Methanol oxidation at platinum electrodes in alkaline solution: comparison between supported catalysts and model system
Samo za registrovane korisnike
2004
Članak u časopisu (Objavljena verzija)
,
Elsevier
Metapodaci
Prikaz svih podataka o dokumentuApstrakt
Methanol oxidation was studied in 0.1 M NaOH at supported Pt electrodes, and compared with the single crystal Pt electrodes, Pt(1 1 1), Pt(1 1 0) and Pt(3 3 2), chosen as model systems, and with a polycrystalline Pt electrode. The supported Pt electrodes were obtained by chemical (Pt–C/GC) and electrochemical (Pt/GC) deposition of the catalyst layer on glassy carbon resulting in the same metal loading of 20 μgPt cm−2. Using STM in air, the average particle size distributions, 3–6 nm at Pt–C/GC and 4–32 nm at Pt/GC were determined. Both supported Pt catalysts were less active than polycrystalline Pt. Negligible differences in the kinetics observed between Pt–C/GC and Pt(1 1 0) and also Pt/GC and Pt(1 1 1) suggested that the activities of supported Pt electrodes could be correlated with the activities of single crystal Pt electrodes oriented as the sites dominating in the Pt particles in catalyst deposits. The electrocatalytic activities of the electrodes studied increase in the sequence...: Pt(3 3 2) > polycrystalline Pt > Pt–C/GC ∼ Pt(1 1 0) > Pt/GC ∼ Pt(1 1 1). On the basis of diagnostic criteria obtained, the chemical reaction between HCOad and OHad giving formate was proposed as the rate limiting step in methanol oxidation.
Ključne reči:
Supported Pt electrodes / Pt polycrystalline / Single crystal Pt electrodes / STM / Reaction mechanismIzvor:
Journal of Electroanalytical Chemistry, 2004, 572, 1, 119-128Izdavač:
- Elsevier
Finansiranje / projekti:
- Ministry of Science, Technology and Development of Serbia, Contract No. H-1796
DOI: 10.1016/j.jelechem.2004.06.007
ISSN: 1572-6657
WoS: 000224287500013
Scopus: 2-s2.0-4544244245
Institucija/grupa
IHTMTY - JOUR AU - Tripković, Amalija AU - Popović, Ksenija AU - Lović, Jelena AU - Jovanović, Vladislava M. AU - Kowal, Andrzej PY - 2004 UR - https://cer.ihtm.bg.ac.rs/handle/123456789/2884 AB - Methanol oxidation was studied in 0.1 M NaOH at supported Pt electrodes, and compared with the single crystal Pt electrodes, Pt(1 1 1), Pt(1 1 0) and Pt(3 3 2), chosen as model systems, and with a polycrystalline Pt electrode. The supported Pt electrodes were obtained by chemical (Pt–C/GC) and electrochemical (Pt/GC) deposition of the catalyst layer on glassy carbon resulting in the same metal loading of 20 μgPt cm−2. Using STM in air, the average particle size distributions, 3–6 nm at Pt–C/GC and 4–32 nm at Pt/GC were determined. Both supported Pt catalysts were less active than polycrystalline Pt. Negligible differences in the kinetics observed between Pt–C/GC and Pt(1 1 0) and also Pt/GC and Pt(1 1 1) suggested that the activities of supported Pt electrodes could be correlated with the activities of single crystal Pt electrodes oriented as the sites dominating in the Pt particles in catalyst deposits. The electrocatalytic activities of the electrodes studied increase in the sequence: Pt(3 3 2) > polycrystalline Pt > Pt–C/GC ∼ Pt(1 1 0) > Pt/GC ∼ Pt(1 1 1). On the basis of diagnostic criteria obtained, the chemical reaction between HCOad and OHad giving formate was proposed as the rate limiting step in methanol oxidation. PB - Elsevier T2 - Journal of Electroanalytical Chemistry T1 - Methanol oxidation at platinum electrodes in alkaline solution: comparison between supported catalysts and model system VL - 572 IS - 1 SP - 119 EP - 128 DO - 10.1016/j.jelechem.2004.06.007 ER -
@article{ author = "Tripković, Amalija and Popović, Ksenija and Lović, Jelena and Jovanović, Vladislava M. and Kowal, Andrzej", year = "2004", abstract = "Methanol oxidation was studied in 0.1 M NaOH at supported Pt electrodes, and compared with the single crystal Pt electrodes, Pt(1 1 1), Pt(1 1 0) and Pt(3 3 2), chosen as model systems, and with a polycrystalline Pt electrode. The supported Pt electrodes were obtained by chemical (Pt–C/GC) and electrochemical (Pt/GC) deposition of the catalyst layer on glassy carbon resulting in the same metal loading of 20 μgPt cm−2. Using STM in air, the average particle size distributions, 3–6 nm at Pt–C/GC and 4–32 nm at Pt/GC were determined. Both supported Pt catalysts were less active than polycrystalline Pt. Negligible differences in the kinetics observed between Pt–C/GC and Pt(1 1 0) and also Pt/GC and Pt(1 1 1) suggested that the activities of supported Pt electrodes could be correlated with the activities of single crystal Pt electrodes oriented as the sites dominating in the Pt particles in catalyst deposits. The electrocatalytic activities of the electrodes studied increase in the sequence: Pt(3 3 2) > polycrystalline Pt > Pt–C/GC ∼ Pt(1 1 0) > Pt/GC ∼ Pt(1 1 1). On the basis of diagnostic criteria obtained, the chemical reaction between HCOad and OHad giving formate was proposed as the rate limiting step in methanol oxidation.", publisher = "Elsevier", journal = "Journal of Electroanalytical Chemistry", title = "Methanol oxidation at platinum electrodes in alkaline solution: comparison between supported catalysts and model system", volume = "572", number = "1", pages = "119-128", doi = "10.1016/j.jelechem.2004.06.007" }
Tripković, A., Popović, K., Lović, J., Jovanović, V. M.,& Kowal, A.. (2004). Methanol oxidation at platinum electrodes in alkaline solution: comparison between supported catalysts and model system. in Journal of Electroanalytical Chemistry Elsevier., 572(1), 119-128. https://doi.org/10.1016/j.jelechem.2004.06.007
Tripković A, Popović K, Lović J, Jovanović VM, Kowal A. Methanol oxidation at platinum electrodes in alkaline solution: comparison between supported catalysts and model system. in Journal of Electroanalytical Chemistry. 2004;572(1):119-128. doi:10.1016/j.jelechem.2004.06.007 .
Tripković, Amalija, Popović, Ksenija, Lović, Jelena, Jovanović, Vladislava M., Kowal, Andrzej, "Methanol oxidation at platinum electrodes in alkaline solution: comparison between supported catalysts and model system" in Journal of Electroanalytical Chemistry, 572, no. 1 (2004):119-128, https://doi.org/10.1016/j.jelechem.2004.06.007 . .