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Effect of urea as a stabiliser in the thermal immersion method to synthesise zinc oxide nanostructures on porous silicon nanostructures

机译:尿素作为稳定剂在热浸渍法中合成多孔硅纳米结构氧化锌纳米结构的稳定剂

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In this work, ZnO nanostructures were prepared using the catalytic immersion method (90 °C) with zinc nitrate hexahydrate (Zn(NO_3)_26H_2O) as a precursor, urea (CH4N2O) as a stabiliser and porous silicon nanostructures (PSi) as a substrate. PSi prepared on p-type Si by using electrochemical etching method. Different molarity concentration ratios of Zn(NO_3)_26H_2O to CH_4N_2O (2:1, 1:2, 1:4 and 1:6) were used in this work. The effects of the urea concentration during the synthesis process were discussed. The ZnO nanostructures were characterised using field emission scanning electron microscope (FESEM), photoluminescence (PL) and I-V probe. Porous nanoflakes were successfully synthesised on a p-type PSi substrate that was prepared by electrochemical etching. High-intensity photoluminescence (PL) at the optimum concentration indicated that urea is a good stabiliser to produce ZnO nanostructures with good crystallinity. The high resistance of ZnO/PSi show that electrical properties of PSi dominant compare to ZnO nanostructures.
机译:在该作品中,使用催化浸渍法(90℃)用硝酸锌六水合物(Zn(NO_3)_26H_2O)作为前体,尿素(CH 4 N 2 O)作为稳定剂和多孔硅纳米结构(PSI)作为基质的ZnO纳米结构。通过使用电化学蚀刻方法对P型SI制备的PSI。在这项工作中使用了Zn(NO_3)_26H_2O至CH_4N_2O(2:1,1:2,1:4和1:4)的不同摩尔浓度比。讨论了尿素浓度在合成过程中的影响。使用现场发射扫描电子显微镜(FESEM),光致发光(PL)和I-V探针表征ZnO纳米结构。在通过电化学蚀刻制备的p型PSI衬底上成功地合成了多孔纳米薄膜。以最佳浓度为高强度光致发光(PL)表明尿素是生产具有良好结晶度的ZnO纳米结构的良好稳定剂。 ZnO / PSI的高性能显示PSI优势与ZnO纳米结构的电性能。

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