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氮掺杂二氧化钛纳米棒阵列的制备和光电转化性能表征

Preparation and Photoelectrical Conversion Performance of Nitrogen-doped Titanium Dioxide Nanorod Arrays

中文摘要英文摘要

本文以氨水为氮源,在掺杂氟的SnO2导电玻璃(SnO2:F,FTO)基底上通过水热法生长出氮掺杂单晶金红石相TiO2纳米棒阵列。X光电子能谱证明,反应物中只有很少量氮元素能进入到TiO2中,以O-Ti-N形态存在。随着氮掺杂浓度的提高,TiO2纳米棒长度增加,(002)晶面相对于未掺杂TiO2生长迅速,然而样品的紫外-可见光吸收谱未发生明显变化,说明半导体的能带位置没有受到氮掺杂的影响。另一方面,氮掺杂大幅度改善了TiO2纳米棒的光电流响应和外量子效率,其最高值分别达到0.15 mA/cm2和3.1%,均为未掺杂TiO2的3.8倍。然而,过量的氮掺杂会导致TiO2纳米棒团聚,导致光致电荷在传输过程的复合现象;过量的氨水还会与其它反应物直接发生水解反应,不利于纳米棒在基底上的生长。

In this paper, nitrogen-doped single crystal rutile TiO2 nanorod arrays were prepared on transparent conductive fluorine-doped tin oxide (FTO) substrates through a facile hydrothermal process, using aqueous ammonia as nitrogen source. X-ray photoelectron spectroscopy analysis demonstrates that only a small amount of nitrogen in reactant was added into TiO2, and formed O-Ti-N structure. With the increase of doping concentration, the length of nanorods and the X-ray diffraction intensity of the (002) plane increased, but the optical absorption of the nanorods remained without obvious changes, indicating the doping had little effect on the bandgap position of TiO2. Moreover, photocurrent response and external quantum efficiency of the nanorods were improved obviously via the doping process, and their highest values reached 0.15 mA/cm2 and 3.1%, respectively, which were about 3.8 times those of undoped TiO2. However, over-doped nitrogen can induce the aggregation of TiO2 nanorods, which leads to the recombination of photogenerated charges. Also, excess ammonia directly reacts with the reactants through the hydrolysis, which thus inhibits the growth of the nanorods on FTO substrate. Above all, nitrogen-doping with desirable concentrations can enhance photoelectrical properties of TiO2 nanorods for their applications in solar cells.

李阳、孙琼、孙先淼、董立峰

物理学化学晶体学

氮掺杂iO2纳米棒阵列形貌表征光电流响应

nitrogen dopingTiO2 nanorod arraymorphology characterizationphotocurrent response

李阳,孙琼,孙先淼,董立峰.氮掺杂二氧化钛纳米棒阵列的制备和光电转化性能表征[EB/OL].(2013-02-06)[2025-08-02].http://www.paper.edu.cn/releasepaper/content/201302-129.点此复制

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