Shape Controlled, Carbon Supported Pt Anodic Catalysts for DFAFC

2015
Authors
Krstajić, MilaStevanović, Sanja

Radmilović, Vuk V.

Rogan, Jelena R.

Gavrilović-Wohlmuther, Aleksandra

Radmilović, Velimir R.

Gojković, Snežana Lj.
Jovanović, Vladislava M.

Conference object (Published version)
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Electrocatalytic activity of platinum-based electrocatalysts used in fuel cells has been well recognized. However, significant attention remains on the particle shape and size control of such nanomaterials. Catalytic activity can be enhanced by alloying Pt with another element (e.g. Ru and Sn), or by supporting Pt on metal oxides, both of which involve a bifunctional effect. It is also possible to achieve better catalytic characteristics by exposing different Pt crystal facets, which alters chemical and electronic interactions (structural effect). In order to synthesize Pt nanoparticles of a pre-determined shape, water in oil microemulsion method was used, with a few modifications: carbon support (Vulcan XC-72R) was added into the microemulsion itself, just after the completion of the reduction reaction of H2PtCl6 with NaBH4 as the reducing agent and this was crucial for further improvements of the catalyst cleaning procedures. Microemulsion consisted of [n-heptane] / [polyethileneglyc...oldodecyether (BRIJ30)] / [0,1M H2PtCl6 in 0, 15, 25 and 35% HCl], so four Pt catalyst were formed using different amounts of HCl in the water phase of the microemulsion. In comparison to previously reported applications of the microemulsion method, where electrochemical treatment of catalysts before its application was necessary, this alteration of cleaning steps made use of the “as prepared” catalysts possible. Catalysts A (0% HCl), B (15% HCl), C (25% HCl) and D (35% HCl) were characterized by thermogravimetric analysis (TGA), X-ray diffraction (XRD) and transmission electron microscopy (TEM), as well as with electrochemical characterization methods (cyclic voltammetry in supporting electrolyte, CO stripping). TEM images confirmed the presence of cubic Pt particles, and indicated their good dispersion on carbon support, while XRD patterns revealed the share of each plane orientation in all investigated catalysts. This acknowledged the influence of HCl in the microemulsion on the shape of Pt particles. Mean particle size was determined both by TEM and XRD investigations, which are in good accordance, and show that average diameters of these four catalysts vary from 3 to 8 nm.
Keywords:
Electrocatalytic activity / platinum-based electrocatalysts / Pt nanoparticlesSource:
5th Regional Symposium on Electrochemistry South-East Europe, RSE-SEE, Program and Book of Abstracts, 2015, 78-78Publisher:
- Academician Evgeni Budevski Institute of Electrochemistry and Energy Systems Bulgarian Academy of Sciences, Sofia, Bulgaria
Note:
- June 07-11, 2015, Pravets, Bulgaria
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IHTMTY - CONF AU - Krstajić, Mila AU - Stevanović, Sanja AU - Radmilović, Vuk V. AU - Rogan, Jelena R. AU - Gavrilović-Wohlmuther, Aleksandra AU - Radmilović, Velimir R. AU - Gojković, Snežana Lj. AU - Jovanović, Vladislava M. PY - 2015 UR - http://www.aseee.eu/index.php/rse-see5-home UR - https://cer.ihtm.bg.ac.rs/handle/123456789/3556 AB - Electrocatalytic activity of platinum-based electrocatalysts used in fuel cells has been well recognized. However, significant attention remains on the particle shape and size control of such nanomaterials. Catalytic activity can be enhanced by alloying Pt with another element (e.g. Ru and Sn), or by supporting Pt on metal oxides, both of which involve a bifunctional effect. It is also possible to achieve better catalytic characteristics by exposing different Pt crystal facets, which alters chemical and electronic interactions (structural effect). In order to synthesize Pt nanoparticles of a pre-determined shape, water in oil microemulsion method was used, with a few modifications: carbon support (Vulcan XC-72R) was added into the microemulsion itself, just after the completion of the reduction reaction of H2PtCl6 with NaBH4 as the reducing agent and this was crucial for further improvements of the catalyst cleaning procedures. Microemulsion consisted of [n-heptane] / [polyethileneglycoldodecyether (BRIJ30)] / [0,1M H2PtCl6 in 0, 15, 25 and 35% HCl], so four Pt catalyst were formed using different amounts of HCl in the water phase of the microemulsion. In comparison to previously reported applications of the microemulsion method, where electrochemical treatment of catalysts before its application was necessary, this alteration of cleaning steps made use of the “as prepared” catalysts possible. Catalysts A (0% HCl), B (15% HCl), C (25% HCl) and D (35% HCl) were characterized by thermogravimetric analysis (TGA), X-ray diffraction (XRD) and transmission electron microscopy (TEM), as well as with electrochemical characterization methods (cyclic voltammetry in supporting electrolyte, CO stripping). TEM images confirmed the presence of cubic Pt particles, and indicated their good dispersion on carbon support, while XRD patterns revealed the share of each plane orientation in all investigated catalysts. This acknowledged the influence of HCl in the microemulsion on the shape of Pt particles. Mean particle size was determined both by TEM and XRD investigations, which are in good accordance, and show that average diameters of these four catalysts vary from 3 to 8 nm. PB - Academician Evgeni Budevski Institute of Electrochemistry and Energy Systems Bulgarian Academy of Sciences, Sofia, Bulgaria C3 - 5th Regional Symposium on Electrochemistry South-East Europe, RSE-SEE, Program and Book of Abstracts T1 - Shape Controlled, Carbon Supported Pt Anodic Catalysts for DFAFC SP - 78 EP - 78 UR - https://hdl.handle.net/21.15107/rcub_cer_3556 ER -
@conference{ author = "Krstajić, Mila and Stevanović, Sanja and Radmilović, Vuk V. and Rogan, Jelena R. and Gavrilović-Wohlmuther, Aleksandra and Radmilović, Velimir R. and Gojković, Snežana Lj. and Jovanović, Vladislava M.", year = "2015", abstract = "Electrocatalytic activity of platinum-based electrocatalysts used in fuel cells has been well recognized. However, significant attention remains on the particle shape and size control of such nanomaterials. Catalytic activity can be enhanced by alloying Pt with another element (e.g. Ru and Sn), or by supporting Pt on metal oxides, both of which involve a bifunctional effect. It is also possible to achieve better catalytic characteristics by exposing different Pt crystal facets, which alters chemical and electronic interactions (structural effect). In order to synthesize Pt nanoparticles of a pre-determined shape, water in oil microemulsion method was used, with a few modifications: carbon support (Vulcan XC-72R) was added into the microemulsion itself, just after the completion of the reduction reaction of H2PtCl6 with NaBH4 as the reducing agent and this was crucial for further improvements of the catalyst cleaning procedures. Microemulsion consisted of [n-heptane] / [polyethileneglycoldodecyether (BRIJ30)] / [0,1M H2PtCl6 in 0, 15, 25 and 35% HCl], so four Pt catalyst were formed using different amounts of HCl in the water phase of the microemulsion. In comparison to previously reported applications of the microemulsion method, where electrochemical treatment of catalysts before its application was necessary, this alteration of cleaning steps made use of the “as prepared” catalysts possible. Catalysts A (0% HCl), B (15% HCl), C (25% HCl) and D (35% HCl) were characterized by thermogravimetric analysis (TGA), X-ray diffraction (XRD) and transmission electron microscopy (TEM), as well as with electrochemical characterization methods (cyclic voltammetry in supporting electrolyte, CO stripping). TEM images confirmed the presence of cubic Pt particles, and indicated their good dispersion on carbon support, while XRD patterns revealed the share of each plane orientation in all investigated catalysts. This acknowledged the influence of HCl in the microemulsion on the shape of Pt particles. Mean particle size was determined both by TEM and XRD investigations, which are in good accordance, and show that average diameters of these four catalysts vary from 3 to 8 nm.", publisher = "Academician Evgeni Budevski Institute of Electrochemistry and Energy Systems Bulgarian Academy of Sciences, Sofia, Bulgaria", journal = "5th Regional Symposium on Electrochemistry South-East Europe, RSE-SEE, Program and Book of Abstracts", title = "Shape Controlled, Carbon Supported Pt Anodic Catalysts for DFAFC", pages = "78-78", url = "https://hdl.handle.net/21.15107/rcub_cer_3556" }
Krstajić, M., Stevanović, S., Radmilović, V. V., Rogan, J. R., Gavrilović-Wohlmuther, A., Radmilović, V. R., Gojković, S. Lj.,& Jovanović, V. M.. (2015). Shape Controlled, Carbon Supported Pt Anodic Catalysts for DFAFC. in 5th Regional Symposium on Electrochemistry South-East Europe, RSE-SEE, Program and Book of Abstracts Academician Evgeni Budevski Institute of Electrochemistry and Energy Systems Bulgarian Academy of Sciences, Sofia, Bulgaria., 78-78. https://hdl.handle.net/21.15107/rcub_cer_3556
Krstajić M, Stevanović S, Radmilović VV, Rogan JR, Gavrilović-Wohlmuther A, Radmilović VR, Gojković SL, Jovanović VM. Shape Controlled, Carbon Supported Pt Anodic Catalysts for DFAFC. in 5th Regional Symposium on Electrochemistry South-East Europe, RSE-SEE, Program and Book of Abstracts. 2015;:78-78. https://hdl.handle.net/21.15107/rcub_cer_3556 .
Krstajić, Mila, Stevanović, Sanja, Radmilović, Vuk V., Rogan, Jelena R., Gavrilović-Wohlmuther, Aleksandra, Radmilović, Velimir R., Gojković, Snežana Lj., Jovanović, Vladislava M., "Shape Controlled, Carbon Supported Pt Anodic Catalysts for DFAFC" in 5th Regional Symposium on Electrochemistry South-East Europe, RSE-SEE, Program and Book of Abstracts (2015):78-78, https://hdl.handle.net/21.15107/rcub_cer_3556 .