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Mild and Selective Hydrogenation of Nitrate to Ammonia in the Absence of Noble Metals
Author(s) -
Lin Wei,
DaJiang Liu,
Bryan A. Rosales,
James W. Evans,
Javier Vela
Publication year - 2020
Publication title -
acs catalysis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 4.898
H-Index - 198
ISSN - 2155-5435
DOI - 10.1021/acscatal.9b05338
Subject(s) - catalysis , chemistry , noble metal , inorganic chemistry , nitrate , nitrite , hydrodesulfurization , transition metal , ammonia , nox , selectivity , oxide , metal , organic chemistry , combustion
Motivated by increased awareness about nitrate contamination of surface waters and its deleterious effects in human and animal health, we sought an alternative, non-noble metal catalyst for the chemical degradation of nitrate. First-row transition metal phosphides recently emerged as excellent alternatives for hydrogen evolution and hydrotreating reactions. We demonstrate that a key member of this family, Ni2P readily hydrogenates nitrate (NO3-) to ammonia (NH3) near ambient conditions with very high selectivity (96%). One of the few non-precious metal-based catalysts for this transformation, and among ca. 1% of catalysts with NH3 selectivity, Ni2P can be recycled multiple times with limited loss of activity. Both nitrite (NO2-) and nitric oxide (NO) interme-diates are also hydrogenated. Density functional theory (DFT) indicates that—in the absence of a catalyst—nitrite hydrogenation is the reaction bottleneck. A variety of adsorbates (H, O, N, NO) induce surface reconstruction with top-layer Ni-rich surf...

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