TY - JOUR
T1 - Solvation geometry engineering for stable high-voltage potassium-ion batteries
AU - Zhang, Zhe
AU - Qi, Wenli
AU - Zhang, Shiwan
AU - Zhu, Jiacheng
AU - Wang, Linlin
AU - Bai, Yue
AU - Chen, Jiale
AU - Chen, Yifan
AU - Hou, Guangqiang
AU - Niu, Xiaogang
AU - Wang, Xuefeng
AU - Chen, Jitao
AU - Ji, Xiao
AU - Zhu, Yujie
N1 - Publisher Copyright:
This journal is © The Royal Society of Chemistry, 2026
PY - 2026/2/24
Y1 - 2026/2/24
N2 - To advance the practical application of potassium-ion batteries (PIBs), the lack of robust electrolytes must be addressed, as the prevailing fluorinated solvents present a cost-prohibitive and environmentally unsustainable solution. Here, we propose an asymmetric alkylation strategy to overcome this limitation, engineering a fluorine-free, high-flash-point, and green ether-based electrolyte. This design reconstitutes the solvent coordination geometry through dual steric hindrance, which concurrently weakens cation–solvent binding and modulates the electronic structure of the solvation cluster. Consequently, the designed electrolyte demonstrates exceptional interfacial compatibility, enabling the high-voltage K2Mn[Fe(CN)6]‖graphite and K2Mn[Fe(CN)6]‖hard carbon full-cells to achieve capacity retention rates of 75.75% after 1400 cycles at 0.33C and 80.09% after 1500 cycles at 0.5C, respectively. Moreover, this stability is preserved at elevated temperatures, with both full-cells exhibiting stable operation over hundreds of cycles. This work establishes an effective electrolyte design strategy for realizing high-performance, cost-effective, and environmentally friendly PIBs.
AB - To advance the practical application of potassium-ion batteries (PIBs), the lack of robust electrolytes must be addressed, as the prevailing fluorinated solvents present a cost-prohibitive and environmentally unsustainable solution. Here, we propose an asymmetric alkylation strategy to overcome this limitation, engineering a fluorine-free, high-flash-point, and green ether-based electrolyte. This design reconstitutes the solvent coordination geometry through dual steric hindrance, which concurrently weakens cation–solvent binding and modulates the electronic structure of the solvation cluster. Consequently, the designed electrolyte demonstrates exceptional interfacial compatibility, enabling the high-voltage K2Mn[Fe(CN)6]‖graphite and K2Mn[Fe(CN)6]‖hard carbon full-cells to achieve capacity retention rates of 75.75% after 1400 cycles at 0.33C and 80.09% after 1500 cycles at 0.5C, respectively. Moreover, this stability is preserved at elevated temperatures, with both full-cells exhibiting stable operation over hundreds of cycles. This work establishes an effective electrolyte design strategy for realizing high-performance, cost-effective, and environmentally friendly PIBs.
UR - https://www.scopus.com/pages/publications/105029459852
U2 - 10.1039/d5ee07550e
DO - 10.1039/d5ee07550e
M3 - Article
AN - SCOPUS:105029459852
SN - 1754-5692
VL - 19
SP - 1374
EP - 1384
JO - Energy and Environmental Science
JF - Energy and Environmental Science
IS - 4
ER -