Roles of the self-reconstruction layer in the catalytic stability of a NiFeP catalyst during the oxygen evolution reaction. Issue 1 (6th December 2022)
- Record Type:
- Journal Article
- Title:
- Roles of the self-reconstruction layer in the catalytic stability of a NiFeP catalyst during the oxygen evolution reaction. Issue 1 (6th December 2022)
- Main Title:
- Roles of the self-reconstruction layer in the catalytic stability of a NiFeP catalyst during the oxygen evolution reaction
- Authors:
- Zhao, Fuzhen
Mao, Xinyu
Zheng, Xin
Liu, Huicong
Zhu, Liqun
Li, Weiping
Wang, Ze
Chen, Haining - Abstract:
- Abstract : Due to the synergistic effect between NiFeP and the self-reconstruction layer, the stability of a NiFeP catalyst during the oxygen evolution reaction is determined by the surface-adhesion O2 bubbles rather than atomic dissolution. Abstract : The roles of the self-reconstruction NiFe–OOH–P layer in the catalytic stability of the NiFeP catalyst during the oxygen evolution reaction (OER), especially in terms of the atomic dissolution and the adsorption behavior of formed bubbles, are seldom studied. Herein, through a systematic study on crystalline (Ni1− x Fe x )3 P, a NiFeP catalyst, it was revealed that although Fe & P dissolve rapidly from the self-reconstruction layer, the self-reconstruction layer could suppress Fe & P dissolution from (Ni1− x Fe x )3 P, tending to form a stable (Ni1− x Fe x )3 P–O/NiOOH heterostructure. DFT simulations demonstrate that the synergistic effect between Fe–O of (Ni1− x Fe x )3 P–O and NiOOH could still efficiently catalyze the OER. Thus, atomic dissolution does not obviously lower the activity. However, the self-reconstruction layer would change the original interface and increase the surface adsorbed bubbles, which determines the degradation of OER performance. Eventually, a superaerophobic heterostructure of (Ni1− x Fe x )3 P/NiFe–OH–P is prepared by changing reconstruction conditions. The catalyst not only exhibits excellent activity with an overpotential of 233 mV at 10 mA cm −2, but also obtains dramatically enhanced stabilityAbstract : Due to the synergistic effect between NiFeP and the self-reconstruction layer, the stability of a NiFeP catalyst during the oxygen evolution reaction is determined by the surface-adhesion O2 bubbles rather than atomic dissolution. Abstract : The roles of the self-reconstruction NiFe–OOH–P layer in the catalytic stability of the NiFeP catalyst during the oxygen evolution reaction (OER), especially in terms of the atomic dissolution and the adsorption behavior of formed bubbles, are seldom studied. Herein, through a systematic study on crystalline (Ni1− x Fe x )3 P, a NiFeP catalyst, it was revealed that although Fe & P dissolve rapidly from the self-reconstruction layer, the self-reconstruction layer could suppress Fe & P dissolution from (Ni1− x Fe x )3 P, tending to form a stable (Ni1− x Fe x )3 P–O/NiOOH heterostructure. DFT simulations demonstrate that the synergistic effect between Fe–O of (Ni1− x Fe x )3 P–O and NiOOH could still efficiently catalyze the OER. Thus, atomic dissolution does not obviously lower the activity. However, the self-reconstruction layer would change the original interface and increase the surface adsorbed bubbles, which determines the degradation of OER performance. Eventually, a superaerophobic heterostructure of (Ni1− x Fe x )3 P/NiFe–OH–P is prepared by changing reconstruction conditions. The catalyst not only exhibits excellent activity with an overpotential of 233 mV at 10 mA cm −2, but also obtains dramatically enhanced stability with a decrease in current density from 120 to 100 mA cm −2 after a 120 h potentiostatic test. … (more)
- Is Part Of:
- Journal of materials chemistry. Volume 11:Issue 1(2023)
- Journal:
- Journal of materials chemistry
- Issue:
- Volume 11:Issue 1(2023)
- Issue Display:
- Volume 11, Issue 1 (2023)
- Year:
- 2023
- Volume:
- 11
- Issue:
- 1
- Issue Sort Value:
- 2023-0011-0001-0000
- Page Start:
- 276
- Page End:
- 286
- Publication Date:
- 2022-12-06
- 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/d2ta06514b ↗
- 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:
- 26014.xml