Red-Light-Driven Biophotochemical Diode Based on a Microorganism-Silicon Nanowire Interface for Stable and Efficient Bias-Free CO<sub>2</sub> Reduction.
basic_science · Level V
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- Record sourced from PubMed, PMID 41284823.
- Also identified by DOI 10.1021/acs.nanolett.5c04698.
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Abstract
Artificial photosynthesis offers a promising route for sustainable liquid fuel and feedstock production, yet integrating efficient CO<sub>2</sub> reduction catalysts with light-harvesting systems remains challenging. Here, we present a biophotochemical diode that couples microorganism-driven CO<sub>2</sub> reduction with glycerol oxidation, enabled by silicon nanowire photoelectrodes under varying red-light intensities. Tuning the biotic-abiotic interface─by increasing biocatalyst loading and adjusting the catholyte pH to mitigate local alkalization─significantly improves performance and stability. The enhanced-loading biocathode maintains a high faradaic efficiency across a wide potential range, even under elevated light intensities. At 60 mW/cm<sup>2</sup>, the system achieves a bias-free current density of 3.5 mA/cm<sup>2</sup>. Long-term stability testing at 40 mW/cm<sup>2</sup> demonstrates stable operation for over 100 h. The photoanode generates valuable C<sub>3</sub> products, primarily glycerate and lactate, enhancing the economic viability. This work showcases the importance of microenvironmental control at the biotic-abiotic interface and establishes a scalable platform for light-driven CO<sub>2</sub> reduction using earth-abundant silicon.