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Department of Energy Science and Engineering
Advanced Energy Materials Laboratory
1. Journal Articles
Strong catalyst support interactions in defect-rich γ-Mo2N nanoparticles loaded 2D-h-BN hybrid for highly selective nitrogen reduction reaction
Yesudoss, David Kumar
;
Lee, Gayoung
;
Shanmugam, Sangaraju
Department of Energy Science and Engineering
Advanced Energy Materials Laboratory
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Title
Strong catalyst support interactions in defect-rich γ-Mo2N nanoparticles loaded 2D-h-BN hybrid for highly selective nitrogen reduction reaction
Issued Date
2021-06
Citation
Yesudoss, David Kumar. (2021-06). Strong catalyst support interactions in defect-rich γ-Mo2N nanoparticles loaded 2D-h-BN hybrid for highly selective nitrogen reduction reaction. Applied Catalysis B: Environmental, 287, 119952. doi: 10.1016/j.apcatb.2021.119952
Type
Article
Author Keywords
Hexagonal boron nitride
;
In-situ nitridation
;
N-vacancy
;
Nitrogen reduction reaction (NRR)
;
gamma-Molybdenum nitride
Keywords
BORON-NITRIDE
;
PHOTOCATALYTIC ACTIVITY
;
GRAPHENE OXIDE
;
AMMONIA
;
N-2
;
ELECTROSYNTHESIS
;
ELECTROCATALYST
;
PHOTOEMISSION
;
NANOSHEETS
ISSN
0926-3373
Abstract
Electrochemical ammonia synthesis by N2 fixation has proven to be a promising alternative to the energy-consuming, befouling Haber-Bosch process. Considering the low faradaic efficiency and sluggish kinetics of Nitrogen Reduction Reaction (NRR), it is significant to design a robust and selective catalyst. Herein, we demonstrate a single step in-situ nitridation method to grow cubic molybdenum nitride (γ-Mo2N) nanoparticles on a 2D hexagonal boron nitride (h-BN) sheets as a potential, cost-effective electrocatalyst for NRR, in which the selectivity for N2 was regulated by interfacially engineering the Mo2N-BN bridge. The maneuverability of h-BN sheets enabled the provocation of N-vacancies governed by the particle size, where the fine-tuning of their significance emanated the highest faradaic efficiency of 61.5 %. Moreover, such non-noble metal-based hybrids delivered a stable performance for 20 h. Therefore, our approach of designing the electronic structure of a catalyst by controlling the defects could be an effective practice for selective NRR. © 2021 Elsevier B.V.
URI
http://hdl.handle.net/20.500.11750/13815
DOI
10.1016/j.apcatb.2021.119952
Publisher
Elsevier BV
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