Microscale electrohydrodynamic printing of in situ reactive features for patterned ZnO nanorods

被引:16
|
作者
Zhang, Bing [1 ,2 ]
He, Jiankang [1 ,2 ]
Li, Jiaxin [1 ,2 ]
Wang, Lei [3 ]
Li, Dichen [1 ,2 ]
机构
[1] Xi An Jiao Tong Univ, State Key Lab Mfg Syst Engn, Xian 710049, Shaanxi, Peoples R China
[2] Xi An Jiao Tong Univ, Rapid Mfg Res Ctr Shaanxi Prov, Xian 710049, Shaanxi, Peoples R China
[3] Fourth Mil Med Univ, Tangdu Hosp, Dept Thorac Surg, Xian 710038, Shaanxi, Peoples R China
基金
中国国家自然科学基金; 国家重点研发计划;
关键词
electrohydrodynamic printing; ZnO nanorods patterns; photoelectrochemical properties; EXPERIMENTAL PARAMETERS; NANOWIRE ARRAYS; ZINC-OXIDE; GROWTH; SHELL; OPTIMIZATION; FABRICATION;
D O I
10.1088/1361-6528/ab3db4
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Patterning of zinc oxide (ZnO) nanorods has attracted considerable interests to enhance the performance of ZnO-based functional devices. Most of the existing techniques for patterned ZnO nanorods are based on conventional microfabrication methods that commonly require cleanroom environment, high-cost equipment and complicated processes. In this study, electrohydrodynamic (EHD) printing strategy was accommodated to fabricate microscale ZnO nanorods patterns based on in situ reactive inks. Smaller working voltage and larger nozzle-to-collector distance facilitated the formation of thinner PEO-Zn(NO3)(2) filaments, which were decomposed into ZnO nanoparticles to serve as the seeding template for the hydrothermal growth of ZnO nanorods. The resultant ZnO nanorods can be flexibly tuned by the EHD printed patterns. The effect of growth time on the size and morphology of ZnO nanorods was investigated. Compared with the spin-coating method, the photoelectrochemical property of patterned ZnO nanorods was well controlled and showed enhanced photoelectrochemical stability. The presented method provides a flexible and rapid way to customize patterned ZnO nanorods that can be potentially used in the fields of optical detectors, biosensors or solar-driven devices.
引用
收藏
页数:10
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