<?xml version="1.0" encoding="UTF-8"?><rdf:RDF xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:dcq="http://purl.org/dc/terms/"><records count="1" morepages="false" start="1" end="1"><record rownumber="1"><dc:product_type>Conference Paper</dc:product_type><dc:title>Electrocatalytic Reduction of Nitrate to Nitrite and Ammonia over Oxide-Derived Silver Electrodes</dc:title><dc:creator>Liu, Hengzhou; Park, Jaeryl; Chen, Yifu; Gu, Shuang; Roling, Luke; Li, Wenzhen</dc:creator><dc:corporate_author/><dc:editor/><dc:description>The nitrogen cycle plays a key role biological, energy, environment, and industrial processes. Breaking natural nitrogen cycle is leading to accumulation of reactive nitrogen chemicals in water and atmosphere, therefore, better management of N-cycle has emerged as an urgent research need in energy and environmental science. Removing excessive nitrate (NO3−) from wastewater has increasingly become an important research topic in light of the growing concerns over the related environmental problems and health issues. In particular, catalytic/electrocatalytic approaches are attractive for NO3− removal, because NO3− from wastewater can be converted to N2 and released back to the atmosphere using renewable H2 or electricity, closing the loop of the global N cycle. However, achieving high product selectivity towards the desirable N2 has proven challenging in the direct NO3−-to-N2 reaction.  In this presentation, we will report our finding on unique and ultra-high electrochemical NO3−-to-NO2−activity on an oxide-derived silver electrode (OD-Ag). Up to 98% selectivity and 95% faradaic efficiency of NO2− were observed and maintained under a wide potential window. Benefiting from overcoming the rate-determining barrier of NO3−-to-NO2−during nitrate reduction, further reduction of accumulated NO2− to NH4+ can be well regulated by the cathodic potential on OD-Ag to achieve a faradaic efficiency of 89%. These indicated the potential controllable pathway to the key nitrate reduction products (NO2−or NH4+) on OD-Ag. DFT computations provided insights into the unique NO2−selectivity on Ag electrodes compared with Cu, showing the critical role of a proton-assisted mechanism. Based on the ultra-high NO3−-to-NO2−activity on OD-Ag, we designed a novel electrocatalytic-catalytic combined process for denitrifying real-world NO3−-containing agricultural wastewater, leading to 95+% of NO3− conversion to N2 with minimal NOx gases. Importantly, NO2− derived from nitrate may serve as a crucial reactive platform for distributed production of various nitrogen products, such as NO, NH2OH, NH3, and urea.</dc:description><dc:publisher/><dc:date>2021-08-22</dc:date><dc:nsf_par_id>10302838</dc:nsf_par_id><dc:journal_name>262nd ACS National Meeting</dc:journal_name><dc:journal_volume/><dc:journal_issue/><dc:page_range_or_elocation/><dc:issn/><dc:isbn/><dc:doi>https://doi.org/</dc:doi><dcq:identifierAwardId>2036944</dcq:identifierAwardId><dc:subject/><dc:version_number/><dc:location/><dc:rights/><dc:institution/><dc:sponsoring_org>National Science Foundation</dc:sponsoring_org></record></records></rdf:RDF>