TY - JOUR
T1 - Metal-assisted hydrogen storage on Pt-decorated single-walled carbon nanohorns
AU - Liu, Yun
AU - Brown, Craig M.
AU - Neumann, Dan A.
AU - Geohegan, David B.
AU - Puretzky, Alexander A.
AU - Rouleau, Christopher M.
AU - Hu, Hui
AU - Styers-Barnett, David
AU - Krasnov, Pavel O.
AU - Yakobson, Boris I.
PY - 2012/11
Y1 - 2012/11
N2 - The catalytic dissociation of hydrogen molecules by metal nanoparticles and spillover of atomic hydrogen onto various supports is a well-established phenomenon in catalysis. However, the mechanisms by which metal catalyst nanoparticles can assist in enhanced hydrogen storage on high-surface area supports are still under debate. Experimental measurements of metal-assisted hydrogen storage have been hampered by inaccurate estimation of atomically stored hydrogen deduced from comparative measurements between metal-decorated and undecorated samples. Here we report a temperature cycling technique combined with inelastic neutron scattering (INS) measurements of quantum rotational transitions of molecular H 2 to more accurately quantify adsorbed hydrogen aided by catalytic particles using single samples. Temperature cycling measurements on single-wall carbon nanohorns (SWCNHs) decorated with 2-3 nm Pt nanoparticles showed 0.17% mass fraction of metal-assisted hydrogen storage (at ≈0.5 MPa) at room temperature. Temperature cycling of Pt-decorated SWCNHs using a Sievert's apparatus also indicated metal-assisted hydrogen adsorption of ≈0.08% mass fraction at 5 MPa at room temperature. No additional metal-assisted hydrogen storage was observed in SWCNH samples without Pt nanoparticles cycled to room temperature. The possible formation of C-H bonds due to spilled-over atomic hydrogen was also investigated using both INS and density functional theory calculations.
AB - The catalytic dissociation of hydrogen molecules by metal nanoparticles and spillover of atomic hydrogen onto various supports is a well-established phenomenon in catalysis. However, the mechanisms by which metal catalyst nanoparticles can assist in enhanced hydrogen storage on high-surface area supports are still under debate. Experimental measurements of metal-assisted hydrogen storage have been hampered by inaccurate estimation of atomically stored hydrogen deduced from comparative measurements between metal-decorated and undecorated samples. Here we report a temperature cycling technique combined with inelastic neutron scattering (INS) measurements of quantum rotational transitions of molecular H 2 to more accurately quantify adsorbed hydrogen aided by catalytic particles using single samples. Temperature cycling measurements on single-wall carbon nanohorns (SWCNHs) decorated with 2-3 nm Pt nanoparticles showed 0.17% mass fraction of metal-assisted hydrogen storage (at ≈0.5 MPa) at room temperature. Temperature cycling of Pt-decorated SWCNHs using a Sievert's apparatus also indicated metal-assisted hydrogen adsorption of ≈0.08% mass fraction at 5 MPa at room temperature. No additional metal-assisted hydrogen storage was observed in SWCNH samples without Pt nanoparticles cycled to room temperature. The possible formation of C-H bonds due to spilled-over atomic hydrogen was also investigated using both INS and density functional theory calculations.
UR - http://www.scopus.com/inward/record.url?scp=84864420584&partnerID=8YFLogxK
U2 - 10.1016/j.carbon.2012.06.028
DO - 10.1016/j.carbon.2012.06.028
M3 - Article
AN - SCOPUS:84864420584
SN - 0008-6223
VL - 50
SP - 4953
EP - 4964
JO - Carbon
JF - Carbon
IS - 13
ER -