Abstract

Photosynthetic organisms, membranes and complexes are attractive starting materials for solar energy conversion (SEC). Our overall goal is to develop methods to perform SEC using these materials in simple, inexpensive and a fashion that will be non-polluting and will not compete with the growth of food materials. I will describe here how the remarkable photocatalytic activity of the photosynthetic apparatus can provide overall water splitting with oxygen and hydrogen production in Bio-Photo-Electro-Chemical (BPEC) cells via the simplest and cleanest of processes wither in the absence or presence of added electron transport molecules. With plant thylakoids, electrons are shuttled by FeCN to a transparent FTO electrode, yielding a photocurrent density of 0.5 mA·cm-2. Hydrogen evolution occurs at the cathode at a bias as low as 0.8 V. A tandem cell comprising the BPEC cell with the thylakoid membranes and a Si photovoltaic module achieves overall water splitting with solar to hydrogen conversion efficiency of 0.3% (Pinhassi et al. Nature Communications 2016). With cyanobacterial cells, following a brief treatment that does not induce loss of cell viability, electrons from both the respiratory and photosynthetic systems are transferred directly to a graphite electrode, utilizing endogenous electron carriers (Saper et al. Nature Communications 2018). The current produced can be used for hydrogen production at low additional bias for significantly longer durations than the plant thylakoids.Another route is to isolate the photosynthetic complexes and chemically connect them to the electrochemical cell. One of the issues with this strategy is the small number of light absorbing chromophores connected to the complex, lowering the photochemical efficiency. Connection of isolated light harvesting complexes can help to overcome this deficiency. Photosystem II (PSII) is the only enzyme that catalyzes light-induced water oxidation being the basis for its application as a biophotoanode in various bio-photovoltaics and photo-bioelectrochemical cells. However, the absorption spectrum of PSII limits the quantum efficiency in the range of visible light, due to a gap in the green absorption region of chlorophylls (500 - 650 nm). To overcome this limitation, we have stabilized the interaction between PSII and Phycobilisomes (PBSs) – the cyanobacterial light harvesting complex, in vitro. The PBS of different cyanobacteria were analyzed for their ability to transfer energy to Thermosynechococcus elongatus (Te) PSII by fluorescence spill-over and photocurrent action spectra. Integration of the PBS-PSII super-complexes within an Os-complex-modified hydrogel on macro-porous indium tin oxide electrodes (MP-ITO) resulted in notably improved, wavelength dependent, incident photon-to-electron conversion efficiencies (IPCE). IPCE values in the green gap were doubled from 3 % to 6 % compared to PSII electrodes without PBS and a maximum IPCE up to 10.9 % at 670 nm was achieved. Figure 1

Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call