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Symmetrical waveform alternating current driven electron enrichment for enhanced oxygen evolution reaction.
Jinhui Hao1, Zhenghao Zhang1, Yitian Wu1
1School ofChemistry and Chemical Engineering, Jiangsu University, Zhenjiang, China. jinhu1_hao@ujs.edu.cn.
Symmetrical alternating current activation engineers nickel iron oxide hydroxide (NiFeOxHy) for enhanced oxygen evolution reaction (OER) performance. This method boosts current and stability by optimizing material properties.
Area of Science:
- Materials Science
- Electrochemistry
- Catalysis
Background:
- The oxygen evolution reaction (OER) is crucial for many energy conversion technologies.
- Developing efficient and stable electrocatalysts for OER remains a significant challenge.
- Current methods for catalyst activation often involve harsh conditions or complex procedures.
Purpose of the Study:
- To develop a novel activation method for NiFeOxHy electrocatalysts.
- To investigate the effect of symmetrical alternating current activation on OER performance.
- To understand the underlying mechanisms responsible for performance enhancement.
Main Methods:
- Symmetrical-waveform alternating current (AC) pulses were used for *in situ* activation of NiFeOxHy.
- Electrochemical characterization techniques were employed to evaluate OER activity and stability.
- Surface analysis was performed to understand the structural and electronic changes in the catalyst.
Main Results:
- AC activation created electron-enriched NiFeOxHy lattices.
- The engineered catalyst exhibited improved intermediate adsorption, conductivity, and mass transport.
- A 33.8% higher current density was achieved at 2.3 V *vs.* RHE compared to untreated catalysts.
- The activated catalyst demonstrated excellent stability over 200 hours.
Conclusions:
- Symmetrical-waveform AC activation is an effective strategy for enhancing NiFeOxHy electrocatalysts.
- The electron-enriched lattice structure is key to the improved OER performance.
- This activation method offers a promising route for developing advanced OER catalysts.
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