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Supramolecular Zinc Porphyrin Photocatalyst with Strong Reduction Ability and Robust Built-In Electric Field for Highly Efficient Hydrogen Production

机译:超分子锌卟啉光催化剂,具有强大的减少能力和坚固的内置电场,用于高效氢气生产

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摘要

The ultrathin 2D self-assembled tetrakis (4-carboxyphenyl) zinc porphyrin (SA-ZnTCPP) is successfully fabricated for photocatalytic hydrogen production. The H-2 evolution rate is 3487.3 mu mol g(-1) h(-1) under wide-spectrum (300-698 nm), which is increased by approximate to 85 times compared with metal-free self-assembled tetrakis (4-carboxyphenyl) porphyrin (SA-TCPP). The significant promotion in photocatalytic activity of SA-ZnTCPP comes from the deep conduction band (-1.01 V) contributed by the elevation of orbital energy level of porphyrin after Zn2+ coordination. In addition, the strong built-in electric field boosts the rapid separation and mobility of photogenerated carriers. Consequently, the strong reduction driving force and faster electron transfer kinetics result in highly efficient photocatalytic hydrogen production of SA-ZnTCPP. This work improves the understanding of the structure-property relationship of metalloporphyrin-based supramolecular photocatalysts and provides a general strategy at the molecular level for performance optimization of photocatalysts.
机译:超薄2D自组装的四(4-羧基苯基)锌卟啉(SA-ZnTCPP)被成功制造用于光催化氢气产生。 H-2进化速率为3487.3μmMolg(-1)H(-1),在宽频谱(300-698nm)下,与无金属自组装的Tetrakis相比,通过近似为85次增加(4 - 羧基苯基)卟啉(SA-TCPP)。 SA-ZnTCPP的光催化活性的显着促进来自深度传导带(-1.01 v),通过Zn2 +协调后卟啉轨道能量水平的升高。此外,强大的内置电场促进了光生载体的快速分离和迁移率。因此,强大的减少驱动力和更快的电子转移动力学导致SA-ZnTCPP的高效光催化氢产生。这项工作改善了对基于金属卟啉的超分子光催化剂结构性质关系的理解,并在光催化剂的性能优化的分子水平下提供了一般策略。

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