2008
DOI: 10.1016/j.jpowsour.2008.05.087
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Physical and electrochemical characterizations of PtPb/C catalyst prepared by pyrolysis of platinum(II) and lead(II) acetylacetonate

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Cited by 42 publications
(30 citation statements)
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“…An interesting comparison of the catalytic activity of disordered PtRu (SA D PtRu ) with that of ordered PtPb (SA O PtPb ) for MOR and FAOR was carried out by Huang et al and Liu et al From the results of Huang et al, the value of the (SA O PtPb /SA D PtRu ) FAOR /(SA O PtPb /SA D PtRu ) MOR ratio obtained by the values of SA O PtPb /SA D PtRu for FAOR and MOR at the same potential (‐0.1 V vs Hg/Hg 2 SO 4 for the FAOR and 0.1 V vs Hg/Hg 2 SO 4 for the MOR) was 1.79. The value of the (MA O PtPb /MA D PtRu ) FAOR /(MA O PtPb /MA D PtRu ) MOR ratio from the averaged values of MA O PtPb /MA D PtRu for FAOR and MOR by the data of Liu et al was 1.74: considering that the value of ECSA is the same for FAOR and MOR; the (MA O PtPb /MA D PtRu ) FAOR /(MA O PtPb /MA D PtRu ) MOR ratio is same as the (SA O PtPb /SA D PtRu ) FAOR /(SA O PtPb /SA D PtRu ) MOR ratio, and both the values of (SA O PtPb /SA D PtRu ) FAOR /(SA O PtPb /SA D PtRu ) MOR ratio were in excellent agreement with the averaged (SA O /SA D ) FAOR /(SA O /SA D ) MOR values of ordered/disordered catalysts previously reported (1.71). Thus, it is reasonable to suppose that the higher (SA O PtPb /SA D PtRu ) FAOR ratio than the (SA O PtPb /SA D PtRu ) MOR ratio should be due to a structural effect (intermetallic vs alloy) rather than to a chemical effect (PtPb vs PtRu).…”
Section: Activity Of Binary Pt–m (M = 1st and 2nd Row Transition Metamentioning
confidence: 99%
“…An interesting comparison of the catalytic activity of disordered PtRu (SA D PtRu ) with that of ordered PtPb (SA O PtPb ) for MOR and FAOR was carried out by Huang et al and Liu et al From the results of Huang et al, the value of the (SA O PtPb /SA D PtRu ) FAOR /(SA O PtPb /SA D PtRu ) MOR ratio obtained by the values of SA O PtPb /SA D PtRu for FAOR and MOR at the same potential (‐0.1 V vs Hg/Hg 2 SO 4 for the FAOR and 0.1 V vs Hg/Hg 2 SO 4 for the MOR) was 1.79. The value of the (MA O PtPb /MA D PtRu ) FAOR /(MA O PtPb /MA D PtRu ) MOR ratio from the averaged values of MA O PtPb /MA D PtRu for FAOR and MOR by the data of Liu et al was 1.74: considering that the value of ECSA is the same for FAOR and MOR; the (MA O PtPb /MA D PtRu ) FAOR /(MA O PtPb /MA D PtRu ) MOR ratio is same as the (SA O PtPb /SA D PtRu ) FAOR /(SA O PtPb /SA D PtRu ) MOR ratio, and both the values of (SA O PtPb /SA D PtRu ) FAOR /(SA O PtPb /SA D PtRu ) MOR ratio were in excellent agreement with the averaged (SA O /SA D ) FAOR /(SA O /SA D ) MOR values of ordered/disordered catalysts previously reported (1.71). Thus, it is reasonable to suppose that the higher (SA O PtPb /SA D PtRu ) FAOR ratio than the (SA O PtPb /SA D PtRu ) MOR ratio should be due to a structural effect (intermetallic vs alloy) rather than to a chemical effect (PtPb vs PtRu).…”
Section: Activity Of Binary Pt–m (M = 1st and 2nd Row Transition Metamentioning
confidence: 99%
“…Among these elements, Pb seems to have stronger promoting effects. A number of studies have devoted to enhanced electrooxidation of small organic molecules by Pb addition [21][22][23][24][25]. The promoting effects of Pb in the Pd-based catalysts can be attributed to the geometric effect, the electronic effect and the bifunctional mechanism [21].…”
Section: Introductionmentioning
confidence: 99%
“…A number of Pt alloy, inter-metallic, or surface modified catalysts (Pt/Ru, Pt/Pd, Pt/Au, and Pt/Pb), have been reported as the anode catalysts for DFAFCs, and these catalysts have shown better cell performance than pure platinum [6,7,14,19,20,33]. As well, a few Pd-based bi-metallic catalysts (Pd/Au, Pd/P, and Pd/Pt) have also been demonstrated in DFAFC systems, and have shown better cell performance than pure palladium [15,26,27].…”
Section: Introductionmentioning
confidence: 99%