TY - JOUR
T1 - Ultrasensitive Detection of Volatile Organic Compounds by a Pore Tuning Approach Using Anisotropically Shaped SnO2 Nanocrystals
AU - Kida, Tetsuya
AU - Suematsu, Koichi
AU - Hara, Kazuyoshi
AU - Kanie, Kiyoshi
AU - Muramatsu, Atsushi
N1 - Funding Information:
This work was supported by a Grant-in-Aid for Scientific Research (B) (No. 26288107) from the Ministry of Education, Culture, Sports, Science and Technology of Japan. This work was also financially supported by Industrial Technology Research Grant Program in 2011 (No. 11b15004d) from New Energy and Industrial Technology Development Organization (NEDO).
Publisher Copyright:
© 2016 American Chemical Society.
PY - 2016/12/28
Y1 - 2016/12/28
N2 - Gas sensing with oxide nanostructures is increasingly important to detect gaseous compounds for safety monitoring, process controls, and medical diagnostics. For such applications, sensor sensitivity is one major criterion. In this study, to sensitively detect volatile organic compounds (VOCs) at very low concentrations, we fabricated porous films using SnO2 nanocubes (13 nm) and nanorods with different rod lengths (50-500 nm) that were synthesized by a hydrothermal method. The sensor response to H2 increased with decreasing crystal size; the film made of the smallest nanocubes showed the best sensitivity, which suggested that the H2 sensing is controlled by crystal size. In contrast, the responses to ethanol and acetone increased with increasing crystal size and resultant pore size; the highest sensitivity was observed for a porous film using the longest nanorods. Using the Knudsen diffusion-surface reaction equation, the gas sensor responses to ethanol and acetone were simulated and compared with experimental data. The simulation results proved that the detection of ethanol and acetone was controlled by pore size. Finally, we achieved ultrahigh sensitivity to ethanol; the sensor response (S) exceeded S = 100 000, which corresponds to an electrical resistance change of 5 orders of magnitude in response to 100 ppm of ethanol at 250 °C. The present approach based on pore size control provides a basis for designing highly sensitive films to meet the criterion for practical sensors that can detect a wide variety of VOCs at ppb concentrations.
AB - Gas sensing with oxide nanostructures is increasingly important to detect gaseous compounds for safety monitoring, process controls, and medical diagnostics. For such applications, sensor sensitivity is one major criterion. In this study, to sensitively detect volatile organic compounds (VOCs) at very low concentrations, we fabricated porous films using SnO2 nanocubes (13 nm) and nanorods with different rod lengths (50-500 nm) that were synthesized by a hydrothermal method. The sensor response to H2 increased with decreasing crystal size; the film made of the smallest nanocubes showed the best sensitivity, which suggested that the H2 sensing is controlled by crystal size. In contrast, the responses to ethanol and acetone increased with increasing crystal size and resultant pore size; the highest sensitivity was observed for a porous film using the longest nanorods. Using the Knudsen diffusion-surface reaction equation, the gas sensor responses to ethanol and acetone were simulated and compared with experimental data. The simulation results proved that the detection of ethanol and acetone was controlled by pore size. Finally, we achieved ultrahigh sensitivity to ethanol; the sensor response (S) exceeded S = 100 000, which corresponds to an electrical resistance change of 5 orders of magnitude in response to 100 ppm of ethanol at 250 °C. The present approach based on pore size control provides a basis for designing highly sensitive films to meet the criterion for practical sensors that can detect a wide variety of VOCs at ppb concentrations.
KW - gas sensor
KW - Knudsen diffusion
KW - nanocubes
KW - nanorods
KW - pore control
KW - SnO
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U2 - 10.1021/acsami.6b13006
DO - 10.1021/acsami.6b13006
M3 - Article
AN - SCOPUS:85007603314
SN - 1944-8244
VL - 8
SP - 35485
EP - 35495
JO - ACS applied materials & interfaces
JF - ACS applied materials & interfaces
IS - 51
ER -