Abstract
We present the rational design of a nanostructured Ti₃C₂Tₓ-MXene@NiAl-layered double hydroxide (NiAl-LDH) hybrid electrode prepared via an in situ growth strategy. Uniform deposition of nanoscale NiAl-LDH on few-layer Ti₃C₂Tₓ-MXene formed a robust interfacial structure with strong electronic coupling. DFT calculations and electrochemical analyses reveal enhanced conductivity, faster ion transport, and improved structural stability. As a result, the electrode delivers a high specific capacitance of 1570.1 F g−1 at 1 A g−1 and retains 92.8% capacitance after 5000 cycles at 10 A g−1.An asymmetric supercapacitor using the NiAl-LDH@Ti3C2Tx cathode and an activated carbon anode in 1 M KOH operates up to 1.6 V, achieving 62.8 Wh kg−1 at 1500 W kg−1 and maintaining 90.2% capacity retention with nearly 100% coulombic efficiency over 5000 cycles. Overall, this work demonstrates that NiAl-LDH@Ti3C2Tx hybridization effectively balances energy density and durability, offering a scalable route for advanced electrochemical energy storage.
| Original language | English |
|---|---|
| Article number | 121049 |
| Journal | Journal of Energy Storage |
| Volume | 154 |
| DOIs | |
| State | Published - 10 Apr 2026 |
| 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
- Asymmetric supercapacitor
- DFT calculations
- High Energy density
- Nanocomposite structure
- NiAl layered double hydroxide
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