Lithium Ion Electro-Insertion and Spectroelectrochemical Properties of Films from Hexaniobate


Autoria(s): REZENDE, Alex R.; BIZETO, Marcos A.; CONSTANTINO, Vera R. L.; HUGUENIN, Fritz
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

20/10/2012

20/10/2012

2009

Resumo

Layer-by-layer (LbL) films from K(2)Nb(6)O(17)(2-) and polyallylamine (PAH) and dip-coating films of H(2)K(2)Nb(6)O(17) were prepared on a fluorine-doped tin-oxide (FTO)-coated glass. The atomic force microscopy (AFM) images were carried out for morphological characterization of both materials. The real surface area and the roughness factor were determined on the basis of pseudocapacitive processes involved in the electroreduction/electrooxidation of gold layers deposited on these films. Next, lithium ion insertion into these materials was examined by means of electrochemical and spectroelectrochemical measurements. More specifically, cyclic voltammetry and current pulses under visible light beams were used to investigate mass transport and chromogenic properties. The lithium ion diffusion coefficient (D(Li)) within the LbL matrix is significantly higher than that within the dip-coating film, ensuring high storage capacity of lithium ions in the self-assembled electrode. Contrary to the LbL film, the potentiodynamic profile of absorbance change (Delta A) as a function of time is not similar to that obtained in the case of current density for the dip-coating film. Aiming at analyzing the rate of the coloration front associated with lithium ion diffusion, a spectroelectrochemical method based on the galvanostatic intermittent titration technique (GITT) was employed so as to determine the ""optical"" diffusion coefficient (D(op)). In the dip-coating film, the method employed here revealed that the lithium ion rate is higher in diffusion pathways formed from K(2)Nb(6)O(17)(2-) sites that contribute more significantly to Delta A. Meanwhile, the presence of PAH contributed to the increased ionic mobility in diffusion pathways in the LbL film, with low contribution to the electrochromic efficiency. These results aided a better understanding of the potentiodynamic profile of the temporal change of absorbance and current density during the insertion/deinsertion of lithium ions into the electrochromic materials.

FAPESP[05/00106-7]

Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

FAPESP[2005/60596-8]

Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

CNPq[555436/2006-3]

Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)

CNPq[550581/2005-7]

Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)

CNPq[301149/2006-2]

Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)

IMMP/MCT, and IMMC/MCT

IMMP/MCT, and IMMC/MCT

Identificador

JOURNAL OF PHYSICAL CHEMISTRY C, v.113, n.25, p.10868-10876, 2009

1932-7447

http://producao.usp.br/handle/BDPI/31180

10.1021/jp901006u

http://dx.doi.org/10.1021/jp901006u

Idioma(s)

eng

Publicador

AMER CHEMICAL SOC

Relação

Journal of Physical Chemistry C

Direitos

restrictedAccess

Copyright AMER CHEMICAL SOC

Palavras-Chave #THIN-FILMS #ELECTROCHEMICAL PROPERTIES #WO3 #DEVICES #INTERCALATION #BATTERIES #OXIDE #K4NB6O17 #V2O5 #PHOTOLUMINESCENCE #Chemistry, Physical #Nanoscience & Nanotechnology #Materials Science, Multidisciplinary
Tipo

article

original article

publishedVersion