A Solid-Solution Approach for Redox Active Metal-Organic Frameworks with Tunable Redox Conductivity.

Systematically tuning the conductivity of metal-organic frameworks (MOFs) is key to synergizing their attractive synthetic control and porosity with electrochemical attributes useful in energy and sensing technologies. A priori control of charge transfer is possible by exploiting the solid-solution properties of MOFs together with electronic self-exchange enabled by redox pendants. Here we introduce a new strategy for preparing redox-active MOF thin-film electrodes with finely tuned redox pendant content. Varying the ratios of alkyl-ferrocene containing redox-active and inactive links during MOF synthesis enabled the fabrication of electrodes with tunable redox conductivity. The prepared MOF electrodes display maximum electron conductivity of 1.10 mS m-1, with crystallographic and electrochemical stability upon thousands of redox cycles. Electroanalytical studies demonstrated that the conductivity follows solution-like diffusion-controlled behavior with nonlinear electron diffusion coefficients consistent with charge hopping and percolation models of spatially fixed redox centers. Our studies create new prospects in the design and synthesis of redox-active MOFs with targeted properties for the design of advanced electrochemical devices.

Modulation of the Electrochemical Reactivity of Solubilized Redox Active Polymers via Polyelectrolyte Dynamics.

Redox active polymers (RAPs) are electrochemically versatile materials that find key applications in energy storage, sensing, and surface modification. In spite of the ubiquity of RAP-modified electrodes, a critical knowledge gap exists in the understanding of the electrochemistry of soluble RAPs and their relation to polyelectrolyte dynamics. Here, we explore for the first time the intersection between polyelectrolyte behavior and the electrochemical response that highly soluble and highly substituted RAPs with viologen, ferrocene, and nitrostyrene moieties elicit at electrodes. This comprehensive study of RAP electrolytes over several orders of magnitude in concentration and ionic strength reveals distinct signatures consistent with surface confined, colloidal, and bulk-like electrochemical behavior. These differences emerge across polyelectrolyte packing regimes and are strongly modulated by changes in RAP coil size and electrostatic interactions with the electrode. We found that, unlike monomer motifs, simple changes in the ionic strength caused variations over 1 order of magnitude in the current measured at the electrode. In addition, the thermodynamics of adsorbed RAP films were also affected, giving rise to standard reduction potential shifts leading to redox kinetic effects as a result of the mediating nature of the RAP film in equilibrium with the solution. Full electrochemical characterization via transient and steady-state techniques, including the use of ultramicroelectrodes and the rotating disk electrode, were correlated to dynamic light scattering, ellipsometry, and viscometric analysis. These methods helped elucidate the relationship between electrochemical behavior and RAP coil size, film thickness, and polyelectrolyte packing regime. This study underscores the role of electrostatics in modulating the reactivity of redox polyelectrolytes.

Interrogating Charge Storage on Redox Active Colloids via Combined Raman Spectroscopy and Scanning Electrochemical Microscopy.

Redox active colloids (RACs) are dispersible, cross-linked polymeric materials that incorporate a high concentration of redox-active motifs, making them attractive for next-generation size-exclusion redox flow batteries. In order to tap into their full potential for energy storage, it is essential to understand their internal charge mobility, capacity, and cyclability. Here we focus on using a combined suite of Raman spectroscopy and scanning electrochemical microscopy (SECM) tools for evaluating three important parameters that govern charge storage in viologen-RACs: their intraparticle redox active concentration, their reduction/oxidation mechanism, and their charge transfer rate. We addressed RACs using SECM imaging and single-particle experiments, from which the intraparticle diffusion and concentration parameters were elucidated. By using Raman spectroscopy coupled to surface interrogation SECM, we further evaluated their reversible redox properties within monolayer films of 80- and 135-nm-sized RACs. Most notably we have confirmed that the concentration and redox mechanisms are essentially unchanged when varying the RAC size. As expected, we see that larger particles inherently require longer times for electrolysis independent of the methodology used for their study. Our simulations further verify the internal concentration of RACs and suggest that their porosity enables solution redox active mediators to penetrate and titrate charge in their interior. The combined methodology presented here sets an important analytical precedent in decoupling the charge storage properties of new bulk materials for polymer batteries starting from probing low-dimensional assemblies and single particles using nano- and spectroelectrochemical approaches.

Redox Active Colloids as Discrete Energy Storage Carriers.

Versatile and readily available battery materials compatible with a range of electrode configurations and cell designs are desirable for renewable energy storage. Here we report a promising class of materials based on redox active colloids (RACs) that are inherently modular in their design and overcome challenges faced by small-molecule organic materials for battery applications, such as crossover and chemical/morphological stability. RACs are cross-linked polymer spheres, synthesized with uniform diameters between 80 and 800 nm, and exhibit reversible redox activity as single particles, as monolayer films, and in the form of flowable dispersions. Viologen-based RACs display reversible cycling, accessing up to 99% of their capacity and 99 ± 1% Coulombic efficiency over 50 cycles by bulk electrolysis owing to efficient, long-distance intraparticle charge transfer. Ferrocene-based RACs paired with viologen-based RACs cycled efficiently in a nonaqueous redox flow battery employing a simple size-selective separator, thus demonstrating a possible application that benefits from their colloidal dimensions. The unprecedented versatility in RAC synthetic and electrochemical design opens new avenues for energy storage.

Impact of electrolyte composition on the reactivity of a redox active polymer studied through surface interrogation and ion-sensitive scanning electrochemical microscopy.

Elucidating the impact of interactions between the electrolyte and electroactive species in redox active polymers is key to designing better-performing electrodes for electrochemical energy storage and conversion. Here, we present on the improvement of the electrochemical activity of poly(para-nitrostyrene) (PNS) in solution and as a film by exploiting the ionic interactions between reduced PNS and K(+), which showed increased reactivity when compared to tetrabutylammonium (TBA(+))- and Li(+)-containing electrolytes. While cyclic voltammetry enabled the study of the effects of cations on the electrochemical reversibility and the reduction potential of PNS, scanning electrochemical microscopy (SECM) provided new tools to probe the ionic and redox reactivity of this system. Using an ion-sensitive Hg SECM tip allowed to probe the ingress of ions into PNS redox active films, while surface interrogation SECM (SI-SECM) measured the specific kinetics of PNS and a solution phase mediator in the presence of the tested electrolytes. SI-SECM measurements illustrated that the interrogation kinetics of PNS in the presence of K(+) compared to TBA(+) and Li(+) are greatly enhanced under the same surface concentration of adsorbed radical anion, exhibiting up to a 40-fold change in redox kinetics. We foresee using this new application of SECM methods for elucidating optimal interactions that enhance polymer reactivity for applications in redox flow batteries.

Electrochemical lithiation-induced polymorphism of anthraquinone derivatives observed by operando X-ray diffraction.

The use of organic molecules represents a very attractive and promising alternative for electrical energy storage applications. Quinones, in general, and anthraquinones, in particular, are especially attractive due to their ability to reversibly exchange multiple electrons per formula unit. When used as the active electrode material in a real lithium-ion battery (LIB), crystalline anthraquinone powders reversibly change crystal packing as a function of state-of-charge (redox state), with well-defined voltage plateaus appearing concomitantly with new phases. Operando powder X-ray diffraction (XRD) is a powerful method for screening the structural stability of organic cathode candidates and for understanding electrochemically-induced structural transformations within organic molecular crystals. Herein we explore the electrochemical lithiation-induced polymorphism of anthraquinone (AQ) and three related derivatives. We believe that this analysis can serve as a model for studying organic charge storage within crystalline small-molecule candidates.

Cation-Dependent Stabilization of Electrogenerated Naphthalene Diimide Dianions in Porous Polymer Thin Films and Their Application to Electrical Energy Storage.

Porous polymer networks (PPNs) are attractive materials for capacitive energy storage because they offer high surface areas for increased double-layer capacitance, open structures for rapid ion transport, and redox-active moieties that enable faradaic (pseudocapacitive) energy storage. Here we demonstrate a new attractive feature of PPNs--the ability of their reduced forms (radical anions and dianions) to interact with small radii cations through synergistic interactions arising from densely packed redox-active groups, only when prepared as thin films. When naphthalene diimides (NDIs) are incorporated into PPN films, the carbonyl groups of adjacent, electrochemically generated, NDI radical anions and dianions bind strongly to K(+), Li(+), and Mg(2+), shifting the formal potentials of NDI's second reduction by 120 and 460 mV for K(+) and Li(+)-based electrolytes, respectively. In the case of Mg(2+), NDI's two redox waves coalesce into a single two-electron process with shifts of 240 and 710 mV, for the first and second reductions, respectively, increasing the energy density by over 20 % without changing the polymer backbone. In contrast, the formal reduction potentials of NDI derivatives in solution are identical for each electrolyte, and this effect has not been reported for NDI previously. This study illustrates the profound influence of the solid-state structure of a polymer on its electrochemical response, which does not simply reflect the solution-phase redox behavior of its monomers.

Rapid and efficient redox processes within 2D covalent organic framework thin films.

Two-dimensional covalent organic frameworks (2D COFs) are ideally suited for organizing redox-active subunits into periodic, permanently porous polymer networks of interest for pseudocapacitive energy storage. Here we describe a method for synthesizing crystalline, oriented thin films of a redox-active 2D COF on Au working electrodes. The thickness of the COF film was controlled by varying the initial monomer concentration. A large percentage (80-99%) of the anthraquinone groups are electrochemically accessible in films thinner than 200 nm, an order of magnitude improvement over the same COF prepared as a randomly oriented microcrystalline powder. As a result, electrodes functionalized with oriented COF films exhibit a 400% increase in capacitance scaled to electrode area as compared to those functionalized with the randomly oriented COF powder. These results demonstrate the promise of redox-active COFs for electrical energy storage and highlight the importance of controlling morphology for optimal performance.

Single layer graphene as an electrochemical platform.

Over the past decade, there has been a great deal of interest in graphene with regards to its electrochemical behavior. Previous studies have focused on understanding fundamental processes such as charge transfer and molecular transport at the graphene-electrolyte interface as well as on applications of graphene in electronic, optical, and mechanical systems. We present illustrative examples of large area, single layer graphene platforms for applications such as optical and sensing devices as well as microfluidic systems. Three examples of graphene modified with thin polymer films are discussed. We have explored the use of graphene as an electrochemical platform for surface-generated electrogenerated chemiluminescence (ECL) using poly-[Ru(v-bpy)3](2+), where v-bpy is 4-vinyl, 4'-methyl 2,2'-bipyridine, as a model system. We found that while graphene can sustain ECL conditions, there was film degradation during ECL, as demonstrated by a decrease in ECL intensity upon potential cycling even in the presence of a graphene coating ("graphene blanket"). Using poly 3,4-ethylenedioxythiophene (EDOT), we demonstrate a facile method of fabricating electrochromic electrodes from large area graphene. The oxidation of NADH at graphene was catalyzed using an electrodeposited layer of 3,4-dihydroxybenzaldehyde as an effective redox mediator. In addition, we describe the fabrication and characterization of a microfluidic device based on a solution-gated field effect transistor which was able to detect changes of 60 mV per pH unit change in an inverted cell design. On the other hand, a 29 mV shift in the Dirac point per unit pH change was measured with our microfluidic devices, and a ca. 10% FET conductance change was measured when we continuously changed the pH in solution from 6.91 to 7.64 in the microfluidic channel, demonstrating local microfluidic pH sensing (albeit non-Nerstian) in real time.

Increasing the gravimetric energy density of organic based secondary battery cathodes using small radius cations (Li+ and Mg2+).

One of the major challenges in electrochemical energy storage (EES) is increasing the gravimetric capacity and energy density of the cathode material. Here we demonstrate how to increase the gravimetric energy density of electrical energy storage devices based on the use of organic materials through exploitation of the strong ionic coupling between a reduced carbonyl functionality and small cations such as lithium (Li(+)) and magnesium (Mg(2+)). Binding of the cation to the reduced carbonyl results in a positive shift of the formal reduction potential of the carbonyl couple. This has the effect of increasing the cell voltage which, in turn, results in an increase in the energy density. We show how this interaction can be used to dramatically increase, by up to a factor of 2, the energy density for a selected case study using 1,2-di(thiophen-2-yl)ethane-1,2-dione (DTED). We have carried out electrochemical and computational studies in order to understand the thermodynamic (positive shift of 250 mV and 1 V in the formal potential for the first and second reductions, respectively, of the carbonyl groups of DTED) and kinetic effects between small radii cations (Li(+) and Mg(2+)) and the reduced carbonyl functionality of carbonyl-based organic molecules (C-bOMs).