TY - JOUR
T1 - Mesoporous Polymeric Cyanamide-Triazole-Heptazine Photocatalysts for Highly-Efficient Water Splitting
AU - Wu, Chongbei
AU - Yu, Guanhang
AU - Yin, Yue
AU - Wang, Yuze
AU - Chen, Li
AU - Han, Qing
AU - Tang, Junwang
AU - Wang, Bo
N1 - Publisher Copyright:
© 2020 Wiley-VCH GmbH
PY - 2020/9/1
Y1 - 2020/9/1
N2 - Conjugated polymers are promising light harvesters for water reduction/oxidation due to their simple synthesis and adjustable bandgap. Herein, both cyanamide and triazole functional groups are first incorporated into a heptazine-based carbon nitride (CN) polymer, resulting in a mesoporous conjugated cyanamide-triazole-heptazine polymer (CTHP) with different compositions by increasing the quantity of cyanamide/triazole units in the CN backbone. Varying the compositions of CTHP modulates its electronic structures, mesoporous morphologies, and redox energies, resulting in a significantly improved photocatalytic performance for both H2 and O2 evolution under visible light irradiation. A remarkable H2 evolution rate of 12723 µmol h−1 g−1 is observed, resulting in a high apparent quantum yield of 11.97% at 400 nm. In parallel, the optimized photocatalyst also exhibits an O2 evolution rate of 221 µmol h−1 g−1, 9.6 times higher than the CN counterpart, with the value being the highest among the reported CN-based bifunctional photocatalysts. This work provides an efficient molecular engineering approach for the rational design of functional polymeric photocatalysts.
AB - Conjugated polymers are promising light harvesters for water reduction/oxidation due to their simple synthesis and adjustable bandgap. Herein, both cyanamide and triazole functional groups are first incorporated into a heptazine-based carbon nitride (CN) polymer, resulting in a mesoporous conjugated cyanamide-triazole-heptazine polymer (CTHP) with different compositions by increasing the quantity of cyanamide/triazole units in the CN backbone. Varying the compositions of CTHP modulates its electronic structures, mesoporous morphologies, and redox energies, resulting in a significantly improved photocatalytic performance for both H2 and O2 evolution under visible light irradiation. A remarkable H2 evolution rate of 12723 µmol h−1 g−1 is observed, resulting in a high apparent quantum yield of 11.97% at 400 nm. In parallel, the optimized photocatalyst also exhibits an O2 evolution rate of 221 µmol h−1 g−1, 9.6 times higher than the CN counterpart, with the value being the highest among the reported CN-based bifunctional photocatalysts. This work provides an efficient molecular engineering approach for the rational design of functional polymeric photocatalysts.
KW - conjugated polymers
KW - hydrogen evolution reaction
KW - oxygen evolution reaction
KW - photocatalysts
KW - water splitting
UR - http://www.scopus.com/inward/record.url?scp=85089312358&partnerID=8YFLogxK
U2 - 10.1002/smll.202003162
DO - 10.1002/smll.202003162
M3 - Article
C2 - 32790004
AN - SCOPUS:85089312358
SN - 1613-6810
VL - 16
JO - Small
JF - Small
IS - 37
M1 - 2003162
ER -