Z-Schematic Artificial Leaf Structure for Biosolar Oxyfunctionalization of Hydrocarbons AITranslate
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The natural Z-schematic photosynthesis is a promising catalytic model for solar-to-chemical conversion. Here, we construct a Z-schematic, wireless photoelectrocatalytic (PEC) system (i.e., artificial leaf) for biocatalytic oxyfunctionalization of hydrocarbons. The monolithic leaf structure consists of a tandem photoanode|photocathode configuration that uses sunlight as the sole energy source to drive redox reactions. Under solar light, the ferric oxyhydroxide-coated, molybdenum-doped bismuth vanadate (FeOOH|Mo:BVO) photoanode extracts electrons from H2O electron feedstock and transfers the electrons to the conjugated polyterthiophene (pTTh) photocathode. Meanwhile, the pTTh photocathode absorbs FeOOH|Mo:BVO-filtered light for O2 reduction to H2O2. The in situ generated H2O2 activates unspecific peroxygenases (UPOs) to drive enantioselective C–H oxyfunctionalization (e.g., hydroxylation and epoxidation). Furthermore, we solve HO•-mediated inactivation of UPOs using a cellulose membrane, which increases enzymatic productivity with a benchmark total turnover number of 193 000 among PEC and photocatalytic platforms that trigger UPO-mediated synthesis.
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DOI:https://doi.org/10.1021/acsenergylett.3c00587
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The natural Z-schematic photosynthesis is a promising catalytic model for solar-to-chemical conversion. Here, we construct a Z-schematic, wireless photoelectrocatalytic (PEC) system (i.e., artificial leaf) for biocatalytic oxyfunctionalization of hydrocarbons. The monolithic leaf structure consists of a tandem photoanode|photocathode configuration that uses sunlight as the sole energy source to drive redox reactions. Under solar light, the ferric oxyhydroxide-coated, molybdenum-doped bismuth vanadate (FeOOH|Mo:BVO) photoanode extracts electrons from H2O electron feedstock and transfers the electrons to the conjugated polyterthiophene (pTTh) photocathode. Meanwhile, the pTTh photocathode absorbs FeOOH|Mo:BVO-filtered light for O2 reduction to H2O2. The in situ generated H2O2 activates unspecific peroxygenases (UPOs) to drive enantioselective C–H oxyfunctionalization (e.g., hydroxylation and epoxidation). Furthermore, we solve HO•-mediated inactivation of UPOs using a cellulose membrane, which increases enzymatic productivity with a benchmark total turnover number of 193 000 among PEC and photocatalytic platforms that trigger UPO-mediated synthesis.
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| GB/T 7714-2015 | [1] Chung Hyun Lee, Jinhyun Kim, Chan Beum Park. ACS Energy Letters, 2023(8). DOI:10.1021/acsenergylett.3c00587. |
| MLA | [1] Chung Hyun Lee, et al., ACS Energy Letters, no. 8, 2023, https://doi.org/10.1021/acsenergylett.3c00587. |
| APA | [1] Chung Hyun Lee, Jinhyun Kim, & Chan Beum Park. (2023). ACS Energy Letters(8). https://doi.org/10.1021/acsenergylett.3c00587 |
| IEEE | [1] Chung Hyun Lee, Jinhyun Kim, and Chan Beum Park, ACS Energy Letters, no. 8, 2023, doi: 10.1021/acsenergylett.3c00587. |
