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无金属光催化石墨相氮化碳在 p 型黄铜矿上作为复合光阴极用于光致氢析出。

Metal-free photocatalytic graphitic carbon nitride on p-type chalcopyrite as a composite photocathode for light-induced hydrogen evolution.

机构信息

Helmholtz-Zentrum Berlin GmbH, Hahn-Meitner-Platz 1, 14109 Berlin, Germany.

出版信息

ChemSusChem. 2012 Jul;5(7):1227-32. doi: 10.1002/cssc.201100691. Epub 2012 Jun 15.

DOI:10.1002/cssc.201100691
PMID:22707459
Abstract

Recently, it has been shown that an abundant material, polymeric carbon nitride, can produce hydrogen from water under visible-light irradiation in the presence of a sacrificial donor. We present herein the preparation and characterization of graphitic carbon nitride (g-C(3)N(4)) films on p-type semiconducting CuGaSe(2) chalcopyrite thin-film substrates by thermal condensation of a dicyandiamide precursor under inert-gas conditions. Structural and surface morphological studies of the carbon nitride films suggest a high porosity of g-C(3)N(4) thin films consisting of a network of nanocrystallites. Photoelectrochemical investigations show light-induced hydrogen evolution upon cathodic polarization for a wide range of proton concentrations in the aqueous electrolyte. Additionally, synchrotron radiation-based photoelectron spectroscopy has been applied to study the surface/near-surface chemical composition of the utilized g-C(3)N(4) film photocathodes. For the first time, it has been shown that g-C(3)N(4) films coated on p-type CuGaSe(2) thin films can be successfully applied as new photoelectrochemical composite photocathodes for light-induced hydrogen evolution.

摘要

最近,研究表明在可见光照射下,在牺牲供体的存在下,丰富的聚合碳氮化物可以将水转化为氢气。本文通过在惰性气体条件下热缩合双氰胺前体,在 p 型半导体 CuGaSe(2)黄铜矿薄膜衬底上制备和表征了石墨相氮化碳(g-C(3)N(4))薄膜。氮化碳薄膜的结构和表面形貌研究表明,g-C(3)N(4)薄膜具有高孔隙率,由纳米晶网络组成。光电化学研究表明,在宽范围的质子浓度的水溶液电解质中,在阴极极化时会发生光诱导的氢气析出。此外,还应用基于同步辐射的光电子能谱研究了所使用的 g-C(3)N(4)薄膜光电阴极的表面/近表面化学组成。首次表明,涂覆在 p 型 CuGaSe(2)薄膜上的 g-C(3)N(4)薄膜可以成功地用作光诱导析氢的新型光电化学复合光电阴极。

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