One-dimensional titanium dioxide nanotube arrays for hydrogen generation

IF 2 4区 化学 Q3 CHEMISTRY, MULTIDISCIPLINARY
Swarna Lakshmi Rajendran, Viswanathan Alagan
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Abstract

The ever-increasing global energy demand has necessitated alternate sources of energy. Photoelectrochemical water splitting proved to be a viable method of green hydrogen production. In the present study, four different one-dimensional titanium dioxide nanotube arrays (TNAs) were fabricated by varying the time duration of the second anodization. The highly ordered TNAs proved to be potential photoanodes for photoelectrochemical water splitting, for production of hydrogen. The fabricated TNAs were confirmed as stable anatase crystal structures using X-ray diffraction and Raman spectroscopy analysis. The TNAs showed an increase in length with an increase in anodization time. The morphological studies revealed the formation of the one-dimensional tube-like morphology of TNAs with lengths varying from 1.41 μm to 6.35 μm. The increased length and one-dimensional nanotube formation implied an increased number of active sites and an increased surface-to-volume ratio. The observed increase in photocurrent may be attributed to increased electrode–electrolyte interfacial area, where charge and mass transport occured. The band-gap of the TNAs showed a minimal progressive decrease with an increase in anodization time. The oxidation states of the constituent elements were confirmed using X-ray photoelectron spectroscopy. Contact angle measurement indicated a transition from slight hydrophobicity to slight hydrophilicity with an increase in the anodization time of the TNAs. Electrochemical studies of TNAs exhibited increased photo-response with an increase in anodization time. The influence of anodization time on the characteristics of TNAs is explored in this study.

Graphical abstract

TiO2 Nanotube Arrays (TNAs) were synthesized by two – step anodization method, by varying second anodization time. The TNAs were tested for their efficacy as photo-anode, following exhaustive characterization techniques. The activity of the potential photoanodes for PEC water splitting was analyzed using LSV, CA, EIS and Tafel plots

用于制氢的一维二氧化钛纳米管阵列
不断增长的全球能源需求使替代能源成为必要。光电化学水分解是一种可行的绿色制氢方法。在本研究中,通过改变二次阳极氧化的时间,制备了四种不同的一维二氧化钛纳米管阵列。高度有序的tna被证明是光电化学水分解和制氢的潜在光阳极。通过x射线衍射和拉曼光谱分析,证实所制备的tna为稳定的锐钛矿晶体结构。随着阳极氧化时间的延长,tna的长度增加。形貌研究表明,tna形成了长度为1.41 ~ 6.35 μm的一维管状结构。长度的增加和一维纳米管的形成意味着活性位点数量的增加和表面体积比的增加。观察到的光电流的增加可能归因于电极-电解质界面面积的增加,在那里发生了电荷和质量传输。随着阳极氧化时间的增加,tna的带隙逐渐减小。用x射线光电子能谱法确定了组成元素的氧化态。接触角测量表明,随着氧化时间的增加,tna由轻微疏水性转变为轻微亲水性。电化学研究表明,随着阳极氧化时间的增加,tna的光响应增强。本研究探讨了阳极氧化时间对tna特性的影响。摘要采用改变二次阳极氧化时间的两步阳极氧化法合成了tio2纳米管阵列(tna)。在详尽的表征技术之后,测试了tna作为光阳极的功效。利用LSV、CA、EIS和Tafel图分析了潜在光阳极对PEC水分解的活性
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来源期刊
Journal of Chemical Sciences
Journal of Chemical Sciences CHEMISTRY, MULTIDISCIPLINARY-
CiteScore
3.10
自引率
5.90%
发文量
107
审稿时长
1 months
期刊介绍: Journal of Chemical Sciences is a monthly journal published by the Indian Academy of Sciences. It formed part of the original Proceedings of the Indian Academy of Sciences – Part A, started by the Nobel Laureate Prof C V Raman in 1934, that was split in 1978 into three separate journals. It was renamed as Journal of Chemical Sciences in 2004. The journal publishes original research articles and rapid communications, covering all areas of chemical sciences. A significant feature of the journal is its special issues, brought out from time to time, devoted to conference symposia/proceedings in frontier areas of the subject, held not only in India but also in other countries.
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