3D Ni and Co redox-active metal–organic frameworks based on ferrocenyl diphosphinate and 4, 4′-bipyridine ligands as efficient electrocatalysts for the hydrogen evolution reaction. Issue 9 (19th February 2020)
- Record Type:
- Journal Article
- Title:
- 3D Ni and Co redox-active metal–organic frameworks based on ferrocenyl diphosphinate and 4, 4′-bipyridine ligands as efficient electrocatalysts for the hydrogen evolution reaction. Issue 9 (19th February 2020)
- Main Title:
- 3D Ni and Co redox-active metal–organic frameworks based on ferrocenyl diphosphinate and 4, 4′-bipyridine ligands as efficient electrocatalysts for the hydrogen evolution reaction
- Authors:
- Khrizanforova, Vera
Shekurov, Ruslan
Miluykov, Vasily
Khrizanforov, Mikhail
Bon, Volodymyr
Kaskel, Stefan
Gubaidullin, Aidar
Sinyashin, Oleg
Budnikova, Yulia - Abstract:
- Abstract : New 3D Ni and Co redox-active metal–organic frameworks based on ferrocenyl diphosphinate and 4, 4′-bipyridine ligands have been explored as efficient electrocatalysts with superior long-term durability in a hydrogen evolution reaction. Abstract : New 3D Ni and Co redox-active metal–organic frameworks based on ferrocenyl diphosphinate and 4, 4′-bipyridine ligands have been synthesized, characterized by single crystal X-ray diffraction and spectroscopic techniques and explored as stable electrocatalysts capable of meeting two important parameters: the overpotential and Tafel slope (TS) in the hydrogen evolution reaction (HER). The electrochemical studies suggest that the reaction kinetics of a Ni-MOF (1 ) catalyst is more favorable than that of a Co-MOF (2 ) catalyst. Particularly, Ni-MOF exhibits better HER performance with an overpotential of 350 mV at a current density of 10 mA cm −2, a small TS of 60 mV dec −1 and superior long-term durability (of up to 10 000 cycles), ranking it among the most active non-noble metal-based molecular electrocatalysts. The introduction of a 4, 4′-bpy linker in 2 significantly changes the catalytic properties in an organic or aqueous environment compared to 1D cobalt polymers based on ferrocenyl diphosphinate. For Co-MOF 2, there is a significant decrease in the overvoltage by ∼440 mV in comparison with the 1D Co polymer in an organic medium and by 50 mV in an aqueous medium. The TS changes from 120 to 65 mV dec −1 when moving fromAbstract : New 3D Ni and Co redox-active metal–organic frameworks based on ferrocenyl diphosphinate and 4, 4′-bipyridine ligands have been explored as efficient electrocatalysts with superior long-term durability in a hydrogen evolution reaction. Abstract : New 3D Ni and Co redox-active metal–organic frameworks based on ferrocenyl diphosphinate and 4, 4′-bipyridine ligands have been synthesized, characterized by single crystal X-ray diffraction and spectroscopic techniques and explored as stable electrocatalysts capable of meeting two important parameters: the overpotential and Tafel slope (TS) in the hydrogen evolution reaction (HER). The electrochemical studies suggest that the reaction kinetics of a Ni-MOF (1 ) catalyst is more favorable than that of a Co-MOF (2 ) catalyst. Particularly, Ni-MOF exhibits better HER performance with an overpotential of 350 mV at a current density of 10 mA cm −2, a small TS of 60 mV dec −1 and superior long-term durability (of up to 10 000 cycles), ranking it among the most active non-noble metal-based molecular electrocatalysts. The introduction of a 4, 4′-bpy linker in 2 significantly changes the catalytic properties in an organic or aqueous environment compared to 1D cobalt polymers based on ferrocenyl diphosphinate. For Co-MOF 2, there is a significant decrease in the overvoltage by ∼440 mV in comparison with the 1D Co polymer in an organic medium and by 50 mV in an aqueous medium. The TS changes from 120 to 65 mV dec −1 when moving from 1D Cofcd H p to a 3D structure of 2 . Thus, a 4, 4′-bpy linker reduces the overvoltage and gives more favorable HER kinetics (lower TS). These results provide important guidelines for the rational design of non-precious metal electrocatalysts. … (more)
- Is Part Of:
- Dalton transactions. Volume 49:Issue 9(2020)
- Journal:
- Dalton transactions
- Issue:
- Volume 49:Issue 9(2020)
- Issue Display:
- Volume 49, Issue 9 (2020)
- Year:
- 2020
- Volume:
- 49
- Issue:
- 9
- Issue Sort Value:
- 2020-0049-0009-0000
- Page Start:
- 2794
- Page End:
- 2802
- Publication Date:
- 2020-02-19
- Subjects:
- Chemistry, Inorganic -- Periodicals
Chemistry, Physical and theoretical -- Periodicals
Chemistry, Inorganic -- Periodicals
546.05 - Journal URLs:
- http://pubs.rsc.org/en/journals/journalissues/dt#!issueid=dt043040&type=current&issnprint=1477-9226 ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/c9dt04834k ↗
- Languages:
- English
- ISSNs:
- 1477-9226
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3517.830000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 12944.xml