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Efficient and economical water splitting would be a technological breakthrough that could underpin a hydrogen economy. A version of water splitting occurs in photosynthesis, but hydrogen is not produced. The reverse of water splitting is the basis of the hydrogen fuel cell. Water splitting using solar radiation has not been commercialized.
The light-harvesting system of PSI uses multiple copies of the same transmembrane proteins used by PSII. The energy of absorbed light (in the form of delocalized, high-energy electrons) is funneled into the reaction center, where it excites special chlorophyll molecules (P700, with maximum light absorption at 700 nm) to a higher energy level.
The oxidation of water is catalyzed in photosystem II by a redox-active structure that contains four manganese ions and a calcium ion; this oxygen-evolving complex binds two water molecules and contains the four oxidizing equivalents that are used to drive the water-oxidizing reaction (Kok's S-state diagrams).
The photocatalyst must have a bandgap large enough to split water; in practice, losses from material internal resistance and the overpotential of the water splitting reaction increase the required bandgap energy to 1.6–2.4 eV to drive water splitting. [2] The process of water-splitting is a highly endothermic process (ΔH > 0).
This occurs by oxidation of water in the case of oxygenic photosynthesis. The electron-deficient reaction center of photosystem II (P680*) is the strongest biological oxidizing agent yet discovered, which allows it to break apart molecules as stable as water. [4] The water-splitting reaction is catalyzed by the oxygen-evolving complex of ...
The antenna complex contains hundreds of chlorophyll molecules which funnel the excitation energy to the center of the photosystem. At the reaction center, the energy will be trapped and transferred to produce a high energy molecule. [2] The main function of PSII is to efficiently split water into oxygen molecules and protons.
The water-splitting reaction occurs on the lumenal side of the thylakoid membrane and is driven by the light energy captured by the photosystems. This oxidation of water conveniently produces the waste product O 2 that is vital for cellular respiration. The molecular oxygen formed by the reaction is released into the atmosphere.
2 surfaces that were plasma etched for 10 seconds and subsequent surface modifications with ODP showed a water contact angle greater than 150 . The surface was converted into a superhydrophilic surface (water contact angle = 0 ) upon UV illumination, due to rapid decomposition of octadecylphosphonic acid coating resulting from TiO 2 photocatalysis.