Multi-high valence state metal doping in NiFe hydroxide toward superior oxygen evolution reaction activity. Issue 6 (24th January 2023)
- Record Type:
- Journal Article
- Title:
- Multi-high valence state metal doping in NiFe hydroxide toward superior oxygen evolution reaction activity. Issue 6 (24th January 2023)
- Main Title:
- Multi-high valence state metal doping in NiFe hydroxide toward superior oxygen evolution reaction activity
- Authors:
- Sari, Fitri Nur Indah
Frenel, Gally
Lee, Alex Chinghuan
Huang, Yan-Jia
Su, Yen-Hsun
Ting, Jyh-Ming - Abstract:
- Abstract : FeNiVTiCr hydroxide, fabricated through a facile Ni-corrosion method at room temperature, is demonstrated to be an outstanding OER electrocatalyst, outperforming commercial electrocatalysts. Abstract : In this study, we demonstrate multi-high valence 3d transition metal (TM) doping to boost the oxygen evolution reaction (OER) activity and stability of NiFe hydroxide. Self-supported NiFe hydroxides with multiple high valence 3d TM (V 4+, V 5+, Ti 3+, Ti 4+, Co 3+, and Cr 3+ ) doping are fabricated using a facile Ni-corrosion method at room temperature without the use of any additional oxidizing agent. The high-valence metal dopants effectively tune the electronic structure of Ni. In situ Raman, ex situ electron energy-loss spectroscopy, and density functional theory calculations reveal that Cr is advantageous for the formation of oxyhydroxide with the longest Ni–O bond length, facilitating the decomposition of *OOH intermediate species for the generation of O2 . Additionally, Ti contributes to charge transfer. The optimized NiFe hydroxide with V, Ti, and Cr dopants (FNVTiCr) outperforms the benchmark RuO2 and reported Ni-based catalyst by exhibiting an overpotential of 240 mV at 100 mA cm −2 and stability for 70 h. Notably, an alkaline electrolyzer with an FNVTiCr anode and Pt/C cathode is also demonstrated with an ultralow cell voltage of 1.49 V to generate a current density of 10 mA cm −2, which is stable for 100 h, surpassing the benchmark industrial catalyst.Abstract : FeNiVTiCr hydroxide, fabricated through a facile Ni-corrosion method at room temperature, is demonstrated to be an outstanding OER electrocatalyst, outperforming commercial electrocatalysts. Abstract : In this study, we demonstrate multi-high valence 3d transition metal (TM) doping to boost the oxygen evolution reaction (OER) activity and stability of NiFe hydroxide. Self-supported NiFe hydroxides with multiple high valence 3d TM (V 4+, V 5+, Ti 3+, Ti 4+, Co 3+, and Cr 3+ ) doping are fabricated using a facile Ni-corrosion method at room temperature without the use of any additional oxidizing agent. The high-valence metal dopants effectively tune the electronic structure of Ni. In situ Raman, ex situ electron energy-loss spectroscopy, and density functional theory calculations reveal that Cr is advantageous for the formation of oxyhydroxide with the longest Ni–O bond length, facilitating the decomposition of *OOH intermediate species for the generation of O2 . Additionally, Ti contributes to charge transfer. The optimized NiFe hydroxide with V, Ti, and Cr dopants (FNVTiCr) outperforms the benchmark RuO2 and reported Ni-based catalyst by exhibiting an overpotential of 240 mV at 100 mA cm −2 and stability for 70 h. Notably, an alkaline electrolyzer with an FNVTiCr anode and Pt/C cathode is also demonstrated with an ultralow cell voltage of 1.49 V to generate a current density of 10 mA cm −2, which is stable for 100 h, surpassing the benchmark industrial catalyst. This multi-high valence 3d TM doping approach provides a strategy for designing a low-cost, effective, and stable Ni-based catalyst. … (more)
- Is Part Of:
- Journal of materials chemistry. Volume 11:Issue 6(2023)
- Journal:
- Journal of materials chemistry
- Issue:
- Volume 11:Issue 6(2023)
- Issue Display:
- Volume 11, Issue 6 (2023)
- Year:
- 2023
- Volume:
- 11
- Issue:
- 6
- Issue Sort Value:
- 2023-0011-0006-0000
- Page Start:
- 2985
- Page End:
- 2995
- Publication Date:
- 2023-01-24
- Subjects:
- Materials -- Research -- Periodicals
Chemistry, Analytic -- Periodicals
Environmental sciences -- Research -- Periodicals
543.0284 - Journal URLs:
- http://pubs.rsc.org/en/journals/journalissues/ta ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/d2ta07681k ↗
- Languages:
- English
- ISSNs:
- 2050-7488
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5012.205100
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 26024.xml