P25@CoAl layered double hydroxide heterojunction nanocomposites for CO^sub 2^ photocatalytic reduction

Artificial photosynthesis driven by inorganic photocatalysts offers a promising route to renewable solar fuels, however efficient CO2 photoreduction remains a challenge. A family of hierarchical nanocomposites, comprising P25 nanoparticles encapsulated within microporous CoAl-layered double hydroxid...

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Veröffentlicht in:Applied catalysis. B, Environmental Environmental, 2017-07, Vol.209, p.394
Hauptverfasser: Kumar, Santosh, Isaacs, Mark A, Trofimovaite, Rima, Durndell, Lee, Parlett, Christopher MA, Douthwaite, Richard E, Coulson, Ben, Cockett, Martin CR, Wilson, Karen, Lee, Adam F
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Sprache:eng
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Zusammenfassung:Artificial photosynthesis driven by inorganic photocatalysts offers a promising route to renewable solar fuels, however efficient CO2 photoreduction remains a challenge. A family of hierarchical nanocomposites, comprising P25 nanoparticles encapsulated within microporous CoAl-layered double hydroxides (CoAl-LDHs) were prepared via a one-pot hydrothermal synthesis. Heterojunction formation between the visible light absorbing CoAl-LDH and UV light absorbing P25 semiconductors extends utilisation of the solar spectrum, while the solid basicity of the CoAl-LDH increases CO2 availability at photocatalytic surfaces. Matching of the semiconductor band structures and strong donor-acceptor coupling improves photoinduced charge carrier separation and transfer via the heterojunction. Hierarchical P25@CoAl-LDH nanocomposites exhibit good activity and selectivity (>90%) for aqueous CO2 photoreduction to CO, without a sacrificial hole acceptor. This represents a facile and cost-effective strategy for the design and development of LDH-based nanomaterials for efficient photocatalysis for renewable solar fuel production from particularly CO2 and water.
ISSN:0926-3373
1873-3883