Electrodeposition Of Ag Research Articles

Electrodeposition of Copper-Silver Alloys from Aqueous Solutions: A Prospective Process for Miscellaneous Usages

The electrodeposition of copper (Cu), silver (Ag), and their alloys has been a subject of interest since the 19th century. Primarily due to their exceptional features such as good mechanical hardness and electrical conductivity, high resistance to corrosion, and electromigration, Cu–Ag electrodeposits continue to be investigated and developed to improve their properties for different applications. This paper reviews the state of the art in the field of electroplated Cu–Ag alloys in an aqueous solution, with particular emphasis on the observed properties and variety of electrochemical processes used to produce high-quality materials. Moreover, this review paper focuses on the experimental conditions employed for Cu–Ag electrodeposition, intending to understand the basis and manipulate the processes to obtain coatings with superior characteristics and for attractive usage. Finally, the most trending applications of these coatings are discussed depending on different parameters of electrodeposition to provide prospects for potential research.

Electrochemical Liquid‐Liquid‐Solid Growth of Ag‐In Crystals with Liquid Indium Alloy Electrodes

AbstractSynthesis of intermetallic crystals by electrodeposition of Ag from alkaline aqueous electrolytes containing AgCN onto liquid metal electrodes via an electrochemical liquid‐liquid‐solid (ec‐LLS) process has been performed. X‐ray diffraction, scanning electron microscopy, and transmission electron microscopy were performed to identify crystalline products. Ec‐LLS experiments performed with pure liquid Hg and Ga electrodes resulted in the formation of polycrystalline Ag2Ga and Ag2Hg3. Experiments performed with In‐containing liquid metals preferentially yielded Ag9In4 and AgIn2 products with liquid Hg0.35In0.65 and Ga0.86In0.14, respectively. The product distribution with liquid Hg0.35In0.65 depended on the level of Ag supersaturation during the electrodeposition. A mechanism that accounts for the aforementioned observations is presented and discussed. This work described the formation of Ag−In intermetallic phases by the isothermal electroreduction of Ag into different liquid metal solvents via ec‐LLS. Electrodeposition of Ag into a pure Ga or pure Hg liquid metal pool yielded precisely the compounds predicted from isothermal cross‐sections of the respective binary phase diagrams. These compounds were not found when using liquid Hg or Ga containing appreciable In. The smaller enthalpy of formation for AgIn2 was consistent with its synthesis in Ga0.86In0.14. However, the observed product of Ag9In4 in Hg‐containing liquid metals could not be rationalized solely from thermodynamic factors. Instead, this observation was consistent with a kinetic pathway based on the lability of Hg‐metal bonds and nearly identical crystal structures of Ag9In4 and Ag2Hg3. Site exchange of Hg for In is consistent with our prior observations[23] of In exchange into Hg−Pd structures during Pd electrodeposition. This mechanism is not based on any direct role of electrochemistry other than aspects that dictate the operative supersaturation of the metal solute.

MeNPs-PEDOT Composite-Based Detection Platforms for Epinephrine and Quercetin.

The development of low-cost, sensitive, and simple analytical tools for biomolecule detection in health status monitoring is nowadays a growing research topic. Sensing platforms integrating nanocomposite materials as recognition elements in the monitoring of various biomolecules and biomarkers are addressing this challenging objective. Herein, we have developed electrochemical sensing platforms by means of a novel fabrication procedure for biomolecule detection. The platforms are based on commercially available low-cost conductive substrates like glassy carbon and/or screen-printed carbon electrodes selectively functionalized with nanocomposite materials composed of Ag and Au metallic nanoparticles and an organic polymer, poly(3,4-ethylenedioxythiophene). The novel fabrication method made use of alternating currents with controlled amplitude and frequency. The frequency of the applied alternating current was 100 mHz for the polymer deposition, while a frequency value of 50 mHz was used for the in situ electrodeposition of Ag and Au nanoparticles. The selected frequency values ensured the successful preparation of the composite materials. The use of readily available composite materials is intended to produce cost-effective analytical tools. The judicious modification of the organic conductive matrix by various metallic nanoparticles, such as Ag and Au, extends the potential applications of the sensing platform toward a range of biomolecules like quercetin and epinephrine, chosen as benchmark analytes for proof-of-concept antioxidant and neurotransmitter detection. The sensing platforms were tested successfully for quercetin and epinephrine determination on synthetic and real samples. Wide linear response ranges and low limit-of-detection values were obtained for epinephrine and quercetin detection.

NMP limits silver particle size to solve deposited film breakup problems

Metal based electroreflective devices (MERDs) have gained wide attention in recent years in the fields of smart windows and automotive glass due to their excellent photo-thermal modulation capability in the visible and near-infrared wavelength bands due to their high reflectivity. However, the high porosity due to the island-like growth of silver particles makes the devices susceptible to electrodeposited film breakage during prolonged energization or bleaching. This will seriously affect the effectiveness and stability of the device. In this paper, it is shown that the problem of Ag electrodeposition film fragmentation can be effectively overcome by replacing dimethyl sulfoxide solvent by N-methylpyrrolidone (NMP). The optical constants during film deposition were tested by the spectroscopic ellipsometry technique, and the porosity was calculated (reduced by 21.6%). The results show that MERDs with NMP as the solvent have more and more dispersed silver deposition sites, which leads to lower porosity of the silver deposited film during the deposition process. In addition, the lower turn-on voltage, greater contrast, longer memory effect, and greater coloring efficiency reveal that they are more promising for energy-saving applications.

Snowflake relocated Cu2O electrocatalyst on an Ag backbone template for the production of liquid C2+ chemicals from CO2.

In this study, we performed the CO2 reduction reaction (CO2RR) using a structural composite catalyst of cuprous oxide (Cu2O) and silver (Ag) that was simultaneously electrodeposited. While the underneath Ag electrodeposits maintained their spiky backbone structures even after the CO2RR, the Cu2O deposits were reduced to Cu(111) and relocated on the backbone template. The structural changes in Cu2O to Cu increase the active area of the Cu-Ag interface, resulting in a remarkable production rate of 125.01 μmol h-1 of liquid C2+ chemicals via the stabilization of the C-C coupling of the key intermediate species of acetaldehyde. This study provides new insights into designing a bimetallic catalyst for producing sustainable C2+ products from CO2 without any selectivity towards the production of methane.

Improvement on solar selective absorption properties of anodic aluminum oxide photonic crystal films by electrodeposition of silver

Solar selective absorption films based on anodic aluminum oxide (AAO) photonic crystals were prepared by an anodization under periodic current-pulses, subsequently with an alternating current electrodeposition of Co and Ag in sequence. The phase structure, microstructure, and solar selective absorption properties of the Co–Ag electrodeposited film were investigated in comparison with a Co electrodeposited counterpart. Moreover, the stability of the properties against thermal annealing was examined for the two films. A one-dimensional photonic crystal structure was verified for the AAO part in both films, with the first-order photonic bandgap occurring at around 4 μm, while the metals were confirmed to be deposited at the bottom of the AAO part in the form of nanoparticles. For the Co–Ag electrodeposited film, the Ag nanoparticles were deposited over those of Co. The Ag electrodeposition not only was contributive to the solar selective absorption properties, but also substantially improved the stability of the properties against thermal annealing. The Co–Ag electrodeposited film exhibited an infrared emissivity of 0.12, a solar absorptivity of 0.94, and a spectral selectivity of 7.83 before experiencing thermal annealing, while retained a decent spectral selectivity of 6.00 after being annealed in air at 300 °C for 24 h.

Demonstration of Feasibility Using Ionic Liquid as Electrolyte for Electrochemical Deposition and Recovery of Silver from Silver Oxide

Silver oxide (Ag₂O) is soluble in the hydrophobic protic amide-type ionic liquid (IL), protonated-betaine bis((trifluoromethyl)sulfonyl)amide ([Hbet][TFSA]). Cyclic voltammetric behavior of Ag(I) showed a single redox couple, and NMR spectra implied that Ag⁺ might be coordinated with the [TFSA] anions in more extent than with the deprotonated [Hbet] ions (i.e. [bet]; a Zwitterion). By changing the scan rates and cycle numbers of potential scan utilized for the cyclic voltammetric electrodeposition, different particle sizes and distribution densities of silver nanoparticles (AgNPs) could be electrodeposited on glassy carbon disc electrode (GCE), which showed activities towards the electrochemical reduction of nitrate and oxidation of hydrazine, respectively, in alkaline solutions. The high faradic efficiencies (F.E.) of Ag electrodeposition using the contents of Ag₂O coin batteries as the Ag source implied that it may be possible to develop a process for recovering Ag from spent Ag₂O coin batteries based on the electrochemical system reported here.

Isotope effects in the electrodeposition of Ag and Pd

The influence of solvent and its isotope in electrochemical deposition of silver and palladium on pencil graphite from H2O, D2O and MeCN was examined via cyclic voltammetry, chronoamperometry and SEM imaging. The evaluation of the nucleation process was done by comparing the current transients to Scharifker–Hills model of nucleation and the process for all samples was deemed to be progressive and mostly under diffusion control. Kinetic parameters were extracted from I/t curves by curve fitting to Heerman–Tarallo model and it was found that for silver and palladium electrodeposition the isotope of the solvent has a noticeable effect on nucleation rate constant with only a limited effect on the number density of nucleation sites.

Application of Anodic Titanium Oxide Modified with Silver Nanoparticles as a Substrate for Surface-Enhanced Raman Spectroscopy.

The formation of nanostructured anodic titanium oxide (ATO) layers was explored on pure titanium by conventional anodizing under two different operating conditions to form nanotube and nanopore morphologies. The ATO layers were successfully developed and showed optimal structural integrity after the annealing process conducted in the air atmosphere at 450 °C. The ATO nanopore film was thinner (1.2 +/- 0.3 μm) than the ATO nanotube layer (3.3 +/- 0.6 μm). Differences in internal pore diameter were also noticeable, i.e., 88 +/- 9 nm and 64 +/- 7 nm for ATO nanopore and nanotube morphology, respectively. The silver deposition on ATO was successfully carried out on both ATO morphologies by silver electrodeposition and Ag colloid deposition. The most homogeneous silver deposit was prepared by Ag electrodeposition on the ATO nanopores. Therefore, these samples were selected as potential surface-enhanced Raman spectroscopy (SERS) substrate, and evaluation using pyridine (aq.) as a testing analyte was conducted. The results revealed that the most intense SERS signal was registered for nanopore ATO/Ag substrate obtained by electrodeposition of silver on ATO by 2.5 min at 1 V from 0.05M AgNO3 (aq.) (analytical enhancement factor, AEF ~5.3 × 104) and 0.025 M AgNO3 (aq.) (AEF ~2.7 × 102). The current findings reveal a low-complexity and inexpensive synthesis of efficient SERS substrates, which allows modification of the substrate morphology by selecting the parameters of the synthesis process.

Antimicrobial activity of porous metal injection molded (MIM) 316L stainless steel by Zn, Cu and Ag electrodeposition

Porous 316L stainless steel samples were functionalized with electrodeposited zinc, copper, and silver coatings for antimicrobial activity against gram-positive bacteria Staphylococcus aureus (S. aureus). Porous stainless steel samples were created by combining metal injection molding (MIM) with a powder space holder (PSH) technique using sodium chloride (20 wt%) as a space holder material. Galvanostatic (0.10 A) electrodeposition was used for zinc, copper, and silver deposition, and antimicrobial activity of functionalized samples was evaluated using a touch test protocol with S. aureus. All electrodeposited samples completely prevented the growth of S. aureus. These results confirm that metal depositions only in the pores of the porous 316L were sufficient to inhibit the growth of S. aureus completely.

Non-Cyanide Thick Silver Electrodeposition Base on Instantaneous Nucleation for 3D Microstructures with High Performance

To meet the diversified development of electronics, it is essential to develop 3D metal microstructures with high performance. However, 3D thick silver forming is still a challenge due to high internal stresses and various defects. Here we proposed a method for the thick Ag electrodeposition with low-stress and high chemical stability for 3D Ag-based microstructures. We carried out systematic studies through electrochemical measurements, morphological characterization, micro-texture analysis, internal and stability examination. The results show that the nucleation mechanism of electroplating Ag is transformed from progressive nucleation to instantaneous nucleation through the coordinated control of current density and temperature. Higher temperature and lower deposition potential are preferred to form the large-grained crystallization. Additionally, the external parameters for fabricating Ag coating were optimized, and the correlation between micro-texture and internal stress was also verified. The feasibility of thick Ag preparation process was demonstrated by extending the electroplating time, showing excellent performance. Finally, 3D Ag micropillar arrays with the height of 577 μm and the high aspect ratio close to 3 were fabricated by MEMS processing techniques, displaying satisfied 3D forming ability. This work presents a new approach for manufacturing the 3D Ag microstructures and lays foundation for the multi-functionalization Ag-based devices.

Silver nanoparticles in electrochemical immunosensing and the emergence of silver-gold galvanic exchange detection.

Nanoparticle-based electrochemical immunosensors demonstrate high sensitivity toward biomarker detection due to the large surface area of the nanoparticles and their ability to amplify the signal of the target molecule. Additionally, they have a fast response time, relatively lower cost, and can be easily miniaturized for point-of-care applications. Among noble metals, silver nanoparticles (AgNPs) have been extensively used in electrochemical sensors due to their unique properties, such as catalytic activity and excellent electrical conductivity. This Feature Article describes six approaches for incorporating AgNPs in electrochemical platforms, featuring the most recent developments in the silver-gold galvanic exchange-based detection strategy. With a few exceptions, many of these detection methods use AgNP oxidation into Ag+ ions, followed by electrodeposition of Ag+ ions onto the working electrode as zero-valent Ag metal and a final stripping step using a voltammetric technique. Combining these steps provides desirable low detection limits and good sensitivity for various biomarkers. A few other methods involved the reduction of Ag+ ions and depositing them as Ag metal onto the electrode using a reagent mixture so that the striping analysis could be performed. Typically, this reagent mixture includes Ag+ ions, a reducing agent, or an enzyme substrate. Besides, AgNPs have also been directly used to modify the surface of electrodes to facilitate kinetically favored redox-mediated electrochemical reactions. In addition to Ag detection methods, this report will also provide recent examples to illustrate how the size and shape of AgNPs impact the detection limits and sensitivity of an electrochemical assay. Finally, we discuss recent developments in lab-on-a-chip type immunosensors designed explicitly for Ag-based metalloimmunoassay detection, and we envision that this article will provide a comprehensive summary of the operational principles and new insights into such immunoassay systems.

Evaluation of a surface roughness-dependent trimodal switchable mirror using a dry deposition method

We used a nanoparticle deposition system (NPDS) to fabricate surface roughness-dependent trimodal switchable mirrors using a non-electrochromic antimony-doped tin oxide (ATO) film with dry-deposited micro- and nano-sized ATO particles. The devices switched among transparent, mirror and black states. Reversible Ag electrodeposition onto flat ITO glass and the rough surface of the ATO film obviated the need for an electrochromic material. NPDS creates very rough films by supersonically spraying powder onto a substrate. The roughness of the micro-sized ATO film was greater than that of the nano-sized ATO film. As both films were sufficiently rough, a completely black state could be achieved by both devices (0% transmittance over the entire visible wavelength), attributable to light scattering. In contrast, the electrochemical properties of devices with the micro-sized ATO film were superior to those of devices using the nano-sized ATO film because the greater roughness increased the active surface. The charge transfer resistance of devices with the micro-sized film (38 Ω) was lower than that of devices with the nano-sized film (44 Ω). The charge capacity of devices with the micro-sized film (109.87 mC/cm2) was much higher than that of devices with the nano-sized (95.59 mC/cm2). The cyclic transmittance of the device using the micro-sized ATO film was evaluated over 500 cycles with 0% diminution for its durability. Therefore, a trimodal switchable mirror was demonstrated by controlling the surface roughness of a non-electrochromic film. • Dry deposition of particles can control surface roughness of the film. • Trimodal switchable mirror was achieved successfully without electrochromic film. • The electrode with rough surface forms complete black state by light scattering. • Performance of switchable mirror device was compared depending on surface roughness.

Nanoscale Manipulating Silver Adatoms for Aqueous Plasmonic Electrochromic Devices

AbstractPlasmonic colors are attractive building blocks for flat panel displays due to their broad color gamut and unprecedented subwavelength resolution. The exploration of reversible silver (Ag) electrodeposition for switchable plasmonic colors is considered as a promising strategy toward dynamically reconfigurable color displays. To date, the current reversible Ag electrodeposition‐based electrochromic devices are energy‐inefficient as the platforms are realized in nonaqueous electrolytes that require high working voltage. However, the high working voltage in an aqueous electrolyte leads to uncontrolled nucleation growth of Ag particles, thus rendering its application for color displays impractical. Herein, the first demonstration of the manipulation of Ag adatoms for aqueous plasmonic electrochromic devices through underpotential deposition is presented. It is shown that the Ag nanoparticles underpotential deposition not only enables a reversible voltage‐activated wide range of dynamic plasmonic color change of 100 nm, but also facilitates size control of the grown Ag nanoparticles. These findings provide a favorable and novel platform for low energy‐consumption tunable photonic and nanoplasmonic devices, as well as a simple and reliable process for rapid, scalable, and green preparation of tunable plasmonic Ag nanoparticles.

Bistable Silver Electrodeposition‐Based Electrochromic Device with Reversible Three‐State Optical Transformation By Using WO3 Nanoislands Modified ITO Electrode

AbstractA bistable electrochromic (EC) device which can reversibly transform between transparent, mirror, and black states based on reversible metal Ag electrodeposition is achieved by introducing 1) a (3‐mercaptopropyl) trimethoxysilane (MPTMS)‐treated indium‐tin‐oxide (ITO) glass electrode modified with WO3 nanoislands (WNs) as the rough surface and 2) ionic liquids (IL) into electrolyte to form an anion‐blocking layer, toward achieving long‐term memory performance. Typically, the EC cell is packaged by sandwiching gel electrolyte between the flat and WNs‐modified ITO electrodes. Under opposite voltages, this smart device can transfer from transparent to black (+2.5 V/9.4 s) or mirror (−2.5 V/8.3 s) state by depositing Ag on the WNs‐modified or flat ITO electrode surface, respectively. The assembled device exhibits over 80% mirror reflectance and below 10% transmittance of black state. After power off, both the black and mirror states remain bistability for a long time (>30 min) when IL are introduced into electrolyte for the EC device. The electrical double layer in the highly viscous electrolyte with IL contributes to form a barrier to bromide ions, which protects the Ag layer from dissolution at open circuit. This multifunctional energy‐efficient EC device has shown great potential and competitiveness for numerous applications compared to conventional EC devices.

Cyanide-free silver electrodeposition with polyethyleneimine and 5,5-dimethylhydantoin as organic additives for an environmentally friendly formulation

The influence of polyethyleneimine (PEI) as additive for cyanide-free silver bath, in combination with 5,5-dimethylhydantoin (DMH) as complexing agent, is studied. Cyclic voltammetry (CV) measurements are used to characterize the electrochemical behaviour of the Ag/DMH complex. The Ag electrodeposition from the cyanide-free silver-plating bath is analysed by CVs and the process is optimized varying the PEI concentration. Chronoamperometry is then used to investigate the electrodeposition mechanism, which is found to be a three-dimensional diffusion-controlled nucleation and growth mechanism, according to the Scharifker–Mostany’s model. Smoother, brighter and blue coloured silver deposits are obtained in the presence of PEI in a Hull’s cell test, at low density current. Eventually, the influence of nitrate anion is also investigated. The presence of nitrate increases the range of current density allowing for an effective Ag deposition.

Ag-O-Co Interface Modulation-Amplified Luminol Cathodic Electrogenerated Chemiluminescence.

It remains a great challenge to develop effective strategies for improving the weak cathodic electrogenerated chemiluminescence (ECL) of the luminol-dissolved O2 system. Interface modulation between metal and supports is an attractive strategy to improve oxygen reduction reaction (ORR) activity. Therefore, the design of electrocatalysts via interface modulation would provide new opportunities for the ECL amplification involving reactive oxygen species (ROSs). Herein, we have fabricated an Ag single-atom catalyst with an oxygen-bridged interface (Ag-O-Co) through the electrodeposition of Ag on a CoAl layered double hydroxide (LDH) modified indium tin oxide (ITO) electrode (Ags/LDH/ITO). Interestingly, it was found that the cathodic ECL intensity of the luminol-dissolved O2 system at the Ags/LDH/ITO electrode was extraordinarily enhanced in comparison with those at bare ITO and other Ag nanoparticle-based electrodes. The enhanced ECL performances of the Ags/LDH/ITO electrode were attributed to the increasing amounts of ROSs by electrocatalytic ORR in the Ag-O-Co interface. The electron redistribution of Ag and Co bimetallic sites could accelerate electron transfer, promote the adsorption of O2, and sufficiently activate O2 through a four-electron reaction pathway. Finally, the luminol cathodic ECL intensity was greatly improved. Our findings can provide inspiration for revealing the interface effects between metal and supports, and open up a new avenue to improve the luminol cathodic ECL.

Pulse electrodeposition of Ag, Cu nanoparticles on TiO2 nanoring/nanotube arrays for enhanced photoelectrochemical water splitting

In this paper, plasmonic Ag and Cu nanoparticles were co-deposited on TiO2 nanoring/nanotube arrays (TiO2 R/T) by using two-step pulse electrodeposition method for investigating the optical and photoelectrochemical properties, in comparison to monometallic Ag, Cu decoration. By optimizing the electrodeposition cycle times and electrolyte concentration, bimetallic Ag–Cu/TiO2 R/T-0.5 with moderate densities and sizes of Ag and Cu nanoparticles was fabricated and shows great photocatalytic potential, in which, Ag mainly facilitates the generation of hot electrons by absorbing visible light and Cu plays an important role in accelerating the separation and transportation of hot electrons. The hydrogen production rate was tested as 425 μL h−1 cm−2, which is about 1.34-fold enhanced H2 production over TiO2 R/T. Furthermore, molecular dynamics simulations were made for analyzing the interface electrostatic properties between plasmonic nanoparticles of Ag or Cu and the semiconductor TiO2. It is calculated that bimetallic Ag–Cu/TiO2/H2O system has larger interfacial Helmholtz potential than monometallic Ag/TiO2/H2O, Cu/TiO2/H2O and pure TiO2/H2O systems, accelerating the four-electron reaction occurring at the semiconductor/electrolyte interface. This research put forward a feasible and simple pulse electrodeposition method to fabricate bimetallic photoanodes for enhanced hydrogen evolution and an important analysis method of semiconductor/ metal/electrolyte interface characteristics.

TiO2-Ag AND NATURAL DYE CO-PIGMENTED WITH SALICYLIC ACID FOR DYE-SENSITIZED SOLAR CELL (DSSC) APPLICATION

The Dye-Sensitized Solar Cell (DSSC) is still inefficient. Because low efficiency is caused by electron recombination, this study reduced it by the electrodeposition of Ag metal against TiO2. XRD was used to determine the crystal structure, size, and effect of Ag electrodeposition on TiO2. SEM-EDS was used to investigate the surface morphology and the presence of Ag metal in the TiO2-Ag layer. Anthocyanins were used as dyes. To improve thermal stability and achieve a bathochromic effect, the anthocyanin used was co-pigmented with salicylic acid. The anthocyanin extract used in this study was obtained from the red grape peel (Vitis Vinifera), jengkol peel (Pithecellobium jiringa), senduduk fruit (Melastoma malabathricum L), and mangosteen peel (Garcinia Mangostana L). The dyes were identified using UV-Vis and FTIR. The electrical properties of the resulting DSSC were measured using a multi-meter. According to this study, the electrodeposition of Ag on the TiO2 layer could improve DSSC efficiency. The highest efficiency was achieved in DSSC with TiO2-Ag and co-pigmented dye using mangosteen peel as the dye source

Ionic Liquid Electrolyte-Based Switchable Mirror with Fast Response and Improved Durability.

Electrochemically tunable devices based on reversible metal electrodeposition have attracted extensive attention for energy-saving smart windows, information displays, digital signage, and variable reflectance mirrors, owing to their excellent optical modulation characteristics, low operation voltage, and superb electrochemical stability. Here, we study the effects of ionic liquid (IL)-based electrolytes on electrodeposition of the reversible electrochemical mirrors (REMs) by changing the organic cations of the ILs to obtain devices with the desired spectroelectrochemical and electrodeposited properties. Spectroelectrochemical measurements and scanning electron microscopy images show that organic cations drastically affect the switching speed and cycling durability, which we proposed on the basis of the difference in the absorption energies between cations and Ag(111) surfaces. Higher adsorption energy indicates strong adhesion between organic cations and Ag(111) surfaces, and this strong adsorption would prevent aggregation and agglomeration during the nucleation of Ag nanoparticles (AgNPs), leading to a denser and more compact electrodeposited Ag film and faster switching speeds (3.3 s for coloring and 14.3 s for bleaching). These findings allow us to fabricate dynamic devices that exhibit reversibly switchable light modulation at fast switching speeds and excellent cycling stability over thousands of cycles without attenuation. The combination of rapid switching and durable cycling stability enables tunable windows, which are based on reversible electrodeposition of metal Ag and IL-based electrolytes, make REM devices a competitive and promising alternative to traditional intelligent response materials.