4.7 Article

Enhanced interfacial electron transfer between semiconductor and non-photosynthetic microorganism under visible light

Journal

BIOELECTROCHEMISTRY
Volume 147, Issue -, Pages -

Publisher

ELSEVIER SCIENCE SA
DOI: 10.1016/j.bioelechem.2022.108195

Keywords

Carbon nitride; Non -photosynthetic microorganism; Extracellular electron transfer; Riboflavin

Funding

  1. National Key Research and Development Plan of China [2018YFC1800502]
  2. Na- tional Science Fund for Distinguished Young Scholars [22025603]
  3. National Natural Science Foundation of China [21802133, 22106161]
  4. China Postdoctoral Science Research Foundation [2018M642574]

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This study found that electron transfer at the biotic-abiotic interface can be enhanced under visible light. Non-photosynthetic microorganisms can capture and utilize visible light by transferring electrons to the valence band of carbon nitride, and this electron transfer is facilitated by the cyclic conversion of riboflavin.
Under visible light, non-photosynthetic microorganism/semiconductor has recently shown promising applica-tions in biofuel production, bioenergy generation and pollutant removal. However, the understanding of electron transfer mechanism at the biotic-abiotic interface is limited. Herein, mixed culture/carbon nitride and pure culture (Stenotrophomonas maltophilia HP14)/carbon nitride were constructed to reveal the energy conversion pathway under visible light. Enhanced electron transfer was observed on the biotic-abiotic interface. The photocurrent of non-photosynthetic S. maltophilia HP14/g-C3N4/ITO with riboflavin addition was 10.2-fold higher than that of g-C3N4/ITO control. As the electron donor, S. maltophilia HP14 transfer bio-electrons to self-secreted riboflavin and valence band of semiconductor. Riboflavin (RF) accept bio-electrons and photo -generated electrons to form 1,5-dihydroflavin (RFH2). While RFH2 is able to transfer electrons to the valence band of carbon nitride and transform into RF again. However, riboflavin is not stable under visible light irradiation, which may lead to a decreased photocurrent. This study demonstrated the role of redox active com-pounds at the microorganism/semiconductor interface and described a possibility for non-photosynthetic microorganisms to capture and utilize visible light.

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