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Article: Piezoelectricity regulated ohmic contact in M/BaTiO3 (M = Ru, Pd, Pt) for charge collision and hydrogen free radical production in ammonia electrosynthesis

TitlePiezoelectricity regulated ohmic contact in M/BaTiO3 (M = Ru, Pd, Pt) for charge collision and hydrogen free radical production in ammonia electrosynthesis
Authors
KeywordsCharge collision
Electrochemical NO3− reduction
Hydrogen radicals
Ohmic contact
Piezoelectric effect
Issue Date2023
Citation
Materials Today, 2023, v. 66, p. 17-25 How to Cite?
AbstractElectrochemical nitrate reduction reaction (NO3RR) is a promising alternative technique for NH3 generation toward the energy-consuming Haber-Bosch process. Nevertheless, it remains hindered by the competitive hydrogen evolution reaction (HER). Herein, the piezoelectric effect of electron-rich BaTiO3 with oxygen vacancies is introduced to promote NO3RR performance. Combining with metal particles (Ru, Pd and Pt), the catalyst achieves a maximal Faradaic efficiency of 95.3% and NH3 yield rate of 6.87 mg h−1 mgcat.−1. Upon piezoelectricity, the interface between metal nanoparticles and BaTiO3 is effectively modulated from Schottky contact to ohmic contact, which leads to unobstructed electron transfer. Abundant hydrogen radicals (·H) can be then produced from the collision between plentiful electrons and polar water molecules adsorbed on the polar surface. Such ·H can significantly facilitate the hydrogenation of reaction intermediates in NO3RR. Meanwhile, this process suppresses the Volmer-Heyrovsky step, therefore inhibiting the HER within a wide range of external potential. This work suggests a new strategy for promoting the performance of multi-electron-involved catalytic reactions.
Persistent Identifierhttp://hdl.handle.net/10722/360234
ISSN
2023 Impact Factor: 21.1
2023 SCImago Journal Rankings: 5.949

 

DC FieldValueLanguage
dc.contributor.authorZhang, Shaoce-
dc.contributor.authorChen, Dong-
dc.contributor.authorGuo, Ying-
dc.contributor.authorZhang, Rong-
dc.contributor.authorZhao, Yuwei-
dc.contributor.authorHuang, Zhaodong-
dc.contributor.authorFan, Jun-
dc.contributor.authorHo, Johnny C.-
dc.contributor.authorZhi, Chunyi-
dc.date.accessioned2025-09-10T09:05:48Z-
dc.date.available2025-09-10T09:05:48Z-
dc.date.issued2023-
dc.identifier.citationMaterials Today, 2023, v. 66, p. 17-25-
dc.identifier.issn1369-7021-
dc.identifier.urihttp://hdl.handle.net/10722/360234-
dc.description.abstractElectrochemical nitrate reduction reaction (NO<inf>3</inf>RR) is a promising alternative technique for NH<inf>3</inf> generation toward the energy-consuming Haber-Bosch process. Nevertheless, it remains hindered by the competitive hydrogen evolution reaction (HER). Herein, the piezoelectric effect of electron-rich BaTiO<inf>3</inf> with oxygen vacancies is introduced to promote NO<inf>3</inf>RR performance. Combining with metal particles (Ru, Pd and Pt), the catalyst achieves a maximal Faradaic efficiency of 95.3% and NH<inf>3</inf> yield rate of 6.87 mg h<sup>−1</sup> mg<inf>cat.</inf><sup>−1</sup>. Upon piezoelectricity, the interface between metal nanoparticles and BaTiO<inf>3</inf> is effectively modulated from Schottky contact to ohmic contact, which leads to unobstructed electron transfer. Abundant hydrogen radicals (·H) can be then produced from the collision between plentiful electrons and polar water molecules adsorbed on the polar surface. Such ·H can significantly facilitate the hydrogenation of reaction intermediates in NO<inf>3</inf>RR. Meanwhile, this process suppresses the Volmer-Heyrovsky step, therefore inhibiting the HER within a wide range of external potential. This work suggests a new strategy for promoting the performance of multi-electron-involved catalytic reactions.-
dc.languageeng-
dc.relation.ispartofMaterials Today-
dc.subjectCharge collision-
dc.subjectElectrochemical NO3− reduction-
dc.subjectHydrogen radicals-
dc.subjectOhmic contact-
dc.subjectPiezoelectric effect-
dc.titlePiezoelectricity regulated ohmic contact in M/BaTiO3 (M = Ru, Pd, Pt) for charge collision and hydrogen free radical production in ammonia electrosynthesis-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1016/j.mattod.2023.03.011-
dc.identifier.scopuseid_2-s2.0-85159293913-
dc.identifier.volume66-
dc.identifier.spage17-
dc.identifier.epage25-
dc.identifier.eissn1873-4103-

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