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Hierarchical hyper-branched titania nanorods with tuneable selectivity for CO 2 photoreduction.

Authors :
Stelios G
Tan JZY
Maroto-Valer MM
Source :
RSC advances [RSC Adv] 2021 Sep 28; Vol. 11 (51), pp. 32022-32029. Date of Electronic Publication: 2021 Sep 28 (Print Publication: 2021).
Publication Year :
2021

Abstract

Utilising captured CO <subscript>2</subscript> and converting it into solar fuels can be extremely beneficial in reducing the constantly rising CO <subscript>2</subscript> concentration in the atmosphere while simultaneously addressing energy crisis issues. Hence, many researchers have focused their work on the CO <subscript>2</subscript> photoreduction reaction for the last 4 decades. Herein, the titania hyper-branched nanorod (HBN) thin films, with a novel hierarchical dendritic morphology, revealed enhanced CO <subscript>2</subscript> photoreduction performance. The HBNs exhibited enhanced photogenerated charge production (66%), in comparison with P25 (39%), due to the unique hyper-branched morphology. Furthermore, the proposed HBN thin films exhibited a high degree of control over the product selectivity, by undergoing a facile phase-altering treatment. The selectivity was shifted from 91% towards CO, to 67% towards CH <subscript>4</subscript> . Additionally, the HBN samples showed the potential to surpass the conversion rates of the benchmark P25 TiO <subscript>2</subscript> in both CO and CH <subscript>4</subscript> production. To further enhance the selectivity and overall performance of the HBNs, RuO <subscript>2</subscript> was incorporated into the synthesis, which enhanced the CH <subscript>4</subscript> selectivity from 67% to 74%; whereas the incorporation of CuO revealed a selectivity profile comparative to P25.<br />Competing Interests: There are no conflicts to declare.<br /> (This journal is © The Royal Society of Chemistry.)

Details

Language :
English
ISSN :
2046-2069
Volume :
11
Issue :
51
Database :
MEDLINE
Journal :
RSC advances
Publication Type :
Academic Journal
Accession number :
35495501
Full Text :
https://doi.org/10.1039/d1ra05414g