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Nanostructured thin-film tungsten trioxide photoanodes for solar water and sea-water splitting

机译:用于太阳能水和海水分裂的纳米结构薄膜钨陶瓷

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About 3 μm thick tungsten trioxide film electrodes consisting of partly sintered, 40-80 nm in diameter, particles deposited on conducting glass substrates exhibit high photon-to-current conversion efficiencies for the photooxidation of water, exceeding 70% at 400 nm. This is facilitated by a ca. 40% film porosity resulting in high contact area with the electrolyte. It is shown that the activity of the WO_3 electrodes towards photooxidation of water is enhanced by addition of even small amounts of halide (Cl~-, Br~-) ions to the acidic electrolyte. Photoelectrolysis experiments performed either in acidic electrolytes containing chloride or bromide anions or in a 0.5 M NaCl solution, under simulated 1.5 AM solar illumination, demonstrated long term stability of the photocurrents. Oxygen remains the main product of the photoanodic reaction even in a 0.5 M NaCl solution, a composition close to the sea water, with chlorine accounting for ca. 20% of current efficiency.
机译:大约3μm厚的三氧化钨膜电极由部分烧结,直径为40-80nm,沉积在导电玻璃基板上的颗粒表现出高的光子 - 电流转化效率,用于水的光氧化,超过400nm。这是由CA促进的。 40%薄膜孔隙率导致具有电解质的高接触区域。结果表明,通过向酸性电解质添加甚至少量的卤化物(Cl〜 - ,Br〜 - )离子来增强WO_3电极朝向水的光氧化。在模拟1.5AM太阳能照射下,在含氯化物或溴化物阴离子或0.5M NaCl溶液中进行的光电解实验,表现出光电流的长期稳定性。氧气仍然是光电反应的主要产物,即使在0.5M NaCl溶液中,靠近海水的组合物,氯算用于CA。 20%的当前效率。

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