A. Cao
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5 records found
1
Recently various porous organic frameworks (POFs, crystalline or amorphous materials) have been discovered, and used for a wide range of applications, including molecular separations and catalysis. Silicon nanowires (SiNWs) have been extensively studied for diverse applications, including as transistors, solar cells, lithium ion batteries and sensors. Here we demonstrate the functionalization of SiNW surfaces with POFs and explore its effect on the electrical sensing properties of SiNW-based devices. The surface modification by POFs was easily achieved by polycondensation on amine-modified SiNWs. Platinum nanoparticles were formed in these POFs by impregnation with chloroplatinic acid followed by chemical reduction. The final hybrid system showed highly enhanced sensitivity for methanol vapour detection. We envisage that the integration of SiNWs with POF selector layers, loaded with different metal nanoparticles will open up new avenues, not only in chemical and biosensing, but also in separations and catalysis.
Chemical Sensors based on Si Nanowires
Surface modifications for the detection of ions, explosives and chemical vapors
(SiNW-FETs) have proven to be a promising platform for molecular
recognition in miniature sensors. In this work, we present a novel nanoFET
device for the sensitive and selective detection of explosives based on affinity
layers of metal−organic polyhedra (MOPs). The judicious selection of the
geometric and electronic characteristics of the assembly units (organic ligands
and unsaturated metal site) embedded within the MOP cage allowed for the
formation of multiple charge-transfer (CT) interactions to facilitate the selective
explosive inclusion. Meanwhile, the host-stabilized CT complex inside the cage
acted as an effective molecular gating element to strongly modulate the electrical conductance of the silicon nanowires. By grafting the MOP cages onto a SiNWFET device, the resulting sensor showed a good electrical sensing capability to various explosives, especially 2,4,6-trinitrotoluene (TNT), with a detection limit below the nanomolar level. Importantly, coupling MOPswhich have tunable structures and propertiesto SiNW-based devices may open up new avenues for a wide range of sensing applications, addressing
various target analytes. ...
(SiNW-FETs) have proven to be a promising platform for molecular
recognition in miniature sensors. In this work, we present a novel nanoFET
device for the sensitive and selective detection of explosives based on affinity
layers of metal−organic polyhedra (MOPs). The judicious selection of the
geometric and electronic characteristics of the assembly units (organic ligands
and unsaturated metal site) embedded within the MOP cage allowed for the
formation of multiple charge-transfer (CT) interactions to facilitate the selective
explosive inclusion. Meanwhile, the host-stabilized CT complex inside the cage
acted as an effective molecular gating element to strongly modulate the electrical conductance of the silicon nanowires. By grafting the MOP cages onto a SiNWFET device, the resulting sensor showed a good electrical sensing capability to various explosives, especially 2,4,6-trinitrotoluene (TNT), with a detection limit below the nanomolar level. Importantly, coupling MOPswhich have tunable structures and propertiesto SiNW-based devices may open up new avenues for a wide range of sensing applications, addressing
various target analytes.
The electrocatalytic reduction of CO2 on Au-Pt bimetallic catalysts with different compositions was evaluated, offering a platform for uncovering the correlation between the catalytic activity and the surface composition of bimetallic electrocatalysts. The Au-Pt alloy films were synthesized by a magnetron sputtering co-deposition technique with tunable composition. It was found that the syngas ratio (CO:H2) on the Au-Pt films is able to be tuned by systematically controlling the binary composition. This tunable catalytic selectivity is attributed to the variation of binding strength of COOH and CO intermediates, influenced by the surface electronic structure (d-band center energy) which is linked to the surface composition of the bimetallic films. Notably, a gradual shift of the d-band center away from the Fermi level was observed with increasing Au content, which correspondingly reduces the binding strength of the COOH and CO intermediates, leading to the distinct catalytic activity for the reduction of CO2 on the compositionally variant Au-Pt bimetallic films. In addition, the formation of formic acid in the bimetallic systems at reduced overpotentials and higher yield indicates that synergistic effects can facilitate reaction pathways for products that are not accessible with the individual components.