Brown coloring electrochromic devices based on NiO-TiO2 layers

被引:27
作者
Al-Kahlout, A.
Pawlicka, A.
Aegerter, M.
机构
[1] INM, Dept Coating Technol, D-66123 Saarbrucken, Germany
[2] Univ Sao Paulo, Dept Quim Fis, Inst Quim Sao Carlos, BR-13560970 Sao Carlos, SP, Brazil
基金
巴西圣保罗研究基金会;
关键词
electrochromic devices; sol-gel layers; NiO-TiO2; films; CeO2-TiO2; starch-based electrolyte; KOH electrolyte;
D O I
10.1016/j.solmat.2006.06.053
中图分类号
TE [石油、天然气工业]; TK [能源与动力工程];
学科分类号
0807 ; 0820 ;
摘要
Brown coloring electrochromic 5 x 10 cm(2) windows with the configuration K-glass/NiO-TiO2/ electrolyte/CeO2-TiO2/K-glass have been prepared and characterized by optoelectrochemical techniques (cyclic voltammetry, chronoamperometry and galvanostatic measurements). The electrochromic layers have been prepared by the sol-gel technique. As electrolyte either a I M aqueous KOH solution or a newly developed starch-based gel impregnated with KOH have been used. The CeO2-TiO2 Sol gel layers sintered at 550 degrees C have been previously characterized in I M aqueous KOH electrolyte as a function of the thickness up to 2000 cycles and showed a highly reversible behavior without any corrosion effect. The NiO-TiO2 sol-gel layers sintered at 300 degrees C have been extensively characterized in the same electrolyte up to about 7000 cycles. All windows present a deep brown color characteristic of the presence of Ni3+ (NiOOH) species, that is fully reversible for several thousands of cycles with a rather-fast kinetics (< 30 s). The transmittance of the bleached state however slowly decreases with cycling (permanent coloration). The full-bleached condition can be nevertheless recovered by applying a negative potential for a long duration. Deeper coloration is usually obtained by cycling the windows galvanostatically with a current density of 20 mu A/cm(2). The lifetime of the windows is however limited because of the degradation of the NiO-based layers due to the not fully reversible exchange of OH- that turns the layers mechanically fragile and leads eventually to their complete removal from the substrate. Windows working satisfactorily up to 7000 and 17 000 cycles have been obtained using aqueous KOH electrolyte and starch KOH gel electrolyte, respectively. Memory tests showed that the devices bleach at the open circuit potential from T=39% (colored state) to about T=50% in 60 min. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:3583 / 3601
页数:19
相关论文
共 22 条
[11]   THE ELECTROCHROMIC PROCESS IN NONSTOICHIOMETRIC NICKEL-OXIDE THIN-FILM ELECTRODES [J].
DECKER, F ;
PASSERINI, S ;
PILEGGI, R ;
SCROSATI, B .
ELECTROCHIMICA ACTA, 1992, 37 (06) :1033-1038
[12]  
Granqvist C. G., 1995, HDB INORGANIC ELECTR
[13]   Grey, brown and blue coloring sol-gel electrochromic devices [J].
Heusing, S ;
Sun, DL ;
Otero-Anaya, J ;
Aegerter, MA .
THIN SOLID FILMS, 2006, 502 (1-2) :240-245
[14]  
Larsson AL, 2004, MATER LETT, V58, P2517, DOI 10.1016/j,matlet.2004.03.023
[15]   All solid state electrochromic devices on glass and polymeric foils [J].
Lechner, R ;
Thomas, LK .
SOLAR ENERGY MATERIALS AND SOLAR CELLS, 1998, 54 (1-4) :139-146
[16]   Electrochromic behavior of Ni-W oxide electrodes [J].
Lee, SH ;
Joo, SK .
SOLAR ENERGY MATERIALS AND SOLAR CELLS, 1995, 39 (2-4) :155-166
[17]  
Monk P. M. S., 1995, ELECTROCHROMISM FUND
[18]   Durability of electrochromic glazing [J].
Nagai, J ;
McMeeking, GD ;
Saitoh, Y .
SOLAR ENERGY MATERIALS AND SOLAR CELLS, 1999, 56 (3-4) :309-319
[19]   Electrochromic coatings-applications and manufacturing issues [J].
O'Brien, NA ;
Gordon, J ;
Mathew, H ;
Hichwa, BP .
THIN SOLID FILMS, 1999, 345 (02) :312-318
[20]  
SCHMIDT H, 1994, Patent No. 9528663