TY - JOUR
T1 - Simple tactic polycondensation synthesis of Z-scheme quasi-polymeric g-C3N4/CaFe2O4 composite for enhanced photocatalytic water depollution via p-n heterojunction
AU - Shenoy, Sulakshana
AU - Chuaicham, Chitiphon
AU - Okumura, Takamasa
AU - Sekar, Karthikeyan
AU - Sasaki, Keiko
N1 - Funding Information:
The authors are grateful to the Japan Society for the Promotion of Science (JSPS) for funding the research grants ( JP21F21342 , JP22H00266 ) to KS and a postdoctoral fellowship for foreign researchers (JP 21P21342) to SS. The HRTEM analysis was carried out at the Ultramicroscopy Research Center (URC) at Kyushu University, which the authors gratefully acknowledge. The authors would like to express their gratitude to the Kyushu University Nanotech Center for giving access to XPS measurements and BET analysis. This work received funding from Advanced Research Infrastructure for Materials and Nanotechnology Grant Number (JPMXP1222KU1012) in Japan sponsored by the Ministry of Education, Culture, Sports, Science and Technology (MEXT) and the Institute for Catalysis at Hokkaido University (No. 21A1001), Japan.
Funding Information:
The authors are grateful to the Japan Society for the Promotion of Science (JSPS) for funding the research grants (JP21F21342, JP22H00266) to KS and a postdoctoral fellowship for foreign researchers (JP 21P21342) to SS. The HRTEM analysis was carried out at the Ultramicroscopy Research Center (URC) at Kyushu University, which the authors gratefully acknowledge. The authors would like to express their gratitude to the Kyushu University Nanotech Center for giving access to XPS measurements and BET analysis. This work received funding from Advanced Research Infrastructure for Materials and Nanotechnology Grant Number (JPMXP1222KU1012) in Japan sponsored by the Ministry of Education, Culture, Sports, Science and Technology (MEXT) and the Institute for Catalysis at Hokkaido University (No. 21A1001), Japan.
Publisher Copyright:
© 2022 Elsevier B.V.
PY - 2023/2/1
Y1 - 2023/2/1
N2 - Ferrites are promising photocatalysts as they absorb a considerable fraction of visible light. Herein, a novel in-situ simple tactic polycondensation method was used to produce n-type porous graphitic carbon nitride nanosheets over p-type CaFe2O4 particles resulting in a “quasi-polymeric” heterojunction. An interfacial electron trap state was created, as represented by an energy-resolved distribution of electron trap patterns in the g-C3N4/CaFe2O4, which traps excited electrons and prevents charge carrier recombination. When the CaFe2O4 precursor content in the g-C3N4/CaFe2O4composite was optimized, the degradation rates of ciprofloxacin and phenol are 2.3 and 2.1-fold higher in comparison to pristine g-C3N4, respectively. The g-C3N4/CaFe2O4 composite efficiently absorbed visible light and could separate and transport charge carriers through the p-n heterojunction. The efficient interfacial charge transport and separation achieved in the composite were validated using photoluminescence spectra and photoelectrochemical characterizations. Based on scavenger studies and electron spin resonance analysis, the most active radical species for the aforementioned pollutant degradation are holes and superoxide anion radicals. Mott-Schottky measurements and X-ray photoelectron spectroscopy confirmed the photocatalytic reaction mechanism is a Z-scheme charge carrier transport route based on the p-n heterojunction. Therefore, the g-C3N4/CaFe2O4 heterojunction offers a lot of promise for pollutant degradation that is both efficient and long-term.
AB - Ferrites are promising photocatalysts as they absorb a considerable fraction of visible light. Herein, a novel in-situ simple tactic polycondensation method was used to produce n-type porous graphitic carbon nitride nanosheets over p-type CaFe2O4 particles resulting in a “quasi-polymeric” heterojunction. An interfacial electron trap state was created, as represented by an energy-resolved distribution of electron trap patterns in the g-C3N4/CaFe2O4, which traps excited electrons and prevents charge carrier recombination. When the CaFe2O4 precursor content in the g-C3N4/CaFe2O4composite was optimized, the degradation rates of ciprofloxacin and phenol are 2.3 and 2.1-fold higher in comparison to pristine g-C3N4, respectively. The g-C3N4/CaFe2O4 composite efficiently absorbed visible light and could separate and transport charge carriers through the p-n heterojunction. The efficient interfacial charge transport and separation achieved in the composite were validated using photoluminescence spectra and photoelectrochemical characterizations. Based on scavenger studies and electron spin resonance analysis, the most active radical species for the aforementioned pollutant degradation are holes and superoxide anion radicals. Mott-Schottky measurements and X-ray photoelectron spectroscopy confirmed the photocatalytic reaction mechanism is a Z-scheme charge carrier transport route based on the p-n heterojunction. Therefore, the g-C3N4/CaFe2O4 heterojunction offers a lot of promise for pollutant degradation that is both efficient and long-term.
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U2 - 10.1016/j.cej.2022.139758
DO - 10.1016/j.cej.2022.139758
M3 - Article
AN - SCOPUS:85140463927
VL - 453
JO - Chemical Engineering Journal
JF - Chemical Engineering Journal
SN - 1385-8947
M1 - 139758
ER -