Neat Polythiophene Film: Their Very High Photoelectrochemical Performance Allowing Completely Solar-Driven Water-Splitting

Kouki Oka, H. Nishide, B. Winther‐Jensen
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Abstract

π-Conjugated polymers are emerging as appealing photoelectrode materials for the photoelectrochemical hydrogen evolution reaction via water-splitting, which has otherwise been extensively explored using inorganic semiconductors. Herein we report the very high performance of a pure organic semiconductor film as a catalyst for hydrogen production via visible-light-driven water-splitting. The neat and unsubstituted polythiophene film, characterised with a well-filled grain morphology of the crystalline polymer, was prepared by a facile polymerisation method. The high photovoltage of 1.38 V vs. RHE at pH 12 enables solar-driven one-electron-per-photon water-splitting in combination with a traditional water-oxidation catalyst to produce hydrogen and oxygen separately. The very high photoelectrocatalytic hydrogen evolution rate of 1.02 mol(H2) h-1g-1 or 0.75 mA/cm2 at 0 V vs. RHE was also achieved with high durability. This study opens a new window for π-conjugated polymers for ultimately sustainable hydrogen production.
整齐的聚噻吩薄膜:其非常高的光电化学性能允许完全由太阳能驱动的水分解
π共轭聚合物作为一种极具吸引力的光电极材料,已被广泛地应用于无机半导体中,用于水裂解的光电化学析氢反应。在此,我们报告了一种纯有机半导体薄膜作为催化剂,通过可见光驱动的水分解制氢的非常高的性能。整齐和未取代的聚噻吩薄膜,其特征是晶体聚合物的颗粒形态填充良好,通过易聚合方法制备。在pH值为12时,1.38 V vs. RHE的高光电压使太阳能驱动的单电子/光子水分解与传统的水氧化催化剂相结合,分别产生氢和氧。与RHE相比,在0 V下,光电催化析氢速率为1.02 mol(H2) h-1g-1或0.75 mA/cm2,并且具有很高的耐久性。该研究为π共轭聚合物最终实现可持续制氢打开了一扇新的窗口。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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