TY - JOUR
T1 - Dependence on Size of Supported Rh Nanoclusters in the Decomposition of Ethanol
AU - Hsia, Yu Yao
AU - Liu, Tzu Yu
AU - Lai, Yu Ling
AU - Hsu, Yao Jane
AU - Wang, Jeng Han
AU - Luo, Meng Fan
N1 - Publisher Copyright:
© 2025 The Authors. Published by American Chemical Society.
PY - 2025/2/6
Y1 - 2025/2/6
N2 - The decomposition of ethanol on Rh nanoclusters supported on thin film Al2O3/NiAl(100) was significantly enhanced with a decreased size of the clusters. The process started with the O-H bond scission, followed predominantly by the Cα-H bond scission to form surface acetaldehyde as a major intermediate and subsequently by further Cα-H and C-C bond scission, and ultimately produced gaseous CO, CH4, and H2. The gaseous production per adsorbed ethanol increased by 3.5-8.8 times (for varied products) when decreasing the cluster diameter from 3.5 to 1.1 nm, indicating a size-dependent reaction probability. The reaction probability of adsorbed ethanol remained near 35% on the clusters of a diameter ≥1.8 nm, whereas it was promoted with decreased cluster diameter <1.8 nm, up to nearly 100%. The promoted reactivity arose largely from the increased concentration of corner Rh atoms on small clusters, where the activation energy for the scission of the O-H bond of adsorbed ethanol, the initial dehydrogenation, became evidently smaller than that for the competing desorption. Moreover, the heavily produced surface CO obstructed the dehydrogenation of methyl intermediates, leading to the pronounced production of gaseous CH4 on small clusters, contrasting with a limited one on Rh single crystals.
AB - The decomposition of ethanol on Rh nanoclusters supported on thin film Al2O3/NiAl(100) was significantly enhanced with a decreased size of the clusters. The process started with the O-H bond scission, followed predominantly by the Cα-H bond scission to form surface acetaldehyde as a major intermediate and subsequently by further Cα-H and C-C bond scission, and ultimately produced gaseous CO, CH4, and H2. The gaseous production per adsorbed ethanol increased by 3.5-8.8 times (for varied products) when decreasing the cluster diameter from 3.5 to 1.1 nm, indicating a size-dependent reaction probability. The reaction probability of adsorbed ethanol remained near 35% on the clusters of a diameter ≥1.8 nm, whereas it was promoted with decreased cluster diameter <1.8 nm, up to nearly 100%. The promoted reactivity arose largely from the increased concentration of corner Rh atoms on small clusters, where the activation energy for the scission of the O-H bond of adsorbed ethanol, the initial dehydrogenation, became evidently smaller than that for the competing desorption. Moreover, the heavily produced surface CO obstructed the dehydrogenation of methyl intermediates, leading to the pronounced production of gaseous CH4 on small clusters, contrasting with a limited one on Rh single crystals.
UR - https://www.scopus.com/pages/publications/85217025153
UR - https://www.scopus.com/pages/publications/85217025153#tab=citedBy
U2 - 10.1021/acs.jpcc.4c08214
DO - 10.1021/acs.jpcc.4c08214
M3 - Article
AN - SCOPUS:85217025153
SN - 1932-7447
VL - 129
SP - 2502
EP - 2511
JO - Journal of Physical Chemistry C
JF - Journal of Physical Chemistry C
IS - 5
ER -