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Ariel University Center
Ruthenium based non platinum catalysts for oxygen reduction in acid solution Alex Schechter Ariel University Center ISRAEL הכנס ה-7 למקורות אנרגיה מתקדמים 26 January 2011 אוניברסיטת ת"א
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Methanol fueled Electric vehicle
Fuel cell
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Membrane/ Separator/ Electrolyte
DMFC Concept Membrane/ Separator/ Electrolyte 6e- In Air – O2 Water + Methanol Residue 3H2O CO2 Out Methanol solution In 6H+ Anode Cathode
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Pt Short Comings in PEMFC and DMFC
Slow oxygen reduction kinetics is the main contributor to efficiency loses (70%) in H2/Air PEMFC Pt is Pt alloys show the best performance but very high cost (USD/oz 1651 Oct. 2010), estimated 0.8g/kW mostly in the cathode In DMFC ,Pt poisoning by methanol (“crossover”) further decrease ORR rate, increase the over potential and cathode loading by a factor of~ 10
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Promissing Non-Pt catalyst
Oxide based catalyst Macro cycles (M=Co ,Fe, Mn) Chevrel phase Ruthenium chevrel phases with Se, S, Te and N Oxide based mainly for SOFC Macro cycles: The structure can be compared to the one of the functional group of chlorophyll or hemoglobin. Newer days they were heat treated to improve the stability and the ORR activity. Than embedded metallic catalytically active centers are formed Chevrel phases: Generally referred as “ternary molybdenum chalcogenides” but named after the scientist Chevrel General structure MxMo6X8 (M = Fe, Cu, Ag…, X = Se, S, Te) Electro catalytic properties first discovered by Alonso-Vante & Tributsch in 1986 → Show good performance and selectivity! → Based on these Chevrel phases the nanostructured RuSe cluster catalyst which we deal with developed → Mainly RuxSey/C catalyst but also RuxSzSey/C → There from now on the presentation is only about Ru-catalyst Wolf Vielstich: Handbook of Fuel Cells Alonso-Vante N, Bogdanoff P, Tributsch H (2000) J Catal190:240
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Cluster charge transfer Ru2Mo6Se8
W. Jaegermann, C. Pettenkoffer, N. Alonso-Vante, Th. Schwazlose and H. Tributsch, Ber. Bunsenges. Phys. Chem., 94,513 (1990)
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Conventional Synthesis methods of RuxLy (L=S,Se,Te)
Precursors- Ru3CO12, RuCl3 Elemental S/Se/Te powder Methods- Reflux 12-48hours in Xylene or ethylene glycol Thermolysis ºC
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RuSe catalyst Mechanisms
Carbonyl – cluster theory The surfaces of Ru particles are occupied by small Ru selenide clusters Theory: Selenium acts as a electron bridge and a changing Tafel slope also indicates a modification in structure. Theory: For low Se contents (<40%) → at higher concentrations hexagonal Ru cores are covered by laminar structures of Ru selenide shells → but generally the processes are not understood in detail so far M. Bron: J of Electroanalytical Chem 500:510 Tributsch H, Bron M, Hilgendorff M, Schulenburg H, Dorbandt I,Eyert V, Bogdanoff P, Fiechter S (2001) J Appl Electrochem ,31:739
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Objectives Find an effective method of preparing RuxSey
Characterize these materials Study oxygen reduction reaction (ORR) on RuxSey in aspects related to fuel cells
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Microwave Synthesis of Nano-Catalysts
C2H4(OH)2 C2H4(OH)O· + H· H· H+ + e- Ru3+ +3e- Ru Eo= 0.703V H2SeO3 + 4H+ + 4e- Se + 3H2O Eo= 0.74V
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Electron Microscopy of RuxSey
HRSEM TEM RuCl3 : elemental Se powder 2:1 (molar)
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Ru and Se values are given in atomic percent
EDX Mapping Ru2Se from Se powder Ru2Se from H2SeO3 Ru and Se values are given in atomic percent
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Simultaneous DSC /TGA analysis (Ru2Se)
H2SeO3 Se powder
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In Ru:Se 2:1 (33%Se) Ru2Se17.3 (EDX) + 3.3%Se (STA) + 12.4%Se washed
Quantitative Analysis of Se Powder in RuxSey Melting Se 3.3% elemental Se In Ru:Se 2:1 (33%Se) Ru2Se17.3 (EDX) + 3.3%Se (STA) %Se washed
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XRD patterns of RuxSey nano-catalysts
Elemental Se powder H2SeO3 RuSe2 321 RuSe2 311 RuSe2 111 RuSe2 210 Ru10Se Ru10Se Ru2Se Ru2Se RuSe2 RuSe2
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Rotating Ring Disc Electrode (RRDE)
The Levich equation: The Koutecky-Levich equation:
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LSV of O2 reduction on RDE
RuxSey N2 O2 0 rpm O2 300 rpm O2 600 rpm O2 900 rpm O rpm O rpm O rpm O rpm Current Amp cm-2 x10-4 MoxRuySez Current Amp cm-2 x10-4
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RRDE result of Ru80Se20 Ring Current A/cm2 Disc
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Tafel plots of O2 reduction on Ru2Se and Pt
RDE electrodes in 0.5M H2SO4 solution. Scan rate=2 mV/sec, ω=1800 rpm.
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ik and B (@E=200 mV) values calculated from the Koutecky-Levich plots
Nano catalyst ik (A/cm2) B (A/rpm-1/2) RuxSey 0.0278 RuxSy 0.0133 RuxTey 0.0091 MoxRuySez 0.0022 MoxRuySz 0.0036 MoxRuyTez 0.0118
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Hydrogen Peroxide Oxidation on RRDE Pt ring
Disk Current microAmp/cm2 Disk Potential [V vs. Ag/AgCl]
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Tafel slopes vs. Se molar percent (EDX) in RuxSey (H2SeO3)
η = mV η = mV
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Exchange current density vs. Se molar percent in RuxSey (H2SeO3)
η = mV η = mV Se content affect the number of active sites and not in the activation energy
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ORR Mechanism x(k1,k2) Only (2)&(3): x=0 Only (2): k1=0, k30
All reactions A. Damjanovic, M. A. Genshaw, and J. O’M. Bockris, J. Chem. Phys., 45, 4057 (1966)
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Rough Surfaces in RRDE-ORR Mechanism Study
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Kinetic constants of ORR on Ru2Se
Rate constants mole/sec k2
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oxygen reduction on Ru2Se versus Pt in the Presence of methanol @0.4 V
Methanol Oxidation
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Ru2Se/C Electrode in 1M MeOH/5M H3PO4 at 60°C
1st day Current Amp/cm2 4th day 7th day
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Stability of ORR Activity of Ru2Se Catalyst
Pt Ru 2 Se (powder Se) Se (H SeO 3 ) Measured at 0.3 V ,during storage in 5M H3PO4 60C
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Fuel cell Testing in DMFC: Pt versus RuxSey
Conditions: T= 25oC, 1M CH3OH, air 150 ml/min
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State of the art comparison
Power Per Gram of Cathode Catalyst Pt RuxSey
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Summary RuxSey synthesis can be controlled by microwave
Optimum ORR kinetics is seen in Ru2Se (~35% Se) Mostly 4e- oxygen reaction occur, distinctly at high over potential Unlike previous reports – RuSe presents high stability and excellent methanol tolerance Further inmprovment of catalytic performance is required to compete with Pt.
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Acknowledgments Dr. Hanan Teller Dr. Oleg Stanevsky Dr. Maria Rylov
Mr. Phillip Hoffhimer Mr. Avinoam Burnstien Mrs. Mietal Gor Mr. Victor Moltenan Mr. Rami Kriger Funding: Israeli Ministry of National Infrastructures
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Thank You
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