Key points are not available for this paper at this time.
The integration of microbial nitrogen (N2) fixation with photochemical processes using inorganic light-absorbing nanomaterials is a burgeoning field in sustainable energy production. Here, we explore the synergistic combination of inorganic semiconductor nanowires (NWs) with whole-cell microorganisms to create an inorganic-bacterial biohybrid system. Specifically, we employ Cu2O@TiO2 NWs with a core/shell structure to harness sunlight and generate photoexcited electrons. Azotobacter vinelandii, serving as a biocatalyst, adsorbs onto these NWs and facilitates the reception of photoexcited electrons, thereby enhancing the efficiency of the photoelectrochemical N2 fixation reaction (PEC-NRR). The biohybrid system achieves an impressive ammonia (NH3) yield of (1.49 ± 0.05) × 10-9 mol s-1 cm-2 (5.36 ± 0.18 μmol h-1 cm-2). The enhancement in NH3 synthesis within the Cu2O@TiO2 NWs/A. vinelandii biohybrid is attributed to the increased concentrations of nicotinamide adenine dinucleotide-hydrogen (NADH) and adenosine 5'-triphosphate (ATP), as well as the overexpression of N2-fixing genes like nifH and nifD within the nitrogenase enzyme complex. This study underscores the potential of inorganic-bacterial biohybrid systems in solar-chemical conversion, paving the way for more diverse and functional approaches to harnessing solar energy for sustainable chemical production.
Zhou et al. (2025) studied this question.