钨酸盐
异质结
材料科学
检出限
二氧化钛
安培法
光电子学
电极
分解水
电化学
纳米技术
催化作用
无机化学
光催化
化学
生物化学
物理化学
冶金
色谱法
作者
Hui Xu,Hongyuan Shang,Qingyun Liu,Cheng Wang,Junwei Di,Chunyan Chen,Liujun Jin,Yukou Du
标识
DOI:10.1016/j.jcis.2020.07.120
摘要
A novel dual mode sensing platform is constructed for highly selective detection of H2S, attributing to the efficient electrochemical (EC) and photoelectrochemical (PEC) signal responses of the TiO2/Bi2WO6/Ag heterojunction. On the one hand, TiO2/Bi2WO6/Ag heterojunction with excellent catalytic performance for the reduction of H2O2 could be employed act as a probe, providing a remarkable EC response through an amperometric i-t method. On the other hand, this hybrid provides a photoelectric beacon with a favorable energy-band configuration. More interestingly, the EC and PEC responses of the functionalized electrodes are proportionately decreased in response to the generation of Bi2S3 and Ag2S nanoparticles upon exposure to sulfide ions. The decreased EC and PEC signals could be ascribed to the poor catalytic properties and the recombination of photoexcited electron – hole pairs of the Bi2S3 and Ag2S. Under the optimal conditions, the dual mode sensor exhibits a wide linear response in the range from 0.5 μM to 300 μM with a detection limit of 0.08 μM for the detection of H2S. Enabled by this unique sensitization mechanism, the proposed sensing platform displays an excellent analytical performance with good selectivity, reproducibility and stability, which providing an alternative pathway of H2S detecting in practical application.
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