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Novel K2Ti8O17 Anode via Na+/Al3+ Co-Intercalation Mechanism for Rechargeable Aqueous Al-Ion Battery with Superior Rate Capability

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A promising aqueous aluminum ion battery (AIB) was assembled using a novel layered K2Ti8O17 anode against an activated carbon coated on a Ti mesh cathode in an AlCl3-based aqueous electrolyte. The intercalation/deintercalation mechanism endowed the layered K2Ti8O17 as a promising anode for rechargeable aqueous AIBs. NaAc was introduced into the AlCl3 aqueous electrolyte to enhance the cycling stability of the assembled aqueous AIB. The as-designed AIB displayed a high discharge voltage near 1.6 V, and a discharge capacity of up to 189.6 mAh g−1. The assembled AIB lit up a commercial light-emitting diode (LED) lasting more than one hour. Inductively coupled plasma–optical emission spectroscopy (ICP-OES), high-resolution transmission electron microscopy (HRTEM), and X-ray absorption near-edge spectroscopy (XANES) were employed to investigate the intercalation/deintercalation mechanism of Na+/Al3+ ions in the aqueous AIB. The results indicated that the layered structure facilitated the intercalation/deintercalation of Na+/Al3+ ions, thus providing a high-rate performance of the K2Ti8O17 anode. The diffusion-controlled electrochemical characteristics and the reduction of Ti4+ species during the discharge process illustrated the intercalation/deintercalation mechanism of the K2Ti8O17 anode. This study provides not only insight into the charge–discharge mechanism of the K2Ti8O17 anode but also a novel strategy to design rechargeable aqueous AIBs.
Title: Novel K2Ti8O17 Anode via Na+/Al3+ Co-Intercalation Mechanism for Rechargeable Aqueous Al-Ion Battery with Superior Rate Capability
Description:
A promising aqueous aluminum ion battery (AIB) was assembled using a novel layered K2Ti8O17 anode against an activated carbon coated on a Ti mesh cathode in an AlCl3-based aqueous electrolyte.
The intercalation/deintercalation mechanism endowed the layered K2Ti8O17 as a promising anode for rechargeable aqueous AIBs.
NaAc was introduced into the AlCl3 aqueous electrolyte to enhance the cycling stability of the assembled aqueous AIB.
The as-designed AIB displayed a high discharge voltage near 1.
6 V, and a discharge capacity of up to 189.
6 mAh g−1.
The assembled AIB lit up a commercial light-emitting diode (LED) lasting more than one hour.
Inductively coupled plasma–optical emission spectroscopy (ICP-OES), high-resolution transmission electron microscopy (HRTEM), and X-ray absorption near-edge spectroscopy (XANES) were employed to investigate the intercalation/deintercalation mechanism of Na+/Al3+ ions in the aqueous AIB.
The results indicated that the layered structure facilitated the intercalation/deintercalation of Na+/Al3+ ions, thus providing a high-rate performance of the K2Ti8O17 anode.
The diffusion-controlled electrochemical characteristics and the reduction of Ti4+ species during the discharge process illustrated the intercalation/deintercalation mechanism of the K2Ti8O17 anode.
This study provides not only insight into the charge–discharge mechanism of the K2Ti8O17 anode but also a novel strategy to design rechargeable aqueous AIBs.

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