Abstract
It is highly desirable to enhance the photogenerated charge separation of g-C(3)N(4) by constructing efficient heterojunctions, especially with an additional organic constitution for solar-hydrogen conversion. Herein, g-C(3)N(4) nanosheets have been modified controllably with nano-sized poly(3-thiophenecarboxylic acid) (PTA) through in situ photopolymerization and then coordinated with Fe(III) via the -COOH groups of modified PTA, forming an interface of tightly contacted nanoheterojunctions between the Fe(III)-coordinated PTA and g-C(3)N(4). The resulting ratio-optimized nanoheterojunction displays a ~4.6-fold enhancement of the visible-light photocatalytic H(2) evolution activity compared to bare g-C(3)N(4). Based on the surface photovoltage spectra, measurements of the amount of •OH produced, photoluminescence (PL) spectra, photoelectrochemical curves, and single-wavelength photocurrent action spectra, it was confirmed that the improved photoactivity of g-C(3)N(4) is attributed to the significantly promoted charge separation by the transfer of high-energy electrons from the lowest unoccupied molecular orbital (LUMO) of g-C(3)N(4) to the modified PTA via the formed tight interface, dependent on the hydrogen bond interaction between the -COOH of PTA and the -NH(2) of g-C(3)N(4), and the continuous transfer to the coordinated Fe(III) with -OH favorable for connection with Pt as the cocatalyst. This study demonstrates a feasible strategy for solar-light-driven energy production over the large family of g-C(3)N(4) heterojunction photocatalysts with exceptional visible-light activities.