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Stable acidic H2O2 electrosynthesis via in situ Ti-N bridging sites
Yuxiang Zhang1, Shan Ding1,2, Sheng Chen1
1Key Laboratory for Soft Chemistry and Functional Materials (Ministry of Education), School of Chemistry and Chemical Engineering, Nanjing University of Science and Technology, Ministry of Education, Nanjing, 210094, China. 18068841629@njust.edu.cn.
We developed a stable MIL-125@Ppy catalyst for acidic hydrogen peroxide electrosynthesis, achieving high yields and long operation times. This breakthrough addresses catalyst instability, paving the way for efficient H2O2 production.
Area of Science:
- Electrochemistry
- Materials Science
- Catalysis
Background:
- Acidic hydrogen peroxide (H2O2) electrosynthesis is crucial for various industrial applications.
- Catalyst instability remains a significant challenge, limiting efficiency and operational lifespan.
Purpose of the Study:
- To develop a novel catalyst for stable and efficient acidic H2O2 electrosynthesis.
- To investigate the mechanism behind catalyst stabilization.
Main Methods:
- Electrochemical synthesis of H2O2 using the MIL-125@Ppy catalyst.
- Spectroscopic analysis (e.g., in situ spectroscopy) to probe reaction intermediates and active sites.
- Long-term stability testing under acidic conditions (pH=1).
Main Results:
- The MIL-125@Ppy catalyst achieved a high H2O2 yield rate of 69.5 mol gcat−1 h−1.
- A high faradaic efficiency of 82.2% was maintained for over 50 hours of operation.
- Spectroscopic data revealed the formation of Ti-N bridge sites that stabilize the *OOH intermediate.
Conclusions:
- The MIL-125@Ppy catalyst offers a promising solution for stable and efficient acidic H2O2 electrosynthesis.
- The identified Ti-N bridge sites are key to the catalyst's enhanced stability and selectivity.
- This work advances the development of robust electrocatalysts for chemical production.
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