TY - JOUR
T1 - A graphitic carbon nitride metal-free visible light photocatalyst with controllable carbon self-doping towards efficient hydrogen evolution
AU - Lei, Lin
AU - Wang, Weijia
AU - Xie, Zhengfeng
AU - Wu, Xiaobo
AU - Yadav, Arun Kumar
AU - Müller-Buschbaum, Peter
AU - Fan, Huiqing
N1 - Publisher Copyright:
© The Royal Society of Chemistry.
PY - 2021/10/21
Y1 - 2021/10/21
N2 - Controlling molecular defects via element doping is an effective strategy for tailoring electronic structures and charge separation in photocatalysts. However, the rational design of self-doped catalysts is generally confronted with the need for expensive reagents, high dopant ratios and environmentally unfriendly materials. Herein, carbon self-doped graphitic carbon nitride (DCN-x) is obtained via one-pot thermal polymerization of urea and d-mannitol. The sp2-hybridized nitrogen atoms are partially substituted by carbon atoms from dopants. The corresponding defects provide the photocatalyst with extended light harvesting up to 600 nm, a tunable optical bandgap, and the formation of more delocalized electrons with a uniform distribution at the defect scope of a C-C bond. In addition, increased band-tail states are found in DCN-3, which greatly enhance charge separation. A high photocatalytic hydrogen evolution rate of 3180 μmol g-1 h-1 is achieved under visible light irradiation (λ > 420 nm), which is about 5.3 fold higher than that of pristine g-C3N4. This work provides a green and economical method to synthesize g-C3N4 with controllable carbon self-doping sites for efficient energy conversion related applications.
AB - Controlling molecular defects via element doping is an effective strategy for tailoring electronic structures and charge separation in photocatalysts. However, the rational design of self-doped catalysts is generally confronted with the need for expensive reagents, high dopant ratios and environmentally unfriendly materials. Herein, carbon self-doped graphitic carbon nitride (DCN-x) is obtained via one-pot thermal polymerization of urea and d-mannitol. The sp2-hybridized nitrogen atoms are partially substituted by carbon atoms from dopants. The corresponding defects provide the photocatalyst with extended light harvesting up to 600 nm, a tunable optical bandgap, and the formation of more delocalized electrons with a uniform distribution at the defect scope of a C-C bond. In addition, increased band-tail states are found in DCN-3, which greatly enhance charge separation. A high photocatalytic hydrogen evolution rate of 3180 μmol g-1 h-1 is achieved under visible light irradiation (λ > 420 nm), which is about 5.3 fold higher than that of pristine g-C3N4. This work provides a green and economical method to synthesize g-C3N4 with controllable carbon self-doping sites for efficient energy conversion related applications.
UR - http://www.scopus.com/inward/record.url?scp=85117370571&partnerID=8YFLogxK
U2 - 10.1039/d1se01244d
DO - 10.1039/d1se01244d
M3 - Article
AN - SCOPUS:85117370571
SN - 2398-4902
VL - 5
SP - 5227
EP - 5235
JO - Sustainable Energy and Fuels
JF - Sustainable Energy and Fuels
IS - 20
ER -