Abstract
In this work, rhombohedral KTi2(PO4)3 is introduced to investigate the related theoretical, structural, and electrochemical properties in K cells. The suggested KTi2(PO4)3 modified by electro-conducting carbon brings about a flat voltage profile at ≈1.6 V, providing a large capacity of 126 mAh (g-phosphate)−1, corresponding to 98.5% of the theoretical capacity, with 89% capacity retention for 500 cycles. Structural analyses using electrochemical performance measurements, first-principles calculations, ex situ X-ray absorption spectroscopy, and operando X-ray diffraction provide new insights into the reaction mechanism controlling the (de)intercalation of potassium ions into the host KTi2(PO4)3 structure. It is observed that a biphasic redox process by Ti4+/3+ occurs upon discharge, whereas a single-phase reaction followed by a biphasic process occurs upon charge. Along with the structural refinement of the electrochemically reduced K3Ti2(PO4)3 phase, these new findings provide insight into the reaction mechanism in Na superionic conductor (NASICON)-type KTi2(PO4)3. The present approach can also be extended to the investigation of other NASICON-type materials for potassium-ion batteries.
| Original language | English |
|---|---|
| Article number | 2001090 |
| Journal | Small |
| Volume | 16 |
| Issue number | 20 |
| DOIs | |
| State | Published - 1 May 2020 |
| Externally published | Yes |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 7 Affordable and Clean Energy
Keywords
- first-principles calculations
- insertion
- KTi(PO)
- potassium-ion batteries
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