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Copper-surface-mediated synthesis of acetylenic carbon-rich nanofibers for active metal-free photocathodes

机译:铜表面介导的无活性金属光阴极的炔属富碳纳米纤维的合成

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摘要

The engineering of acetylenic carbon-rich nanostructures has great potential in many applications, such as nanoelectronics, chemical sensors, energy storage, and conversion, etc. Here we show the synthesis of acetylenic carbon-rich nanofibers via copper-surface-mediated Glaser polycondensation of 1,3,5-triethynylbenzene on a variety of conducting (e.g., copper, graphite, fluorine-doped tin oxide, and titanium) and non-conducting (e.g., Kapton, glass, and silicon dioxide) substrates. The obtained nanofibers (with optical bandgap of 2.51 eV) exhibit photocatalytic activity in photoelectrochemical cells, yielding saturated cathodic photocurrent of ca. 10 µA cm−2 (0.3–0 V vs. reversible hydrogen electrode). By incorporating thieno[3,2-b]thiophene units into the nanofibers, a redshift (ca. 100 nm) of light absorption edge and twofold of the photocurrent are achieved, rivalling those of state-of-the-art metal-free photocathodes (e.g., graphitic carbon nitride of 0.1–1 µA cm−2). This work highlights the promise of utilizing acetylenic carbon-rich materials as efficient and sustainable photocathodes for water reduction
机译:乙炔富碳纳米结构的工程在许多应用中具有巨大潜力,例如纳米电子学,化学传感器,能量存储和转换等。在这里,我们展示了通过铜表面介导的Glaser缩聚反应合成乙炔富碳纳米纤维。在各种导电(例如,铜,石墨,氟掺杂的氧化锡和钛)和非导电(例如,Kapton,玻璃和二氧化硅)基板上的1,3,5-三乙炔基苯。所获得的纳米纤维(带隙为2.51 eV)在光电化学电池中表现出光催化活性,产生的饱和阴极光电流为。 10 µA cm −2 (相对于可逆氢电极为0.3–0 V)。通过将噻吩并[3,2-b]噻吩单元结合到纳米纤维中,实现了光吸收边缘的红移(约100 edgenm)和光电流的两倍,可与最先进的无金属光电阴极相媲美。 (例如,0.1–1 µA cm -2 的石墨氮化碳)。这项工作突出了利用炔属富碳材料作为高效,可持续的光阴极减少水的前景

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