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Underpotential deposition(UPD) of Cu on an Au electrode followed by redox replacement reaction(RRR) of CuUPD with a Pt source(H2PtCl6 or K2PtCl4) yielded Au-supported Pt adlayers(for short,Pt(CuUPD-Pt4+)n/Au for H2PtCl6,or Pt(CuUPD-Pt2+)n/Au for K2PtCl4,where n denotes the number of UPD-redox replacement cycles).The electrochemical quartz crystal microbalance(EQCM) technique was used for the first time to quantitatively study the fabricated electrodes and estimate their mass-normalized specific electrocatalytic activity(SECA) for methanol oxidation in alkaline solution.In comparison with Pt(CuUPD-Pt2+)n/Au,Pt(CuUPD-Pt4+)n/Au exhibited a higher electrocatalytic activity,and the maximum SECA was obtained to be as high as 35.7 mA ?g?1 at Pt(CuUPD-Pt4+)3/Au.The layer-by-layer architecture of Pt atoms on Au is briefly discussed based on the EQCM-revealed redox replacement efficiency,and the calculated distribution percentages of bare Au sites agree with the experimental results deduced from the charge under the AuOx-reduction peaks.The EQCM is highly recommended as an efficient technique to quantitatively examine various electrode-supported catalyst adlayers,and the highly efficient catalyst adlayers of noble metals are promising in electrocatalysis relevant to biological,energy and environmental sciences and technologies.
Underpotential deposition (UPD) of Cu on an Au electrode followed by redox replacement reaction (RRR) of CuUPD with a Pt source (H2PtCl6 or K2PtCl4) yielded Au-supported Pt adlayers (for short, Pt (CuUPD- Pt4 +) n / Au for H2PtCl6, or Pt (CuUPD-Pt2 +) n / Au for K2PtCl4 where n denotes the number of UPD-redox replacement cycles). Electrochemical quartz crystal microbalance (EQCM) technique was used for the first time to quantitatively study the fabricated electrodes and estimate their mass-normalized specific electrocatalytic activity (SECA) for methanol oxidation in alkaline solution.In comparison with Pt (CuUPD-Pt2 +) n / Au, Pt (CuUPD- Pt4 +) n / Au exhibited a higher electrocatalytic activity, and the maximum SECA was at as high as 35.7 mA • g • 1 at Pt (CuUPD-Pt4 +) 3 / Au. The layer-by-layer architecture of Pt atoms on Au is briefly based on the EQCM-revealed redox replacement efficiency, and the calculated distribution percentages of bare Au sites agree with the experimental results deduced from the charge under the AuOx-reduction peaks.The EQCM is highly recommended as an efficient technique to quantitatively examine various electrode-supported catalyst adlayers, and the highly efficient catalyst adlayers of noble metals are promising in electrocatalysis relevant to biological, energy and environmental sciences and technologies.