Single atom tungsten doped ultrathin α-Ni(OH)2 for enhanced electrocatalytic water oxidation
Junqing Yan,
Lingqiao Kong,
Yujin Ji,
Jai White,
Youyong Li (),
Jing Zhang,
Pengfei An,
Shengzhong Liu (),
Shuit-Tong Lee and
Tianyi Ma ()
Additional contact information
Junqing Yan: Shaanxi Normal University
Lingqiao Kong: Shaanxi Normal University
Yujin Ji: Soochow University
Jai White: University of Newcastle
Youyong Li: Soochow University
Jing Zhang: Chinese Academy of Sciences
Pengfei An: Chinese Academy of Sciences
Shengzhong Liu: Shaanxi Normal University
Shuit-Tong Lee: Soochow University
Tianyi Ma: University of Newcastle
Nature Communications, 2019, vol. 10, issue 1, 1-10
Abstract:
Abstract Electrocatalytic water oxidation is a rate-determining step in the water splitting reaction. Here, we report one single atom W6+ doped Ni(OH)2 nanosheet sample (w-Ni(OH)2) with an outstanding oxygen evolution reaction (OER) performance that is, in a 1 M KOH medium, an overpotential of 237 mV is obtained reaching a current density of 10 mA/cm2. Moreover, at high current density of 80 mA/cm2, the overpotential value is 267 mV. The corresponding Tafel slope is measured to be 33 mV/dec. The d0 W6+ atom with a low spin-state has more outermost vacant orbitals, resulting in more water and OH− groups being adsorbed on the exposed W sites of the Ni(OH)2 nanosheet. Density functional theory (DFT) calculations confirm that the O radical and O-O coupling are both generated at the same site of W6+. This work demonstrates that W6+ doping can promote the electrocatalytic water oxidation activity of Ni(OH)2 with the highest performance.
Date: 2019
References: Add references at CitEc
Citations: View citations in EconPapers (7)
Downloads: (external link)
https://www.nature.com/articles/s41467-019-09845-z Abstract (text/html)
Related works:
This item may be available elsewhere in EconPapers: Search for items with the same title.
Export reference: BibTeX
RIS (EndNote, ProCite, RefMan)
HTML/Text
Persistent link: https://EconPapers.repec.org/RePEc:nat:natcom:v:10:y:2019:i:1:d:10.1038_s41467-019-09845-z
Ordering information: This journal article can be ordered from
https://www.nature.com/ncomms/
DOI: 10.1038/s41467-019-09845-z
Access Statistics for this article
Nature Communications is currently edited by Nathalie Le Bot, Enda Bergin and Fiona Gillespie
More articles in Nature Communications from Nature
Bibliographic data for series maintained by Sonal Shukla () and Springer Nature Abstracting and Indexing ().