Journal
CHEMELECTROCHEM
Volume 8, Issue 6, Pages 1204-1210Publisher
WILEY-V C H VERLAG GMBH
DOI: 10.1002/celc.202100147
Keywords
chlorine evolution reaction; IrO2; doping; density functional theory
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By doping Nd into IrO2 catalysts, the CER performance can be significantly improved while reducing the usage of Ir, demonstrating higher mass activity and stability.
The chlorine evolution reaction (CER) is extensively used in disinfection, chlorine products, and water treatment. However, CER catalysts based on noble metals are expensive, limiting their industrial application. For the purpose of enhancing the CER performance with low usage of Ir, Nd-doped IrO2 electrocatalysts supported on Ti plates were fabricated by using the sol-gel method. The optimal Ti/Ir0.8Nd0.2Ox electrode exhibited excellent CER performance with a low potential of 1.52 V vs. RHE at 100 mA cm(-2) and a great stability of over 210 h in 5 M NaCl solution. Notably, the mass activity of Ti/Ir0.8Nd0.2Ox (96.5 A g(Ir)(-1) at 1.5 V vs RHE) was twice as high as that of Ti/IrO2, which was the highest among noble metal electrodes reported. Density functional theory calculations indicated that the doping of Nd could clearly decrease the loss of Gibbs free energy for the rate-determining step (desorption of chlorine).
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