Enhancement in hydrogen evolution using Au-TiO2 hollow spheres with microbial devices modified with conjugated oligoelectrolytes

Objective: Although photoelectrochemical (PEC) water splitting heralds the emergence of the hydrogen economy, the need for external bias and low efficiency stymies the widespread application of this technology. By coupling water splitting (in a PEC cell) to a microbial fuel cell (MFC) using Escheric...

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Published inNPJ biofilms and microbiomes Vol. 1; no. 1; p. 15020
Main Authors Ngaw, Chee Keong, Wang, Victor Bochuan, Liu, Zhengyi, Zhou, Yi, Kjelleberg, Staffan, Zhang, Qichun, Tan, Timothy Thatt Yang, Loo, Say Chye Joachim
Format Journal Article
LanguageEnglish
Published London Nature Publishing Group UK 21.10.2015
Nature Publishing Group
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Summary:Objective: Although photoelectrochemical (PEC) water splitting heralds the emergence of the hydrogen economy, the need for external bias and low efficiency stymies the widespread application of this technology. By coupling water splitting (in a PEC cell) to a microbial fuel cell (MFC) using Escherichia coli as the biocatalyst, this work aims to successfully demonstrate a sustainable hybrid PEC–MFC platform functioning solely by biocatalysis and solar energy, at zero bias. Through further chemical modification of the photo-anode (in the PEC cell) and biofilm (in the MFC), the performance of the hybrid system is expected to improve in terms of the photocurrent generated and hydrogen evolved. Methods: The hybrid system constitutes the interconnected PEC cell with the MFC. Both PEC cell and MFC are typical two-chambered systems housing the anode and cathode. Au-TiO 2 hollow spheres and conjugated oligoelectrolytes were synthesised chemically and introduced to the PEC cell and MFC, respectively. Hydrogen evolution measurements were performed in triplicates. Results: The hybrid PEC–MFC platform generated a photocurrent density of 0.35 mA/cm 2 (~70× enhancement) as compared with the stand-alone P25 standard PEC cell (0.005 mA/cm 2 ) under one-sun illumination (100 mW/cm 2 ) at zero bias (0 V vs. Pt). This increase in photocurrent density was accompanied by continuous H 2 production. No H 2 was observed in the P25 standard PEC cell whereas H 2 evolution rate was ~3.4 μmol/h in the hybrid system. The remarkable performance is attributed to the chemical modification of E. coli through the incorporation of novel conjugated oligoelectrolytes in the MFC as well as the lower recombination rate and higher photoabsorption capabilities in the Au-TiO 2 hollow spheres electrode. Conclusions: The combined strategy of photo-anode modification in PEC cells and chemically modified MFCs shows great promise for future exploitation of such synergistic effects between MFCs and semiconductor-based PEC water splitting. Bacteria-enhanced photoelectrochemical devices for water splitting A novel hybrid cell uses solar power and a biofilm catalyst to generate hydrogen from water. Joachim Loo of Singapore's Nanyang Technological University and colleagues in Singapore and Australia have developed a hybrid platform that significantly improves on existing technology, generating a stronger photocurrent and higher hydrogen yields. The team combined modified photoelectrochemical (PEC) cells, which split water using solar energy but require an external power supply, with microbial fuel cells (MFCs), which use chemically modified Escherichia coli as a biocatalyst to create a complementary unit. This platform generated a photocurrent density seventy times higher than that of a standard PEC cell. With further development, this technology could help to lessen society's need for fossil fuels, paving the way for the emergence of hydrogen fuel-based economies.
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These authors contributed equally to this work.
SCJL and TTYT initiated the project and conceived the experiments. ZL was involved in the synthesis of the photo-anode while YZ synthesised the conjugated oligoelectrolytes used in this study. SK and QZ contributed to the analysis of the experimental data. CKN and VBW performed all the measurements and co-wrote the manuscript together.
ISSN:2055-5008
2055-5008
DOI:10.1038/npjbiofilms.2015.20