Login / Signup

Co-doping regulation on Ni-based electrocatalysts to adjust the selectivity of oxygen reduction reaction for Zn-air batteries and H 2 O 2 production.

Songhan HuKai WangXinxin XuQiang Wang
Published in: Dalton transactions (Cambridge, England : 2003) (2024)
Although Ni-based materials are widely used as electrocatalysts, it remains necessary to further explore their selectivity towards the four- or two-electron oxygen reduction reaction (ORR). Herein, it is proposed to synthesize NiO@NCNTs (NCNTs = N-doped carbon nanotubes) using a metal-organic framework (MOF), [Ni(BZIDA)(H 2 O)] n (NiMOF, BZIDA = benzimidazole-5,6-dicarboxylic acid), as a precursor after calcination with dicyandiamide (DCDA). Regarding NiO@NCNTs, small NiO particles are distributed in NCNTs derived from DCDA homogeneously. NiO@NCNTs act as a typical two-electron electrocatalyst. The H 2 O 2 production rate of NiO@NCNTs reaches 0.5 mol g -1 h -1 at 0.46 V ( vs. RHE). After the doping of Co 2+ in NiMOF, Co/NiO@NCNTs were synthesized using a similar method, with the four-electron character shown in ORR. A Zn-air battery was assembled by applying Co/NiO@NCNTs as the cathode material. When discharge occurs at 5 and 10 mA cm -2 , its specific capacitance reaches 779.3 and 832.2 mA h g -1 with an energy density of 928.6 and 948.5 W h kg -1 , respectively. Theoretical calculations suggest a variation in ORR selectivity between NiO@NCNTs and Co/NiO@NCNTs, which results from their different interactions with OOH*. This study demonstrates the effect of the structure on ORR selectivity for Ni-based electrocatalysts.
Keyphrases
  • metal organic framework
  • carbon nanotubes
  • heavy metals
  • transition metal
  • solar cells
  • molecular dynamics simulations
  • risk assessment
  • molecular docking