Abstract
Graphitic carbon nitride (CNx) is a promising photocatalyst with visible-light sensitivity, attractive
band-edge positions, tunable electronic structure, and eco-friendliness. However, their applications
are limited by a low catalytic activity due to inefficient charge separation and insufficient visiblelight absorption. Here we show a new method to generate the electron polarization of CNx toward
the edge via the chemical conjugation of catechol to CNx for enhanced photochemical activity.
The electron-attracting property of catechol/quinone pairs induces the accumulation of photoexcited electrons at the edge of conjugated catechol-CNx hybrid nanostructure (Cat-CNx), ,
serving as an electron hot spot, as demonstrated by positive open-circuit photovoltage, which
increases electron transfer through the conjugated catechol while suppressing charge
recombination in the CNx. The catechol conjugation also widens the photoactive spectrum via the
larger range delocalization of π-electrons. Accordingly, Cat-CNx reveals a 6.3 higher reductive
photocurrent density than CNx. Gold ion reduction dramatically increased due to the enhanced
electron transfer activity of Cat-CNx in cooperation with the inherent hydrophilicity and metal
chelating property of catechols. Cat-CNx exhibits a 4.3 higher maximum adsorption capacity for
gold ions under simulated sun light illumination compared to CNx. This work suggests that the post-modification of CNx’s π-conjugated system is a promising route to handle varied
shortcomings and broaden availability of CNx.
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