File Download

There are no files associated with this item.

  Links for fulltext
     (May Require Subscription)
Supplementary

Article: Electrochemical nitrate reduction in acid enables high-efficiency ammonia synthesis and high-voltage pollutes-based fuel cells

TitleElectrochemical nitrate reduction in acid enables high-efficiency ammonia synthesis and high-voltage pollutes-based fuel cells
Authors
Issue Date2023
Citation
Nature Communications, 2023, v. 14, n. 1, article no. 8036 How to Cite?
AbstractMost current research is devoted to electrochemical nitrate reduction reaction for ammonia synthesis under alkaline/neutral media while the investigation of nitrate reduction under acidic conditions is rarely reported. In this work, we demonstrate the potential of TiO2 nanosheet with intrinsically poor hydrogen-evolution activity for selective and rapid nitrate reduction to ammonia under acidic conditions. Hybridized with iron phthalocyanine, the resulting catalyst displays remarkably improved efficiency toward ammonia formation owing to the enhanced nitrate adsorption, suppressed hydrogen evolution and lowered energy barrier for the rate-determining step. Then, an alkaline-acid hybrid Zn-nitrate battery was developed with high open-circuit voltage of 1.99 V and power density of 91.4 mW cm–2. Further, the environmental sulfur recovery can be powered by above hybrid battery and the hydrazine-nitrate fuel cell can be developed for simultaneously hydrazine/nitrate conversion and electricity generation. This work demonstrates the attractive potential of acidic nitrate reduction for ammonia electrosynthesis and broadens the field of energy conversion.
Persistent Identifierhttp://hdl.handle.net/10722/360273

 

DC FieldValueLanguage
dc.contributor.authorZhang, Rong-
dc.contributor.authorLi, Chuan-
dc.contributor.authorCui, Huilin-
dc.contributor.authorWang, Yanbo-
dc.contributor.authorZhang, Shaoce-
dc.contributor.authorLi, Pei-
dc.contributor.authorHou, Yue-
dc.contributor.authorGuo, Ying-
dc.contributor.authorLiang, Guojin-
dc.contributor.authorHuang, Zhaodong-
dc.contributor.authorPeng, Chao-
dc.contributor.authorZhi, Chunyi-
dc.date.accessioned2025-09-10T09:06:00Z-
dc.date.available2025-09-10T09:06:00Z-
dc.date.issued2023-
dc.identifier.citationNature Communications, 2023, v. 14, n. 1, article no. 8036-
dc.identifier.urihttp://hdl.handle.net/10722/360273-
dc.description.abstractMost current research is devoted to electrochemical nitrate reduction reaction for ammonia synthesis under alkaline/neutral media while the investigation of nitrate reduction under acidic conditions is rarely reported. In this work, we demonstrate the potential of TiO<inf>2</inf> nanosheet with intrinsically poor hydrogen-evolution activity for selective and rapid nitrate reduction to ammonia under acidic conditions. Hybridized with iron phthalocyanine, the resulting catalyst displays remarkably improved efficiency toward ammonia formation owing to the enhanced nitrate adsorption, suppressed hydrogen evolution and lowered energy barrier for the rate-determining step. Then, an alkaline-acid hybrid Zn-nitrate battery was developed with high open-circuit voltage of 1.99 V and power density of 91.4 mW cm<sup>–2</sup>. Further, the environmental sulfur recovery can be powered by above hybrid battery and the hydrazine-nitrate fuel cell can be developed for simultaneously hydrazine/nitrate conversion and electricity generation. This work demonstrates the attractive potential of acidic nitrate reduction for ammonia electrosynthesis and broadens the field of energy conversion.-
dc.languageeng-
dc.relation.ispartofNature Communications-
dc.titleElectrochemical nitrate reduction in acid enables high-efficiency ammonia synthesis and high-voltage pollutes-based fuel cells-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1038/s41467-023-43897-6-
dc.identifier.pmid38052852-
dc.identifier.scopuseid_2-s2.0-85178436433-
dc.identifier.volume14-
dc.identifier.issue1-
dc.identifier.spagearticle no. 8036-
dc.identifier.epagearticle no. 8036-
dc.identifier.eissn2041-1723-

Export via OAI-PMH Interface in XML Formats


OR


Export to Other Non-XML Formats