Revealing the activity of Co3Mo3N and Co3Mo3N0.5 as electrocatalysts for the hydrogen evolution reaction. Issue 2 (17th December 2021)
- Record Type:
- Journal Article
- Title:
- Revealing the activity of Co3Mo3N and Co3Mo3N0.5 as electrocatalysts for the hydrogen evolution reaction. Issue 2 (17th December 2021)
- Main Title:
- Revealing the activity of Co3Mo3N and Co3Mo3N0.5 as electrocatalysts for the hydrogen evolution reaction
- Authors:
- Sun, Youyi
Wang, Lewen
Guselnikova, Olga
Semyonov, Oleg
Fraser, James
Zhou, Yecheng
López, Núria
Ganin, Alexey Y. - Abstract:
- Abstract : The ability of Co3 Mo3 N to act as catalyst for the hydrogen evolution reaction at low overpotential is demonstrated. The identity of catalytic sites is established using DFT simulations. Abstract : The hydrogen evolution reaction (HER) from water is governed by the electrocatalysts used. Multiple factors such as crystal structure, composition and morphology dictate the final catalytic performance. However, as multicomponent materials are developed to replace noble metals in the HER, it has become increasingly difficult to identify intrinsically active materials. Hence, there is an imperative for phase-pure catalysts to be synthesized and tested without obscuring contributions from impurities or substrates. Herein, we demonstrate that phase-pure, unsupported Co3 Mo3 N achieves a competitively low overpotential (OVP) of 108 ± 8 mV at 10 mA cm −2 in 0.5 M H2 SO4 . Density functional theory (DFT) reveals weakly binding metal sites as the catalytic centres for the HER in the nitride. Remarkably, the N-deficient Co3 Mo3 N0.5 shows similar electrochemical properties but has limited chemical stability under cathodic bias. Thus, even though nitrogen sites play only a minor role in catalytic performance, their occupancy is crucial for the stability of nitride catalysts in the corrosive electrolyte. The composite of Co3 Mo3 N on Ni-foam sustains 10 ± 1 mA cm −2 at an applied potential of just 20 mV over extended time, highlighting the utility of nitrides for the futureAbstract : The ability of Co3 Mo3 N to act as catalyst for the hydrogen evolution reaction at low overpotential is demonstrated. The identity of catalytic sites is established using DFT simulations. Abstract : The hydrogen evolution reaction (HER) from water is governed by the electrocatalysts used. Multiple factors such as crystal structure, composition and morphology dictate the final catalytic performance. However, as multicomponent materials are developed to replace noble metals in the HER, it has become increasingly difficult to identify intrinsically active materials. Hence, there is an imperative for phase-pure catalysts to be synthesized and tested without obscuring contributions from impurities or substrates. Herein, we demonstrate that phase-pure, unsupported Co3 Mo3 N achieves a competitively low overpotential (OVP) of 108 ± 8 mV at 10 mA cm −2 in 0.5 M H2 SO4 . Density functional theory (DFT) reveals weakly binding metal sites as the catalytic centres for the HER in the nitride. Remarkably, the N-deficient Co3 Mo3 N0.5 shows similar electrochemical properties but has limited chemical stability under cathodic bias. Thus, even though nitrogen sites play only a minor role in catalytic performance, their occupancy is crucial for the stability of nitride catalysts in the corrosive electrolyte. The composite of Co3 Mo3 N on Ni-foam sustains 10 ± 1 mA cm −2 at an applied potential of just 20 mV over extended time, highlighting the utility of nitrides for the future design of stable and active HER catalytic systems. … (more)
- Is Part Of:
- Journal of materials chemistry. Volume 10:Issue 2(2022)
- Journal:
- Journal of materials chemistry
- Issue:
- Volume 10:Issue 2(2022)
- Issue Display:
- Volume 10, Issue 2 (2022)
- Year:
- 2022
- Volume:
- 10
- Issue:
- 2
- Issue Sort Value:
- 2022-0010-0002-0000
- Page Start:
- 855
- Page End:
- 861
- Publication Date:
- 2021-12-17
- 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/d1ta08389a ↗
- 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:
- 21453.xml