AVS 62nd International Symposium & Exhibition
    Thin Film Monday Sessions
       Session TF+AS+SS-MoM

Paper TF+AS+SS-MoM3
Coordination-Based Molecular Assemblies as Electrochromic Materials: Ultra-High Switching Stability and Coloration Efficiencies[1]

Monday, October 19, 2015, 9:00 am, Room 111

Session: Self-Assembled Monolayers, Layer-by-Layer, etc.
Presenter: Michal Lahav, Weizmann Institute of Science, Israel
Correspondent: Click to Email

Layer-by-Layer (LbL) deposition, combined with metal-ligand coordination, has served as a powerful tool for generating functional architectures.[2] Such systems might find interesting applications in molecular electronics, sensor, solar cells and data storage. More significantly, owing to their interesting electrochromic (EC) behavior, they are promising candidates for use in smart windows and display devices. In this study we used a dip-coating process to generate molecular assemblies (MA) from metal polypyridyl complexes cross-linked with PdCl2. These polypyridyl complexes are considered ideal chromophores for fabricating electrochromic materials, due to their excellent stability and light absorption that greatly depends on their oxidation state.[3],[4] The number of pyridine moieties of the chromophores is varied to control (i) the materials’ stability, (ii) color, (iii) redox-chemistry, and (iv) the film growth (i.e., linear vs. exponential). We also observed that minor structural differences (i.e., the pyridine-bipyridine bond order) at the molecular level become apparent when the stability and electrochromic properties are examined (Figure 1). The MAs exhibit high coloration efficiencies and are extremely stable: they are thermally robust and have exceptionally high (spectro)electrochemical activity. Furthermore, we demonstrated the formation of a first-generation solid-state set-up.[1],[5]

1) S. Shankar, M. Lahav, M. E. van der Boom, J. Am. Chem. Soc. 2015, 137, Just Accepted Manuscript.

2) R. J. Mortimer, Annu. Rev. Mater. Res., 2011, 41, 241.

3) G. de Ruiter, M. Lahav, M. E. van der Boom, Acc. Chem. Res., 2014, 47, 3407-3416.

4) G. de Ruiter, M. Lahav, H. Keisar, M. E. van der Boom, Angew. Chem., Int. Ed. 2013, 52, 704-709.

5) M. E. van der Boom, M. Lahav, S. Shankar, US Patent 61/906,565, 2013.