Access to this article is restricted until 12 months after publication by request of the publisher.. Restriction lift date: 2018-11-20
Natural carbonized sugar as a low-temperature ammonia sensor material: experimental, theoretical and computational studies
No Thumbnail Available
Ghule, Balaji G.
Shaikh, Shoyebmohamad F.
Ekar, Satish U.
Nakate, Umesh Tukaram
Gunturu, Krishna Chaitanya
Kim, Kwang Ho
American Chemical Society
Carbonized sugar (CS) has been synthesized via microwave-assisted carbonization of market-quality tabletop sugar bearing in mind the advantages of this synthesis method, such as being useful, cost-effective, and eco-friendly. The as-prepared CS has been characterized for its morphology, phase purity, type of porosity, pore-size distribution, and so on. The gas-sensing properties of CS for various oxidizing and reducing gases are demonstrated at ambient temperature, where we observe good selectivity toward liquid ammonia among other gases. The highest ammonia response (50%) of a CS-based sensor was noted at 80 °C for 100 ppm concentration. The response and recovery times of the CS sensor are 180 and 216 s, respectively. This unveiling ammonia-sensing study is explored through a plausible theoretical mechanism, which is further well-supported by computational modeling performed using density function theory. The effect of relative humidity on the CS sensor has also been studied at ambient temperature, which demonstrated that the minimum and maximum (20–100%) relative humidity values revealed 16 and 62% response, respectively.
Carbonized sugar , Structural analysis , Surface morphology , Ammonia sensor , Density function theory
Ghule, B., Shaikh, S. F., Ekar, S., Nakate, U. T., Gunturu, K. C., Shinde, N., Naushad, M., Kim, K. H., O'Dwyer, C. and Mane, R. (2017) 'Natural carbonized sugar as a low-temperature ammonia sensor material: experimental, theoretical and computational studies', ACS Applied Materials and Interfaces, 9(49), pp. 43051–43060. doi:10.1021/acsami.7b13122
© 2017, American Chemical Society. This document is the Accepted Manuscript version of a Published Work that appeared in final form in ACS Applied Materials and Interfaces © American Chemical Society, after peer review and technical editing by the publisher. To access the final edited and published work see http://pubs.acs.org/doi/10.1021/acsami.7b13122