| Citation: |
Hai Yang, Fuxiang He, Jialong Shen, Zhihao Chen, Yu Yao, Lixin He, Yan Yu. 2D Nb2O5@2D metallic RuO2 heterostructures as highly reversible anode materials for lithium-ion batteries[J]. Energy Lab, 2023, 1(1): 220007. doi: 10.54227/elab.20220007
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2D Nb2O5@2D metallic RuO2 heterostructures as highly reversible anode materials for lithium-ion batteries
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Abstract
Constructing two-dimensional (2D) heterostructured materials by stacking different 2D materials could combine the merits of the individual building blocks while getting rid of the associated shortcomings. Orthorhombic Nb2O5 (T-Nb2O5) is one of the greatly promising candidates for durable and safety anode for Li-ion batteries (LIBs), but it usually exhibits poor electrochemical performance due to the low electronic conductivity. Herein, we realize excellent lithium storage performance of T-Nb2O5 by designing 2D Nb2O5@2D metallic RuO2 heterostructures (Nb2O5@RuO2). The presence of 2D metallic RuO2 leads to enhanced electronic conductivity. The 2D Nb2O5@RuO2 heterostructures possess very short diffusion length of ions/electrons, easy penetration of liquid electrolyte, and high conductivity transport of electrons through the 2D metallic RuO2 to 2D Nb2O5. The Nb2O5@RuO2 delivers remarkable rate performance (133 mAh g−1 and 106 mAh g−1 at 50 C and 100 C) and excellent long-life capacity (97 mAh g−1 after
10000 cycles at 50 C). Moreover, Nb2O5@RuO2//LiFePO4 full batteries also display high rate capability of 140 mAh g−1 and 90 mAh g−1 at 20 C and 50 C, respectively. Theoretical calculation results show that the 2D Nb2O5@RuO2 heterostructures possess more large adsorption ability for Li+ than that of Nb2O5, indicating an excellent lithium storage performance.-
Keywords:
- Nb2O5 /
- RuO2 /
- 2D nanomaterials /
- Lithium-ion battery /
- Heterostructures
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References
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Hai Yang, Fuxiang He, Jialong Shen, Zhihao Chen, Yu Yao, Lixin He, Yan Yu. 2D Nb2O5@2D metallic RuO2 heterostructures as highly reversible anode materials for lithium-ion batteries[J]. Energy Lab, 2023, 1(1): 220007. doi: 10.54227/elab.20220007
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Figure 1.
Schematic illustrations of a the synthesis process of Nb2O5@RuO2. b, The lithium ions and electrons transportation process. SEM images of c KNb3O8 and d NaRuO2. TEM images of e TBA-Nb3O8 and f TBA-RuO2.
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Figure 2.
a, b SEM, c, d TEM, e, f HRTEM, g HADDF-STEM images and corresponding h Nb, i Ru and j O elemental mapping of Nb2O5@RuO2.
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Figure 3.
a, CV curves for first four cycles at a scan rate of 0.1 mV s−1. b, Galvanostatic charge/discharge curves for first three cycles at 1 C. c, Cycling stability at 5 C. d, Long-term cycling stability at 50 C of Nb2O5@RuO2. e, Rate capacity at different rates as indicated of Nb2O5@RuO2 and Nb2O5. f, A comparison of rate performance of Nb2O5@RuO2 with some other reported Nb2O5 anode materials.
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Figure 4.
a, CV curves of Nb2O5@RuO2 at various scan rates. b, Relationship between the peak currents and scan rates in logarithmic format. c, Capacitive contribution of Nb2O5@RuO2 at a scan rate of 10 mV s−1. d, Contribution ratio of the capacitive and diffusion-controlled capacity versus scan rate.
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Figure 5.
a, Schematic illustration of the Nb2O5/LiFePO4 full cell. b, The charge/discharge curves of full cells at various current densities. c, Rate performance. d, long cycle performance for 500 cycles at 20 C.
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Figure 6.
a, Structure of the unlithiated model of Nb2O5 (left) and lithiated Nb2O5 (right). b, Structure of the unlithiated model of Nb2O5@RuO2 (left) and lithiated Nb2O5@RuO2 (right). c, The adsorption energies of Li ions on Nb2O5 and Nb2O5@RuO2 labeled in a and b. The Li ions migration barriers in Nb2O5 and Nb2O5@RuO2 along d path 1 and e path 2.
