TY - JOUR
T1 - Active sites on Cu/SiO2 prepared using the atomic layer epitaxy technique for a low-temperature water-gas shift reaction
AU - Chen, Ching Shiun
AU - Lin, Jarrn Horng
AU - Lai, Tzu Wen
AU - Li, Bao Hui
PY - 2009/4/1
Y1 - 2009/4/1
N2 - The atomic layer epitaxy (ALE) technique has been used to prepare uniform copper nanoparticles dispersed on a silica support (ALE-Cu/SiO2 with 2.85 ± 0.32 nm), which are highly active in the water-gas shift reaction. Infrared spectra of CO adsorption are employed to study the active sites on ALE-Cu/SiO2 surface, suggesting that two major active sites are found on the copper surface, namely defect sites and highly dispersed Cu particles and/or isolated Cu atoms sites. We report here that the defect sites on these small Cu particles or isolated Cu atoms provide high activity for the water gas shift reaction. The high efficiency of the water gas shift reaction on the ALE-Cu/SiO2 catalyst may be ascribed to its strong activity in promoting H2O dissociation. Nanoscale Cu particles may be involved in strong interactions with the SiO2 support, leading to a partially electropositive state as a result of interactions with oxygen atoms at the surface of the support, even if the copper is reduced.
AB - The atomic layer epitaxy (ALE) technique has been used to prepare uniform copper nanoparticles dispersed on a silica support (ALE-Cu/SiO2 with 2.85 ± 0.32 nm), which are highly active in the water-gas shift reaction. Infrared spectra of CO adsorption are employed to study the active sites on ALE-Cu/SiO2 surface, suggesting that two major active sites are found on the copper surface, namely defect sites and highly dispersed Cu particles and/or isolated Cu atoms sites. We report here that the defect sites on these small Cu particles or isolated Cu atoms provide high activity for the water gas shift reaction. The high efficiency of the water gas shift reaction on the ALE-Cu/SiO2 catalyst may be ascribed to its strong activity in promoting H2O dissociation. Nanoscale Cu particles may be involved in strong interactions with the SiO2 support, leading to a partially electropositive state as a result of interactions with oxygen atoms at the surface of the support, even if the copper is reduced.
KW - Atomic layer epitaxy
KW - Carbon monoxide adsorption
KW - Copper
KW - Infrared spectroscopy
KW - Temperature-programmed desorption
KW - Water-gas shift reaction
UR - https://www.scopus.com/pages/publications/62249104413
U2 - 10.1016/j.jcat.2009.02.004
DO - 10.1016/j.jcat.2009.02.004
M3 - 文章
AN - SCOPUS:62249104413
SN - 0021-9517
VL - 263
SP - 155
EP - 166
JO - Journal of Catalysis
JF - Journal of Catalysis
IS - 1
ER -