A Reversible MnO2 Deposition-Enabled Multicolor Electrochromic Device with Efficient Tunability of Ultraviolet-Visible Light.

Electrochromic technology offers exciting opportunities for smart applications such as energy-saving and interactive systems. However, achieving dual-band regulation together with the multicolor function is still an unmet challenge for electrochromic devices. Herein, an ingenious electrochromic strategy based on reversible manganese oxide (MnO2) electrodeposition, different from traditional ion intercalation/deintercalation-type electrochromic materials is proposed. Such a deposition/dissolution-based MnO2 brings an intriguing electrochromic feature of dual-band regulation for the ultraviolet (UV) and visible lights with high optical modulation (93.2% and 93.6% at 400 and 550 nm, respectively) and remarkable optical memory. Moreover, a demonstrative smart window assembled by MnO2 and Cu electrodes delivers the electrochromic properties of effective dual-band regulation accompanied by multicolor changes (transparent, yellow, and brown). The robust redox deposition/dissolution process endows the MnO2-based electrochromic device with excellent rate capability and an areal capacity of 570 mAh m-2 at 0.1 mA cm-2. It is believed that the metal oxide-based reversible electrodeposition strategy would be an attractive and promising electrochromic technology and provide a train of thought for the development of multifunctional electrochromic devices and applications.

An Electrochromic Hydrogen-Bonded Organic Framework Film.

Hydrogen-bonded organic frameworks (HOFs) possess various merits, such as high porosity, tunable structure, facile modification, and ready regeneration. These properties have yet to be explored in the context of new functional HOF materials. The facile and inexpensive electrophoretic deposition (EPD) method applied in this study generated a transparent HOF film at room temperature in just 2 min and is applicable to other HOFs. The resulting film exhibited reversible electrochromism with the advantage of long cycle life (>500 cycles). More strikingly, this all-organic film could be readily regenerated (through rinsing with DMF and redeposition) and showed tunable electrochromic behavior (through low-cost postsynthetic modification) with the ability to undergo successive color changes, which is difficult to achieve with conventional electrochromic materials. An electrochromic device was manufactured to further demonstrate the application potential of the film.

Fabrication of Lanthanide-Functionalized Hydrogen-Bonded Organic Framework Films for Ratiometric Temperature Sensing by Electrophoretic Deposition.

Developing a noncontact ratiometric luminescent temperature sensor with high sensitivity, widely available emission range, and reliable performance is a challenge in materials science. Herein, we demonstrated that this goal can be achieved by fabricating a lanthanide-functionalized hydrogen-bonded organic framework film (named the Eu@HOF-TCBP film). The unbonded carboxylic groups that existed in the structure not only enable lanthanide ions to bind with the framework for bringing dual emission but also allow for preparing a hydrogen-bonded organic framework (HOF) film through the facile electrophoretic deposition. The obtained film exhibits ratiometric temperature sensing performance in the range of 297-377 K with a maximum relative sensitivity of 5.787% K-1 and shows repeated use without sensitivity loss. Moreover, the material can be easily recycled and refabricated with consistent performance, demonstrating its unique merits of easy recyclability and regeneration as an HOF material. We believe that the reported strategies for preparing a dual-emitting HOF and fabricating a thin film will open a window for HOF applications.

Dual-Emitting UiO-66(Zr&Eu) Metal-Organic Framework Films for Ratiometric Temperature Sensing.

A novel dual-emitting metal-organic framework based on Zr and Eu, named as UiO-66(Zr&Eu), was built using a clever strategy based on secondary building units. With the use of polymers, the obtained UiO-66(Zr&Eu) was subsequently deposited as thin films that can be utilized as smart thermometers. The UiO-66(Zr&Eu) polymer films can be used for the detection of temperature changes in the range of 237-337 K due to the energy transfer between the lanthanide ions (Eu in clusters) and the luminescent ligands, and the relative sensitivity reaches 4.26% K-1 at 337 K. Moreover, the sensitivity can be improved to 19.67% K-1 by changing the film thickness. In addition, the temperature-sensing performance of the films is superior to that of the powders, and the sensor can be reused 3 times without loss of performance.

C-QDs@UiO-66-(COOH)2 Composite Film via Electrophoretic Deposition for Temperature Sensing.

Temperature plays a crucial role in both scientific research and industry. However, traditional temperature sensors, such as liquid-filled thermometers, thermocouples, and transistors, require contact to obtain heat equilibrium between the probe and the samples during the measurement. In addition, traditional temperature sensors have limitations when being used to detect the temperature change of fast-moving samples at smaller scales. Herein, the carbon quantum dots (C-QDs) functionalized metal-organic framework (MOF) composite film, a novel contactless solid optical thermometer, has been prepared via electrophoretic deposition (EPD). Instead of terephthalic acid (H2BDC), 1',2',4',5'-benzenetetracarboxylic (H4BTEC) acid was employed to construct a UiO-66 framework to present two uncoordinated carboxylic groups decorated on the pore surface. The uncoordinated carboxylic groups can generate negative charges, which facilitates the deposition of film on the positive electrode during the EPD process. Moreover, UiO-66-(COOH)2 MOFs can absorb C-QDs from the solution and prevent C-QDs from aggregating, and the well-dispersed C-QDs impart fluorescence characteristics to composites. As-synthesized composite film was successfully used to detect temperature change in the range of 97-297 K with a relative sensitivity up to 1.3% K-1 at 297 K.

Preparation of Dual-Emitting Ln@UiO-66-Hybrid Films via Electrophoretic Deposition for Ratiometric Temperature Sensing.

Engineering novel dual-emitting metal-organic frameworks (MOFs) with wide emission ranges for application as ratiometric temperature sensors is still a challenge. In this paper, two novel dual-emitting MOFs with intergrated lanthanide metals and luminescent ligand in a UiO-66-type structure, named Ln@UiO-66-Hybrid, were prepared via the combination of postsynthetic modification and postsynthetic exchange methods. Subsequently, the as-synthesized MOFs were deposited onto fluorine tin oxide substrates through electrophoretic deposition by taking advantage of the charges from the unmodified carboxylic groups of the MOFs. The as-prepared Tb@UiO-66-Hybrid and Eu@UiO-66-Hybrid films were applied to detect temperature changes. The resulting Tb@UiO-66-Hybrid film exhibited good temperature-sensing properties with a relative sensitivity of up to 2.76% K-1 in the temperature range of 303-353 K. In addition, the Eu@UiO-66-Hybrid film showed excellent temperature-sensing performance based on the energy transfer between the luminescent ligand (H2NDC) and europium ions with a relative sensitivity of up to 4.26% K-1 in the temperature range of 303-403 K.

Facile and Rapid Growth of Nanostructured Ln-BTC Metal-Organic Framework Films by Electrophoretic Deposition for Explosives sensing in Gas and Cr 3+ Detection in Solution.

Until now, it has been a challenge to prepare lanthanide metal-organic framework films on traditional substrates, like zinc plate, indium oxide (ITO), and fluorine-doped tin oxide (FTO) glasses in a rapid and facile method. In this paper, continuous and dense Ln-BTC MOFs films on unmodified low-cost substrates have been rapidly and easily fabricated though the newly developed electrophoretic deposition (EPD) method in 5 min. Moreover, the as-prepared luminescent films were successfully used for the detection of nitrobenzene (NB), trinitrotoluene (TNT) in gas phases, as well as NB, Cr3+ ions for detection in solution.

Patterned growth of luminescent metal-organic framework films: a versatile electrochemically-assisted microwave deposition method.

Electrochemically-assisted microwave deposition technology, a facile method for the fabrication of luminescent metal-organic framework (LMOF) films, is presented herein. This method was further developed into a versatile method for preparing patterned LMOF films. The strategy based on this method can spatially locate microcrystals of MOFs on a surface, which provides great promise in anti-counterfeiting barcode applications.