TY - JOUR
T1 - Seed-mediated synthesis of dendritic platinum nanostructures with high catalytic activity for aqueous-phase hydrogenation of acetophenone
AU - Yuan, Yuan
AU - Kaneti, Yusuf Valentino
AU - Liu, Minsu
AU - Jin, Fangzhu
AU - Kennedy, Danielle Frances
AU - Jiang, Xuchuan
AU - Huang, Jun
AU - Yu, Aibing
N1 - Publisher Copyright:
© 2015 Science Press and Dalian Institute of Chemical Physics.
PY - 2015/9
Y1 - 2015/9
N2 - This work reports a facile and efficient seed-mediated method for the synthesis of dendritic platinum (Pt) nanoparticles (NPs) at low temperatures of 55-60 °C in water, using L-ascorbic acid as a reducing agent and sodium citrate as a capping agent. It is found that the dendritic Pt NPs (10-150 nm) are composed of tiny Pt nanocrystals, which nucleate and grow through the introduced smaller Pt seeds with diameters of 3-5 nm. Further investigation shows that the dendritic Pt nanostructures display excellent catalytic performance in an aqueous-phase aromatic ketone hydrogenation reaction, including: (i) acetophenone conversion rate of > 90%, with smaller dendritic Pt NPs (10-46 nm) offering a higher conversion efficiency; (ii) high chemoselectivity toward carbonyl group (90.6%-91.5%), e.g., the selectivity to 1-phenylethanol is ∼90.1% with nearly 100% acetophenone conversion for 10 nm dendritic Pt NPs within 60 min, under mild reaction conditions (20 °C, 1.5 bar H2 pressure, and 1.5 mol% catalyst). The high catalytic activity, selectivity and stability of the dendritic Pt nanostructures under the organic solvent-free conditions make them promising for many potential applications in green catalytic conversion of hydrophilic biomass derived compounds.
AB - This work reports a facile and efficient seed-mediated method for the synthesis of dendritic platinum (Pt) nanoparticles (NPs) at low temperatures of 55-60 °C in water, using L-ascorbic acid as a reducing agent and sodium citrate as a capping agent. It is found that the dendritic Pt NPs (10-150 nm) are composed of tiny Pt nanocrystals, which nucleate and grow through the introduced smaller Pt seeds with diameters of 3-5 nm. Further investigation shows that the dendritic Pt nanostructures display excellent catalytic performance in an aqueous-phase aromatic ketone hydrogenation reaction, including: (i) acetophenone conversion rate of > 90%, with smaller dendritic Pt NPs (10-46 nm) offering a higher conversion efficiency; (ii) high chemoselectivity toward carbonyl group (90.6%-91.5%), e.g., the selectivity to 1-phenylethanol is ∼90.1% with nearly 100% acetophenone conversion for 10 nm dendritic Pt NPs within 60 min, under mild reaction conditions (20 °C, 1.5 bar H2 pressure, and 1.5 mol% catalyst). The high catalytic activity, selectivity and stability of the dendritic Pt nanostructures under the organic solvent-free conditions make them promising for many potential applications in green catalytic conversion of hydrophilic biomass derived compounds.
KW - Acetophenone conversion
KW - Aqueous-phase hydrogenation
KW - Dendritic Pt nanoparticles
KW - Seed mediated synthesis
UR - https://www.scopus.com/pages/publications/84944733680
U2 - 10.1016/j.jechem.2015.09.001
DO - 10.1016/j.jechem.2015.09.001
M3 - 文章
AN - SCOPUS:84944733680
SN - 2095-4956
VL - 24
SP - 660
EP - 668
JO - Journal of Energy Chemistry
JF - Journal of Energy Chemistry
IS - 5
ER -