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Photoassisted CO 2 Conversion to Fuels
Author(s) -
RemiroBuenamañana Sonia,
García Hermenegildo
Publication year - 2019
Publication title -
chemcatchem
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.497
H-Index - 106
eISSN - 1867-3899
pISSN - 1867-3880
DOI - 10.1002/cctc.201801409
Subject(s) - fossil fuel , photocatalysis , context (archaeology) , artificial photosynthesis , nanotechnology , materials science , graphene , renewable energy , catalysis , energy transformation , nanoparticle , semiconductor , chemical engineering , chemistry , organic chemistry , physics , optoelectronics , paleontology , thermodynamics , engineering , electrical engineering , biology
In the context of the on‐going change from fossil fuels to renewable energy sources, there is much interest in decreasing atmospheric CO 2 emissions. One of the possibilities is to use CO 2 as feedstock of fuels and chemicals. While some catalytic CO 2 transformations are well known processes, they consume a considerable amount of energy to occur at significant rates and in the classical processes this energy is again produced by burning fossil fuels. For this reason, there is much current interest in developing light assisted CO 2 transformations, including, but not limited to, artificial photosynthesis. Rather than a comprehensive review, the present article describes a range of approaches for CO 2 activation based either on the direct CO 2 excitation with deep UV light or on the use of solar photocatalysts. Due to the extension of the field, this article is focused on two photocatalyst types, namely, TiO 2 containing plasmonic Au nanoparticles and graphene‐semiconductor heterojunctions. It will be emphasized the opportunities that bimetallic plasmonic nanoparticles offer to implement on commercial TiO 2 visible light photoresponse and selectivity towards CO 2 reduction. It will also be commented that adsorption of Cu 2 O onto defective graphene increases the photocatalytic activity of the copper semiconductor over one order of magnitude for CO 2 photomethanation. The last section includes some comments about possible alternatives to go beyond the current efficiencies in light assisted CO 2 conversion with the aim of triggering new research in the area.