(36g) Flame Spray Pyrolysis Designed Defective Catalysts for Carbon Dioxide Conversion | AIChE

(36g) Flame Spray Pyrolysis Designed Defective Catalysts for Carbon Dioxide Conversion


Lovell, E. - Presenter, University of New South Wales
Amal, R., ARC Centre for Functional Nanomaterials
Scott, J., University of New South Wales

Emma Lovell Normal Emma Lovell 2 49 2019-04-12T20:09:00Z 2019-04-12T20:09:00Z 1 337 1925 16 4 2258 16.00

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Spray Pyrolysis Designed Defective Catalysts for Carbon Dioxide Conversion

" arial>Rahman Daiyan, Salina
Jantarang, Jonathan Horlyck, Jason Scott and Rose Amal

and Catalysis Research Group, School of Chemical Engineering, the University of
New South Wales, Sydney, Australia, 2052


line-height:107%;font-family:" arial>

line-height:107%;font-family:" arial>Given the current state of
play globally with respect to climate change the mitigation of anthropogenic carbon
dioxide emissions is of key societal importance. The valorization of carbon
dioxide to invaluable industrial chemicals and fuels, such as methane and formate,
has the dual benefit of consuming destructive CO2 whilst simultaneously
producing valuable products. The catalytic conversion of carbon dioxide can be done
using thermal catalytic and electrocatalytic pathways. In both
of these conversion routes, surface defect sites and oxygen vacancies are
proposed to play a significant role in the activation of CO2.

line-height:107%;font-family:" arial>Flame spray pyrolysis (FSP) is
a scalable and reproducible method of synthesizing nanomaterials which allows for
control over size, morphology, crystallinity and surface chemistry by simply
tuning the flame input parameters. Given these properties, FSP has vast potential
to produce materials for CO2 conversion, both thermal and electro-catalytically.

line-height:107%;font-family:" arial>In this work, we utilized FSP
as a powerful tool to tune the surface defects of a range of metal oxides which
were used as catalysts for CO2 reduction reactions. By varying input
parameters and post-processing methods, we were able to effectively tune the surface
defect sites and oxygen vacancies for a range of materials, including SnO2
and ZnO, for the electrocatalytic reduction of carbon
dioxide (CO2RR). By doing so, we were able to control selectivity
and maximise current density. Ultimately this enabled insights into the role of
defect sites in electrocatalytic CO2 reduction reactions. Further,
we utilised FSP to design CeO2-based catalyst supports to
systematically control the surface oxygen vacancies of Ni/CeO2
catalysts for the (photo)thermal conversion of CO2 to CH4.
In tuning these, we were able to understand the role of CeO2 surface
oxygen vacancies in the methanation of carbon dioxide.