模拟太阳辐照下 ITIES 光催化剂辅助电子转移的抑制作用--支撑电解质的作用

IF 3.5 4区 化学 Q2 ELECTROCHEMISTRY
Edwin Avella, Andrea Folli, Angel Cuesta
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引用次数: 0

摘要

在两种不相溶电解质溶液(ITIES)的界面上进行光催化剂辅助电荷转移已经得到证实。然而,其实际应用需要了解其在太阳照射下的性能。我们以 TCNQ 7,7,8,8-Tetracyanoquinodimethane (TCNQ) 为电子清除剂,以双(三苯基膦亚基)四(4-氯苯基)硼酸铵 (BTPPA-TPBCl) 为有机相电解质,研究了光催化剂在太阳照射下辅助 ITIES 处的水氧化。在 ITIES 上组装光催化剂纳米粒子后,没有观察到水的氧化能力增强。含有光催化剂的光电流与不含光催化剂的光电流相似,但存在 TCNQ。有光催化剂和无光催化剂时观察到的光电流都是由于 TCNQ⋅- 与有机电解质发生反应或与水发生界面氧化作用而产生的。前者在正电位时占主导地位,并由于 TCNQ⋅- 在 ITIES 上的转移而产生正向光电流。后者在负电位时占主导地位,产生负光电流。电子顺磁共振(EPR)检测到了 TCNQ⋅-,并发现其通过与 BTPPA+ 形成加合物而得到稳定,这必然有助于使 TCNQ 的光活性成为即使有光催化剂的情况下的主要过程。这些发现突出表明,有必要研究其他合适的电子清除剂-支撑电解质组合,以便在太阳能的光电催化转换中使用 ITIES。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Inhibition of Photocatalyst-Assisted Electron Transfer at ITIES Under Simulated Solar Irradiation-the Role of Supporting Electrolyte

Inhibition of Photocatalyst-Assisted Electron Transfer at ITIES Under Simulated Solar Irradiation-the Role of Supporting Electrolyte

Inhibition of Photocatalyst-Assisted Electron Transfer at ITIES Under Simulated Solar Irradiation-the Role of Supporting Electrolyte

Photocatalyst-assisted charge transfer at the interface between two immiscible electrolyte solutions (ITIES) has been previously proven. However, its practical application requires information on its performance under solar irradiation. We investigated photocatalyst-assisted oxidation of water at ITIES under solar irradiation using TCNQ 7,7,8,8-Tetracyanoquinodimethane (TCNQ) as electron scavenger and bis(triphenylphosphoranylidene) ammonium tetrakis(4-chlorophenyl)borate (BTPPA-TPBCl) as organic phase electrolyte. No enhancement of water oxidation after assembling photocatalyst nanoparticles at the ITIES was observed. Photocurrents with photocatalyst were similar to those without but in the presence of TCNQ. Photocurrents observed both with and without photocatalyst are shown to be due to photogeneration of TCNQ⋅, either by reaction with the organic electrolyte or by interfacial oxidation of water. The former dominates at positive potentials and results in a positive photocurrent due to transfer of TCNQ⋅ across the ITIES. The latter dominates at negative potentials and results in a negative photocurrent. Electron paramagnetic resonance (EPR) detected TCNQ⋅ and revealed its stabilisation by formation of an adduct with BTPPA+, which must contribute to making the photoactivity of TCNQ the dominant process even with photocatalyst. These findings highlight the necessity of research on alternative suitable electron scavenger-supporting electrolyte combinations for implementing ITIES in the photoelectrocatalytic conversion of solar energy.

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来源期刊
ChemElectroChem
ChemElectroChem ELECTROCHEMISTRY-
CiteScore
7.90
自引率
2.50%
发文量
515
审稿时长
1.2 months
期刊介绍: ChemElectroChem is aimed to become a top-ranking electrochemistry journal for primary research papers and critical secondary information from authors across the world. The journal covers the entire scope of pure and applied electrochemistry, the latter encompassing (among others) energy applications, electrochemistry at interfaces (including surfaces), photoelectrochemistry and bioelectrochemistry.
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