Efficient use of resources in energy converting applications

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Efficient use of resources in energy converting applications (en)
Authors

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Investigation of tungsten carbide supported Pd or Pt as anode catalysts for PEM fuel cells

Nikolić, Vladimir M.; Žugić, Dragana; Perović, Ivana M.; Šaponjić, Aleksandra; Babić, Biljana M.; Pašti, Igor A.; Marčeta Kaninski, Milica

(2013)

TY  - JOUR
AU  - Nikolić, Vladimir M.
AU  - Žugić, Dragana
AU  - Perović, Ivana M.
AU  - Šaponjić, Aleksandra
AU  - Babić, Biljana M.
AU  - Pašti, Igor A.
AU  - Marčeta Kaninski, Milica
PY  - 2013
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/5665
AB  - In this contribution, we present results of electrochemical characterization of prepared tungsten carbide supported palladium and platinum and Vulcan XC-72 supported palladium. These catalysts were employed as anode catalysts in PEMFC and results are compared to commercial platinum catalyst. Platinum seems to be irreplaceable as a proton exchange membrane fuel cell (PEMFC) catalyst for both the anode and the cathode, yet the high price and limited natural resources are holding back the commercialization of the PEMFCs. Tungsten carbide is recognized as promising catalyst support having the best conductivity among interstitial carbides. Higher natural resources and significantly lower price make palladium good candidate for replacement of the platinum catalyst. The presented results show that all prepared catalysts are very active for the hydrogen oxidation reaction. Linear sweep voltammetry curves of Pd/C and Pd/WC show existence of peaks at 0.07 V vs. RHE, which is assigned to absorbed hydrogen. H-2 vertical bar Pd/WC vertical bar Nafion117 vertical bar Pt/C vertical bar O-2 fuel cell has almost the same efficiency and similar power output as commercial platinum catalyst. Copyright (C) 2013, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.
T2  - International Journal of Hydrogen Energy
T1  - Investigation of tungsten carbide supported Pd or Pt as anode catalysts for PEM fuel cells
VL  - 38
IS  - 26
SP  - 11340
EP  - 11345
DO  - 10.1016/j.ijhydene.2013.06.094
ER  - 
@article{
author = "Nikolić, Vladimir M. and Žugić, Dragana and Perović, Ivana M. and Šaponjić, Aleksandra and Babić, Biljana M. and Pašti, Igor A. and Marčeta Kaninski, Milica",
year = "2013",
abstract = "In this contribution, we present results of electrochemical characterization of prepared tungsten carbide supported palladium and platinum and Vulcan XC-72 supported palladium. These catalysts were employed as anode catalysts in PEMFC and results are compared to commercial platinum catalyst. Platinum seems to be irreplaceable as a proton exchange membrane fuel cell (PEMFC) catalyst for both the anode and the cathode, yet the high price and limited natural resources are holding back the commercialization of the PEMFCs. Tungsten carbide is recognized as promising catalyst support having the best conductivity among interstitial carbides. Higher natural resources and significantly lower price make palladium good candidate for replacement of the platinum catalyst. The presented results show that all prepared catalysts are very active for the hydrogen oxidation reaction. Linear sweep voltammetry curves of Pd/C and Pd/WC show existence of peaks at 0.07 V vs. RHE, which is assigned to absorbed hydrogen. H-2 vertical bar Pd/WC vertical bar Nafion117 vertical bar Pt/C vertical bar O-2 fuel cell has almost the same efficiency and similar power output as commercial platinum catalyst. Copyright (C) 2013, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.",
journal = "International Journal of Hydrogen Energy",
title = "Investigation of tungsten carbide supported Pd or Pt as anode catalysts for PEM fuel cells",
volume = "38",
number = "26",
pages = "11340-11345",
doi = "10.1016/j.ijhydene.2013.06.094"
}
Nikolić, V. M., Žugić, D., Perović, I. M., Šaponjić, A., Babić, B. M., Pašti, I. A.,& Marčeta Kaninski, M.. (2013). Investigation of tungsten carbide supported Pd or Pt as anode catalysts for PEM fuel cells. in International Journal of Hydrogen Energy, 38(26), 11340-11345.
https://doi.org/10.1016/j.ijhydene.2013.06.094
Nikolić VM, Žugić D, Perović IM, Šaponjić A, Babić BM, Pašti IA, Marčeta Kaninski M. Investigation of tungsten carbide supported Pd or Pt as anode catalysts for PEM fuel cells. in International Journal of Hydrogen Energy. 2013;38(26):11340-11345.
doi:10.1016/j.ijhydene.2013.06.094 .
Nikolić, Vladimir M., Žugić, Dragana, Perović, Ivana M., Šaponjić, Aleksandra, Babić, Biljana M., Pašti, Igor A., Marčeta Kaninski, Milica, "Investigation of tungsten carbide supported Pd or Pt as anode catalysts for PEM fuel cells" in International Journal of Hydrogen Energy, 38, no. 26 (2013):11340-11345,
https://doi.org/10.1016/j.ijhydene.2013.06.094 . .
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27
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Is platinum necessary for efficient hydrogen evolution? - DFT study of metal monolayers on tungsten carbide

Vasić Anićijević, Dragana D.; Nikolić, Vladimir M.; Marčeta Kaninski, Milica; Pašti, Igor A.

(2013)

TY  - JOUR
AU  - Vasić Anićijević, Dragana D.
AU  - Nikolić, Vladimir M.
AU  - Marčeta Kaninski, Milica
AU  - Pašti, Igor A.
PY  - 2013
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/5780
AB  - In this work WC-supported metal monolayers (Cu, Ru, Rh, Pd, Ag, Ir, Pt and Au) are investigated using Density Functional Theory in order to establish general trends regarding monolayer stability, electronic structure and reactivity. Using calculated hydrogen metal bond energies and available data on the exchange current densities (j(0)) for hydrogen evolution reaction (HER) volcano-type curve is obtained enabling prediction of HER j(0) for the entire series of M-ML/WC systems not considered so far as HER electrocatalysts. Among investigated surfaces, Cu-ML/WC(0001) and Rh-ML/WC(0001) are identified as promising HER electrocatalysts with (i) HER exchange current density matching the one of Pt and (ii) stability in electrochemical environment under HER conditions. Provided results point to a general conclusion that Pt might not be necessary for efficient catalysis of hydrogen electrode reactions superior catalysts can be obtained by rational design approach with suitable choice of overlayer/support system not involving Pt at all. Copyright (C) 2013, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.
T2  - International Journal of Hydrogen Energy
T1  - Is platinum necessary for efficient hydrogen evolution? - DFT study of metal monolayers on tungsten carbide
VL  - 38
IS  - 36
SP  - 16071
EP  - 16079
DO  - 10.1016/j.ijhydene.2013.09.079
ER  - 
@article{
author = "Vasić Anićijević, Dragana D. and Nikolić, Vladimir M. and Marčeta Kaninski, Milica and Pašti, Igor A.",
year = "2013",
abstract = "In this work WC-supported metal monolayers (Cu, Ru, Rh, Pd, Ag, Ir, Pt and Au) are investigated using Density Functional Theory in order to establish general trends regarding monolayer stability, electronic structure and reactivity. Using calculated hydrogen metal bond energies and available data on the exchange current densities (j(0)) for hydrogen evolution reaction (HER) volcano-type curve is obtained enabling prediction of HER j(0) for the entire series of M-ML/WC systems not considered so far as HER electrocatalysts. Among investigated surfaces, Cu-ML/WC(0001) and Rh-ML/WC(0001) are identified as promising HER electrocatalysts with (i) HER exchange current density matching the one of Pt and (ii) stability in electrochemical environment under HER conditions. Provided results point to a general conclusion that Pt might not be necessary for efficient catalysis of hydrogen electrode reactions superior catalysts can be obtained by rational design approach with suitable choice of overlayer/support system not involving Pt at all. Copyright (C) 2013, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.",
journal = "International Journal of Hydrogen Energy",
title = "Is platinum necessary for efficient hydrogen evolution? - DFT study of metal monolayers on tungsten carbide",
volume = "38",
number = "36",
pages = "16071-16079",
doi = "10.1016/j.ijhydene.2013.09.079"
}
Vasić Anićijević, D. D., Nikolić, V. M., Marčeta Kaninski, M.,& Pašti, I. A.. (2013). Is platinum necessary for efficient hydrogen evolution? - DFT study of metal monolayers on tungsten carbide. in International Journal of Hydrogen Energy, 38(36), 16071-16079.
https://doi.org/10.1016/j.ijhydene.2013.09.079
Vasić Anićijević DD, Nikolić VM, Marčeta Kaninski M, Pašti IA. Is platinum necessary for efficient hydrogen evolution? - DFT study of metal monolayers on tungsten carbide. in International Journal of Hydrogen Energy. 2013;38(36):16071-16079.
doi:10.1016/j.ijhydene.2013.09.079 .
Vasić Anićijević, Dragana D., Nikolić, Vladimir M., Marčeta Kaninski, Milica, Pašti, Igor A., "Is platinum necessary for efficient hydrogen evolution? - DFT study of metal monolayers on tungsten carbide" in International Journal of Hydrogen Energy, 38, no. 36 (2013):16071-16079,
https://doi.org/10.1016/j.ijhydene.2013.09.079 . .
59
49
61

Uticaj volfram-karbidnih i ugljeničnih nosača anodnih katalizatora na karakteristike PEM gorivne ćelije

Nikolić, Vladimir M.

(Универзитет у Београду, Факултет за физичку хемију, 2013)

TY  - THES
AU  - Nikolić, Vladimir M.
PY  - 2013
UR  - http://eteze.bg.ac.rs/application/showtheses?thesesId=3885
UR  - https://fedorabg.bg.ac.rs/fedora/get/o:13048/bdef:Content/download
UR  - http://vbs.rs/scripts/cobiss?command=DISPLAY&base=70036&RID=44737807
UR  - http://nardus.mpn.gov.rs/123456789/6559
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/7304
AB  - Gorivne ćelije su elektrohemijski izvori struje koji direktno prevode hemijsku energiju goriva u električnu energiju. Vodonične gorivne ćelije (eng. Proton Exchange Membrane Fuel Cell, PEMFC) kao gorivo koriste vodonik, a kao oksidans kiseonik ili vazduh, a pored dobijene električne energije jedini prateći proizvodi su voda i toplota. Poslednjih godina se intenzivno razvijaju sistemi koji koriste PEMFC namenjeni snabdevanju električnom energijom pojedinačnih domaćinstava ili zgrada. Ovakvi sistemi (eng. Micro Combined Heat and Power, μCHP) koriste dobijenu toplotu, nastalu proizvodnjom električne energije, za grejanje/ hlađenje pojedinačnih domaćinstava ili zgrada. Kako centralnu komponentu μCHP sistema čine PEM gorivne ćelije, visoka cena komponenti PEMFC i opadanje performansi tokom dugotrajnog rada usporavaju široku primenu u decentralizaciji energetskih sistema. Oko 50% cene PEMFC čini cena korišćenog katalizatora, a promene u strukturi katalizatora nastale oksidacijom nosača katalizatora i niskom tolerancijom na nečistoće u gorivu direktno utiču na dugotrajnost upotrebe μCHP sistema za snabdevanje električnom energijom i toplotom. U okviru ove disertacije je razvijen i karakterisan interaktivan nosač katalizatora na bazi nanopraha volfram-karbida. Ovakav materijal služi kao nosač nekoliko različitih katalizatora (Pt, Pd, Pt-Pd i Pt-Ru). Pored ovoga pripremljen je i neplatinski katalizator na bazi kobalta. Rezultati fizičko-hemijske karakterizacije su korelisani sa elektrohemijskim merenjima, kako bi se dobio uvid u ponašanje sintetisanih katalizatora. Kinetika reakcije oksidacije vodonika je ispitana korišćenjem klasičnih metoda elektrohemije. Pokazano je da je reakcija oksidacije vodonika veoma brza na svim ispitivanim katalizatorima, tj. da je kinetički kontrolisana do nadnapona od 50 mV. Interakcija čestica Pt ili Pd sa nosačem od WC je opisana, i doprinos ove interakcije jasno ukazuje na mogućnost sniženja količine plemenitog metala na WC nosaču, što dovodi do sniženja cene katalizatora za PEMFC. Ispitivanje uticaja ugljen-monoksida na reakciju HOR je vršeno u smeši H2+ 2% CO, na svim pripremljenim katalizatorima, kao i komercijalnim Pt/C (40%) i Pt-Ru/C (50%)...
AB  - Fuel cells are electrochemical power sources that directly transform chemical energy of fuels into electricity. Hydrogen fuel cells (Proton Exchange Membrane Fuel Cell, PEMFC) are fueled by hydrogen and oxygen as the oxidant, and in addition to the generated electric power only following products are water and heat.In recent years there are intensively developed systems using PEMFC dedicated for electricity supply individual households or buildings. Such systems (Micro Combined Heat and Power, μCHP) use the resulting heat from power generation for heating / cooling purposes of individual households or buildings. As the central component of the μCHP system is PEM fuel cell, high cost of PEMFC components and the decline in performance over the long term are slowing the wide application in the decentralized energy systems. About 50% of the PEMFC price arises from the catalyst used, and changes in the catalyst structure originated from oxidation of catalyst support and catalyst low tolerance to impurities in the fuel directly affect the lifetime of the μCHP system. This PhD thesis deals wuth the development and characterization of an interactive catalyst support based on tungsten carbide nanopowders. This material serves as a catalyst support for a number of different catalysts (Pt, Pd, Pt-Pd and Pt-Ru). In addition a non-nobel anode catalyst based on cobalt is prepared. The results of physico-chemical characterization are correlated with the electrochemical measurements, in order to gain insight into the behavior of synthesized catalysts. Kinetics of hydrogen oxidation was investigated using the traditional methods of electrochemistry. It is shown that the hydrogen oxidation reaction (HOR) is very fast at all tested catalysts, ie. that is kinetically controlled by the overvoltage of 50 mV. The interaction of Pt particles or Pd with WC catalyst support is described, and the contribution of this interaction clearly indicates the possibility of decreasing the amount of precious metal, which leads to catalyst price reduction for the PEMFC. Influence of the carbon monoxide on the HOR kinetics was investigated using a mixture H2 + 2% CO, at all prepared catalysts and commercial Pt/C (40%) and Pt-Ru/C (50%) catalysts. It is shown that...
PB  - Универзитет у Београду, Факултет за физичку хемију
T2  - Универзитет у Београду
T1  - Uticaj volfram-karbidnih i ugljeničnih nosača anodnih katalizatora na karakteristike PEM gorivne ćelije
T1  - Influence of the tungsten carbide and carbon anode catalyst supports on PEM fuel cell performance
UR  - https://hdl.handle.net/21.15107/rcub_nardus_6559
ER  - 
@phdthesis{
author = "Nikolić, Vladimir M.",
year = "2013",
abstract = "Gorivne ćelije su elektrohemijski izvori struje koji direktno prevode hemijsku energiju goriva u električnu energiju. Vodonične gorivne ćelije (eng. Proton Exchange Membrane Fuel Cell, PEMFC) kao gorivo koriste vodonik, a kao oksidans kiseonik ili vazduh, a pored dobijene električne energije jedini prateći proizvodi su voda i toplota. Poslednjih godina se intenzivno razvijaju sistemi koji koriste PEMFC namenjeni snabdevanju električnom energijom pojedinačnih domaćinstava ili zgrada. Ovakvi sistemi (eng. Micro Combined Heat and Power, μCHP) koriste dobijenu toplotu, nastalu proizvodnjom električne energije, za grejanje/ hlađenje pojedinačnih domaćinstava ili zgrada. Kako centralnu komponentu μCHP sistema čine PEM gorivne ćelije, visoka cena komponenti PEMFC i opadanje performansi tokom dugotrajnog rada usporavaju široku primenu u decentralizaciji energetskih sistema. Oko 50% cene PEMFC čini cena korišćenog katalizatora, a promene u strukturi katalizatora nastale oksidacijom nosača katalizatora i niskom tolerancijom na nečistoće u gorivu direktno utiču na dugotrajnost upotrebe μCHP sistema za snabdevanje električnom energijom i toplotom. U okviru ove disertacije je razvijen i karakterisan interaktivan nosač katalizatora na bazi nanopraha volfram-karbida. Ovakav materijal služi kao nosač nekoliko različitih katalizatora (Pt, Pd, Pt-Pd i Pt-Ru). Pored ovoga pripremljen je i neplatinski katalizator na bazi kobalta. Rezultati fizičko-hemijske karakterizacije su korelisani sa elektrohemijskim merenjima, kako bi se dobio uvid u ponašanje sintetisanih katalizatora. Kinetika reakcije oksidacije vodonika je ispitana korišćenjem klasičnih metoda elektrohemije. Pokazano je da je reakcija oksidacije vodonika veoma brza na svim ispitivanim katalizatorima, tj. da je kinetički kontrolisana do nadnapona od 50 mV. Interakcija čestica Pt ili Pd sa nosačem od WC je opisana, i doprinos ove interakcije jasno ukazuje na mogućnost sniženja količine plemenitog metala na WC nosaču, što dovodi do sniženja cene katalizatora za PEMFC. Ispitivanje uticaja ugljen-monoksida na reakciju HOR je vršeno u smeši H2+ 2% CO, na svim pripremljenim katalizatorima, kao i komercijalnim Pt/C (40%) i Pt-Ru/C (50%)..., Fuel cells are electrochemical power sources that directly transform chemical energy of fuels into electricity. Hydrogen fuel cells (Proton Exchange Membrane Fuel Cell, PEMFC) are fueled by hydrogen and oxygen as the oxidant, and in addition to the generated electric power only following products are water and heat.In recent years there are intensively developed systems using PEMFC dedicated for electricity supply individual households or buildings. Such systems (Micro Combined Heat and Power, μCHP) use the resulting heat from power generation for heating / cooling purposes of individual households or buildings. As the central component of the μCHP system is PEM fuel cell, high cost of PEMFC components and the decline in performance over the long term are slowing the wide application in the decentralized energy systems. About 50% of the PEMFC price arises from the catalyst used, and changes in the catalyst structure originated from oxidation of catalyst support and catalyst low tolerance to impurities in the fuel directly affect the lifetime of the μCHP system. This PhD thesis deals wuth the development and characterization of an interactive catalyst support based on tungsten carbide nanopowders. This material serves as a catalyst support for a number of different catalysts (Pt, Pd, Pt-Pd and Pt-Ru). In addition a non-nobel anode catalyst based on cobalt is prepared. The results of physico-chemical characterization are correlated with the electrochemical measurements, in order to gain insight into the behavior of synthesized catalysts. Kinetics of hydrogen oxidation was investigated using the traditional methods of electrochemistry. It is shown that the hydrogen oxidation reaction (HOR) is very fast at all tested catalysts, ie. that is kinetically controlled by the overvoltage of 50 mV. The interaction of Pt particles or Pd with WC catalyst support is described, and the contribution of this interaction clearly indicates the possibility of decreasing the amount of precious metal, which leads to catalyst price reduction for the PEMFC. Influence of the carbon monoxide on the HOR kinetics was investigated using a mixture H2 + 2% CO, at all prepared catalysts and commercial Pt/C (40%) and Pt-Ru/C (50%) catalysts. It is shown that...",
publisher = "Универзитет у Београду, Факултет за физичку хемију",
journal = "Универзитет у Београду",
title = "Uticaj volfram-karbidnih i ugljeničnih nosača anodnih katalizatora na karakteristike PEM gorivne ćelije, Influence of the tungsten carbide and carbon anode catalyst supports on PEM fuel cell performance",
url = "https://hdl.handle.net/21.15107/rcub_nardus_6559"
}
Nikolić, V. M.. (2013). Uticaj volfram-karbidnih i ugljeničnih nosača anodnih katalizatora na karakteristike PEM gorivne ćelije. in Универзитет у Београду
Универзитет у Београду, Факултет за физичку хемију..
https://hdl.handle.net/21.15107/rcub_nardus_6559
Nikolić VM. Uticaj volfram-karbidnih i ugljeničnih nosača anodnih katalizatora na karakteristike PEM gorivne ćelije. in Универзитет у Београду. 2013;.
https://hdl.handle.net/21.15107/rcub_nardus_6559 .
Nikolić, Vladimir M., "Uticaj volfram-karbidnih i ugljeničnih nosača anodnih katalizatora na karakteristike PEM gorivne ćelije" in Универзитет у Београду (2013),
https://hdl.handle.net/21.15107/rcub_nardus_6559 .