TY - JOUR
T1 - Two-step carbothermal welding to access atomically dispersed pd1 on three-dimensional zirconia nanonet for direct indole synthesis
AU - Zhao, Yafei
AU - Zhou, Huang
AU - Chen, Wenxing
AU - Tong, Yujing
AU - Zhao, Chao
AU - Lin, Yue
AU - Jiang, Zheng
AU - Zhang, Qingwei
AU - Xue, Zhenggang
AU - Cheong, Weng Chon
AU - Jin, Benjin
AU - Zhou, Fangyao
AU - Wang, Wenyu
AU - Chen, Min
AU - Hong, Xun
AU - Dong, Juncai
AU - Wei, Shiqiang
AU - Li, Yadong
AU - Wu, Yuen
N1 - Publisher Copyright:
Copyright © 2019 American Chemical Society.
PY - 2019/6/12
Y1 - 2019/6/12
N2 - Herein, we report a novel carbothermal welding strategy to prepare atomically dispersed Pd sites anchored on a three-dimensional (3D) ZrO2 nanonet (Pd1@ZrO2) via two-step pyrolysis, which were evolved from isolated Pd sites anchored on linker-derived nitrogen-doped carbon (Pd1@NC/ZrO2). First, the NH2-H2BDC linkers and Zr6-based [Zr6(μ3-O)4(μ3-OH)4]12+ nodes of UiO-66-NH2 were transformed into amorphous N-doped carbon skeletons (NC) and ZrO2 nanoclusters under an argon atmosphere, respectively. The NC supports can simultaneously reduce and anchor the Pd sites, forming isolated Pd1-N/C sites. Then, switching the argon to air, the carbonaceous skeletons are gasified and the ZrO2 nanoclusters are welded into a rigid and porous nanonet. Moreover, the reductive carbon will result in abundant oxygen (O) defects, which could help to capture the migratory Pd1 species, leaving a sintering-resistant Pd1@ZrO2 catalyst via atom trapping. This Pd1@ZrO2 nanonet can act as a semi-homogeneous catalyst to boost the direct synthesis of indole through hydrogenation and intramolecular condensation processes, with an excellent turnover frequency (1109.2 h-1) and 94% selectivity.
AB - Herein, we report a novel carbothermal welding strategy to prepare atomically dispersed Pd sites anchored on a three-dimensional (3D) ZrO2 nanonet (Pd1@ZrO2) via two-step pyrolysis, which were evolved from isolated Pd sites anchored on linker-derived nitrogen-doped carbon (Pd1@NC/ZrO2). First, the NH2-H2BDC linkers and Zr6-based [Zr6(μ3-O)4(μ3-OH)4]12+ nodes of UiO-66-NH2 were transformed into amorphous N-doped carbon skeletons (NC) and ZrO2 nanoclusters under an argon atmosphere, respectively. The NC supports can simultaneously reduce and anchor the Pd sites, forming isolated Pd1-N/C sites. Then, switching the argon to air, the carbonaceous skeletons are gasified and the ZrO2 nanoclusters are welded into a rigid and porous nanonet. Moreover, the reductive carbon will result in abundant oxygen (O) defects, which could help to capture the migratory Pd1 species, leaving a sintering-resistant Pd1@ZrO2 catalyst via atom trapping. This Pd1@ZrO2 nanonet can act as a semi-homogeneous catalyst to boost the direct synthesis of indole through hydrogenation and intramolecular condensation processes, with an excellent turnover frequency (1109.2 h-1) and 94% selectivity.
UR - http://www.scopus.com/inward/record.url?scp=85069621957&partnerID=8YFLogxK
U2 - 10.1021/jacs.9b03182
DO - 10.1021/jacs.9b03182
M3 - Article
C2 - 31188590
AN - SCOPUS:85069621957
SN - 0002-7863
VL - 141
SP - 10590
EP - 10594
JO - Journal of the American Chemical Society
JF - Journal of the American Chemical Society
IS - 27
ER -