微尺度高温合成聚合物氮化碳光电阴极

Ayelet Tashakory, Sanjit Mondal, Venugopala Rao Battula, Gabriel Mark, Tirza Shmila, Michael Volokh, Menny Shalom
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引用次数: 0

摘要

聚合氮化碳(CN)已成为分水光电化学电池(PEC)中一种前景广阔的光阳极材料。然而,目前在基底上沉积氮化萘层的方法通常包括在 500-550 °C 下长时间加热,这可能会导致氮化萘单体升华或分解,并破坏基底,从而导致氮化萘薄膜不均匀。本文介绍了一种简单、快速、可扩展且节能的合成均匀氯化萘薄膜的方法。将预先设计好的 CN 单体薄膜置于比标准煅烧程序更高的温度下几分钟。短时间的加热过程可形成均匀的氯化萘层,该层与基底接触良好,在 PEC 中具有良好的光阳极活性。在中性和酸性溶液中,最佳 CN 光阳极在 1.23 相对于可逆氢电极时的光电流密度为 ≈200 μA cm-2,在碱性溶液中为 120 μA cm-2。
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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Minute-Scale High-Temperature Synthesis of Polymeric Carbon Nitride Photoanodes
Polymeric carbon nitride (CN) has emerged as a promising photoanodic material in water-splitting photoelectrochemical cells (PEC). However, the current deposition methods of CN layers on substrates usually include a long heating process at 500−550 °C, which might cause sublimation or decomposition of the CN monomers and destruction of the substrate, leading to a nonuniform CN film. Herein, a simple, fast, and scalable energy-economic procedure to synthesize homogenous CN films is introduced. The predesigned CN monomers film is subjected for several minutes to higher temperatures than the standard calcination procedure. The short heating process allows the formation of a uniform CN layer, with excellent contact with the substrate and good activity as a photoanode in PEC. The optimal CN photoanode reaches photocurrent densities of ≈200 μA cm−2 at 1.23 versus reversible hydrogen electrode in neutral and acidic solutions and 120 μA cm−2 in a basic solution.
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