Author
Listed:
- Benjamin Rui Peng Yip
(National University of Singapore
National University of Singapore)
- Chaofan Chen
(Delft University of Technology)
- Yan Jiang
(National University of Singapore
National University of Singapore)
- David Ohayon
(National University of Singapore
National University of Singapore)
- Guillermo C. Bazan
(National University of Singapore
National University of Singapore)
- Xuehang Wang
(Delft University of Technology)
Abstract
Despite the development of various pseudocapacitive materials, full-cell pseudocapacitors have yet to surpass the power density of conventional electric double layer capacitors, primarily due to the lack of high-rate positive pseudocapacitive materials. This work reports a solid-state conjugated polyelectrolyte that achieves high-rate charge storage as a positive electrode, facilitated by a co-ion desorption mechanism. The conjugated polyelectrolyte retains 70% of its capacitance at 100 A g−1 with a mass loading of 2.8 mg cm−2 and exhibits a long cycling life of 100,000 cycles in a Swagelok cell configuration. Increasing the electrode thickness fourfold has minimal impact on ion diffusivity and accessibility, yielding a high areal capacitance of 915 mF cm−2. When paired with a high-rate negative pseudocapacitive electrode Ti3C2Tx, the device leverages the redox-active potentials of both materials, achieving a device voltage of 1.5 V and supports operation rates up to 10 V s−1 or 50 A g−1. This configuration enables the pseudocapacitor to deliver an areal power of 160 mW cm−2, while significantly increasing the areal energy (up to 71 μWh cm−2). The high areal performance, combined with the additive-free and water-based fabrication process, makes pseudocapacitors promising for on-chip and wearable energy storage applications.
Suggested Citation
Benjamin Rui Peng Yip & Chaofan Chen & Yan Jiang & David Ohayon & Guillermo C. Bazan & Xuehang Wang, 2025.
"Aqueous asymmetric pseudocapacitor featuring high areal energy and power using conjugated polyelectrolytes and Ti3C2Tx MXene,"
Nature Communications, Nature, vol. 16(1), pages 1-12, December.
Handle:
RePEc:nat:natcom:v:16:y:2025:i:1:d:10.1038_s41467-025-63034-9
DOI: 10.1038/s41467-025-63034-9
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