Spontaneous Surface Flattening via Layer-by-Layer Assembly of Interdiffusing Polyelectrolyte Multilayers

被引:12
作者
Kim, Young Hun [1 ]
Lee, Yong Man [2 ]
Park, Juhyun [3 ]
Ko, Min Jae [4 ]
Park, Jong Hyeok [1 ]
Jung, Woncheol [5 ]
Yoo, Pil J. [1 ,2 ]
机构
[1] Sungkyunkwan Univ, Sch Chem Engn, Suwon 440746, South Korea
[2] Sungkyunkwan Univ, SKKU Adv Inst Nanotechnol SAINT, Suwon 440746, South Korea
[3] Chung Ang Univ, Sch Chem Engn & Mat Sci, Seoul 156756, South Korea
[4] Korea Inst Sci & Technol, Solar Cell Ctr, Seoul 136791, South Korea
[5] Samsung Elect, Mat Res Ctr, SAIT, Yongin 446712, South Korea
关键词
SENSITIZED SOLAR-CELLS; EXPONENTIAL-GROWTH; TIO2; FILMS; FLUORESCENCE RECOVERY; WEAK POLYELECTROLYTES; OPTICAL-PROPERTIES; THIN-FILMS; ADSORPTION; DIFFUSION; MEMBRANES;
D O I
10.1021/la103282m
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
We report a facile means to achieve planarization of nonflat or patterned surfaces by utilizing the layer-by-layer (LbL) assembly of highly diffusive polyelectrolytes. The polyelectrolyte pair of linear polyethylenimine (LPEI) and poly(acrylic acid) (PAA) is known to maintain intrinsic diffusive mobility atop or even inside ionically complexed films prepared by LbL deposition. Under highly hydrated and swollen conditions during the sequential film buildup process, the LbL-assembled him of LPEI/PAA undergoes a topological self-deformation for minimizing surface area to satisfy the minimum-energy state or the surface, which eventually induces surface planarization along with spontaneous filling of surface textures or nonflat structures. This result is clearly different from other cases of applying nondiffusive polyelectrolytes onto patterned surfaces or confined structures, wherein surface roughening or incomplete filling is developed with the LbL assembly. Therefore, the approach proposed in this study can readily allow for surface planarization with the deposition of a relatively thin layer or polyelectrolyte multilayers. In addition. this strategy of planarization was extended to the surface modification of indium tin oxide (ITO) substrate. where surface smoothing and enhanced optical transmittance were obtained without sacrificing the electronic conductivity. Furthermore. we investigated the potential applicability or surface-treated ITO substrates as photoelectrodes or dye-sensitized solar cells prepared at room temperature. As a result, an enhanced photoconversion efficiency and improved device characteristics were obtained because of the synergistic role of polyelectrolyte deposition in improving the optical properties and acting as a blocking layer to prevent electron recombination with the electrolytes.
引用
收藏
页码:17756 / 17763
页数:8
相关论文
共 59 条
[1]   Layer-by-layer assembly of polyelectrolytes in nanopores [J].
Alem, Halima ;
Blondeau, Francoise ;
Glinel, Karine ;
Demoustier-Champagne, Sophie ;
Jonas, Alain M. .
MACROMOLECULES, 2007, 40 (09) :3366-3372
[2]  
[Anonymous], 1992, INTERMOLECULAR SURFA
[3]   Multiple Functionalities of Polyelectrolyte Multilayer Films: New Biomedical Applications [J].
Boudou, Thomas ;
Crouzier, Thomas ;
Ren, Kefeng ;
Blin, Guillaume ;
Picart, Catherine .
ADVANCED MATERIALS, 2010, 22 (04) :441-467
[4]   Nanoengineering of inorganic and hybrid hollow spheres by colloidal templating [J].
Caruso, F ;
Caruso, RA ;
Möhwald, H .
SCIENCE, 1998, 282 (5391) :1111-1114
[5]   pH-Responsive Reversibly Swellable Nanotube Arrays [J].
Chia, Khek-Khiang ;
Rubner, Michael F. ;
Cohen, Robert E. .
LANGMUIR, 2009, 25 (24) :14044-14052
[6]  
Cho J, 2001, ADV MATER, V13, P1076, DOI 10.1002/1521-4095(200107)13:14<1076::AID-ADMA1076>3.0.CO
[7]  
2-M
[8]   Effect of layer integrity of spin self-assembled multilayer films on surface Wettability [J].
Cho, J ;
Char, K .
LANGMUIR, 2004, 20 (10) :4011-4016
[9]   Influence of the degree of ionization on weak polyelectrolyte multilayer assembly [J].
Choi, J ;
Rubner, MF .
MACROMOLECULES, 2005, 38 (01) :116-124
[10]   An ultraviolet-curable mold for sub-100-nm lithography [J].
Choi, SJ ;
Yoo, PJ ;
Baek, SJ ;
Kim, TW ;
Lee, HH .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2004, 126 (25) :7744-7745