Ni(OH)2 microspheres in situ self-grown on ultra-thin layered g-C3N4 as a heterojunction electrocatalyst for oxygen evolution reaction. (20th December 2021)
- Record Type:
- Journal Article
- Title:
- Ni(OH)2 microspheres in situ self-grown on ultra-thin layered g-C3N4 as a heterojunction electrocatalyst for oxygen evolution reaction. (20th December 2021)
- Main Title:
- Ni(OH)2 microspheres in situ self-grown on ultra-thin layered g-C3N4 as a heterojunction electrocatalyst for oxygen evolution reaction
- Authors:
- Li, Tong
Ma, Xinxia
Wu, Jiang
Chu, Fenghong
Qiao, Lingxia
Song, Yubao
Wu, Maoliang
Lin, Jia
Peng, Lin
Chen, Zhongwei - Abstract:
- Abstract: Oxygen evolution reaction (OER), as a part reaction of the overall water splitting, is deemed as a prospective technology for large-scale energy storage. However, the sluggish kinetics (large overpotential) and the expensive cost of noble metal-based electrocatalysts (RuO2 and IrO2 ) restrain the widespread usage of OER. Hence, the discovery of non-precious metal-based electrocatalysts with tiny overpotential, satisfactory current density and outstanding stability has become urgent. In this work, we have prepared ultra-thin layered g-C3 N4 by a two-step thermal peeling method and synthesized Ni(OH)2 /g-C3 N4 composite by a simple one-step solvothermal method. Benefiting from the layered g-C3 N4 as substrate, the overpotential of Ni(OH)2 /g-C3 N4 composite was just 240 mV at 10 mA cm −2, which gives an unexpected improvement in the electrochemical performance of the composite samples compared to pure Ni(OH)2 ( η = 460 mV). Additionally, the formation of heterojunction effectively reduces the resistance to electron transport in OER, the resistance of Ni(OH)2 /g-C3 N4 ( Rct = 38.8 Ω) is far smaller than those of bare Ni(OH)2 ( Rct = 41.6 Ω) and layered g-C3 N4 ( Rct = 43.6 Ω) at the open circuit potential. Ni(OH)2 /g-C3 N4 composite samples display outstanding electrochemical stability, maintaining 85% of initial current density for 12 h. Moreover, density functional theory (DFT) demonstrates that Δ G 3 of Ni(OH)2 /g-C3 N4 composite ( η = 0.46 V) is much lowerAbstract: Oxygen evolution reaction (OER), as a part reaction of the overall water splitting, is deemed as a prospective technology for large-scale energy storage. However, the sluggish kinetics (large overpotential) and the expensive cost of noble metal-based electrocatalysts (RuO2 and IrO2 ) restrain the widespread usage of OER. Hence, the discovery of non-precious metal-based electrocatalysts with tiny overpotential, satisfactory current density and outstanding stability has become urgent. In this work, we have prepared ultra-thin layered g-C3 N4 by a two-step thermal peeling method and synthesized Ni(OH)2 /g-C3 N4 composite by a simple one-step solvothermal method. Benefiting from the layered g-C3 N4 as substrate, the overpotential of Ni(OH)2 /g-C3 N4 composite was just 240 mV at 10 mA cm −2, which gives an unexpected improvement in the electrochemical performance of the composite samples compared to pure Ni(OH)2 ( η = 460 mV). Additionally, the formation of heterojunction effectively reduces the resistance to electron transport in OER, the resistance of Ni(OH)2 /g-C3 N4 ( Rct = 38.8 Ω) is far smaller than those of bare Ni(OH)2 ( Rct = 41.6 Ω) and layered g-C3 N4 ( Rct = 43.6 Ω) at the open circuit potential. Ni(OH)2 /g-C3 N4 composite samples display outstanding electrochemical stability, maintaining 85% of initial current density for 12 h. Moreover, density functional theory (DFT) demonstrates that Δ G 3 of Ni(OH)2 /g-C3 N4 composite ( η = 0.46 V) is much lower than that of bare Ni(OH)2 ( η = 0.64 V). These undeniable results demonstrate that Ni(OH)2 /g-C3 N4 composite materials is promising alternative materials to replace precious metal-based OER electrocatalysts in the field of water splitting. Graphical abstract: Image, graphical abstract … (more)
- Is Part Of:
- Electrochimica acta. Volume 400(2021)
- Journal:
- Electrochimica acta
- Issue:
- Volume 400(2021)
- Issue Display:
- Volume 400, Issue 2021 (2021)
- Year:
- 2021
- Volume:
- 400
- Issue:
- 2021
- Issue Sort Value:
- 2021-0400-2021-0000
- Page Start:
- Page End:
- Publication Date:
- 2021-12-20
- Subjects:
- Oxygen evolution reaction -- Water splitting -- Electrocatalyst -- Ni(OH)2/g-C3N4
Electrochemistry -- Periodicals
Electrochemistry, Industrial -- Periodicals
541.37 - Journal URLs:
- http://www.sciencedirect.com/science/journal/00134686 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.electacta.2021.139473 ↗
- Languages:
- English
- ISSNs:
- 0013-4686
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3698.950000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 20172.xml