Carbon impurity-free, novel Mn, N co-doped porous Mo2C nanorods for an efficient and stable hydrogen evolution reaction. Issue 9 (6th August 2019)
- Record Type:
- Journal Article
- Title:
- Carbon impurity-free, novel Mn, N co-doped porous Mo2C nanorods for an efficient and stable hydrogen evolution reaction. Issue 9 (6th August 2019)
- Main Title:
- Carbon impurity-free, novel Mn, N co-doped porous Mo2C nanorods for an efficient and stable hydrogen evolution reaction
- Authors:
- Zhou, Yajun
Xu, Jieyu
Lian, Cheng
Ge, Lin
Zhang, Lingxia
Li, Liang
Li, Yunheng
Wang, Min
Liu, Honglai
Li, Yongsheng - Abstract:
- Abstract : Carbon impurity-free, novel Mn, N co-doped porous Mo2 C nanorods reduce the hydrogen adsorption energy, functioning as efficient HER electrocatalysts. Abstract : Heteroatom doping is an effective way to modulate the electronic configuration and optimize the electroactivity over a series of electrocatalytic materials. Here we report novel kinds of Mn, N co-doped porous Mo2 C nanorods for the hydrogen evolution reaction (HER) in acidic solution, which are facilely fabricated based on Mn-modified MoO x -amine precursors. The obtained porous, monocrystalline nanorods without carbon impurities could not only provide abundant catalytic sites, but also facilitate electrolyte penetration and hydrogen release. Furthermore, the fine-tuned electronic structure of Mo2 C nanorods with Mn, N dopants could produce more available active sites and reduce the hydrogen adsorption energy (Δ G H* ). As a result, the optimized Mn, N co-doped Mo2 C nanorods exhibit high HER activity with a low overpotential ( η 10 = 163 mV), a small Tafel slope (66 mV dec −1 ), and excellent long-term stability in acidic electrolyte. EPR and DFT calculations confirm that the high performance originates from new active sites (Mn site), a low charge-transfer resistance and an optimized adsorption–desorption behavior after Mn, N co-doping. This work may provide a new pathway to design and explore efficient non-noble metal water-splitting electrocatalysts via electronic engineering of their compositions andAbstract : Carbon impurity-free, novel Mn, N co-doped porous Mo2 C nanorods reduce the hydrogen adsorption energy, functioning as efficient HER electrocatalysts. Abstract : Heteroatom doping is an effective way to modulate the electronic configuration and optimize the electroactivity over a series of electrocatalytic materials. Here we report novel kinds of Mn, N co-doped porous Mo2 C nanorods for the hydrogen evolution reaction (HER) in acidic solution, which are facilely fabricated based on Mn-modified MoO x -amine precursors. The obtained porous, monocrystalline nanorods without carbon impurities could not only provide abundant catalytic sites, but also facilitate electrolyte penetration and hydrogen release. Furthermore, the fine-tuned electronic structure of Mo2 C nanorods with Mn, N dopants could produce more available active sites and reduce the hydrogen adsorption energy (Δ G H* ). As a result, the optimized Mn, N co-doped Mo2 C nanorods exhibit high HER activity with a low overpotential ( η 10 = 163 mV), a small Tafel slope (66 mV dec −1 ), and excellent long-term stability in acidic electrolyte. EPR and DFT calculations confirm that the high performance originates from new active sites (Mn site), a low charge-transfer resistance and an optimized adsorption–desorption behavior after Mn, N co-doping. This work may provide a new pathway to design and explore efficient non-noble metal water-splitting electrocatalysts via electronic engineering of their compositions and nanostructures. … (more)
- Is Part Of:
- Inorganic chemistry frontiers. Volume 6:Issue 9(2019)
- Journal:
- Inorganic chemistry frontiers
- Issue:
- Volume 6:Issue 9(2019)
- Issue Display:
- Volume 6, Issue 9 (2019)
- Year:
- 2019
- Volume:
- 6
- Issue:
- 9
- Issue Sort Value:
- 2019-0006-0009-0000
- Page Start:
- 2464
- Page End:
- 2471
- Publication Date:
- 2019-08-06
- Subjects:
- Chemistry, Inorganic -- Periodicals
546.05 - Journal URLs:
- http://www.rsc.org/ ↗
http://pubs.rsc.org/en/journals/journalissues/qi#!issues ↗ - DOI:
- 10.1039/c9qi00676a ↗
- Languages:
- English
- ISSNs:
- 2052-1553
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 4515.872000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 11651.xml