hydrogen fuel cells and storage technology (fcast) project
TRANSCRIPT
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UNLV Renewable Energy Symposium 2008 UNLV Renewable Energy Symposium
Aug 20th, 3:15 PM - 3:45 PM
Hydrogen Fuel Cells and Storage Technology (FCAST) Project Hydrogen Fuel Cells and Storage Technology (FCAST) Project
Clemens Heske University of Nevada, Las Vegas, [email protected]
Follow this and additional works at: https://digitalscholarship.unlv.edu/res
Part of the Chemistry Commons, and the Oil, Gas, and Energy Commons
Repository Citation Repository Citation Heske, Clemens, "Hydrogen Fuel Cells and Storage Technology (FCAST) Project" (2008). UNLV Renewable Energy Symposium. 3. https://digitalscholarship.unlv.edu/res/2008/aug20/3
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Hydrogen Fuel Cells and Storage Technology (FCAST) Project
Clemens Heske (lead PI-experiment)Balakrishnan Naduvalath (lead PI-theory)
Department of ChemistryUniversity of Nevada, Las Vegas
Project manager: Robert F. D. PerretUNLV Research Foundation
sponsored by the DOE EERE Hydrogen Research Program through the UNLV Research Foundation, contract number DE-FG36-05GO85028
This presentation does not contain any proprietary, confidential, or otherwise restricted information
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FCAST partnersUNLV Experiment
• Chulsung Bae – Chemistry• Andrew Cornelius – Physics• B.J. Das - Electrical Engineering• David Hatchett – Chemistry• Clemens Heske – Chemistry• Wayne Stolte, Oliver Hemmers, Dennis Lindle – Chemistry
UNLV Theory• Changfeng Chen – Physics• Eunja Kim – Physics• Steven Lepp – Physics• Bala Naduvalath – Chemistry• Tao Pang – Physics• Bernard Zygelman – Physics
External Partners
• United Technologies (UTC) Power• Rice University• Lawrence Berkeley National Lab • Air Products• Hahn-Meitner-Institute, Berlin• Shanghai Jiatong University• Penn State
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Why Hydrogen Economy?
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• We need a new fuel! (sooner or later)
Why Hydrogen Economy?
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• We need a new fuel! (sooner or later)
• This could be: • Biodiesel• Hydrogen• Electricity• Uranium• ...
Why Hydrogen Economy?
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• Hydrogen Production
• Hydrogen Storage
• Hydrogen Delivery
• Hydrogen Consumption
What would a Hydrogen Economy need?
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• Hydrogen Production• Solar (thermal, photoelectrochemical)• Nuclear• Currently: natural gas reforming
• Hydrogen Storage• Nanomaterials, Metal Hydrides, Chemical
Hydrides• Hydrogen Delivery
• Pipelines, Trucks, Tanks, ...• Hydrogen Consumption
• Fuel Cells, Internal Combustion Engine
What would a Hydrogen Economy need?
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• Hydrogen Production• Solar (thermal, photoelectrochemical)• Nuclear• Currently: natural gas reforming
• Hydrogen Storage• Nanomaterials, Metal Hydrides, Chemical
Hydrides• Hydrogen Delivery
• Pipelines, Trucks, Tanks, ...• Hydrogen Consumption
• Fuel Cells, Internal Combustion Engine
What would a Hydrogen Economy need?
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Objectives of FCAST• Perform closely-coupled theoretical and experimental
investigations of– hydrogen adsorption/desorption in various matrices to
establish a solid understanding of optimal storage concepts
– the electronic and geometric structure of metal hydrides, nanomaterials (C, B, N, transition metals, alloys), metal adatoms, and adsorbed hydrogen molecules/atoms
– Fuel cell membranes and catalytic materialsto predict optimized materials and structures for hydrogen storage and fuel cells in the DOE Hydrogen program
• Collaborate closely with external partners
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Task 1: Theory and Experiment of Nanomaterialsfor Storage Applications(New Materials, Hydrogen Uptake, Local Electronic Structure, Adsorption Energies and Geometries, …)
Task 2: Metal Hydrides (Structure, Reversibility, T-and P-Dependence, …)
Task 3: Mesoporous Polymer Nanostructures (Synthesis, Hydrogen Uptake, …)
Task 4: Improved Fuel Cell Membrane
Task 5: Design and Characterization of Improved Fuel Cell Catalytic Materials 10
Approach
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Titanium-decorated Carbon Nanotubes as a Potential High-capacity Hydrogen
Storage MediumT. Yildirim and S. Ciraci, Phys. Rev. Lett. 94, 175501 (2005)
Hydrogen storage in/on nanomaterials
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nanotubes come in bundles
Samples have a size distribution
Samples contain impurities
A local experiment onone individual nanotube would be ideal!
TEM of SWNT
5 nm
Which is the best nanotube for hydrogen storage ?How does hydrogen adsorption/desorption work ?
How can we improve it ?
Single-Walled Carbon NanoTubes (SWNT)
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• Up to 4 H2 are adsorbed on each Ti atom with the binding energy ranging
from 0.1 eV to 0.4 eV per H2. (7.8wt% for double side coverage)
Ti 1H2 2H2 3H2 4H2 5H2
E (eV/H2) 0.60 0.36 0.39 0.09 0.02
The binding energy of H2 on Sc is slightly lower than that on Ti.
Transition-metal decoration and hydrogen storage (Changfeng Chen, Physics, Task 1)
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• Car-Parrinello molecular dynamics simulations indicate that the proposed frameworks are thermodynamically stable up to 20 ps at 300 K and 2 ps at 600K
• Preliminary results indicate that Li-decorated 3D nano-frameworks are promising for hydrogen storage
A novel class of 3D nanoframeworks based on CNTs(Balakrishnan Naduvalath, Chemistry, Eunja Kim, Physics, Task 1)
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• Tin clusters evolve on Pentagonal growth pattern• Second energy difference indicates Ti7 and Ti13 clusters
are highly stable, which agrees well with the experimentalresults
Ti7
Ti9
Ti5
Ti8
Ti15
Ti13
Ti11
Ti10
1.8694 eV
2 ( 1) ( 1) 2 ( )E E n E n E nΔ = + + − −
Second Energy Difference
2.3128 eV
2.5187 eV
2.3562 eV
2.4472 eV2.9270 eV
2.5700 eV
2.8063 eV
Electronic structure of Titanium clusters (B. Naduvalath, Task 1)
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Ti13H20 (μ3)
• Hydrogen multi-center bonds in Ti13Hm• μ3 for m ≤ 20 and μ2 in Ti13H30• Cage expansion due to saturation from
m = 20 – 30 by 6%
Ti13
H20
H30
H20
H30
μ3 μ2
Ti13 cluster and H2 saturation (B. Naduvalath, Task 1)
Ti13H30 (μ2)
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Ti55H120 (μ2 & μ3)
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• How does Hydrogen interact with carbon-based nanomaterials?
• Why is there a “gap” between theory and experiment?
Experiment matrix for Hydrogen storage on (metal-decorated) carbon nanomaterials:
– Carbon (nano)materials: C60, SWNT, HOPG– Metal (co-)adsorbates: Ti, Li– Hydrogenation: molecular, atomic
Surface and interface spectroscopy/microscopy of nanomaterials for hydrogen storage(Clemens Heske, Chemistry, Task 1)
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Soft X-ray spectroscopies
EConduction band
Photoelectron-Spectroscopy (PES)
X-Ray EmissionSpectroscopy ( )XES
e-
e-
e-
Valence band
Core level
h ’’ν
hν
h ’ν
Auger-Electron-Spectroscopy (AES)
e
X-ray Absorption Spectroscopy (XAS)
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High dynamic rangeXPS, UPS, Auger, IPES
High resolutionXPS, UPS, Auger
Sample preparation and distribution
Scanning ProbeMicroscope
Glovebox
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Beamline 8.0 – Advanced Light Source – Lawrence Berkeley National Lab
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Scanning Tunneling Microscopy (STM) / Spectroscopy (STS)
Microscopy
Tunneling tip can be scanned over the sample by piezos
Tunneling current is measured at a tunneling voltage V and kept constant
by a feedback controlling the z-direction→ “topography of electron density”
z-range 150 pm
HOPG 2x2 nm2
controlunitP
iezo
tube
tip Computertunneling voltage
z
V
Spectroscopy
Tunneling voltage V is varied at one spot with constant tip-sample distance→ density of states around EF
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STM on SWCNT – 2 Electro-deposited (6 min, upside down) on HOPG, SWCNT (not cut)
20x20 nm2200x200 nm2 10x10 nm2
Electro deposition worked
Low coverage with long SWCNT
“Small” bundles (e.g. two bundled tubes) and individual tubes are observed
Atomic resolution can be achieved
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Scanning Tunneling Microscopy/Spectroscopy of SWNT with/without Ti decoration (Task 1)
I-V curve and STS of SWNT on Au
STM image of SWNT on Au with atomic resolution
Ti deposited on top of SWNT/Au
200x200 nm2
200x200 nm2
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Atomic Hydrogen Source (AHS)Based on U. Bischler, J. Vac. Sci. Technol. A 11, 458 (1993)
Atomic hydrogen is produced by high temperature thermal cracking of molecular hydrogen via a W capillary tube, submitted to HV and electron bombardment
Atomic Hydrogen Source components:
• Gas Reservoir
• Tungsten Capillary Tube
– 50-mm long, 1.6-mm O.D, 0.6-mm I.D.
– Acceleration Voltage of ~+3 kV
• Tungsten Filament
– 1.7 A, 7.0 V, 12 W
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500 1000 1500 20000.010
0.012
0.014
0.016
9.0x10-8mBar
P AH/P
H2
W Capillary tube Temperature (K)
Atomic/ molecular hydrogen
ratio
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287 286 285 284 283
Inte
nsity
(a.u
.)
Binding Energy (eV)
Sample 2min.RT 2min.1000K 2min.1500K 2min.1800K 2min.1950K 2min.2000K 2min.2050K
C 1sMg K
α XPS
SWNT on In foil
1. No shift in C 1s for molecular hydrogen adsorption (at RT)
2. C 1s shifts to higher binding energy for atomic hydrogen (along with capillary temperature), indicating H adsorption
H/H2 sourcetemperature
XPS: Hydrogenation of SWNT (Task 1)
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290 288 286 284 282 280
Exp. curve Fitted curve Peak I Peak II Peak III
Nor
mal
ized
inte
nsity
(a.u
.)
Binding Energy (eV)290 288 286 284 282 280
Exp. curve Fitted curve Peak I Peak II Peak III
Nor
mal
ized
inte
nsity
(a.u
.)Binding Energy (eV)
2 min. 2050K
XPS: Hydrogenation of SWNT (Task 1)
0 200 400 600 800 1000 1200 1400 1600 1800 2000 2200
0.60
0.65
0.70
0.75
0.80
0.85
0.90
0.95
1.00
AΙΙ
/AΙ
W Capillary tube Temperature (K)(0 stands for original sample)
AI
AII
Sample
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AII/AI
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Gibbs free energy and temperature-pressure phase diagram of lithium alanates (Changfeng Chen, Task 2)
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Apply first-principles electronic structure and lattice dynamics calculations within and beyond the harmonic phonon approximation to examine the thermodynamic phase stability of lithium alanates and predict their reaction pathways and reversibility
Results:• Obtained a comprehensive set of thermodynamic functions over a wide temperature range for LiAlH4, Li3AlH6 and LiH.
• Evaluated decomposition reactions to determine reversibility and suitability for practical use in mobile applications.
• Established the thermodynamic (temperature-pressure) phase diagram for lithium alanatesand identified key operating physical parameters for hydrogen storage and reversible release-recharge process.
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Polyaniline (PANI)/Pd Composites for Hydrogen Storage (David Hatchett, Task 3)
Pd(ii) reduction in PANI
Pd morphology isa function of thenumber of voltammetriccycles
Pd aggregation also possible with potentiometric growth
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PANI/Pd Composites (Task 3)
Pd(iv) Reduction in PANI
Pd thickness is a function of the number of voltammetric cycles
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H Sorption Apparatus (Task 3)
H2 Generator
Carrier inPANI/Pd
GC
TCD
Exhaust
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Hydrogen Sorption in Chemical Composites (Task 3)
Material ASorption is obtainedusing a normal GC witha hydrogen generator
• The first peak remains unchanged relative to the second because it represents the void volume of hydrogen in the tube rather than sorbed hydrogen
• The second peak represent sorbed hydrogen
• A temperature ramp is used to observed desorption
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Hydrogen Sorption Results and Conclusions (Task 3)
• Five composite materials have been produced that show promise for Hydrogen sorption
• Preliminary measurements have been made to verify the sorption properties
• Variations in the chemical composites have been eliminated by treatment with NaBH4 thus reducing any unreduced species
• This material shows the highest sorption suggesting that treatment of the other chemically prepared composites may increase sorption properties 33
ABCD
A+NaBH4
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PEM Fuel Cell
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SummaryFCAST is a joint experimental and theoretical
project to enhance the understanding of hydrogen fuel cells and storage materials
• Joint experimental and theoretical work performed on electronic structure of carbon nanoclusters
• Stable structures of graphitic-BC2N as potential hydrogen storage media identified
• The electronic structure of Ti decorated SWCNTs explored using X-ray and electron spectroscopy. Significant oxidation of Ti leading to TiO2 formation is observed
• Systematically explored hydrogen uptake of transition metal-bonded organometallic systems (Sc, Ti, V) using DFT methods
• Proposed new class of carbon nanoframeworks (thin SWCNTs linked by phenyl spacers) as potential hydrogen storage media
• Investigated electronic structures and bondings in hydrogen saturated Ti and Ti-Al clusters and identified novel bonding motifs which may be harnessed to design novel hydrogen storage systems
• Synthesized bulk quantities of mesoporous PANI/Pd composites for hydrogen storage