Abstract

AbstractThe detection of toxic gases, such as NH3 and CO, in the environment is of high interest in chemical, electronic, and automotive industry as even small amounts can display a health risk for workers. Sensors for the real‐time monitoring of these gases should be simple, robust, reversible, highly sensitive, inexpensive and show a fast response. The indicator supraparticles presented herein can fulfill all of these requirements. They consist of silica nanoparticles, which are assembled to supraparticles upon spray‐drying. Sensing molecules such as Reichardt's dye and a binuclear rhodium complex are loaded onto the microparticles to target NH3 and CO detection, respectively. The spray‐drying technique affords high flexibility in primary nanoparticle size selection and thus, easy adjustment of the porosity and specific surface area of the obtained micrometer‐sized supraparticles. This ultimately enables the fine‐tuning of the sensor sensitivity and response. For the application of the indicator supraparticles in a gas detection device, they can be immobilized on a coating. Due to their microscale size, they are large enough to poke out of thin coating layers, thus guaranteeing their gas accessibility, while being small enough to be applicable to flexible substrates.

Highlights

  • Sensors for the real-time monitoring of NH3 and CO gases should be simple, robust, reversible, highly sensitive, and fine-tuning of the sensor sensitivity and response

  • Due to their microscale size, they are large enough to poke out of thin coating layers, guaranteeing their gas accessibility, while being small enough to be applicable to flexible substrates

  • The measured specific surface area, average pore diameter, and total pore volume determined by gas adsorption and calculated based on the Brunauer, Emmett, and Teller (BET) model, the Barret–Joyner– Halenda (BJH) analysis, and the Gurvich rule, respectively, are shown

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Summary

Composition of Supraparticles as Support Matrix

Four different sizes of primary silica nanoparticle building blocks were assembled to supraparticles upon spray-drying. It can be seen that by changing the primary silica nanoparticle size, the specific surface area of the particles can be varied from about 46 to about 166 m2 g−1, while the average pore diameter ranges from 37 to 160 Å and the total pore volume from 0.125 to 0.185 cm g−1 These three values are modified www.particle-journal.com by the assembly structure, as well as the packing density of one or two nanoparticle types in the microparticle. This is why the smallest size in primary nanoparticles does not automatically lead to the highest specific surface area of Particle A, which would be expected for nonassembled nanoparticles. The higher surface area and smaller pore diameter of Particle G compared to Particle B can be only explained by the assembly structure of Particle G and not by the primary nanoparticle sizes

CO Sensing by Indicator Supraparticles
NH3 Sensing by Indicator Supraparticles
Conclusion
Experimental Section
Conflict of Interest
Full Text
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