About

Log in?

DTU users get better search results including licensed content and discounts on order fees.

Anyone can log in and get personalized features such as favorites, tags and feeds.

Log in as DTU user Log in as non-DTU user No thanks

DTU Findit

Journal article

Gd-induced electronic structure engineering of a NiFe-layered double hydroxide for efficient oxygen evolution

From

Nanjing Normal University1

Department of Physics, Technical University of Denmark2

Catalysis Theory Center, Department of Physics, Technical University of Denmark3

Indiana University Bloomington4

Nanyang Technological University5

Rare earth (RE) elements have drawn increased attention recently as an effective promoter in electrocatalysis because of their partially filled 4f orbitals. Herein, a new type of RE hybrid electrocatalyst, consisting of a gadolinium-doped hierarchal NiFe-layered double hydroxidein situgrown on carbon cloth (Gd-NiFe-LDH@CC), is designed and developedviaa facile one-step hydrothermal approach.

The Gd doping regulates the electronic structure of NiFe-LDH and increases the number of oxygen vacancies, thus tuning the adsorption energies of oxygen intermediate species (e.g.HOO*). With the presence of Gd species, Gd-NiFe-LDH@CC exhibits superior electrocatalytic activity for the OER in an alkaline medium, which requires an overpotential of only 210 mV to afford 10 mA cm−2current density, better than that of NiFe-LDH@CC (250 mV) and commercial RuO2(298 mV).

The robust electrocatalytic stability and satisfactory selectivity (nearly 100% Faraday efficiency) of Gd-NiFe-LDH@CC for the OER are also demonstrated. We ascribe such outstanding OER performance of Gd-NiFe-LDH@CC to the optimized electronic structure, rich oxygen vacancies and hierarchal porous morphology.

Theoretical calculation further demonstrates that the electronic disturbance caused by Gd doping enhances the activity of Ni sites, resulting in stronger binding strength of HOO* at the Ni sites during the OER.

Language: English
Year: 2021
Pages: 2999-3006
ISSN: 20507496 and 20507488
Types: Journal article
DOI: 10.1039/d0ta10740a
ORCIDs: 0000-0003-0411-645X , 0000-0001-6300-0866 and 0000-0003-4468-0821

DTU users get better search results including licensed content and discounts on order fees.

Log in as DTU user

Access

Analysis