TY - JOUR
T1 - Insight into the Effect of the Cl 3p Orbital on g-C3N4Mimicking Photosynthesis under CO2Reduction
AU - Wang, Yi
AU - Tang, Xu
AU - Huo, Pengwei
AU - Yan, Yongsheng
AU - Zhu, Zhi
AU - Dai, Jiangdong
AU - Liu, Zhixiang
AU - Li, Zhanguo
AU - Xi, Hailing
N1 - Publisher Copyright:
© 2021 American Chemical Society.
PY - 2021/5/13
Y1 - 2021/5/13
N2 - Achieving high-efficiency photocatalytic materials to convert CO2 into high-value chemicals is still challenging. Herein, chlorine-doped g-C3N4 photocatalysts (Cl-CN) were successfully synthesized by a simple multiple calcination method. The as-prepared Cl-CN exhibited satisfactory photocatalytic activity in photoreduction of CO2. The CO yield of Cl-CN was about 39.89 μmol/g. The DRS, UPS, and VB-XPS results indicated a narrower band gap, and the negatively shifted CB potential enhanced the CO2 reduction ability. DFT calculations and the partial density of states revealed that the Cl 3p orbital greatly contributed to the CBM and VBM of Cl-CN, which caused the narrower band gap and an upshift of the conduction band by 0.14 eV over that of bulk-CN. The CO2 conversion intermediate was investigated by in situ Fourier transform infrared spectroscopy, and the corresponding reaction mechanism was proposed according to the density functional theory calculations and experimental results, which showed that Cl doping and the C-Cl bond increased the photogenerated carrier lifetime and the CO2 adsorption capacity of Cl-CN. Therefore, this work provides a deeper understanding of the effect of Cl doping on the g-C3N4 electronic structure and its CO2 reduction activity.
AB - Achieving high-efficiency photocatalytic materials to convert CO2 into high-value chemicals is still challenging. Herein, chlorine-doped g-C3N4 photocatalysts (Cl-CN) were successfully synthesized by a simple multiple calcination method. The as-prepared Cl-CN exhibited satisfactory photocatalytic activity in photoreduction of CO2. The CO yield of Cl-CN was about 39.89 μmol/g. The DRS, UPS, and VB-XPS results indicated a narrower band gap, and the negatively shifted CB potential enhanced the CO2 reduction ability. DFT calculations and the partial density of states revealed that the Cl 3p orbital greatly contributed to the CBM and VBM of Cl-CN, which caused the narrower band gap and an upshift of the conduction band by 0.14 eV over that of bulk-CN. The CO2 conversion intermediate was investigated by in situ Fourier transform infrared spectroscopy, and the corresponding reaction mechanism was proposed according to the density functional theory calculations and experimental results, which showed that Cl doping and the C-Cl bond increased the photogenerated carrier lifetime and the CO2 adsorption capacity of Cl-CN. Therefore, this work provides a deeper understanding of the effect of Cl doping on the g-C3N4 electronic structure and its CO2 reduction activity.
UR - http://www.scopus.com/inward/record.url?scp=85106465590&partnerID=8YFLogxK
U2 - 10.1021/acs.jpcc.1c00663
DO - 10.1021/acs.jpcc.1c00663
M3 - 文章
AN - SCOPUS:85106465590
SN - 1932-7447
VL - 125
SP - 9646
EP - 9656
JO - Journal of Physical Chemistry C
JF - Journal of Physical Chemistry C
IS - 18
ER -