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@ARTICLE{Wang:916663,
author = {Wang, Yehong and Wang, Jiapei and Zhang, Yuda and Guo,
Qiang and An, Jie and Liang, Yafei and Wang, Yanan and Cao,
Pengfei and Heggen, Marc and Dunin-Borkowski, Rafal E. and
Zhu, Xiangxue and Li, Xiujie and Wang, Feng},
title = {{R}evealing the {C}atalytic {R}ole of {S}n {D}opant in {CO}
2 ‐{O}xidative {D}ehydrogenation of {P}ropane over
{P}t/{S}n‐{C}e{O} 2 {C}atalyst},
journal = {ChemCatChem},
volume = {14},
number = {23},
issn = {1867-3880},
address = {Weinheim},
publisher = {Wiley-VCH},
reportid = {FZJ-2023-00015},
pages = {1-12},
year = {2022},
abstract = {CO2-oxidative dehydrogenation of propane (CO2-ODHP)
provides a promising route for propylene production.
Sufficient propane conversion and propylene selectivity
remain a great challenge due to the difficulty in activating
inert propane and CO2 simultaneously. Herein, a Sn doped
CeO2 supported Pt (Pt/Sn-CeO2) catalyst in CO2-ODHP reaction
is reported. Sn doping appears to kill two birds with one
stone for propane and CO2 activation. On the one side, it
increases the electron density of Pt species via PtSn alloy
formation, promoting propane adsorption and C−H bond
cleavage. On the other side, it enhances oxygen vacancy
concentrations of CeO2 support, facilitating CO2
dissociation. A higher propylene selectivity $(63.9 \%$ vs
$22.3 \%)$ was obtained on $0.1 wt \%$
$Pt/1.0 wt \%$ Sn-CeO2 than that on $0.1 wt \%$
Pt/CeO2 with a comparable propane conversion $(15.1 \%$ vs
$14.3 \%)$ at 550 °C after 240 min on stream. This
work provides a reference for designing efficient
catalysts.},
cin = {ER-C-1},
ddc = {540},
cid = {I:(DE-Juel1)ER-C-1-20170209},
pnm = {5351 - Platform for Correlative, In Situ and Operando
Characterization (POF4-535)},
pid = {G:(DE-HGF)POF4-5351},
typ = {PUB:(DE-HGF)16},
UT = {WOS:000879602500001},
doi = {10.1002/cctc.202200982},
url = {https://juser.fz-juelich.de/record/916663},
}