Version 2 2024-06-05, 11:01Version 2 2024-06-05, 11:01
Version 1 2018-05-11, 09:49Version 1 2018-05-11, 09:49
journal contribution
posted on 2018-03-14, 00:00authored byB Y Zhang, A Zavabeti, A F Chrimes, F Haque, Luke O'DellLuke O'Dell, H Khan, N Syed, R Datta, Yichao Wang, A S R Chesman, T Daeneke, K Kalantar-zadeh, J Z Ou
Plasmonic biosensors based on noble metals generally suffer from low sensitivities if the perturbation of refractive-index in the ambient is not significant. By contrast, the features of degenerately doped semiconductors offer new dimensions for plasmonic biosensing, by allowing charge-based detection. Here, this concept is demonstrated in plasmonic hydrogen doped molybdenum oxides (HxMoO3), with the morphology of 2D nanodisks, using a representative enzymatic glucose sensing model. Based on the ultrahigh capacity of the molybdenum oxide nanodisks for accommodating H+, the plasmon resonance wavelengths of HxMoO3are shifted into visible-near-infrared wavelengths. These plasmonic features alter significantly as a function of the intercalated H+concentration. The facile H+deintercalation out of HxMoO3provides an exceptional sensitivity and fast kinetics to charge perturbations during enzymatic oxidation. The optimum sensing response is found at H1.55MoO3, achieving a detection limit of 2 × 10−9m at 410 nm, even when the biosensing platform is adapted into a light-emitting diode-photodetector setup. The performance is superior in comparison to all previously reported plasmonic enzymatic glucose sensors, providing a great opportunity in developing high performance biosensors.