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用于光电化学水分解的 Sn/TiO2 纳米棒的可控合成。

Controlled fabrication of Sn/TiO2 nanorods for photoelectrochemical water splitting.

机构信息

State Key Laboratory of Digital Manufacturing Equipment and Technology, Huazhong University of Science and Technology, Wuhan 430074, China.

出版信息

Nanoscale Res Lett. 2013 Nov 5;8(1):462. doi: 10.1186/1556-276X-8-462.

Abstract

In this work, we investigate the controlled fabrication of Sn-doped TiO2 nanorods (Sn/TiO2 NRs) for photoelectrochemical water splitting. Sn is incorporated into the rutile TiO2 nanorods with Sn/Ti molar ratios ranging from 0% to 3% by a simple solvothermal synthesis method. The obtained Sn/TiO2 NRs are single crystalline with a rutile structure. The concentration of Sn in the final nanorods can be well controlled by adjusting the molar ratio of the precursors. Photoelectrochemical experiments are conducted to explore the photocatalytic activity of Sn/TiO2 NRs with different doping levels. Under the illumination of solar simulator with the light intensity of 100 mW/cm2, our measurements reveal that the photocurrent increases with increasing doping level and reaches the maximum value of 1.01 mA/cm2 at -0.4 V versus Ag/AgCl, which corresponds to up to about 50% enhancement compared with the pristine TiO2 NRs. The Mott-Schottky plots indicate that incorporation of Sn into TiO2 nanorod can significantly increase the charge carrier density, leading to enhanced conductivity of the nanorod. Furthermore, we demonstrate that Sn/TiO2 NRs can be a promising candidate for photoanode in photoelectrochemical water splitting because of their excellent chemical stability.

摘要

在这项工作中,我们研究了用于光电化学水分解的掺锡二氧化钛纳米棒(Sn/TiO2 NRs)的可控制备。通过简单的溶剂热合成方法,将 Sn 掺入锐钛矿 TiO2 纳米棒中,Sn/Ti 摩尔比范围为 0%至 3%。所得到的 Sn/TiO2 NRs 为单晶,具有锐钛矿结构。通过调整前体的摩尔比,可以很好地控制最终纳米棒中 Sn 的浓度。进行光电化学实验以探索不同掺杂水平的 Sn/TiO2 NRs 的光催化活性。在 100 mW/cm2 光强的太阳模拟器照射下,我们的测量结果表明,随着掺杂水平的增加,光电流增加,在-0.4 V 相对于 Ag/AgCl 时达到 1.01 mA/cm2 的最大值,与原始 TiO2 NRs 相比,增加了约 50%。Mott-Schottky 图表明,Sn 掺入 TiO2 纳米棒可以显著增加载流子密度,从而提高纳米棒的导电性。此外,我们证明 Sn/TiO2 NRs 由于其优异的化学稳定性,是光电化学水分解中光阳极的有前途的候选材料。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c05/4228341/ca6a6585fc48/1556-276X-8-462-1.jpg

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