TY - JOUR
T1 - Exploring the Fundamental Roles of Functionalized Ligands in Platinum@Metal-Organic Framework Catalysts
AU - Zhang, Wenlei
AU - Ji, Wenlan
AU - Li, Linjie
AU - Qin, Peishan
AU - Khalil, Islam E.
AU - Gu, Zhida
AU - Wang, Peng
AU - Li, Hongfeng
AU - Fan, Yun
AU - Ren, Zhen
AU - Shen, Yu
AU - Zhang, Weina
AU - Fu, Yu
AU - Huo, Fengwei
N1 - Publisher Copyright:
© 2020 American Chemical Society.
PY - 2020/11/25
Y1 - 2020/11/25
N2 - The metal nodes, functionalized ligands, and uniform channels of metal-organic frameworks (MOFs) are typically utilized to regulate the catalytic properties of metal nanoparticles (MNPs). However, though the ligand functionalization could impact the properties of the metal nodes and channels, which might further regulate the catalytic activity and selectivity of MNPs, related research in the design of MNP/MOF catalysts was usually neglected. Herein, we synthesized a series of Pt@UiO-66 composites (Pt@UiO-66-NH2, Pt@UiO-66-SO3H, and Pt@UiO-66) with slightly different organic ligands, which enhanced steric hindrance and contributed to multipathway electron transfer in selective hydrogenation of linear citronellal. The selectivity toward citronellol was gradually improved along with the increased size of functional groups (hydrogen, amino groups, and sulfo groups) on organic ligands, which enhanced steric hindrance provided by channels. In addition, the X-ray photoelectron spectroscopy measurements also revealed that the electronic state of Pt NPs was regulated through multipathway electron transfer from Pt NPs to metal nodes, between organic ligands and Pt NPs/metal nodes. Our research proved that the ligand functionalization altered physiochemical properties of the channels and metal nodes, further together managing the catalytic performance of Pt NPs through enhanced steric hindrance and multi-pathway electron transfer.
AB - The metal nodes, functionalized ligands, and uniform channels of metal-organic frameworks (MOFs) are typically utilized to regulate the catalytic properties of metal nanoparticles (MNPs). However, though the ligand functionalization could impact the properties of the metal nodes and channels, which might further regulate the catalytic activity and selectivity of MNPs, related research in the design of MNP/MOF catalysts was usually neglected. Herein, we synthesized a series of Pt@UiO-66 composites (Pt@UiO-66-NH2, Pt@UiO-66-SO3H, and Pt@UiO-66) with slightly different organic ligands, which enhanced steric hindrance and contributed to multipathway electron transfer in selective hydrogenation of linear citronellal. The selectivity toward citronellol was gradually improved along with the increased size of functional groups (hydrogen, amino groups, and sulfo groups) on organic ligands, which enhanced steric hindrance provided by channels. In addition, the X-ray photoelectron spectroscopy measurements also revealed that the electronic state of Pt NPs was regulated through multipathway electron transfer from Pt NPs to metal nodes, between organic ligands and Pt NPs/metal nodes. Our research proved that the ligand functionalization altered physiochemical properties of the channels and metal nodes, further together managing the catalytic performance of Pt NPs through enhanced steric hindrance and multi-pathway electron transfer.
KW - ligand functionalization
KW - metal nanoparticles
KW - metal-organic frameworks
KW - multi-pathway electron transfer
KW - steric effect
UR - http://www.scopus.com/inward/record.url?scp=85096692665&partnerID=8YFLogxK
U2 - 10.1021/acsami.0c15340
DO - 10.1021/acsami.0c15340
M3 - 文章
C2 - 33169972
AN - SCOPUS:85096692665
SN - 1944-8244
VL - 12
SP - 52660
EP - 52667
JO - ACS Applied Materials and Interfaces
JF - ACS Applied Materials and Interfaces
IS - 47
ER -