TY - JOUR
T1 - Potassium Molten Salt-Mediated In Situ Structural Reconstruction of a Carbon Nitride Photocatalyst
AU - Gupta, Akanksha
AU - Bhoyar, Toshali
AU - Abraham, B. Moses
AU - Kim, Dong Jin
AU - Pasupuleti, Kedhareswara Sairam
AU - Umare, Suresh S.
AU - Vidyasagar, Devthade
AU - Gedanken, Aharon
N1 - Publisher Copyright:
© 2023 American Chemical Society.
PY - 2023/4/19
Y1 - 2023/4/19
N2 - Metal-free polymeric carbon nitride (PCN) materials are at the forefront of photocatalytic applications. Nevertheless, the overall functionality and performance of bulk PCN are limited by rapid charge recombination, high chemical inertness, and inadequate surface-active sites. To address these, here, we employed potassium molten salts (K+X-, where X- is Cl-, Br-, and I-) as a template for the in situ generation of surface reactive sites in thermal pyrolyzed PCN. Theoretical calculations imply that addition of KX salts to PCN-forming monomers causes halogen ions to be doped into C or N sites of PCN with a relative trend of halogen ion doping being Cl < Br < I. The experimental results show that reconstructing C and N sites in PCN develops newer reactive sites that are beneficial for surface catalysis. Interestingly, the photocatalytic H2O2 generation rate of KBr-modified PCN was 199.0 μmol h-1, about three times that of bulk PCN. Owing to the simple and straightforward approach, we expect molten salt-assisted synthesis to have wide exploration in modifying PCN photocatalytic activity.
AB - Metal-free polymeric carbon nitride (PCN) materials are at the forefront of photocatalytic applications. Nevertheless, the overall functionality and performance of bulk PCN are limited by rapid charge recombination, high chemical inertness, and inadequate surface-active sites. To address these, here, we employed potassium molten salts (K+X-, where X- is Cl-, Br-, and I-) as a template for the in situ generation of surface reactive sites in thermal pyrolyzed PCN. Theoretical calculations imply that addition of KX salts to PCN-forming monomers causes halogen ions to be doped into C or N sites of PCN with a relative trend of halogen ion doping being Cl < Br < I. The experimental results show that reconstructing C and N sites in PCN develops newer reactive sites that are beneficial for surface catalysis. Interestingly, the photocatalytic H2O2 generation rate of KBr-modified PCN was 199.0 μmol h-1, about three times that of bulk PCN. Owing to the simple and straightforward approach, we expect molten salt-assisted synthesis to have wide exploration in modifying PCN photocatalytic activity.
KW - HO generation
KW - chromium reduction
KW - molten salts
KW - polymeric carbon nitride
KW - surface sites
UR - https://www.scopus.com/pages/publications/85152204230
U2 - 10.1021/acsami.3c00239
DO - 10.1021/acsami.3c00239
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C2 - 37018662
AN - SCOPUS:85152204230
SN - 1944-8244
VL - 15
SP - 18898
EP - 18906
JO - ACS Applied Materials and Interfaces
JF - ACS Applied Materials and Interfaces
IS - 15
ER -