TY - JOUR
T1 - Binary Metal Single Atom Electrocatalysts with Synergistic Catalytic Activity toward High-Rate and High Areal-Capacity Lithium–Sulfur Batteries
AU - Ma, Lianbo
AU - Qian, Ji
AU - Li, Yongtao
AU - Cheng, Yuwen
AU - Wang, Shanying
AU - Wang, Ziwei
AU - Peng, Cheng
AU - Wu, Konglin
AU - Xu, Jie
AU - Manke, Ingo
AU - Yang, Chao
AU - Adelhelm, Philipp
AU - Chen, Renjie
N1 - Publisher Copyright:
© 2022 Wiley-VCH GmbH.
PY - 2022/12/16
Y1 - 2022/12/16
N2 - Lithium–sulfur (Li–S) batteries with high theoretical energy density have been long considered as an alternative energy storage device to lithium-ion batteries. Nevertheless, the polysulfide shuttle effects trigger fast capacity decay and short battery lifespan, severely hampering their practical utilizations. Herein, an efficient electrocatalyst comprising of nitrogen (N)-coordinated binary metal single atoms (SAs) implanted within a hierarchical porous carbon skeleton (Fe/Co-N-HPC) is constructed to trap and catalyze polysulfides conversion through a separator coating strategy. It is demonstrated that the introduction of Co atom can enrich the electron number of Fe active center, thereby realizing the distinct synergistic catalytic effect of binary metal SAs and improving the bidirectional catalysis of Li–S redox reaction. As a result, Li–S batteries with the Fe/Co-N-HPC-modified separator exhibit outstanding rate capability (740 mAh g−1 at 5.0 C), and superior long-term cyclic stability (694 mAh g−1 after 600 cycles at 1.0 C). Increasing the sulfur loading to 4.8 mg cm−2, a remarkable areal capacity of 6.13 mAh cm−2 is achieved. Furthermore, in situ X-ray diffraction and theoretical simulation results verify the catalysis mechanism of binary metal SAs by changing the rate-determining steps, providing new directions for constructing high-performance Li–S batteries.
AB - Lithium–sulfur (Li–S) batteries with high theoretical energy density have been long considered as an alternative energy storage device to lithium-ion batteries. Nevertheless, the polysulfide shuttle effects trigger fast capacity decay and short battery lifespan, severely hampering their practical utilizations. Herein, an efficient electrocatalyst comprising of nitrogen (N)-coordinated binary metal single atoms (SAs) implanted within a hierarchical porous carbon skeleton (Fe/Co-N-HPC) is constructed to trap and catalyze polysulfides conversion through a separator coating strategy. It is demonstrated that the introduction of Co atom can enrich the electron number of Fe active center, thereby realizing the distinct synergistic catalytic effect of binary metal SAs and improving the bidirectional catalysis of Li–S redox reaction. As a result, Li–S batteries with the Fe/Co-N-HPC-modified separator exhibit outstanding rate capability (740 mAh g−1 at 5.0 C), and superior long-term cyclic stability (694 mAh g−1 after 600 cycles at 1.0 C). Increasing the sulfur loading to 4.8 mg cm−2, a remarkable areal capacity of 6.13 mAh cm−2 is achieved. Furthermore, in situ X-ray diffraction and theoretical simulation results verify the catalysis mechanism of binary metal SAs by changing the rate-determining steps, providing new directions for constructing high-performance Li–S batteries.
KW - binary metal single atoms
KW - catalytic activities
KW - hierarchical porous carbon skeletons
KW - lithium–sulfur batteries
KW - synergistic effects
UR - https://www.scopus.com/pages/publications/85139422901
U2 - 10.1002/adfm.202208666
DO - 10.1002/adfm.202208666
M3 - Article
AN - SCOPUS:85139422901
SN - 1616-301X
VL - 32
JO - Advanced Functional Materials
JF - Advanced Functional Materials
IS - 51
M1 - 2208666
ER -