The
real-world application of an enzyme-based biofuel cell (EBFC)
requires the desirable immobilization of enzymes on the electrode
surface, offering the feasibility of addressing its short lifetime
and low-power density. Nevertheless, an efficient immobilization of
enzymes strongly relies on the preferred scaffolding between the enzyme
and the electrode. Accordingly, the development of a promising route
to attain a tunable scaffold structure is urgently required. Herein,
we present a facile and ecofriendly route for efficiently controlling
the scaffold structure by investigating the interplay of tripolyphosphate
(TPP), chitosan (CS), and Na. A series of glucose oxidase (GOx)-based
anodic electrodes, GOx[CS/TPP]CC, GOx[CS/Na]CC, and GOx[CS/TPP/Na]CC,
are synthesized using CS/TPP, CS/Na, and CS/TPP/Na as the scaffolding
on carbon cloth (CC) followed by the immobilization of GOx for a comparative
study of the microstructure, enzyme loading, and electrochemical property.
It is revealed that the self-pumping EBFC, driven by capillary force,
utilizing GOx[CS/TPP/Na]CC can deliver a higher peak power density
(1.077 mW cm–2) than that utilizing GOx[CS/TPP]CC
(0.776 mW cm–2) and GOx[CS/Na]CC (0.682 mW cm–2). The self-pumping EBFC utilizing GOx[CS/TPP/Na]CC
can retain 89.2% of its beginning performance even after 240 h of
testing, as compared with that utilizing GOx[CS/Na]CC (61.1%). This
enhancement can be attributed to the formation of a desirable scaffold
structure via the cross-linked CS/TPP matrices combined with Na polymers
for the hybrid enzyme immobilization, simultaneously offering the
capability of improving the enzyme-loading efficiency, facilitating
the interaction between the surface electrode and the enzyme, and
preventing the release of the enzyme during the cell operation.