ABSTRACT
The introduction of novel materials with multifunctional chromogenic properties, such as electrochromic/electrofluorochromic (EC/EFC) properties, has recently attracted prospective interest in the development of various optoelectronic devices and smart windows. In this study, a novel Zn(II)-based metallo-supramolecular polymer (polyZn) has been developed as an ON/OFF switchable EFC application with prominent EC behavior. In this regard, the polymeric chain of polyZn was first synthesized by 1:1 complexation in a zigzag manner with Zn(II) ions at the metal center and 4,4'-[bis(2,2':6',2â³-terpyridinyl)benzene]triphenylamine (LTPY-TPA) as the redox-active ditopic ligand. The polyZn exhibits excellent solubility in organic solvents and can form a very good uniform thin film on an indium tin oxide/glass substrate by spin-coating. In a neutral state, transparent polyZn exhibits a bright yellow color to the naked eye (absorption at â¼325 nm). The electroactive triphenylamine (TPA) core of LTPA-TPY, however, undergoes reversible single-electron oxidation when a positive bias of +1.6 V vs Ag/Ag+ is applied, generating radical cations (TPA â TPAâ¢+) with a significant drop in transparency (77%). A noticeable chromic shift in the hue of the film from brilliant yellow to green was observed with the appearance of a near-infrared absorption band at â¼897 nm with a tail of 1300-1600 nm. Interestingly, in addition to this EC phenomenon, the fabricated solid-state polyZn film exhibits intense, high-contrast reddish-orange photoluminescence with λem = 650 nm, which is significantly desired as a molecular probe for bioimaging. Both the TPA core and the redox-inactive Zn(II)-terpyridine core emit orange-red photoluminescence in polyZn, which is significantly quenched upon the oxidation of the film and is re-emitted at 0.0 V vs Ag/Ag+. This ON/OFF EFC transition was sustained for several cycles. This study should motivate to design and create distinctive new unique materials with combined EC/EFC behavior for the fabrication of optoelectronic devices by combining a metal-fluorescent core with a redox-active spacer.
ABSTRACT
Fe-based metallo-supramolecular polymer (polyFe), composed of Fe(II) ions and bis(terpyridyl)benzene, is known as a good electrochromic (EC) material. For the first time, to improve the EC properties, we prepared nanocomposites comprising polyFe and a layered inorganic-imidazoline covalently bonded hybrid (LIIm) by simply mixing them in methanol and then examined the effect of the nanocomposition on EC properties. The obtained blue/purple-colored composites (polyFe/LIIm composites) were demonstrated by scanning electron microscopy (SEM) to comprise a structure of LIIm nanoparticles coated with amorphous polyFe. Interestingly, X-ray diffraction (XRD) measurements suggested that there was no intercalation of polyFe in the interlayer space of LIIm. Ultraviolet-visible (UV-vis) spectroscopy measurements demonstrated that light absorption close to 600 nm was attributed to metal-to-ligand charge transfer (MLCT) from the Fe(II) ion to the bisterpyridine ligand and was influenced by LIIm in the composites. The composites exhibited a pair of redox waves, assigned to the redox between Fe(II) and Fe(III), in the cyclic voltammograms; moreover, the composites were estimated to be diffusion controlled. Thin composite films demonstrated reversible EC changes, triggered by the redox reaction of the metal. Furthermore, the results show that the nano-scale composition of the metallo-supramolecular polymers with LIIm can effectively improve the memory properties without reducing the contrast in transmittance (ΔT) of 70-76% in EC changes after applying 1.2 V vs. Ag/Ag+. The EC properties varied with varying ratios (3/0.1, 0.5, 1, and 5) of the polyFe/LIIm, and the ratio of 3/1 exhibited the longest memory and largest MLCT absorption peak among composites. The results show that the polyFe/LIIm composites are useful EC materials for dimming glass applications, such as smart windows.
ABSTRACT
Low-voltage operation, high durability, and long memory time are demanded for electrochromic (EC) display device applications. Metallo-supramolecular polymers (MSPs), composed of a metal ion and ditopic ligand, are one of the recently developed EC materials, and the ligand modification is expected to tune the redox potential of MSP. In order to lower the redox potential of MSP, tetrakis(N-methylbenzimidazolyl)bipyridine (LBip) was designed as an electronically rich ligand. Ru-based MSP (polyRu-LBip) was successfully synthesized by 1:1 complexation of RuCl2(DMSO)4 with LBip. The molecular weight (Mw) was high (8.8 × 106 Da) enough to provide a simple 1H NMR spectrum, of which the proton peaks could be assigned by the comparison with the spectrum of the corresponding mono-Ru complex. The redox potential (E1/2) between Ru(II/III) was 0.51 V versus Ag/Ag+, which was much lower than the redox potential of previously reported Ru-based MSP with bis(terpyridyl)benzene (0.95 V vs Ag/Ag+). The polymer film exhibited reversible, distinct color changes between violet and light green-yellow upon applying very low potentials of 0 and 0.6 V vs Ag/Ag+, respectively. The appearance and disappearance of the metal-to-ligand charge transfer absorption by the electrochemical redox between Ru(II/III) were confirmed using in situ spectro-electrochemical measurement. A solid-state EC device with polyRu-LBip was revealed to have large optical contrast (ΔT 54%), fast response time (1.37 s for bleaching and 0.67 s for coloration), remarkable coloration efficiency (571 cm2/C), and high durability for the repeated color changes more than 20,000 cycles. The device also showed a long optical memory time of up to 19 h to maintain 40% to the initial contrast under the open circuit conditions. It is considered that the stabilization of the Ru(III) state by LBip suppressed the self-coloring to Ru(II) inside the device.
ABSTRACT
2,6-Divinylpyridine-appended anthracene derivatives flanked by two alkyl chains at the 9,10-position of the core have been designed, synthesized, and characterized by NMR, MALDI-TOF, FTIR, and single-crystal XRD. These anthracene derivatives are able to recognize picric acid (2,4,6-trinitrophenol, PA) selectively down to parts per billion (ppb) level in aqueous as well as nonaqueous medium. Fluorescence emission of these derivatives in solution is significantly quenched by adding trace amounts of PA, even in the presence of other competing analogues, such as 2,4-dinitrophenol (2,4-DNP), 4-nitrophenol (NP), nitrobenzene (NB), benzoic acid (BA), and phenol (PH). The high sensitivity of these derivatives toward PA is considered as a combined effect of the proton-induced intramolecular charge transfer (ICT) as well as electron transfer from the electron-rich anthracene to the electron-deficient PA. Moreover, visual detection of PA has been successfully demonstrated in the solid state by using different substrates.
