异质结
光催化
拉曼光谱
可见光谱
材料科学
氢氧化物
电场
辐照
光化学
电化学
化学
纳米技术
电极
光电子学
催化作用
无机化学
物理化学
物理
光学
有机化学
核物理学
量子力学
作者
Xinxin Han,Bingjie Lu,Xin Huang,Cheng Liu,Shixia Chen,Jingwen Chen,Zheling Zeng,Shuguang Deng,Jun Wang
标识
DOI:10.1016/j.apcatb.2022.121587
摘要
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.
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