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Department of Energy Science and Engineering
Advanced Energy Materials Laboratory
1. Journal Articles
Accelerated N2 Reduction Kinetics in Hybrid Interfaces of NbTiO4 and Nitrogen-doped Carbon Nanorod via Synergistic Electronic Coupling Effect
Yesudoss, David Kumar
;
Byungchan Han
;
Shanmugam, Sangaraju
;
Chun, Hoje
Department of Energy Science and Engineering
Advanced Energy Materials Laboratory
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Title
Accelerated N2 Reduction Kinetics in Hybrid Interfaces of NbTiO4 and Nitrogen-doped Carbon Nanorod via Synergistic Electronic Coupling Effect
Issued Date
2022-05
Citation
Yesudoss, David Kumar. (2022-05). Accelerated N2 Reduction Kinetics in Hybrid Interfaces of NbTiO4 and Nitrogen-doped Carbon Nanorod via Synergistic Electronic Coupling Effect. Applied Catalysis B: Environmental, 304. doi: 10.1016/j.apcatb.2021.120938
Type
Article
Author Keywords
Nitrogen reduction reaction
;
Electrochemical ammonia synthesis
;
Strong catalyst-support interaction
;
NbTiO4
;
Hybrid catalyst
Keywords
Ammonia
;
Calculations
;
Carbon
;
Catalyst selectivity
;
Doping (additives)
;
Electrocatalysts
;
Electron transport properties
;
Hybrid materials
;
Kinetic theory
;
Kinetics
;
Metals
;
Nitrogen fixation
;
Reaction kinetics
;
Strontium titanates
ISSN
0926-3373
Abstract
Electrochemical ammonia synthesis through the atmospheric nitrogen reduction reaction (NRR) is a promising method for sustainable fertilizer and carbon-free hydrogen energy carriers. The inevitable selectivity gap against hydrogen evolution reaction and inert nitrogen (N2) hinders the device-level usage of nitrogen cathodes. In this work, we report engineered electrocatalyst/support interface of NbTiO4 nanoparticles supported on nitrogen-doped carbon nanorods (NbTiO4@NCNR) to catalyze NRR. Insisted by the pitfalls to rationally design N2 reduction catalysts, the strong catalyst-support interaction strategy is adapted to tune the selectivity towards NRR. Electrochemical tests reveal that NbTiO4@NCNR hybrid accelerates a 10-fold increase in N2 selectivity compared to pure metal oxide. Using first-principles calculations, we identify the underlying mechanism of enhanced performance: bridging bonds in the interface as electron transport channels to promote the N2 reduction kinetics. Essentially, this study provides an insight into how to overcome the immense kinetic barrier of NRR using smartly engineered interfaces of hybrid materials. © 2021 Elsevier B.V.
URI
http://hdl.handle.net/20.500.11750/16046
DOI
10.1016/j.apcatb.2021.120938
Publisher
Elsevier BV
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