4.6 Article

Simultaneous optimization of CoIr alloy nanoparticles and 2D graphitic-N doped carbon support in CoIr@CN by Ir doping for enhanced oxygen and hydrogen evolution reactions

Journal

JOURNAL OF MATERIALS CHEMISTRY A
Volume 10, Issue 29, Pages 15543-15553

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/d2ta03496d

Keywords

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Funding

  1. National Natural Science Foundation of China [21902034]
  2. Startup R&D funding from the One-Hundred Young Talents Program of Guangdong University of Technology [220413251]

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This study reports the design of strong metal-support interaction through multiple electronic structure modification, improving the electrocatalytic activity of supported catalysts. A CoIr alloy supported on two dimensional (2D) graphitic-N doped carbon (CoIr@CN) was successfully synthesized through a one-step annealing process, exhibiting reduced Ir loading and enhanced catalytic performance for oxygen evolution reaction (OER) and hydrogen evolution reaction (HER).
Multiple electronic structure modification is propitious for constructing strong metal-support interaction and then improving the electrocatalytic activity of supported catalysts, yet remains a great challenge due to the lack of facile protocols. Herein, we report a CoIr alloy supported on two dimensional (2D) graphitic-N doped carbon (CoIr@CN) through a one-step annealing process from an Ir-doped 2D Co-MOF, which exhibits a remarkably reduced Ir loading (2.69 wt%) and enhanced electrocatalytic activity for oxygen evolution reaction (OER) and hydrogen evolution reaction (HER). Ir plays an essential role of optimizing the properties of metal nanoparticles and simultaneously effecting the calcining process to adjust the N-doping structure, eventually modulating the synergetic effect between alloy nanoparticles and the N-doped carbon support. Owing to the positive effect of such multiple electronic structure optimization, the electron transfer between alloy nanoparticles and N-doped carbon is promoted to enable more moderate adsorption energies of reaction intermediates in both the OER and HER. Impressively, CoIr@CN exhibits a low OER/HER overpotential of 269 mV/70 mV to achieve a current density of 10 mA cm(-2) in 1.0 M KOH, and 25 mV in 0.5 M H2SO4 for HER, as well as a negligible decay of catalytic activity after long-term stability measurements for OER/HER. This study offers an effective way for designing strong metal-support interaction through multiple electronic structure modification, which effectively improves the OER/HER performance of supported catalysts.

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