TY - JOUR
T1 - Novel p- and n-type S-scheme heterojunction photocatalyst for boosted CO2 photoreduction activity
AU - Han, Xinxin
AU - Lu, Bingjie
AU - Huang, Xin
AU - Liu, Cheng
AU - Chen, Shixia
AU - Chen, Jingwen
AU - Zeng, Zheling
AU - Deng, Shuguang
AU - Wang, Jun
N1 - Funding Information:
This research work was supported by the National Natural Science Foundation of China (No. 21908090 , 22008101 , 22108243 , and 22168023 ), the Natural Science Foundation of Jiangxi Province (No. 20202BAB203010 and 20212BAB213038 ) and the Special Fund for Postgraduate Innovation of Jiangxi Province ( YC2020-S116 ).
Publisher Copyright:
© 2022 Elsevier B.V.
PY - 2022/11/5
Y1 - 2022/11/5
N2 - S-scheme photocatalysts are more efficient than the conventional type-II configuration, but the CO2 reduction performances are still unsatisfactory. Herein, we firstly report the layered double hydroxide (LDH) based S-scheme heterostructure photocatalyst (NiIn LDH/In2S3) with n-type NiIn LDH and p-type In2S3. The built-in internal electric field directs the photogenerated electrons flow from the conductive band of In2S3 to the valance band of NiIn LDH, which is confirmed by operando and theoretical experiments. The CO2 photoreduction intermediates are monitored by in-situ Raman spectra, and the density functional calculations disclose the reduced energy barrier for CO desorption on the heterojunction. Therefore, without cocatalysts or sacrificial agents, the NiIn LDH/In2S3 heterojunction delivers a high CO yield rate of 29.43 μmol g−1 h−1 under visible light irradiation, ca. 3.5 and 4.3 times higher than the single counterpart NiIn LDH and In2S3. Notably, this value is the highest among S-scheme CO2 photocatalysts and surpasses most top-ranking benchmarks.
AB - S-scheme photocatalysts are more efficient than the conventional type-II configuration, but the CO2 reduction performances are still unsatisfactory. Herein, we firstly report the layered double hydroxide (LDH) based S-scheme heterostructure photocatalyst (NiIn LDH/In2S3) with n-type NiIn LDH and p-type In2S3. The built-in internal electric field directs the photogenerated electrons flow from the conductive band of In2S3 to the valance band of NiIn LDH, which is confirmed by operando and theoretical experiments. The CO2 photoreduction intermediates are monitored by in-situ Raman spectra, and the density functional calculations disclose the reduced energy barrier for CO desorption on the heterojunction. Therefore, without cocatalysts or sacrificial agents, the NiIn LDH/In2S3 heterojunction delivers a high CO yield rate of 29.43 μmol g−1 h−1 under visible light irradiation, ca. 3.5 and 4.3 times higher than the single counterpart NiIn LDH and In2S3. Notably, this value is the highest among S-scheme CO2 photocatalysts and surpasses most top-ranking benchmarks.
KW - CO photoreduction
KW - Heterojunction
KW - Layered double hydroxide
KW - S-scheme
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U2 - 10.1016/j.apcatb.2022.121587
DO - 10.1016/j.apcatb.2022.121587
M3 - Article
AN - SCOPUS:85132856944
SN - 0926-3373
VL - 316
JO - Applied Catalysis B: Environmental
JF - Applied Catalysis B: Environmental
M1 - 121587
ER -