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用于氧还原的染料敏化光阴极:高效的羟基生成和非质子氧化还原反应。

Dye-sensitized photocathodes for oxygen reduction: efficient HO production and aprotic redox reactions.

作者信息

Sun Jiaonan, Yu Yongze, Curtze Allison E, Liang Xichen, Wu Yiying

机构信息

Department of Chemistry and Biochemistry , The Ohio State University , Columbus , Ohio 43210 , USA . Email:

出版信息

Chem Sci. 2019 Apr 29;10(21):5519-5527. doi: 10.1039/c9sc01626k. eCollection 2019 Jun 7.

Abstract

Dye-sensitized photoelectrochemical cells (DSPECs) can be used to store solar energy in the form of chemical bonds. Hydrogen peroxide (HO) is a versatile energy carrier and can be produced by reduction of O on a dye-sensitized photocathode, in which the design of dye molecules is crucial for the conversion efficiency and electrode stability. Herein, using a hydrophobic donor-double-acceptor dye (denoted as BH4) sensitized NiO photocathode, hydrogen peroxide (HO) can be produced efficiently by reducing O with current density up to 600 μA cm under 1 sun conditions (Xe lamp as sunlight simulator, > 400 nm). The DSPECs maintain currents greater than 200 μA cm at low overpotential (0.42 V RHE) for 18 h with no decrease in the rate of HO production in aqueous electrolyte. Moreover, the BH4 sensitized NiO photocathode was for the first time applied in an aprotic electrolyte for oxygen reduction. In the absence of a proton source, the one-electron reduction of O generates stable, nucleophilic superoxide radicals that can then be synthetically utilized in the attack of an available electrophile, such as benzoyl chloride. The corresponding photocurrent generated by this photoelectrosynthesis is up to 1.8 mA cm. Transient absorption spectroscopy also proves that there is an effective electron transfer from reduced BH4 to O with a rate constant of 1.8 × 10 s. This work exhibits superior photocurrent in both aqueous and non-aqueous systems and reveals the oxygen/superoxide redox mediator mechanism in the aprotic chemical synthesis.

摘要

染料敏化光电化学电池(DSPEC)可用于以化学键的形式存储太阳能。过氧化氢(HO)是一种通用的能量载体,可通过在染料敏化光阴极上还原O来产生,其中染料分子的设计对于转换效率和电极稳定性至关重要。在此,使用疏水性供体-双受体染料(表示为BH4)敏化的NiO光阴极,在1个太阳条件下(以Xe灯作为阳光模拟器,>400 nm),通过还原O可以高效地产生过氧化氢(HO),电流密度高达600 μA cm。DSPEC在低过电位(0.42 V RHE)下保持大于200 μA cm的电流18小时,在水性电解质中HO的产生速率没有降低。此外,BH4敏化的NiO光阴极首次应用于非质子电解质中的氧还原。在没有质子源的情况下,O的单电子还原产生稳定的亲核超氧自由基,然后可以在攻击可用的亲电试剂(如苯甲酰氯)时进行合成利用。这种光电合成产生的相应光电流高达1.8 mA cm。瞬态吸收光谱也证明存在从还原的BH4到O的有效电子转移,速率常数为1.8×10 s。这项工作在水性和非水性系统中都表现出优异的光电流,并揭示了非质子化学合成中的氧/超氧氧化还原介质机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e20d/6544122/29ada8ac717c/c9sc01626k-s1.jpg

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