liu.seSök publikationer i DiVA
Ändra sökning
RefereraExporteraLänk till posten
Permanent länk

Direktlänk
Referera
Referensformat
  • apa
  • ieee
  • modern-language-association-8th-edition
  • vancouver
  • oxford
  • Annat format
Fler format
Språk
  • de-DE
  • en-GB
  • en-US
  • fi-FI
  • nn-NO
  • nn-NB
  • sv-SE
  • Annat språk
Fler språk
Utmatningsformat
  • html
  • text
  • asciidoc
  • rtf
A new strategy for boron cluster-based metal boride (Co2B) synthesis and its applicability to electrocatalytic nitrate reduction
Hubei Univ Sci & Technol, Peoples R China; Wuhan Univ, Peoples R China.
Wuhan Univ, Peoples R China.
Wuhan Univ, Peoples R China.
Wuhan Univ, Peoples R China.
Visa övriga samt affilieringar
2024 (Engelska)Ingår i: Chemical Engineering Journal, ISSN 1385-8947, E-ISSN 1873-3212, Vol. 485, artikel-id 149639Artikel i tidskrift (Refereegranskat) Published
Abstract [en]

To achieve efficient conversion of nitrate to ammonia, it is necessary to design and develop electrode materials with high activity and efficiency for the electrocatalytic reduction reaction of nitrate (NO3RR). Due to its unique semi-metallic properties, the vacancy orbitals of boron are prone to accommodate electrons, so doping element B with transition metals is expected to change the local electronic configuration of the metal, which in turn affects the corresponding catalytic reaction. Here, we propose a new strategy for the preparation of metal borides by using dodecahydro-closo-dodecaborate and Co2+ complexed and calcined to prepare a novel metal boride-Co2B for electrocatalytic nitrate reduction. This modification considerably enhances the performance of NO3RR. Co2B exhibited a Faradaic efficiency of NH4+ (FENH4+) as high as 96.61 % at -0.5 V vs. RHE, achieving a remarkable NH4+ yield of 5.73 mg h-1 mgcat - 1. This study provides a new approach for designing catalysts for environmentallyfriendly ammonia synthesis.

Ort, förlag, år, upplaga, sidor
ELSEVIER SCIENCE SA , 2024. Vol. 485, artikel-id 149639
Nyckelord [en]
Nitrate reduction; Ammonia; Dodecahydro; closo -dodecaborate; Metal boride
Nationell ämneskategori
Organisk kemi
Identifikatorer
URN: urn:nbn:se:liu:diva-202531DOI: 10.1016/j.cej.2024.149639ISI: 001197602800001Scopus ID: 2-s2.0-85185846551OAI: oai:DiVA.org:liu-202531DiVA, id: diva2:1851973
Anmärkning

Funding Agencies|National Natural Science Foundation of China [22179100]; Foundation of Hubei Provincial Department of Education [Q20222805]; Hubei Provincial Department of Science and Technology Project [2023DJC144]; Xianning City Program of Science Technology [2023ZRKX090]; Scientific Research Foundation of Hubei University of Science and Technology [2023HX026, BK202125, 2022ZX07]; Olle Engkvist Byggma stare foundation [212-0178, SNIC 2022-3-34, NAISS 2023/5-77]; Swedish Research Council [2018-05973]

Tillgänglig från: 2024-04-16 Skapad: 2024-04-16 Senast uppdaterad: 2026-03-11

Open Access i DiVA

fulltext(1841 kB)37 nedladdningar
Filinformation
Filnamn FULLTEXT01.pdfFilstorlek 1841 kBChecksumma SHA-512
a5eb44730ae45177c0a7d778c1d5e51f9cb598c11fd2b5063b96d8f11c29992bd18b3d40848e1ada16d94bd78e98e041dcb44f78aa938cc4488d8e9c6b31cb4f
Typ fulltextMimetyp application/pdf

Övriga länkar

Förlagets fulltextScopus

Sök vidare i DiVA

Av författaren/redaktören
Baryshnikov, Glib
Av organisationen
Laboratoriet för organisk elektronikTekniska fakulteten
I samma tidskrift
Chemical Engineering Journal
Organisk kemi

Sök vidare utanför DiVA

GoogleGoogle Scholar
Totalt: 37 nedladdningar
Antalet nedladdningar är summan av nedladdningar för alla fulltexter. Det kan inkludera t.ex tidigare versioner som nu inte längre är tillgängliga.

doi
urn-nbn

Altmetricpoäng

doi
urn-nbn
Totalt: 78 träffar
RefereraExporteraLänk till posten
Permanent länk

Direktlänk
Referera
Referensformat
  • apa
  • ieee
  • modern-language-association-8th-edition
  • vancouver
  • oxford
  • Annat format
Fler format
Språk
  • de-DE
  • en-GB
  • en-US
  • fi-FI
  • nn-NO
  • nn-NB
  • sv-SE
  • Annat språk
Fler språk
Utmatningsformat
  • html
  • text
  • asciidoc
  • rtf