Redox Events Research Articles

57Fe nuclear resonance vibrational spectroscopic studies of tetranuclear iron clusters bearing terminal iron(iii)-oxido/hydroxido moieties.

57Fe nuclear resonance vibrational spectroscopy (NRVS) has been applied to study a series of tetranuclear iron ([Fe4]) clusters based on a multidentate ligand platform (L3-) anchored by a 1,3,5-triarylbenzene linker and pyrazolate or (tertbutylamino)pyrazolate ligand (PzNH t Bu-). These clusters bear a terminal Fe(iii)-O/OH moiety at the apical position and three additional iron centers forming the basal positions. The three basal irons are connected with the apical iron center via a μ4-oxido ligand. Detailed vibrational analysis via density functional theory calculations revealed that strong NRVS spectral features below 400 cm-1 can be used as an oxidation state marker for the overall [Fe4] cluster core. The terminal Fe(iii)-O/OH stretching frequencies, which were observed in the range of 500-700 cm-1, can be strongly modulated (energy shifts of 20-40 cm-1 were observed) upon redox events at the three remote basal iron centers of the [Fe4] cluster without the change of the terminal Fe(iii) oxidation state and its coordination environment. Therefore, the current study provides a quantitative vibrational analysis of how the remote iron centers within the same iron cluster exert exquisite control of the chemical reactivities and thermodynamic properties of the specific iron site that is responsible for small molecule activation.

Homotrinuclear ruthenium(ii) and rhodium(i) complexes of redox-active tris(ferrocenyl)arene-based tris-phosphanes.

Homotrinuclear complexes of the C 3-symmetric tris(ferrocenyl)arene-based tris-phosphanes 1a-d with ruthenium(ii) ([1a-d(Ru)3]) and rhodium(i) ([1a-d(Rh)3]) were prepared and fully characterised. Complexes [1a-d(Ru)3] and [1a-d(Rh)3] are electrochemically active. The nature of the arene core in 1a-d ranging from benzene, 1,3,5-trifluorobenzene and mesitylene to s-triazine allows to fine-tune the exact oxidation potentials for tailoring the electrochemical response. With a BArF 4 --based supporting electrolyte, a distinct separation of the three iron-centred oxidations of the ligand backbone is observable. Under these conditions, these oxidations are mostly reversible but, especially for the third oxidation, already show signs of irreversibility. In general, while the coordinated metal complex fragment does not strongly alter the electrochemical response of the arene-trisferrocenyl core 1a-d, there are observable differences. Rhodium(i) complexes are oxidised at slightly higher potentials than ruthenium(ii) complexes. In both cases, individual oxidation states for the C6H3(CH2)3-based ligand (1d) are difficult to address and the C3N3-based ligand (1c) shows the most complicated and least reversible electrochemistry with severely broadened third oxidations and reduced reversibility in cyclic voltammetry. The most well-suited system for potential applications in redox-switchable catalysis, in all cases, is the C6H3-based ligand (1a), showing entirely reversible and well-separated redox events.

In Situ Investigation of Electrochemically Mediated Carbon Capture and Release Via Quinone Chemistry in Aqueous Media

The development of devices capable of capturing and sequestering carbon dioxide emissions directly from air or at point sources is motivated by mitigating climate change. Electrochemically driven carbon capture and release at ambient temperature and pressure through the formation of complexes with organic redox active molecules [1,2] or via pH swing caused by proton-coupled electron transfer during molecular redox events [3,4] has shown promising results for carbon capture and release in terms of energy cost, scalability and safety compared to the state of the art amine scrubbing technologies [5].Quinones are organic molecules containing an unsaturated six-member ring with two carbonyl groups. They exhibit two potential mechanisms of CO2 capture. (a) Upon electrochemical reduction, the carbonyl groups within quinones provide sites for nucleophilic addition of carbon dioxide which results in the formation of a quinone-CO2 adduct (CO2reversibly bound by quinones). (b) Depending on the pKa of the quinone and the local pH, the electrochemical reduction of the compound can be proton-coupled, creating hydroxide, which captures CO2 as carbonate or bicarbonate.In this work, we introduce in situ electrochemical characterization and in situ fluorescence microscopy to separately quantify the two aforementioned contributions toward capture of CO2 at partial pressures ranging from 0.1 bar to 0.4 mbar. The non-invasive in situ analytical methods introduced in this work are used to distinguish, with sub-second time resolution, between the oxidized, reduced and adduct species by their electrochemical and fluorescence signatures. The results of this study permits us to understand the underlying simultaneous contributions of quinone-CO2 adduct path and the pH-swing path toward carbon capture and release and, additionally, introduces powerful non-invasive methods for gathering insights on similar systems. 1X. Li, X. Zhao, Y. Liu, T.A. Hatton, and Y. Liu, "Redox-tunable lewis bases for electrochemical carbon dioxide capture", Nature Energy 7, 1065 (2022). 2Y. Liu, H.Z. Ye, K.M. Diederichsen, T. Van Voorhis, and T.A. Hatton, "Electrochemically mediated carbon dioxide separation with quinone chemistry in salt-concentrated aqueous media", Nat Commun 11, 2278 (2020). 3S. Jin, M. Wu, Y. Jing, R.G. Gordon, and M.J. Aziz, "Low energy carbon capture via electrochemically induced pH swing with electrochemical rebalancing", Nat Commun 13, 2140 (2022). 4S. Jin, M. Wu, R.G. Gordon, M.J. Aziz, and D.G. Kwabi, "pH swing cycle for CO2 capture electrochemically driven through proton-coupled electron transfer", Energy & Environmental Science 13, 3706 (2020). 5G.T. Rochelle, "Amine scrubbing for CO2 capture", Science 325, 1652.

Effect of Apical Ligands, Substituents and Oxidation States on the Electronic Structure of Co(III) Corrolates

AbstractCobalt(III) corroles are the most commonly studied types of metallocorroles, yet the details of their electronic structure, ground spin states and place of redox events are not always straightforward. Corroles are redox active, potentially non‐innocent ligands, and it has been found through various experimental and computational techniques, that the innocent or non‐innocent behavior is modulated by the apical ligands bound to the cobalt center. In this work, we aim to analyze the effect of corrole substituents and number and type of apical ligands on the electronic structure of cobalt corroles through density functional and wavefunction theories, and to determine the relative energies between closed‐ and open‐shell states. We further perform preliminary analyses on the place of electron abstraction upon oxidation and on the effect of the corrole and apical ligands on the cobalt ligand field splittings. We find that both ligand field and electron‐donating or withdrawing effects determine the relative energies of open‐shell and closed shell singlet states.

A Conformationally Stable π-Expanded X-Type Double Helicene Comprising Dihydropyracylene Units with Multistage Redox Behavior.

A π-expanded X-type double [5]helicene comprising dihydropyracylene moieties was synthesized from commercially available acenaphthene. X-ray crystallographic analysis revealed the unique highly twisted structure of the compound resulting in the occurrence of two enantiomers which were separated by chiral HPLC, owing to their high conformational stability. The compound shows strongly bathochromically shifted UV/vis absorption and emission bands with small Stokes shift and considerable photoluminescence quantum yield and circular polarized luminescence response. The electrochemical studies revealed five facilitated reversible redox events, including three reductions and two oxidations, thus qualifying the compound as chiral multistage redox amphoter. The experimental findings are in line with the computational studies based on density functional theory pointing towards increased spatial extension of the frontier molecular orbitals over the polycyclic framework and a considerably narrowed HOMO-LUMO gap.

Scrutinizing the redox chemistry of group 10 complexes supported by a redox-active bis-phenolate mesoionic carbene

We present the synthesis of an isostructural series of group 10 mesoionic carbene complexes with the general formula [M(MIC)Py] (with M = Ni (1), Pd (2) and Pt (3), Py = pyridine and MIC = bis-phenolate triazolylidene). Their electrochemical properties are investigated, revealing two quasi-reversible oxidations for all compounds, while no reductions are observed. Isolation of the oxidized species has been achieved using either silver triflate or nitrosonium tetrafluoroborate for the nickel and the platinum complex yielding the corresponding mono-cationic complexes [1]X and [3]X (X = OTf or BF4). For the palladium complex, oxidation reactions yielded different products 4 and 5 in which the pyridine and/or the phenol(oxy) donors were found to be labile compared to Ni and Pt. Additionally, for Pt the electron transfer reaction was found to be quite slow and short reaction times led to the isolation of an unusual heterobimetallic silver-platinum complex 6. The location of the redox event has been investigated using EPR spectroscopy and computational methods, which suggest, that the oxidation is mostly centered on one of the phenolate anchors.

Synthesis and Properties of Fluorenone-Containing Cycloparaphenylenes and Their Late-Stage Transformation.

Cycloparaphenylenes (CPPs) are the smallest possible armchair carbon nanotubes, the properties of which strongly depend on their ring size. They can be further tuned by either peripheral functionalization or by replacing phenylene rings for other aromatic units. Here we show how four novel donor-acceptor chromophores were obtained by incorporating fluorenone or 2-(9H-fluoren-9-ylidene)malononitrile into the loops of two differently sized CPPs. Synthetically, we managed to perform late-stage functionalization of the fluorenone-based rings by high-yielding Knoevenagel condensations. The structures were confirmed by X-ray crystallographic analyses, which revealed that replacing a phenylene for a fused-ring-system acceptor introduces additional strain. The donor-acceptor characters of the CPPs were supported by absorption and fluorescence spectroscopic studies, electrochemical studies (displaying the CPPs as multi-redox systems undergoing reversible or quasi-reversible redox events), as well as by computations. The oligophenylene parts were found to comprise the electron donor units of the macrocycles and the fluorenone parts the acceptor units.

Altering the Localization of an Unpaired Spin in a Formal Ni(V) Species.

The participation of both ligand and the metal center in the redox events has been recognized as one of the ways to attain the formal high valent complexes for the late 3d metals, such as Ni and Cu. Such an approach has been employed successfully to stabilize a Ni(III) bisphenoxyl diradical species in which there exist an equilibrium between the ligand and the Ni localized resultant spin. The present work, however, broadens the scope of the previously reported three oxidized equivalent species by conveying the approaches that tend to affect the reported equilibrium in CH3 CN at 233 K. Various spectroscopic characterization revealed that employing exogenous N-donor ligands like 1-methyl imidazole and pyridine favors the formation of the Ni centered localized spin though axial binding. In contrast, due to its steric hinderance, quinoline favors an exclusive ligand localized radical species. DFT studies shed light on the novel intermediates' complex electronic structure. Further, the three oxidized equivalent species with the Ni centered spin was examined for its hydrogen atom abstraction ability stressing their key role in alike reactions.

Nano-size cobalt-doped cerium oxide particles embedded into graphitic carbon nitride for enhanced electrochemical sensing of insecticide fenitrothion in environmental samples: An experimental study with the theoretical elucidation of redox events

In the present work, a nanocomposite, based on embedding Co-doped CeO2 nanoparticles into graphitic carbon nitride (g-C3N4), was applied to functionalize commercial glassy carbon paste. This is the first application of the electrochemical sensor, developed through the proposed procedure, in electrochemical sensing. The sensor was utilized for the electrochemical determination of organophosphate pesticide fenitrothion (FNT). Cyclic voltammetry identified reversible oxidation of FNT (oxidation at 0.18 V and reduction at 0.13 V) and additional reduction at −0.62 V vs. Ag/AgCl in HCl solution (pH = 1). Theoretical calculations were carried out to model and elucidate experimentally observed redox processes. Special attention was devoted to modeling experimental conditions, and based on the obtained results, a detailed redox mechanism of the investigated analyte was proposed. This represents the first complete and unambiguous elucidation of the FNT redox mechanism, supported by joined experimental and theoretical data. Square wave voltammetry (SWV) was utilized for quantification, whereby the FNT oxidation peak was chosen for monitoring the analyte concentration. The developed sensor provided a nanomolar detection limit (3.2 nmol L−1), a wide linear concentration range (from 0.01 to 13.7 μmol L−1), and good precision, repeatability, and selectivity towards FNT. Practical application possibility was explored by testing the sensor performance for examining tap water and apple samples. Recovery tests, conducted during the FNT-spiked sample assays, showed a great application capability of the developed sensor for real-time monitoring of FNT traces in environmental samples.

Hexaguanidino-Triptycenes and Triphenylenes: Electronic Coupling in Molecules Containing Three Redox-Active o-Diguanidinobenzene Units Connected either Directly or Interacting Through Homoconjugation.

Novel redox-active hexaguanidine molecules with multiple redox states were synthesized by connecting three o-diguanidinobenzene units. In 2,3,6,7,14,15-hexaguanidino-triptycenes, the three redox-active o-diguanidinobenzene units are connected through C-C bonds to the sp3 -hybridized bridgehead C atoms, and in 2,3,6,7,10,11-hexaguanidino-triphenylenes they are directly connected. The connectivity difference leads to different electronic coupling between the three redox-active o-diguanidinobenzene units, with homoconjugation being present in the triptycene, but not in the triphenylene compounds. Motivated by the appearance of an intense low-energy electronic transition, we especially analysed the effect of homoconjugation on the electronic structure and charge delocalization in the dicationic redox state of the triptycene derivatives. Then, several trinuclear high-spin cobalt (and copper) complexes were synthesized with the triphenylene and triptycene ligands, and the magnetic coupling and redox properties analysed. By choice of the coligands (hexafluoroacetylacetonate, trifluoroacetylacetonate and acetylacetonate), oxidation could be switched between metal- and ligand-centered redox events, leading to drastic changes in the magnetic or optical properties, especially as a consequence of homoconjugation in the triptycene derivatives.

Lewis Acid Supported Nickel Nitrenoids.

Metalation of the polynucleating ligand F,tbs LH6 (1,3,5-C6 H9 (NC6 H3 -4-F-2-NSiMe2 t Bu)3 ) with two equivalents of Zn(N(SiMe3 )2 )2 affords the dinuclear product (F,tbs LH2 )Zn2 (1), which can be further deprotonated to yield (F,tbs L)Zn2 Li2 (OEt2 )4 (2). Transmetalation of 2 with NiCl2 (py)2 yields the heterometallic, trinuclear cluster (F,tbs L)Zn2 Ni(py) (3). Reduction of 3 with KC8 affords [KC222 ][(F,tbs L)Zn2 Ni] (4) which features a monovalent Ni centre. Addition of 1-adamantyl azide to 4 generates the bridging μ3 -nitrenoid adduct [K(THF)3 ][(F,tbs L)Zn2 Ni(μ3 -NAd)] (5). EPR spectroscopy reveals that the anionic cluster possesses a doublet ground state (S = ). Cyclic voltammetry of 5 reveals two fully reversible redox events. The dianionic nitrenoid [K2 (THF)9 ][(F,tbs L)Zn2 Ni(μ3 -NAd)] (6) was isolated and characterized while the neutral redox isomer was observed to undergo both intra- and intermolecular H-atom abstraction processes. Ni K-edge XAS studies suggest a divalent oxidation state for the Ni centres in both the monoanionic and dianionic [Zn2 Ni] nitrenoid complexes. However, DFT analysis suggests Ni-borne oxidation for 5.

Lewis Acid Supported Nickel Nitrenoids

AbstractMetalation of the polynucleating ligand F,tbsLH6 (1,3,5‐C6H9(NC6H3−4‐F−2‐NSiMe2tBu)3) with two equivalents of Zn(N(SiMe3)2)2 affords the dinuclear product (F,tbsLH2)Zn2 (1), which can be further deprotonated to yield (F,tbsL)Zn2Li2(OEt2)4 (2). Transmetalation of 2 with NiCl2(py)2 yields the heterometallic, trinuclear cluster (F,tbsL)Zn2Ni(py) (3). Reduction of 3 with KC8 affords [KC222][(F,tbsL)Zn2Ni] (4) which features a monovalent Ni centre. Addition of 1‐adamantyl azide to 4 generates the bridging μ3‐nitrenoid adduct [K(THF)3][(F,tbsL)Zn2Ni(μ3‐NAd)] (5). EPR spectroscopy reveals that the anionic cluster possesses a doublet ground state (S = ). Cyclic voltammetry of 5 reveals two fully reversible redox events. The dianionic nitrenoid [K2(THF)9][(F,tbsL)Zn2Ni(μ3‐NAd)] (6) was isolated and characterized while the neutral redox isomer was observed to undergo both intra‐ and intermolecular H‐atom abstraction processes. Ni K‐edge XAS studies suggest a divalent oxidation state for the Ni centres in both the monoanionic and dianionic [Zn2Ni] nitrenoid complexes. However, DFT analysis suggests Ni‐borne oxidation for 5.

Synthesis, characterization, and luminescence properties of salophen-bridged heterotrinuclear Ru–M–Ru (M = Ni, Zn) hybrid complexes composed of coordination and organometallic sites

Six heterotrinuclear complexes, Ni[C5H2NBr{N = COC6H3C≡C(trans-Ru(dppe)2)C≡CC6H4R}2 (1a–c) and Zn[C5H2NBr{N = COC6H3C≡C(trans-Ru(dppe)2)C≡CC6H4R}2] (2a–c), have been prepared by reaction of [(OH)(COH)C6H3C≡C(trans-Ru(dppe)2)C≡CC6H4R] (dppe = 1,2-bis(diphenylphosphino)ethane; R = H, NO2, OCH3) with nickel acetate or zinc acetate, followed by addition of 2,3-diamino-5-bromopyridine. Our synthetic efforts are discussed along with spectroscopic and electronic characterization of the compounds. The complexes were studied by thermal and electrochemical analyses. They are thermally robust and show quasireversible redox events attributed to Ru(II)/Ru(III) and Ni (II)/Ni(III) couples for 1a–c and Ru(II)/Ru(III) couples for 2a–c. All complexes are luminescent, emitting in the blue-green region at room temperature. Their emission is influenced by substituents and the π-acidic character of the coordinated groups. Second harmonic generation efficiencies of the complexes were measured by the Kurtz powder technique, indicating that all complexes are promising for applications as nonlinear optical materials.

Electrochromism in Isoreticular Metal-Organic Framework Thin Films with Record High Coloration Efficiency.

The power of isoreticular chemistry has been widely exploited to engineer metal-organic frameworks (MOFs) with fascinating molecular sieving and storage properties but is underexplored for designing MOFs with tunable optoelectronic properties. Herein, three dipyrazole-terminated XDIs (X = PM (pyromellitic), N (naphthalene), or P (perylene); DI = diimide) with different lengths and electronic properties are prepared and employed as linkers for the construction of an isoreticular series of Zn-XDI MOFs with distinct electrochromism. The MOFs are grown on fluorine-doped tin oxide (FTO) as high-quality crystalline thin films and characterized by X-ray diffraction (XRD) and scanning electron microscopy (SEM). Due to the constituting electronically isolated XDI linkers, each member of the isoreticular thin film series exhibits two reversible one-electron redox events, each at a distinct electrochemical potential. The orientation of the MOFs as thin films as well as their isoreticular nature results in identical cation-coupled electron hopping transport rates in all three materials, as demonstrated by comparable apparent electron diffusion coefficients, Deapp. Upon electrochemical reduction to either the [XDI]•- or [XDI]2- state, each MOF undergoes characteristic changes in its optical properties as a function of linker length and redox state of the linker. Operando spectroelectrochemistry measurements reveal that Zn-PDI@FTO (PDI = perylene diimide) thin films exhibit a record high coloration efficiency of 941 cm2 C-1 at 746 nm, which is attributed to the maximized Faradaic transformations at each electronically isolated PDI unit. The electrochromic response of the thin film is retained to more than 99% over 100 reduction-oxidation cycles, demonstrating the applicability of the presented materials.

Manipulating Ligand Density at the Surface of Polyoxovanadate-Alkoxide Clusters.

We present the post-synthetic modification of a polyoxovanadate-alkoxide (POV-alkoxide) cluster via the reactivity of its cationic form, [V6O7(OCH3)12]1+, with water. This result indicates that cluster oxidation increases the lability of bridging methoxide ligands, affording a ligand exchange reaction that serves to compensate for the increased charge of the cluster core. This synthetic advance affords the isolation of a series of POV-alkoxide clusters with varying degrees of μ2-O2- ligands incorporated at the surface, namely, [V6O8(OCH3)11], [V6O9(OCH3)10], and [V6O10(OCH3)9]. Characterization of the POV-alkoxide clusters is described; changes in the infrared and electronic absorption spectra are consistent with the oxidation of the cluster core. We also examine the consequences of ligand substitution on the redox properties of the series of POV-alkoxide clusters via cyclic voltammetry; decreased alkoxide ligand density translates to a cathodic shift of analogous redox events. Ligand substitution also increases comproportionation constants of the Lindqvist core, indicating electron exchange between vanadium centers is promoted in structures with greater numbers of μ2-O2- ligands.

Sterically Bulky Asymmetric Benzophenone Derivatives as Negolytes in a Non-Aqueous Redox Flow Battery

To increase renewable energy generation to the electrical grid, intermittent energy sources, such as wind and solar energy, need a long-term, large scale energy storage method. Redox flow batteries (RFB) are an attractive solution as they allow for long term storage in various redox states of an organic or inorganic compound. The ideal redox-active compound for a RFB should have a high energy density, which can be achieved through a large potential difference in redox events, high concentration of charge carrier, or by increasing the number of electrons transferred during a given redox event. In particular, nonaqueous RFB (NRFB) are promising for building a system with a large potential difference for redox events due the large electrochemical solvent window (~5 V for acetonitrile) as compared to water (~2 V). While metal complexes featuring redox active ligands have been thoroughly investigated as carriers in NRFBs, they are often too expensive for widespread use. This has led to increasing interest in organic carriers. Benzophenone is a promising candidate for an organic negolyte due to its high solubility in acetonitrile and the presence of a reversible reduction at -2.1 V vs. Ag/Ag+. Unfortunately, the durability of benzophenone during cycling is low. Here, we discuss the degradation products of benzophenone during cycling and show how the incorporation of sterically bulky groups ortho to the benzophenone carbonyl improves durability. We then evaluate the utility of these benzophenone derivatives as negolytes in a NRFB flow cell.

Mixed Isomer Chromium-Chelates for High Concentration Aqueous Flow Battery Electrolytes

Redox flow batteries have attracted attention for their potential for large-scale energy storage, largely due to their ability to decouple power and energy. However, their limited energy density is often cited as a major drawback preventing adoption at scale. Therefore, there is interest in research into increasing the solubility of the active material in these electrolytes. One such method is active materials with multiple redox events. Promising materials are, however, often poorly soluble, and computational studies showed that increasing differences in redox potential between e.g., two redox events will decrease the energy efficiency of the cell.1 Here, two Cr-chelate structural isomer complexes, with redox potentials 100 mV apart are characterized and compared electrochemically. The two chromium complexes are combined in mixed-anion electrolytes to generate an electrolyte of 2 M active species, corresponding to a capacity of 53.6 Ah L−1, significantly higher than the individual isomers could achieve. At 100 mA cm−2 the cell achieved average Coulombic efficiencies of 99.6% and an equilibrium cell potential of 1.65 V at 50% State-of-Charge. Due to high viscosity of the electrolyte, the voltaic efficiency was only 67%. At a 1 M concentration, the equimolar mixed-anion electrolyte had a comparable current efficiency to the individual Cr-isomers (within 0.2%) but lowered voltaic efficiency (75.8% compared to 77.8% and 78.6%). The lowered voltaic efficiency is attributed to inefficiencies caused by non-concerted multiple redox events. The high cell voltage and increased combined electrolyte capacity demonstrate that employing chirality, chelate geometry, and structural isomers in a mixed-anion approach can significantly increase overall active material concentrations, but that there are consequences for cell performance when using multiple molecules with disparate reduction potentials in an electrolyte. This highlights that concerted transitions should be prioritized in order to capitalize on multi-electron redox species.

Exploring the Impact of Successive Redox Events in Thin Films of Metal-Organic Frameworks: An Absorptiometric Approach.

Metal-organic frameworks (MOFs) featuring redox activity are highly appealing for electrocatalytic or charge accumulation applications. An important aspect in this field is the ability to address as many redox centers as possible in the material by an efficient diffusion of charges. Herein, we investigate for the first time the charge diffusion processes occurring upon two sequential one-electron reductions in an MOF thin film. Two pyrazolate-zinc(II)-based MOFs including highly electro-deficient perylene diimide (PDI) ligands were grown on conducting substrates, affording thin films with double n-type electrochromic properties as characterized by spectroelectrochemical analysis. In depth electrochemical and chronoabsorptiometric investigations were carried out to probe the charge diffusion in the MOF layers and highlighted significant differences in terms of diffusion kinetics and material stability between the first and second successive reduction of the redox-active PDI linkers. Our results show that MOFs based on multiredox centers are more sensitive to encumbrance-related issues than their monoredox analogues in the context of electrochemical applications, an observation that further underlines the fundamental aspect of careful pore dimensions toward efficient and fast ion diffusion.

Electronic Rearrangement in Steps of Reductive Elimination of Polar Electrophiles Leads to Refinement of Redox Events

Electronic Rearrangement in Steps of Reductive Elimination of Polar Electrophiles Leads to Refinement of Redox Events

An automated and lightweight framework for electrolyte diagnostics using quantitative microelectrode voltammetry

Voltammetry is a ubiquitous electroanalytical method that can be used to help probe sustainable electrochemical technologies. When conducted with a microelectrode (radius ca. μm), voltammetry enables special interrogation of electrolyte solutions by minimizing distortions and facilitating near-steady-state measurements. Methodologies aimed to evaluate the behavior of redox-active species often leverage well-established, physically-grounded expressions that can be extended to examine electrolyte solutions under non-ideal conditions (e.g., signal convolution from multiple redox events) by simulating the entire voltammogram. To characterize these analyte systems, we first develop closed-form expressions—building on previous work that utilizes oblate spheroidal coordinates—and establish a framework for rapidly evaluating electrolyte composition. We subsequently apply finite difference transient voltammogram models to assess the performance of this workflow. We then validate our findings using model, deterministically-prepared nonaqueous electrolyte solutions containing N-[2-(methoxyethoxy)ethyl]phenothiazine. Overall, we show the toolkit is particularly adept at rapidly (< 1 min) estimating the degree to which an electrolyte solution is charged (its “state-of-charge”) and remains intact (its “state-of-health”). Finally, we highlight potential extensions of this method towards advancing in situ or operando diagnostic methods within operating electrochemical devices.