential of about 1.15 V at a specific current of 560 mA g−1 with a low decay rate of 0.016% per cycle for 225 cycles at 25 °C.
AB - Secondary non-aqueous magnesium-based batteries are a promising candidate for post-lithium-ion battery technologies. However, the uneven Mg plating behavior at the negative electrode leads to high overpotential and short cycle life. Here, to circumvent these issues, we report the preparation of a magnesium/black phosphorus (Mg@BP) composite and its use as a negative electrode for non-aqueous magnesium-based batteries. Via in situ and ex situ physicochemical measurements, we demonstrate that Mg ions are initially intercalated in black phosphorus two-dimensional structures, forming chemically stable MgxP intermediates. After the formation of the intermediates, Mg electrodeposition reaction became the predominant. When tested in the asymmetric coin cell configuration, the Mg@BP composite electrode allowed stable stripping/plating performances for 1600 h (800 cycles), a cumulative capacity of 3200 mAh cm−2, and a Coulombic efficiency of 99.98%. Assembly and testing of the Mg@BP | |nano-CuS coin cell enabled a discharge capacity of 398 mAh g−1 and an average cell discharge potential of about 1.15 V at a specific current of 560 mA g−1 with a low decay rate of 0.016% per cycle for 225 cycles at 25 °C.
UR - http://www.scopus.com/inward/record.url?scp=85205799443&partnerID=8YFLogxK
U2 - 10.1038/s41467-024-52949-4
DO - 10.1038/s41467-024-52949-4
M3 - 文章
C2 - 39375331
AN - SCOPUS:85205799443
SN - 2041-1723
VL - 15
JO - Nature Communications
JF - Nature Communications
IS - 1
M1 - 8680
ER -