We report on mild and selective filling of multiwalled carbon nanotubes (MWCNTs) with Prussian blue (PB) to explore the filling/electrochemistry/mass-transfer in nanochannels and the biosensing mode of nanochannel interior-exterior cooperation. PB-filled MWCNTs (MWCNTs-PB in ) are prepared by filling MWCNTs with the gradually growing PB and then selectively removing the outer-surface PB by careful chemical washing. The prepared MWCNTs-PB in composites possess high filling yield (mass ratio of PB to MWCNTs, (30 ± 3)%) and electroactivity percentage (mass ratio of electroactive PB to total PB, (45 ± 3)%). The MWCNTs-PB in composites on Au electrode exhibit strong and stable electrocatalytic activity of filled PB for H 2 O 2 reduction and electroanalysis. The filling of the MWCNTs with electroactive PB also provides a new experimental platform to deal with the widely concerned issue of mass transfer inside nanochannels. The normalized cyclic voltammetric responses of filled PB on MWCNTs-PB in electrode at relatively low scan rates (below 125 and 75 mV s –1 for mass transfer of K + and K + + H 2 O 2, respectively) were found to be equivalent to those of conventionally electrodeposited PB on MWCNTs/Au and Au electrodes, demonstrating that the mass transfer of K + and H 2 O 2 inside our MWCNTs is comparable to those outside our MWCNTs at the low scan rates. Furthermore, the unoccupied outer surfaces of MWCNTs-PB in are conveniently exploited to bind 4-(1-pyrenyl) butyric acid through π–π stacking interaction and then to anchor glucose oxidase or lactate oxidase through the EDC/NHS chemistry. Thus, we have developed a novel cooperative biosensing mode by combining outer-surface biocatalyzed oxidation of substrate with interior PB-catalyzed reduction of enzymatically generated H 2 O 2, which endows our biosensors with low detection potential (−0.1 V) and satisfactory sensitivity/selectivity.
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Wang et al. (2012) studied this question.
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