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Crystalline phosphides/amorphous oxides composite for energy-saving hydrogen production assisted by efficient urea oxidation reaction
Lulu Qiao1; Anquan Zhu3; Di Liu1; Jinxian Feng1; Yuyun Chen1; Mingpeng Chen1; Pengfei Zhou1; Lihong Yin1; Rucheng Wu1; Kar Wei Ng1; Hui Pan1,2
2023-02-15
Source PublicationChemical Engineering Journal
ISSN1385-8947
Volume424Issue:4Pages:140380
Abstract

Developing active and stable electrocatalysts for urea oxidation reaction (UOR) is of great significance to energy-saving hydrogen production. Herein, we report a crystalline nickel–cobalt phosphides/amorphous phosphorous-incorporated manganese oxides composite (c-CoNiP/a-P-MnO) with a hierarchical structure as an efficient, durable, and multifunctional catalyst for both UOR and hydrogen evolution reaction (HER) in alkaline solution. The c-CoNiP/a-P-MnO electrode shows excellent UOR activity (by indirect mechanism) with the low potentials of 1.24 and 1.35 V at 10 and 100 mA cm, respectively, long-term stability (300 h), and excellent HER performance with a hydrogen production rate of 0.18 mmol h and an average Faraday efficiency (FE) of 97.2 % at 20 mA cm and high stability at 50 mA cm as assisted by UOR. The outstanding catalytic performance is attributed to that: (1) the Co-incorporation into NiP system lowers the oxidation potential of Ni to Ni, leading to the enrichment of UOR-oriented active component (NiOOH) on the surface of the electrode; (2) CoNiP with excellent electrical conductivity and electron-transfer ability serves as the active phase for HER; and (3) the unique configuration of a-P-MnO and c-CoNiP not only boosts the adsorption of reactant molecules to enhance the activity, but also enables long-term stabilities towards UOR and HER. This work highlights that the crystalline/amorphous configuration and the Mn/Co-incorporation greatly optimize the catalytic activity and stability towards both UOR and HER, which opens a new avenue to develop high-performance catalysts for the energy-saving hydrogen production.

KeywordCrystalline/amorphous Configuration Synergistic Electrocatalysis Urea Oxidation Reaction Energy-saving Hydrogen Production
DOI10.1016/j.cej.2022.140380
URLView the original
Indexed BySCIE
Language英語English
WOS Research AreaEngineering
WOS SubjectEngineering ; Environmental Engineering ; Chemical
WOS IDWOS:000895504600006
PublisherELSEVIER SCIENCE SA, PO BOX 564, 1001 LAUSANNE, SWITZERLAND
Scopus ID2-s2.0-85142483160
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Citation statistics
Document TypeJournal article
CollectionFaculty of Science and Technology
INSTITUTE OF APPLIED PHYSICS AND MATERIALS ENGINEERING
DEPARTMENT OF PHYSICS AND CHEMISTRY
Corresponding AuthorKar Wei Ng; Hui Pan
Affiliation1.Institute of Applied Physics and Materials Engineering, University of Macau, Macao SAR 999078, China
2.Department of Physics and Chemistry, Faculty of Science and Technology, University of Macau, Macao SAR, 999078, China
3.Center of Super-Diamond and Advanced Films (COSDAF), Department of Materials Science and Engineering, City University of Hong Kong, Kowloon, Tat Chee Avenue, Hong Kong, China
First Author AffilicationINSTITUTE OF APPLIED PHYSICS AND MATERIALS ENGINEERING
Corresponding Author AffilicationINSTITUTE OF APPLIED PHYSICS AND MATERIALS ENGINEERING;  Faculty of Science and Technology
Recommended Citation
GB/T 7714
Lulu Qiao,Anquan Zhu,Di Liu,et al. Crystalline phosphides/amorphous oxides composite for energy-saving hydrogen production assisted by efficient urea oxidation reaction[J]. Chemical Engineering Journal, 2023, 424(4), 140380.
APA Lulu Qiao., Anquan Zhu., Di Liu., Jinxian Feng., Yuyun Chen., Mingpeng Chen., Pengfei Zhou., Lihong Yin., Rucheng Wu., Kar Wei Ng., & Hui Pan (2023). Crystalline phosphides/amorphous oxides composite for energy-saving hydrogen production assisted by efficient urea oxidation reaction. Chemical Engineering Journal, 424(4), 140380.
MLA Lulu Qiao,et al."Crystalline phosphides/amorphous oxides composite for energy-saving hydrogen production assisted by efficient urea oxidation reaction".Chemical Engineering Journal 424.4(2023):140380.
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