Abstract
The induction of cation dopant into the lattice structure of anode materials is a feasible and effective method to modulate the electronic structure and induce different active sites for Li+ storage. However, it is a challenge to create the cation dopant into the structure of the transition metal oxides anode of the lithium-ion batteries (LIBs). In this work, we propose an in-situ source template thermal reduction of graphite foam (GF) and annealing process for the first time to successfully induce Ti3+ into the titanium niobium oxide (Ti2Nb10O29, TNO) nanocrystal structure denoted as TNO@GF for high-energy/power lithium storage. The induction of Ti3+ could not only prompt the more active sites for Li+ ion storage but also modulate the electronic interaction between the active sites and the intercalated Li+ ion, leading to the favorable Li+ ions intercalation and minimizing the Li+-ion diffusion barriers in the open channel of the ReO3-type structure unit. Due to the combined effect of nanocrystal structure and Ti3+, TNO@GF yields a higher reversible discharge capacity of 328 mAh g−1 at 0.1C, a higher rate capability of 296.3 mAh g−1; and keeps 207.88 mAh g−1 at a high rate of 35 C and shows good cycling stability (217.73 mAh g−1 at the rate of 10 C) with the capacity retention of 83.20 % after 500 cycles. These findings provide insights into cation engineering and its influence on the functional nanomaterials' physicochemical properties, which are not achievable in the perfect crystal for advanced energy storage applications.
| Original language | English |
|---|---|
| Pages (from-to) | 1015-1026 |
| Number of pages | 12 |
| Journal | Journal of Colloid and Interface Science |
| Volume | 623 |
| DOIs | |
| Publication status | Published - Oct 2022 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 7 Affordable and Clean Energy
Keywords
- Carbon-based footprint strategy
- In-situ thermal reduction process
- Lithium-ion batteries
- Nanocrystal
- Ti dopant
- TiNbO
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