Evaluation of the surface activity of silicon in electrolytic media under the influence of hydroxyl radicals

IF 4.1 3区 化学 Q1 CHEMISTRY, ANALYTICAL Journal of Electroanalytical Chemistry Pub Date : 2025-02-14 DOI:10.1016/j.jelechem.2025.119010
C. Heyser , A.M.R. Ramírez , P. Grez , E. Muñoz , A. Sáez-Arteaga , N. Briones , P. Häberle
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Abstract

The purpose of this study is to evaluate the surface activity of silicon by evaluating a voltammetric profile of the substrate in an electrolytic medium. Since the electrical current flowing through the circuit is a measure of the rate at which a redox process occurs at the interface, higher current values will indicate more active substrates. For this study, hydroxyl radicals were generated by photochemical decomposition of H2O2. For this purpose, a H2O2 solution was irradiated with a UV lamp. The experimental conditions that were varied in the process were: illumination time, H2O2 concentration. The presence of the hydroxyl radicals generated through the methodology employed was qualitatively confirmed by fluorescence, using for this purpose (i) a 2′,7′-dichlorodihydrofluorescein diacetate (DCFH-DA) probe and (ii) a “radical scavenger”, which corresponds to an antioxidant species, in this case ascorbic acid. On the other hand, for the voltammetric measurements of the semiconducting substrate after interaction with hydroxyl radicals, a 0,1 M KCl solution was used as electrolyte solution. The experimental conditions studied were: influence of the pH of the medium and influence of different chemical treatments applied to the substrates used after interaction with hydroxyl radicals. From the results obtained, an increase in bothH2O2 concentration and immersion time produces an increase in current in the interphase electrode processes, indicating an activation of the semiconductor electrode surface. Indeed, in the anodic hemicycle, the signal of substrate oxidation appears at −0,75 V, and then from −0,45 V onwards, the oxidation of water. This is an indication that the semiconductor/electrolyte interface is ohmic, since in the absence of illumination (absence of minority carriers, h+) there are oxidation processes. On the other hand, for pH values in the intervals between 2 > pH > 5 and 7 > pH > 13, the slopes are approximately 0 mV/pH and for the interval between 5 > pH > 7, of the order of 60 mV/pH, this being an indication of a change in the nature of the surface functional groups of silicon.
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羟基自由基影响下电解介质中硅表面活性的评价
本研究的目的是通过评估衬底在电解介质中的伏安分布来评估硅的表面活性。由于流经电路的电流是在界面上发生氧化还原过程的速率的量度,因此较高的电流值将表明更活跃的衬底。在本研究中,羟基自由基是由H2O2光化学分解产生的。为此,用紫外灯照射H2O2溶液。实验过程中不同的实验条件有:光照时间、H2O2浓度。通过所采用的方法产生的羟基自由基的存在通过荧光定性确认,为此目的使用(i) 2 ',7 ' -二氯双氢荧光素(DCFH-DA)探针和(ii)“自由基清除剂”,其对应于抗氧化剂,在本例中为抗坏血酸。另一方面,对于半导体衬底与羟基自由基相互作用后的伏安测量,使用0.1 M KCl溶液作为电解质溶液。实验条件研究了介质pH值的影响和不同化学处理对底物与羟基自由基相互作用后的影响。从得到的结果来看,h2o2浓度的增加和浸泡时间的增加会导致相间电极过程中电流的增加,表明半导体电极表面被激活。事实上,在阳极半循环中,衬底氧化的信号出现在- 0.75 V,然后从- 0.45 V开始,水的氧化。这表明半导体/电解质界面是欧姆的,因为在没有照明的情况下(没有少数载流子,h+)存在氧化过程。另一方面,对于2 >;pH值比;5和7 >;pH值比;13,斜率约为0 mV/pH,在5 >之间;pH值比;约为60 mV/pH,这表明硅表面官能团的性质发生了变化。
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来源期刊
CiteScore
7.80
自引率
6.70%
发文量
912
审稿时长
2.4 months
期刊介绍: The Journal of Electroanalytical Chemistry is the foremost international journal devoted to the interdisciplinary subject of electrochemistry in all its aspects, theoretical as well as applied. Electrochemistry is a wide ranging area that is in a state of continuous evolution. Rather than compiling a long list of topics covered by the Journal, the editors would like to draw particular attention to the key issues of novelty, topicality and quality. Papers should present new and interesting electrochemical science in a way that is accessible to the reader. The presentation and discussion should be at a level that is consistent with the international status of the Journal. Reports describing the application of well-established techniques to problems that are essentially technical will not be accepted. Similarly, papers that report observations but fail to provide adequate interpretation will be rejected by the Editors. Papers dealing with technical electrochemistry should be submitted to other specialist journals unless the authors can show that their work provides substantially new insights into electrochemical processes.
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