钇掺入†增强聚合物氮化碳光阳极的活性和稳定性

EES catalysis Pub Date : 2025-04-17 DOI:10.1039/D5EY00064E
Sanjit Mondal, Ayelet Tashakory, Gabriel Mark, Shmuel Barzilai, Angus Pedersen, Michael Volokh, Josep Albero, Hermenegildo García and Menny Shalom
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引用次数: 0

摘要

高分子氮化碳材料(CNs)在水分解光电化学电池中作为光阳极具有广阔的应用前景。然而,电极-水界面的催化活性差限制了它们的性能和寿命,导致光活性低和不必要的自氧化。在这里,我们展示了一种基于掺杂钇团簇的聚合物氮化碳的高性能光阳极,以高法拉第效率实现了水氧化的增强活性和稳定性。加入钇团簇可以增强光捕获、电子导电性、电荷分离和空穴萃取动力学,从而实现高效的水氧化。此外,钇与CN的氮基团之间的强相互作用指导了富钇的一维管状结构的形成,这些管状结构连接了二维CN片。优化后的光阳极光电流密度为275±10 μA cm−2,法拉第析氧效率为90%,性能稳定长达10小时,在碱性介质中实现了高达14%的外量子效率。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Enhanced activity and stability of polymeric carbon nitride photoanodes by yttrium incorporation†

Enhanced activity and stability of polymeric carbon nitride photoanodes by yttrium incorporation†

Polymeric carbon nitride materials (CNs) show promising potential as photoanodes in water-splitting photoelectrochemical cells. However, poor catalytic activity at the electrode–water interface limits their performance and longevity, resulting in low photoactivity and unwanted self-oxidation. Here, we demonstrate a high-performance photoanode based on polymeric carbon nitride doped with yttrium clusters, achieving enhanced activity and stability with high faradaic efficiency for water oxidation. Incorporating yttrium clusters enhances light harvesting, electronic conductivity, charge separation, and hole extraction kinetics, enabling efficient water oxidation. Furthermore, the strong interaction between yttrium and the CN's nitrogen groups guides the formation of yttrium-rich one-dimensional tubular structures that interconnect two-dimensional CN sheets. The optimized photoanode delivers a photocurrent density of 275 ± 10 μA cm−2 with 90% faradaic efficiency for oxygen evolution, demonstrates stable performance for up to 10 hours, and achieves external quantum efficiencies of up to 14% in an alkaline medium.

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