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In situ doping control and electrical transport investigation of single and arrayed CdS nanopillars
Gu, Leilei,Liu, Xi,Kwon, Kyungmook,La, Chih-Chung,Lee, Min Hyung,Yu, Kyoungsik,Chueh, Yu-Lun,Fan, Zhiyong The Royal Society of Chemistry 2013 Nanoscale Vol.5 No.16
<P>Highly aligned intrinsic and indium doped CdS nanopillar arrays were fabricated via a template assisted Solid Source Chemical Vapor Deposition method (SSCVD). The prepared nanopillar arrays were well aligned, dense and uniform in diameter and length. Their geometry can be well defined by the design of the templates. These unique properties make them promising candidates for future photonic and optoelectronic devices. The structure of the prepared nanopillars has been studied by high resolution transmission electron microscopy and their different growth orientation as compared to those grown in free space has been observed and interpreted by the template induced change of the liquid-solid interfacial energy and the surface tension at the edge of the circular interface. To investigate electrical property of CdS nanopillars, vertical nanopillar array devices and horizontal individual nanopillar field-effect transistors have been fabricated and characterized. The measurements showed that the location of the indium doping source significantly affected carrier concentration, conductivity and field-effect mobility of the prepared CdS nanopillars. Particularly, it was found that conductivity could be improved by 4 orders of magnitude and field-effect mobility could be enhanced up to 50 cm(2) V(-1) s(-1) via proper doping control. These results enable further applications of CdS nanopillars in nano-optoelectronic applications such as photodetection and photovoltaics in the future.</P>
Guo Zhou,Haiyan Meng,Yan Cao,Xuejun Kou,Shuxiang Duan,Leilei Fan,Ming Xiao,Fangzhou Zhou,Zhenzi Li,Zipeng Xing 한국공업화학회 2018 Journal of Industrial and Engineering Chemistry Vol.64 No.-
The tiny Ag nanoparticles-uniformly decorated Ti3+ self-doped porous black TiO2 pillars (Ag-TPBTPs) are prepared, which show obvious surface plasmon resonance (SPR) and extend the photoresponse to visible light and near-infrared region (∼1500 nm). The Ag-TPBTPs exhibit excellent solar-driven photocatalytic activities by mineralizing of high-toxic 2,4-dichlorophenol (∼99%), which is three times higher than that of the pristine TiO2. The remarkable solar-driven photocatalytic performance can be ascribed to the porous pillars structure offering more surface active sites, the self-doped Ti3+ and SPR effect of Ag nanoparticles improving the utilization of solar light, and enhancing the spatial separation efficiency of photogenerated charge carriers.
Efficient Photon Capturing with Ordered Three-Dimensional Nanowell Arrays
Leung, Siu-Fung,Yu, Miao,Lin, Qingfeng,Kwon, Kyungmook,Ching, Kwong-Lung,Gu, Leilei,Yu, Kyoungsik,Fan, Zhiyong American Chemical Society 2012 NANO LETTERS Vol.12 No.7
<P>Unique light-matter interaction at nanophotonic regime can be harnessed for designing efficient photonic and optoelectronic devices such as solar cells, lasers, and photodetectors. In this work, periodic photon nanowells are fabricated with a low-cost and scalable approach, followed by systematic investigations of their photon capturing properties combining experiments and simulations. Intriguingly, it is found that a proper periodicity greatly facilitates photon capturing process in the nanowells, primarily owing to optical diffraction. Meanwhile, the nanoengineered morphology renders the nanostructures with a broad-band efficient light absorption. The findings in this work can be utilized to implement a new type of nanostructure-based solar cells. Also, the methodology applied in this work can be generalized to rational design of other types of efficient photon-harvesting devices.</P><P><B>Graphic Abstract</B> <IMG SRC='http://pubs.acs.org/appl/literatum/publisher/achs/journals/content/nalefd/2012/nalefd.2012.12.issue-7/nl3014567/production/images/medium/nl-2012-014567_0006.gif'></P><P><A href='http://pubs.acs.org/doi/suppl/10.1021/nl3014567'>ACS Electronic Supporting Info</A></P>