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自偏压光电化学池用于可见光照射下的自发整体水分解。

Self-biasing photoelectrochemical cell for spontaneous overall water splitting under visible-light illumination.

机构信息

School of Environmental Science and Engineering, Shanghai Jiao Tong University, Shanghai, PR China.

出版信息

ChemSusChem. 2013 Jul;6(7):1276-81. doi: 10.1002/cssc.201200936. Epub 2013 Jun 17.

DOI:10.1002/cssc.201200936
PMID:23775929
Abstract

A self-biasing photoelectrochemical (PEC) cell that could work for spontaneous overall water splitting in a neutral solution was established based on the mismatched Fermi levels between the photoelectrodes. A Pt-catalyst-decorated crystalline silicon photovoltaic cell (Pt/PVC) was prepared and employed as an effective photocathode. This was coupled with a poly(ethylene glycol)-directed WO3/W photoanode prepared by a hydrothermal process. Both of the photoelectrodes showed a response to visible light. The WO3/W photoanode had a positively located valence band edge, the energy level of which was enough for water oxidation, and the Pt/PVC photocathode possessed a negatively located conduction band edge, which was capable of water reduction. More importantly, the Fermi level of the WO3/W photoanode was more positive than that of the Pt/PVC photocathode because of the p-n junction of the PVC that decoupled the band bending and enlarged the photovoltage. Under visible-light irradiation, the WO3/W photoanode provided a negative bias for the Pt/PVC photocathode, and the Pt/PVC photocathode provided a positive bias for the WO3/W photoanode. An interior bias was generated that could relax the strict criteria of overall water splitting by cooperatively separating the hole-electron pairs at both photoelectrodes. In this system, the short-circuit current and the open-circuit voltage increased with increasing light intensity (AM 1.5 illumination) to reach 121 μA cm(-2) and 0.541 V, respectively, at a light intensity of 100 mW cm(-2). Such a combination provides a promising method for the fabrication of self-driven devices for solar-energy storage.

摘要

基于光电极之间不匹配的费米能级,建立了一种能够在中性溶液中自发进行整体水分解的自偏光电化学(PEC)池。制备了一种 Pt 催化剂修饰的结晶硅光伏电池(Pt/PVC)并用作有效的光电阴极。将其与通过水热法制备的聚乙二醇导向的 WO3/W 光阴极耦合。两个光电极都对可见光有响应。WO3/W 光阴极的价带边缘位置为正,其能级足以进行水氧化,而 Pt/PVC 光电阴极的导带边缘位置为负,能够进行水还原。更重要的是,由于 PVC 的 p-n 结解耦了能带弯曲并扩大了光电压,WO3/W 光阴极的费米能级比 Pt/PVC 光电阴极的费米能级更正。在可见光照射下,WO3/W 光阴极对 Pt/PVC 光电阴极施加负偏压,Pt/PVC 光电阴极对 WO3/W 光阴极施加正偏压。产生了内部偏压,通过协同分离两个光电极的空穴-电子对,从而放宽了整体水分解的严格标准。在该系统中,短路电流和开路电压随光强(AM 1.5 照明)的增加而增加,在 100 mW cm-2 的光强下分别达到 121 μA cm-2 和 0.541 V。这种组合为制造自驱动太阳能存储设备提供了一种很有前途的方法。

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