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Peer-reviewedCC BY-NCRSC advances

A FTO/MXene@PdTe₂@TiO₂//PANI composite for the development of light-responsive electrodes for solar-integrated hybrid supercapacitors.

  1. 1Department of Physics, College of Sciences, Princess Nourah bint Abdulrahman University P. O. Box 84428 Riyadh 11671 Saudi Arabia.
  2. 2Department of Physics, Riphah International University, Campus Lahore Islamabad Pakistan [email protected] [email protected].

Abstract

The development of multifunctional electrodes capable of simultaneously harvesting solar energy and storing electrical charge is highly attractive for next-generation self-powered energy systems. Herein, we introduce a ternary MXene@PdTe₂@TiO₂ heterostructure as a multifunctional photo-electrochemical electrode, in which highly conductive MXene, broadband photoresponsive PdTe₂, and semiconducting TiO₂ are synergistically integrated to couple solar-energy harvesting with electrochemical charge storage. The distinctive ternary architecture promotes interfacial charge separation and transfer, facilitates ion diffusion, and accelerates faradaic reaction kinetics, enabling the construction of a photo-electrochemical hybrid asymmetric MXene@PdTe₂@TiO₂//PANI@AC supercapacitor. The resulting MXene@PdTe₂@TiO₂-electrode has a high power conversion efficiency (PCE) of 16%, a high value of fill factor (FF) of 87%, and a maximum open-circuit voltage (V oc) of 0.74 V. The obtained values of Schottky barrier height and ideality factor (Φ = 0.35, and n = 1.22) also prove the positive charge transfer dynamics and minimum ionic recombination loss. The MXene@PdTe₂@TiO₂//PANI@AC hybrid device offered the highest specific charge (Q s) of 279 C g⁻¹, energy density of 45 Wh kg⁻¹ at a power density of 2469.77 W kg⁻¹, and it has a high retention of 98.36% over 10 000 cycles, indicating its good long-term stability of operation under solar illumination because of effective photogenerated electrons by the PdTe₂-TiO₂ synergy. Collectively, these findings indicate that MXene@PdTe₂@TiO₂//PANI@AC is a high-performance photoelectrochemical electrode that couples solar energy harvesting with improved electrochemical charge storage, providing a potential platform for next-generation solar-assisted and photo-rechargeable hybrid energy storage technologies.

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BibTeX
@article{almunyif2026ftomxenepdte₂tio₂pani,
  title = {{A FTO/MXene@PdTe₂@TiO₂//PANI composite for the development of light-responsive electrodes for solar-integrated hybrid supercapacitors.}},
  author = {Amjad A Almunyif and Ahdab Khalid Althukair and Saba Khalil and Amir Muhammad Afzal},
  journal = {RSC advances},
  year = {2026},
  month = oct,
  doi = {10.1039/d6ra05563j},
  url = {https://europepmc.org/article/MED/42846094},
  note = {CC BY-NC},
}
RIS
TY  - JOUR
TI  - A FTO/MXene@PdTe₂@TiO₂//PANI composite for the development of light-responsive electrodes for solar-integrated hybrid supercapacitors.
AU  - Amjad A Almunyif
AU  - Ahdab Khalid Althukair
AU  - Saba Khalil
AU  - Amir Muhammad Afzal
PY  - 2026
DA  - 2026/10/07
JO  - RSC advances
DO  - 10.1039/d6ra05563j
UR  - https://europepmc.org/article/MED/42846094
AB  - The development of multifunctional electrodes capable of simultaneously harvesting solar energy and storing electrical charge is highly attractive for next-generation self-powered energy systems. Herein, we introduce a ternary MXene@PdTe₂@TiO₂ heterostructure as a multifunctional photo-electrochemical electrode, in which highly conductive MXene, broadband photoresponsive PdTe₂, and semiconducting TiO₂ are synergistically integrated to couple solar-energy harvesting with electrochemical charge storage. The distinctive ternary architecture promotes interfacial charge separation and transfer, facilitates ion diffusion, and accelerates faradaic reaction kinetics, enabling the construction of a photo-electrochemical hybrid asymmetric MXene@PdTe₂@TiO₂//PANI@AC supercapacitor. The resulting MXene@PdTe₂@TiO₂-electrode has a high power conversion efficiency (PCE) of 16%, a high value of fill factor (FF) of 87%, and a maximum open-circuit voltage (V oc) of 0.74 V. The obtained values of Schottky barrier height and ideality factor (Φ = 0.35, and n = 1.22) also prove the positive charge transfer dynamics and minimum ionic recombination loss. The MXene@PdTe₂@TiO₂//PANI@AC hybrid device offered the highest specific charge (Q s) of 279 C g⁻¹, energy density of 45 Wh kg⁻¹ at a power density of 2469.77 W kg⁻¹, and it has a high retention of 98.36% over 10 000 cycles, indicating its good long-term stability of operation under solar illumination because of effective photogenerated electrons by the PdTe₂-TiO₂ synergy. Collectively, these findings indicate that MXene@PdTe₂@TiO₂//PANI@AC is a high-performance photoelectrochemical electrode that couples solar energy harvesting with improved electrochemical charge storage, providing a potential platform for next-generation solar-assisted and photo-rechargeable hybrid energy storage technologies.
SN  - 2046-2069
ER  -