Heterojunction engineering is recognized as a promising strategy to modulate the photocatalytic properties of semiconductors.Herein,lead-free Cs_(2)CuBr_(4)perovskite quantum dots(PQDs)were confined in a mesoporous Cu...Heterojunction engineering is recognized as a promising strategy to modulate the photocatalytic properties of semiconductors.Herein,lead-free Cs_(2)CuBr_(4)perovskite quantum dots(PQDs)were confined in a mesoporous CuO framework and a p-n type S-scheme heterojunction of Cs_(2)CuBr_(4)/CuO(CCB/CuO)photocatalyst was fabricated.Experimental characterizations confirmed the effective confinement of the Cs_(2)CuBr_(4)PQDs in the mesoporous CuO framework,which enabled intimate contact in the interface of CCB/CuO heterojunction,thus facilitating the interfacial charge migration and separation between p-type CuO and n-type Cs_(2)CuBr_(4).Owing to the outstanding charge transport property and CO_(2)adsorption capacity,the developed CCB/CuO heterojunction exhibited remarkably enhanced photocatalytic CO_(2)conversion efficiency with an electron consumption rate(R_(electron))of 281.1μmol g^(-1)h^(-1),which was approximately2.8 times higher than that of pristine Cs_(2)CuBr_(4).These findings provide some insights into the rational engineering design of lead-free perovskite-based heterostructures for efficient photocatalytic CO_(2)conversion.展开更多
An efficient room-temperature self-powered,broadband(300 nm–1100 nm)photodetector based on a CuO–TiO_(2)/TiO_(2)/p-Si(100)heterostructure is demonstrated.The CuO–TiO_(2)nanocomposites were grown in a two-zone horiz...An efficient room-temperature self-powered,broadband(300 nm–1100 nm)photodetector based on a CuO–TiO_(2)/TiO_(2)/p-Si(100)heterostructure is demonstrated.The CuO–TiO_(2)nanocomposites were grown in a two-zone horizontal tube furnace on a 40 nm TiO_(2)thin film deposited on a p-type Si(100)substrate.The CuO–TiO_(2)/TiO_(2)/p-Si(100)devices exhibited excellent rectification characteristics under dark and individual photoillumination conditions.The devices showed remarkable photo-response under broadband(300–1100 nm)light illumination at zero bias voltage,indicating the achievement of highly sensitive self-powered photodetectors at visible and near-infrared light illuminations.The maximum response of the devices is observed at 300 nm for an illumination power of 10 W.The response and recovery times were calculated as 86 ms and 78 ms,respectively.Moreover,under a small bias,the devices showed a prompt binary response by altering the current from positive to negative under illumination conditions.The main reason behind this binary response is the low turn-on voltage and photovoltaic characteristics of the devices.Under illumination conditions,the generation of photocurrent is due to the separation of photogenerated electron-hole pairs within the built-in electric field at the CuO–TiO_(2)/TiO_(2)interface.These characteristics make the CuO–TiO_(2)/TiO_(2)broadband photodetectors suitable for applications that require high response speeds and self-sufficient functionality.展开更多
The Bi_(2)MoO_(6)/TiO_(2)and Bi_(2)MoO_(6)/Ag/TiO_(2)composites were solvothermally synthesized and characterized by X-ray diffraction(XRD),X-ray photoelectron spectroscopy(XPS),and(high resolution)transmission electr...The Bi_(2)MoO_(6)/TiO_(2)and Bi_(2)MoO_(6)/Ag/TiO_(2)composites were solvothermally synthesized and characterized by X-ray diffraction(XRD),X-ray photoelectron spectroscopy(XPS),and(high resolution)transmission electron microscopy((HR)TEM).The Bi_(2)MoO_(6)/TiO_(2)and Bi_(2)MoO_(6)/Ag/TiO_(2)composites exhibited higher photocatalytic activity than pure Bi_(2)MoO_(6).100%of the Rh B dye molecules could be decomposed over Bi_(2)MoO_(6)/Ag/TiO_(2)composite in 120 min.The enhanced photocatalytic activity of Bi_(2)MoO_(6)/TiO_(2)and Bi_(2)MoO_(6)/Ag/TiO_(2)composite was attributed to the efficient separation of photoinduced electrons and holes.The mechanism for the enhanced photocatalytic activity is discussed.展开更多
基金financially supported by Natural Science Foundation of Shanghai(No.22ZR1460700)Shanghai Institute of Technology(No.XTCX2022-28)。
文摘Heterojunction engineering is recognized as a promising strategy to modulate the photocatalytic properties of semiconductors.Herein,lead-free Cs_(2)CuBr_(4)perovskite quantum dots(PQDs)were confined in a mesoporous CuO framework and a p-n type S-scheme heterojunction of Cs_(2)CuBr_(4)/CuO(CCB/CuO)photocatalyst was fabricated.Experimental characterizations confirmed the effective confinement of the Cs_(2)CuBr_(4)PQDs in the mesoporous CuO framework,which enabled intimate contact in the interface of CCB/CuO heterojunction,thus facilitating the interfacial charge migration and separation between p-type CuO and n-type Cs_(2)CuBr_(4).Owing to the outstanding charge transport property and CO_(2)adsorption capacity,the developed CCB/CuO heterojunction exhibited remarkably enhanced photocatalytic CO_(2)conversion efficiency with an electron consumption rate(R_(electron))of 281.1μmol g^(-1)h^(-1),which was approximately2.8 times higher than that of pristine Cs_(2)CuBr_(4).These findings provide some insights into the rational engineering design of lead-free perovskite-based heterostructures for efficient photocatalytic CO_(2)conversion.
基金CSIR-09/0973(11599)/2021-EMR-I and SERB(Project no:CRG/2021/000255),Department of Science and Technology,Govt.of India。
文摘An efficient room-temperature self-powered,broadband(300 nm–1100 nm)photodetector based on a CuO–TiO_(2)/TiO_(2)/p-Si(100)heterostructure is demonstrated.The CuO–TiO_(2)nanocomposites were grown in a two-zone horizontal tube furnace on a 40 nm TiO_(2)thin film deposited on a p-type Si(100)substrate.The CuO–TiO_(2)/TiO_(2)/p-Si(100)devices exhibited excellent rectification characteristics under dark and individual photoillumination conditions.The devices showed remarkable photo-response under broadband(300–1100 nm)light illumination at zero bias voltage,indicating the achievement of highly sensitive self-powered photodetectors at visible and near-infrared light illuminations.The maximum response of the devices is observed at 300 nm for an illumination power of 10 W.The response and recovery times were calculated as 86 ms and 78 ms,respectively.Moreover,under a small bias,the devices showed a prompt binary response by altering the current from positive to negative under illumination conditions.The main reason behind this binary response is the low turn-on voltage and photovoltaic characteristics of the devices.Under illumination conditions,the generation of photocurrent is due to the separation of photogenerated electron-hole pairs within the built-in electric field at the CuO–TiO_(2)/TiO_(2)interface.These characteristics make the CuO–TiO_(2)/TiO_(2)broadband photodetectors suitable for applications that require high response speeds and self-sufficient functionality.
基金National Training Programs of Innovation and Entrepreneurship for Undergraduates(Nos.202010357021,202010357296)Anhui Province Key Laboratory of Chemistry for Inorganic/Organic Hybrid Functionalized Materials,Anhui University+1 种基金Anhui Provincial Natural Science Foundation(No.1308085MA04)the Higher Educational Natural Science Foundation of Anhui Province(No.KJ2013A031)。
文摘The Bi_(2)MoO_(6)/TiO_(2)and Bi_(2)MoO_(6)/Ag/TiO_(2)composites were solvothermally synthesized and characterized by X-ray diffraction(XRD),X-ray photoelectron spectroscopy(XPS),and(high resolution)transmission electron microscopy((HR)TEM).The Bi_(2)MoO_(6)/TiO_(2)and Bi_(2)MoO_(6)/Ag/TiO_(2)composites exhibited higher photocatalytic activity than pure Bi_(2)MoO_(6).100%of the Rh B dye molecules could be decomposed over Bi_(2)MoO_(6)/Ag/TiO_(2)composite in 120 min.The enhanced photocatalytic activity of Bi_(2)MoO_(6)/TiO_(2)and Bi_(2)MoO_(6)/Ag/TiO_(2)composite was attributed to the efficient separation of photoinduced electrons and holes.The mechanism for the enhanced photocatalytic activity is discussed.
基金supported by the National Natural Science Foundation of China (Nos.52274295,52104291,51874079)the Natural Science Foundation of Hebei Province,China (Nos.E2022501028,E2022501029,E2021501029,A2021501007,E2018501091,E2020501001,E2022501030)+4 种基金the Hebei Province Key Research and Development Plan Project,China (No.19211302D)Performance Subsidy Fund for Key Laboratory of Dielectric and Electrolyte Functional Material Hebei Province,China (No.22567627H)the Fundamental Research Funds for the Central Universities,China (Nos.N2223009,N2223010,N2123035,N2023040)the Science and Technology Project of Hebei Education Department,China (No.ZD2022158)the Central Guided Local Science and Technology Development Fund Project of Hebei Province,China (No.226Z4401G).
