Mixed-Valence Compounds as a New Route for Electrochromic Devices with High Coloration Efficiency in the Whole Vis-NIR Region
Source abstract
Abstract
Electrochromic devices (ECDs) that allow the modulation of light transmission are very attractive in the research field of energy saving. Here all-in-one gel switchable ECDs based on mixed-valence electroactive compounds were developed. The use of the thienoviologen/ferrocene couple as cathode and anode, respectively, leads to a significant electrochromic band in the visible range (550–800 nm), with a color change from yellow to green, and to a lower band in the NIR region (1000–1700 nm), due to the presence of one electroactive-chromic species. Replacement of the electroactive ferrocene with a fluorene-diarylamine electroactive-chromic species, allows to extend and intensify the absorption in the NIR region, thus affording modulation of the solar radiation from 500 up to 2200 nm. High optical contrast, fast coloration and bleaching times and outstanding coloration efficiencies were measured for all observed absorption bands upon the application of small potential differences (1.4 V < DV < 2 V).
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Research context
OpenAlex topics: Conducting polymers and applications · Transition Metal Oxide Nanomaterials · Perovskite Materials and Applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Chemistry and Chemical Technologies, University of Calabria, Via P. Bucci, Cubo 15D, 87036 Arcavacata di Rende, Italy
Institute of Nanotechnology (CNR-NANOTEC), c/o Campus Ecotekne, via Monteroni, 73100 Lecce, Italy
References (53)
Show source-provided references
1. Masson-Delmotte, V., Zhai, P., Pörtner, H.-O., Roberts, D., Skea, J., Shukla, P.R., Pirani, A., Moufouma-Okia, W., Péan, C., and Pidcock, R. (2018). Global Warming of 1.5 °C. An IPCC Special Report on the Impacts of Global Warming of 1.5 °C Above Pre-industrial Levels and Related Global Greenhouse Gas Emission Pathways, in the Context of Strengthening the Global Response to the Threat of Climate Change, Sustainable Development, and Efforts to Eradicate Poverty, Available online: https://www.ipcc.ch/site/assets/uploads/sites/2/2019/06/SR15_Full_Report_High_Res.pdf.
2. Climate adaptive building shells: State-of-the-art and future challenges. Renew. Sustain
3. Thermal performance of an electrochromic smart window tested in an environmental test cell10.1016/j.enbuild.2010.03.010 ↗
4. Properties, requirements and possibilities of smart windows for dynamic daylight and solar energy control in buildings: A state-of-the-art review10.1016/j.solmat.2009.08.021 ↗
5. Byker, H.J. (1992). Variable Reflectance Motor Vehicle Mirror. (5,128,799), U.S. Patent.
6. Varaprasad, D.V., Habibi, H., Mccabe, I.A., Lynam, N.R., Zhao, M., and Dornan, C.A. (1995). Electrochromic Mirrors and Devices. (5,724,187), U.S. Patent.
7. Electrochromics for smart windows: Oxide-based thin films and device10.1016/j.tsf.2014.02.002 ↗
8. Monk, P.M.S., Mortimer, R.J., and Rosseinsky, D.R. (2007). Electrochromism and Electrochromic Devices, Cambridge University Press.10.1017/CBO9780511550959 ↗
9. Mortimer, R.J., Rosseinsky, D.R., and Monk, P.M.S. (2015). Electrochromic Materials and Devices, Wiley-VCH.
10. Next-Generation Multifunctional Electrochromic Devices10.1021/acs.accounts.6b00183 ↗
11. Color Control in π-Conjugated Organic Polymers for Use in Electrochromic Devices10.1021/cr900129a ↗
12. Electrochemical and electrochromic properties of bilayer polymer films prepared by electrochemical polymerization based on star-shaped thiophene derivatives10.1039/C9NJ01730E ↗
13. Study of electrochromic characteristics in the nearinfrared region of electrochromic devices based on solution-processed amorphous WO3 films10.1016/j.mssp.2018.07.034 ↗
14. Synergistically Enhanced Electrochemical Response of Host−Guest Recognition Based on Ternary Nanocomposites: Reduced Graphene Oxide-Amphiphilic Pillar [5] arene-Gold Nanoparticles10.1021/am403463p ↗
15. Amorphous titanium dioxide film with improved electrochromism in nearinfrared region10.1016/j.optmat.2019.01.034 ↗
16. Coordination-Based Molecular Assemblies as Electrochromic Materials: Ultra-High Switching Stability and Coloration Efficiencies10.1021/jacs.5b00429 ↗
17. Mononuclear and Dinuclear Ruthenium Complexes of 2,3-Di-2-pyridyl-5,6-diphenylpyrazine: Synthesis and Spectroscopic and Electrochemical Studies10.1021/ic101629w ↗
18. Transmissive-to-black fast electrochromic switching from a long conjugated pendant group and a highly dispersed polymer/SWNT10.1039/C7PY01863K ↗
19. Further understanding of the mechanisms of electrochromic devices with variable infrared emissivity based on polyaniline conducting polymers10.1039/C9TC02126D ↗
20. Discrete Donor−Acceptor Conjugated Systems in Neutral and Oxidized States: Implications toward Molecular Design for High Contrast Electrochromics10.1021/acs.chemmater.6b04725 ↗
21. Xu, J.W., Chua, M.H., and Shah, K.W. (2019). Electrochomic and Electrofluorescence Liquid Crystals. Electrochromic Smart Materials: Fabrication and Application, Royal Society of Chemistry.
22. Colorless to All-Black Full-NIR High-Contrast Switching in Solid Electrochromic Films Prepared with Organic Mixed Valence Systems Based on Dibenzofulvene Derivatives10.1021/acs.chemmater.8b01665 ↗
23. Mesomorphic and electrooptical properties of viologens based on non-symmetric alkyl/polyfluoroalkyl functionalization and on an oxadiazolyl-extended bent core10.1039/C9TC01697J ↗
24. Synthesis and thermotropic properties of new green electrochromic ionic liquid crystals10.1039/C9NJ03303C ↗
25. Novel electrochromic gel with high optical contrast in the visible and near-infrared10.1016/j.matchemphys.2013.04.005 ↗
26. Electro-optical properties of neutral and radical ion thienosquaraines10.1002/chem.201601281 ↗
27. Electrochromic organic and polymeric materials for display applications10.1016/j.displa.2005.03.003 ↗
28. Electrochromic Systems and the Prospects for Devices10.1002/1521-4095(200106)13:11<783::AID-ADMA783>3.0.CO;2-D ↗
29. Electrochromic materials10.1039/cs9972600147 ↗
30. Monk, P.M.S. (1998). The Viologens: Physicochemical Properties, Synthesis and Applications of the Salts of 4,4′-Bipyridine, Wiley-VCH.
31. Yolanda, A., Ana, V., Javier, R., and Ramon, T.-Z. (2018). All-in-One Gel-Based Electrochromic Devices: Strengths and Recent Developments. Materials, 11.10.3390/ma11030414 ↗
32. Electrofluorochromism in π-conjugated ionic liquid crystals10.1038/ncomms4105 ↗
33. Mesomorphism and electrochemistry of thienoviologen liquid crystals10.1039/C5CP02350E ↗
34. Star–shaped, dendrimeric and polymeric triarylamines as photoconductors and hole transport materials for electro-optical applications10.1002/1439-2054(20020701)287:7<442::AID-MAME442>3.0.CO;2-H ↗
35. Polyimide memory: A pithy guideline for future applications10.1039/C2PY20632C ↗
36. Novel organosoluble aromatic polyimides bearing pendant methoxy-substituted triphenylamine moieties: Synthesis, electrochromic, and gas separation properties10.1002/pola.23082 ↗
37. Triphenylamine-based polyimides with trimethyl substituents for gas separation membrane and electrochromic applications10.1002/pola.24802 ↗
38. Multicolored near-infrared electrochromic polyimides: Synthesis, electrochemical, and electrochromic properties10.1016/j.dyepig.2013.08.019 ↗
39. Photoelectrochemical and electrochromic properties of polyimide/graphene oxide composites10.1016/j.carbon.2013.10.021 ↗
40. High glass transitions of new polyamides, polyimides, and poly(amide-imide) s containing a triphenylamine group: Synthesis and characterization10.1021/ma001523u ↗
41. Organic Mixed-Valence Compounds: A Playground for Electrons and Holes10.1002/anie.201100944 ↗
42. Colorless Triphenylamine-Based Aliphatic Thermoset Epoxy for Multicolored and Near-Infrared Electrochromic Applications10.1021/am405803z ↗
43. A mixed-valence bis(diarylamino)stilbene: Crystal structure and comparison of electronic coupling with biphenyl and tolane analogues10.1039/B415018J ↗
44. Orthogonal electronic coupling in multicentre arylamine mixed-valence compounds based on a dibenzofulvene-thiophene conjugated bridge10.1039/C7CC03156D ↗
45. Synthesis and Characterization of New Conjugation-extended Viologens Involving a Central Aromatic Linking Group10.1039/c39920000620 ↗
46. Switching from columnar to calamitic mesophases in a new class of rod-like thienoviologens10.1039/c3tc00853c ↗
47. High-Performance Electrofluorochromic Switching Devices Using a Novel Arylamine-Fluorene Redox-Active Fluorophore10.1021/acsami.9b01656 ↗
48. Synthesis, characterization and photoconductive properties of optically activemethacrylic polymers bearing side-chain 9-phenylcarbazole moieties10.1016/j.polymer.2009.11.054 ↗
49. Highly fluorescent thienoviologen-based polymer gels for single layer electrofluorochromic devices10.1002/adfm.201403611 ↗
50. Experimental and theoretical characterization of a new synthesized extended viologen10.1016/j.cplett.2012.09.042 ↗
51. A novel bis(dihydroxypropyl) viologen-based all-in-one electrochromic device with high cycling stability and coloration efficiency10.1016/j.electacta.2018.12.135 ↗
52. Multifunctional hydrogel enables extremely simplified electrochromic devices for smart windows and ionic writing boards10.1039/C8MH00856F ↗
53. Solution-processable electrochromic materials and devices: Roadblocks and strategies towards large-scale applications10.1039/C9TC02861G ↗