Jewell Carly F, Subramanian Ashwanth, Nam Chang-Yong, Finke Richard G
Department of Chemistry, Colorado State University, Fort Collins, Colorado 80523, United States.
Department of Materials Science and Chemical Engineering, Stony Brook University, Stony Brook, New York 11794, United States.
ACS Appl Mater Interfaces. 2022 Jun 8;14(22):25326-25336. doi: 10.1021/acsami.2c02692. Epub 2022 May 25.
In 2017, we reported a dye-sensitized, photoelectrolysis cell consisting of fluorine-doped tin oxide (FTO)-coated glass covered by SnO nanoparticles coated with ,'-bis(phosphonomethyl)-3,4,9,10-perylenediimide (PMPDI) dye and then a photoelectrochemically deposited CoO water oxidation catalyst (WOCatalyst), FTO/nano-SnO/PMPDI/CoO. This system employed nanostructured SnO stabilized by a polyethyleneglycol bisphenol A epichlorohydrin (PEG-BAE) copolymer and other C-containing additives based on a literature synthesis to achieve a higher surface area and thus greater PMPDI dye absorption and resultant light collection. Surprisingly, the addition of the well-established WOCatalyst CoO resulted in a in the photocurrent, an unexpected . Two primary questions addressed in the present study are (1) what is the source of this "anti-catalyst" effect? and (2) are the findings of broader interest? Reflection on the synthesis of nano-SnO stabilized by PEG-BAE, and the large, ca. 10:1 ratio of C to Sn in synthesis, led to the hypothesis that even the annealing step at 450 °C in of the FTO/SnO anode precursors was unlikely to remove all the carbon initially present. Indeed, residual carbon impurities are shown to be the culprit in the presently observed "anti-catalyst" effect. The implication and anticipated broader impact of the results of answering the two abovementioned questions are also presented and discussed along with a section entitled "Perspective and Suggestions for the Field Going Forward."
2017年,我们报道了一种染料敏化光电解池,它由氟掺杂氧化锡(FTO)涂层玻璃组成,该玻璃覆盖有涂有,'-双(膦酰甲基)-3,4,9,10-苝二酰亚胺(PMPDI)染料的SnO纳米颗粒,然后是光电化学沉积的CoO水氧化催化剂(WOCatalyst),即FTO/纳米-SnO/PMPDI/CoO。该系统采用由聚乙二醇双酚A环氧氯丙烷(PEG-BAE)共聚物和其他基于文献合成的含碳添加剂稳定的纳米结构SnO,以实现更高的表面积,从而实现更大的PMPDI染料吸收和由此产生的光收集。令人惊讶的是,添加成熟的WOCatalyst CoO导致光电流下降,这是一个意想不到的结果。本研究中解决的两个主要问题是:(1)这种“反催化剂”效应的来源是什么?(2)这些发现是否具有更广泛的意义?对由PEG-BAE稳定的纳米-SnO的合成以及合成中约10:1的大碳锡比的思考,导致了这样的假设,即即使在FTO/SnO阳极前驱体的450°C退火步骤也不太可能去除最初存在的所有碳。事实上,残留的碳杂质被证明是目前观察到的“反催化剂”效应的罪魁祸首。还介绍并讨论了回答上述两个问题的结果的含义和预期的更广泛影响,以及题为“该领域未来的展望和建议”的部分。