摘要
The coupling modes of dyes with corresponding supports play key roles in the performance of dye-sensitized heterogeneous photocatalytic systems. Herein, a solvothermal method was developed to synthesize a typical kind of dye-sensitized metal-organic frameworks (MOFs), Eosin Y (EY)-sensitized UiO-66-NH2, in which EY was anchored on UiO-66-NH2 via the bidentately bridging configuration of Zr⟵O-C = O→Zr. Such a coupling mode of chemical bonding strengthened the linking between EY and UiO-66-NH2, increased the content of EY on UiO-66-NH2, and facilitated the transfer of photogenerated electrons from EY to UiO-66-NH2. Correspondingly, the H2 evolution rate of EY-sensitized UiO-66-NH2 via solvothermal treatment (2760 μmol g−1 h-1) was 8 times as that via room-temperature sensitization, with apparent quantum efficiency (AQE) ∼17.6 % at 500 nm. The as-obtained AQE and excellent stability performance exceeds most dye-sensitized photocatalytic systems for H2 production. This work provides valuable information about developing dye-based or MOFs-based materials for efficient photocatalytic application.
| 源语言 | 英语 |
|---|---|
| 文章编号 | 119385 |
| 期刊 | Applied Catalysis B: Environmental |
| 卷 | 280 |
| DOI | |
| 出版状态 | 已出版 - 1月 2021 |
学术指纹
探究 'Eosin Y bidentately bridged on UiO-66-NH2 by solvothermal treatment towards enhanced visible-light-driven photocatalytic H2 production' 的科研主题。它们共同构成独一无二的指纹。引用此
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