TY - JOUR
T1 - Ordered and Ultralong Graphitic Carbon Nitride Nanotubes Obtained via In-Air CVD for Enhanced Photocatalytic Hydrogen Evolution
AU - Wu, Xiaobo
AU - Fan, Huiqing
AU - Wang, Weijia
AU - Lei, Lin
AU - Chang, Xinye
N1 - Publisher Copyright:
© 2021 American Chemical Society.
PY - 2021/11/22
Y1 - 2021/11/22
N2 - Metal-free graphitic carbon nitride (g-C3N4) has become one of the most up-and-coming photocatalyst candidates for the hydrogen evolution reaction. However, the improvement in photocatalytic property is strongly suppressed by the limited active reaction sites due to the bulk microstructure of g-C3N4. On this basis, we exploit a moderate and economical approach to prepare an ordered and one-dimensionally ultralong carbon nitride nanotube (CN-NT) via the in-air chemical vapor deposition (CVD) with SiO2 nanofiber templates synthesized by electrostatic spinning. Due to the uniform size, fluffiness, and easy removal, SiO2 nanofiber templates are conducive to prepare ordered and tubular CN-NT. The obtained CN-NT sample exhibits an excellent photocatalytic hydrogen evolution rate (HER) of 4605.2 μmol·h-1·g-1 under visible light, which is 33.4 times higher than that of the original bulk g-C3N4. The apparent quantum efficiency reaches 6.49% at 420 nm. The enhancement in the photocatalytic activity is ascribed to the increased specific surface area, faster electron transfer pathway, advanced light absorption ability, and furthermore the lower recombination rate of photogenerated electrons.
AB - Metal-free graphitic carbon nitride (g-C3N4) has become one of the most up-and-coming photocatalyst candidates for the hydrogen evolution reaction. However, the improvement in photocatalytic property is strongly suppressed by the limited active reaction sites due to the bulk microstructure of g-C3N4. On this basis, we exploit a moderate and economical approach to prepare an ordered and one-dimensionally ultralong carbon nitride nanotube (CN-NT) via the in-air chemical vapor deposition (CVD) with SiO2 nanofiber templates synthesized by electrostatic spinning. Due to the uniform size, fluffiness, and easy removal, SiO2 nanofiber templates are conducive to prepare ordered and tubular CN-NT. The obtained CN-NT sample exhibits an excellent photocatalytic hydrogen evolution rate (HER) of 4605.2 μmol·h-1·g-1 under visible light, which is 33.4 times higher than that of the original bulk g-C3N4. The apparent quantum efficiency reaches 6.49% at 420 nm. The enhancement in the photocatalytic activity is ascribed to the increased specific surface area, faster electron transfer pathway, advanced light absorption ability, and furthermore the lower recombination rate of photogenerated electrons.
KW - electrostatic spinning
KW - graphitic carbon nitride
KW - one-dimensional nanotube
KW - photocatalysis
KW - photocatalytic hydrogen evolution
UR - http://www.scopus.com/inward/record.url?scp=85118670961&partnerID=8YFLogxK
U2 - 10.1021/acsaem.1c02846
DO - 10.1021/acsaem.1c02846
M3 - 文章
AN - SCOPUS:85118670961
SN - 2574-0962
VL - 4
SP - 13263
EP - 13271
JO - ACS Applied Energy Materials
JF - ACS Applied Energy Materials
IS - 11
ER -