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Article: Enhanced Nitrite Electrovalorization to Ammonia by a NiFe Layered Double Hydroxide

TitleEnhanced Nitrite Electrovalorization to Ammonia by a NiFe Layered Double Hydroxide
Authors
Issue Date2022
PublisherWiley. The Journal's web site is located at http://www.eurjic.org
Citation
European Journal of Inorganic Chemistry, 2022 How to Cite?
AbstractThe development of non-precious metal (NPM) electrocatalysts for efficient nitrite-to-ammonia upcycling is key to enabling a sustainable society. Here, an earth-abundant NiFe layered double hydroxide (LDH) is prepared to electrochemically reduce nitrite with a Faradaic efficiency as high as 85 %, an ammonia selectivity reaching 98 %, and an ammonia yield rate up to 351 μmol h−1 mgcat−1, rivaling the performance metrics of state-of-the-art NPM catalysts. NiFe LDH further displays excellent stability after 10 consecutive electrolysis runs with its nanostructure unperturbed. By conducting electroreduction of nitrite in a range of solutions, the electrolyte identity is found to play an important role in dictating the overall nitrite removal activity. Through a comparative study with MgFe and NiAl inorganic solids, Ni and Fe are demonstrated to boost nitrite valorization rate as well as ammonia selectivity and yield in a synergistic manner. Taken together, these low-cost catalysts provide a promising strategy for one-step conversion of nitrite into ammonia exclusively with implications in next-generation wastewater treatment and green industrial commodity production.
Persistent Identifierhttp://hdl.handle.net/10722/315647
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorWANG, W-
dc.contributor.authorTse, CME-
dc.date.accessioned2022-08-19T09:01:48Z-
dc.date.available2022-08-19T09:01:48Z-
dc.date.issued2022-
dc.identifier.citationEuropean Journal of Inorganic Chemistry, 2022-
dc.identifier.urihttp://hdl.handle.net/10722/315647-
dc.description.abstractThe development of non-precious metal (NPM) electrocatalysts for efficient nitrite-to-ammonia upcycling is key to enabling a sustainable society. Here, an earth-abundant NiFe layered double hydroxide (LDH) is prepared to electrochemically reduce nitrite with a Faradaic efficiency as high as 85 %, an ammonia selectivity reaching 98 %, and an ammonia yield rate up to 351 μmol h−1 mgcat−1, rivaling the performance metrics of state-of-the-art NPM catalysts. NiFe LDH further displays excellent stability after 10 consecutive electrolysis runs with its nanostructure unperturbed. By conducting electroreduction of nitrite in a range of solutions, the electrolyte identity is found to play an important role in dictating the overall nitrite removal activity. Through a comparative study with MgFe and NiAl inorganic solids, Ni and Fe are demonstrated to boost nitrite valorization rate as well as ammonia selectivity and yield in a synergistic manner. Taken together, these low-cost catalysts provide a promising strategy for one-step conversion of nitrite into ammonia exclusively with implications in next-generation wastewater treatment and green industrial commodity production.-
dc.languageeng-
dc.publisherWiley. The Journal's web site is located at http://www.eurjic.org-
dc.relation.ispartofEuropean Journal of Inorganic Chemistry-
dc.rightsSubmitted (preprint) Version This is the pre-peer reviewed version of the following article: [FULL CITE], which has been published in final form at [Link to final article using the DOI]. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Use of Self-Archived Versions. Accepted (peer-reviewed) Version This is the peer reviewed version of the following article: [FULL CITE], which has been published in final form at [Link to final article using the DOI]. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Use of Self-Archived Versions.-
dc.titleEnhanced Nitrite Electrovalorization to Ammonia by a NiFe Layered Double Hydroxide-
dc.typeArticle-
dc.identifier.emailTse, CME: ecmtse@hku.hk-
dc.identifier.authorityTse, CME=rp02452-
dc.identifier.doi10.1002/ejic.202200291-
dc.identifier.hkuros335882-
dc.identifier.isiWOS:000831090700001-

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