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![Protein Film Infrared Electrochemistry Demonstrated for Study of H2 Oxidation by a [NiFe] Hydrogenase](/_next/image?url=https%3A%2F%2Fcloudfront.jove.com%2FCDNSource%2Fteasers%2F55858.jpg&w=3840&q=50)
Protein Film Infrared Electrochemistry Demonstrated for Study of H2 Oxidation by a [NiFe] Hydrogenase
Published on: December 4, 2017
Direct Insight into the Role of Cationic Lactam Nitrogen on Oxygen Electroreduction
Guanbin Ding1, Jun Ma2, Yuefeng Liu2
1State Key Laboratory of Pollution Control and Resources Reuse, School of Environmental Science and Engineering, Tongji University, 1239 Siping Road, Shanghai 200092, P. R. China.
Abstract:
Nitrogen-doped carbon catalysts are promising metal-free candidates for the oxygen reduction reaction (ORR). However, the identification of genuine active species remains challenging due to the complexity of local N environments, where the role of lactam has long been overlooked. Herein, N-doped nanodiamond (NND) and carbon nanotubes (NCNT) as metal-free model catalysts are fabricated for ORR. Spectroscopic analyses and temperature-programmed desorption (TPD) measurements reveal the dominance of lactam in an sp3-hybridized carbon framework of NND, whereas NCNT is mainly composed of pyridinic and graphitic N, providing clear chemical tools for active site investigation. Through electrochemical Coulombic screening experiments, it was demonstrated that ORR on NND mainly proceeds via lactam-derived cationic N intermediates, while NCNT could expedite the reaction through anionic intermediates associated with pyridinic N. Further postreaction characterizations evidence the formation of cationic N+ in NND, which interacts strongly with neighboring carbon atoms (e.g., C-O-) to participate in ORR actively. Taken together, this work not only highlights the pivotal role of cationic lactam N toward ORR but also gives insights into the future design of metal-free carbon catalysts via fine N engineering.
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