2 research outputs found
Amine-Functionalized Graphene/CdS Composite for Photocatalytic Reduction of CO<sub>2</sub>
This
study provides a significant enhancement in CO<sub>2</sub> photoconversion
efficiency by the functionalization of a reduced
graphene oxide/cadmium sulfide composite (rGO/CdS) with amine. The
amine-functionalized graphene/CdS composite (AG/CdS) was obtained
in two steps. First, graphene oxide (GO) was selectively deposited
via electrostatic interaction with CdS nanoparticles modified with
3-aminopropyltriethoxysilane. Subsequently, ethylenediamine (NH<sub>2</sub>C<sub>2</sub>H<sub>4</sub>NH<sub>2</sub>) was grafted by an <i>N</i>,<i>N</i>′-dicyclohexylcarbodiimide coupling
reaction between the amine group of ethylenediamine and the carboxylic
group of GO. As a result, a few layers of amine-functionalized graphene
wrapped CdS uniformly, forming a large interfacial area. Under visible
light, the photocurrent through the AG/CdS significantly increased
because of enhanced charge separation in CdS. The CO<sub>2</sub> adsorption
capacity on AG/CdS was 4 times greater than that on rGO/CdS at 1 bar.
These effects resulted in a methane formation rate of 2.84 μmol/(g
h) under visible light and CO<sub>2</sub> at 1 bar, corresponding
to 3.5 times that observed for rGO/CdS. Interestingly, a high methane
formation rate (1.62 μmol/(g h)) was observed for AG/CdS under
CO<sub>2</sub> at low pressure (0.1 bar), corresponding to a value
20 times greater than that observed for the rGO/CdS. Thus, the enhanced
performance for photocatalytic reduction of CO<sub>2</sub> on the
AG/CdS is due to the improved CO<sub>2</sub> adsorption related to
the amine groups on amine-functionalized graphene, which sustains
the strong absorption of visible light and superior charge-transfer
properties in comparison with those of graphene
Rational Design of Aminopolymer for Selective Discrimination of Acidic Air Pollutants
Strong
acidic gases such as CO<sub>2</sub>, SO<sub>2</sub>, and
NO<sub>2</sub> are harsh air pollutants with major human health threatening
factors, and as such, developing new tools to monitor and to quickly
sense these gases is critically required. However, it is difficult
to selectively detect the acidic air pollutants with single channel
material due to the similar chemistry shared by acidic molecules.
In this work, three acidic gases (i.e., CO<sub>2</sub>, SO<sub>2</sub>, and NO<sub>2</sub>) are selectively discriminated using single
channel material with precise moiety design. By changing the composition
ratio of primary (1°), secondary (2°), and tertiary (3°)
amines of polyethylenimine (PEI) on CNT channels, unprecedented high
selectivity between CO<sub>2</sub> and SO<sub>2</sub> is achieved.
Using in situ FT-IR characterizations, the distinct adsorption phenomenon
of acidic gases on each amine moiety is precisely demonstrated. Our
approach is the first attempt at controlling gas adsorption selectivity
of solid-state sensor via modulating chemical moiety level within
the single channel material. In addition, discrimination of CO<sub>2</sub>, SO<sub>2</sub>, and NO<sub>2</sub> with the single channel
material solid-state sensor is first reported. We believe that this
approach can greatly enhance air pollution tracking systems for strong
acidic pollutants and thus aid future studies on selective solid-state
gas sensors