NiFe-Layered Double Hydroxides/Lead-free Cs2AgBiBr6 Perovskite 2D/2D Heterojunction for Photocatalytic CO2 Conversion
Designing of heterojunction photocatalysts with appropriate interfacial contact plays crucial roles in enhancing the interfacial charge transfer/separation. A two-dimensional (2D)/2D face-to-face heterojunction is an ideal option since this architecture with a large contact area can provide abundant...
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Published in | Inorganic chemistry Vol. 62; no. 4; pp. 1752 - 1761 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
American Chemical Society
30.01.2023
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Online Access | Get full text |
ISSN | 0020-1669 1520-510X 1520-510X |
DOI | 10.1021/acs.inorgchem.2c04374 |
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Summary: | Designing of heterojunction photocatalysts with appropriate interfacial contact plays crucial roles in enhancing the interfacial charge transfer/separation. A two-dimensional (2D)/2D face-to-face heterojunction is an ideal option since this architecture with a large contact area can provide abundant reactive centers and promote the interfacial charge transfer/separation between layers. Herein, a novel 2D/2D heterojunction of NiFe-layered double hydroxides (NiFe-LDH)/Cs2AgBiBr6 (CABB) was fabricated by electrostatic self-assembly of NiFe-LDH and CABB nanosheets. This unique 2D/2D architecture endowed NiFe-LDH/CABB with a large contact area and a short charge transport distance, assuring remarkable interfacial charge transfer/separation rates. As a result, the 2D/2D NiFe-LDH/CABB heterojunction exhibited significant improvement in photocatalytic CO2 reduction under visible light than the pristine counterparts. Based on density functional theory calculations and various characterizations, a step scheme charge-transfer mechanism was proposed. This investigation sheds light on the designing and manufacturing of highly efficient 2D/2D heterostructure photocatalysts for artificial photosynthesis. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0020-1669 1520-510X 1520-510X |
DOI: | 10.1021/acs.inorgchem.2c04374 |