Carbonyl-Based Redox-Active Compounds as Organic Electrodes for Batteries: Escape from Middle-High Redox Potentials and Further Improvement?

Extracting─from the vast space of organic compounds─the best electrode candidates for achieving energy material breakthrough requires the identification of the microscopic causes and origins of various macroscopic features, including notably electrochemical and conduction properties. As a first guess of their capabilities, molecular DFT calculations and quantum theory of atoms in molecules (QTAIM)-derived indicators were applied to explore the family of pyrano[3,2-b]pyran-2,6-dione (PPD, i.e., A0) compounds, expanded to A0 fused with various kinds of rings (benzene, fluorinated benzene, thiophene, and merged thiophene/benzene). A glimpse of up-to-now elusive key incidences of introducing oxygen in vicinity to the carbonyl redox center within 6MRs─as embedded in the A0 core central unit common to all A-type compounds─has been gained. Furthermore, the main driving force toward achieving modulated low redox potential/band gaps thanks to fusing the aromatic rings for the A compound series was discovered.

Atomic Group Decomposition of Charge Transfer Excitation Global Indexes.

A model for decomposing the Le Bahers, Adamo, and Ciofini Charge Transfer (CT) Excitations global indexes ( J. Chem. Theory Comput. 2011, 7, 2498-2506) into molecular subdomains contributions is presented and a software, DOCTRINE (atomic group Decomposition Of the Charge TRansfer INdExes) for the implementation of this novel model has been coded. Although our method applies to any fuzzy or to any disjoint exhaustive partitioning of the real space, it is here applied using a definition of chemically relevant molecular subdomains based on the Atoms in Molecules Bader basins. This choice has the relevant advantage of associating intra or inter subdomain contributions to rigorously defined quantum objects, yet bearing a clear chemical meaning. Our method allows for a quantitative evaluation of the subdomain contributions to the charge transfer, the charge transfer excitation length and the dipole moment change upon excitation. All these global indexes may be obtained either from the electron density increment or the electron density depletion upon excitation. However, the subdomain contributions obtained from the two distributions generally differ, therefore allowing to distinguish whether the contribution to a given property of a given subdomain is dominated by one of the two distributions or if both are playing a significant role. As a toy system for the first application of our model, a typical [D-π-A, π = conjugated bridge] compound belonging to the merocyanine dyes family is selected, and the first four excited states of this compound in a strongly polar protic solvent and in a weakly polar solvent are thoroughly investigated.

Seeking for Optimal Excited States in Photoinduced Electron-Transfer Processes─The Case Study of Brooker's Merocyanine.

Material design enters an era in which control of electrons in atoms, molecules, and materials is an essential property to be predicted and thoroughly understood in view of discovering new compounds with properties optimized toward specific optical/optoelectronic applications. π-electronic delocalization and charge separation/recombination enter notably into the set of features that are highly desirable to tailor. Diverse domains are particularly relying on photoinduced electron-transfer (PET), including fields of paramount importance such as energy production through light-harvesting, efficient chemoreceptive sensors, or organic field-effect transistors. In view of completing the arsenal of strategies in this area, we selected Brooker's merocyanine─a typical [D-π-A] compound─as the case study and examined from time-dependent density functional theory the opportunity offered by selected excited states to reach a suited manipulation of the charge transfer (CT) extent. In addition to the consideration of diagnostic tools able to spot the charge amount (i.e., magnitude of electron fraction) transferred upon excitation (qCT), the spatial extent associated with such an electronic transition or CT length (DCT), as well as the corresponding variation in dipole moment between the ground and the excited states (µCT), further analysis of the excitation process was undertaken. The advantage of going beyond the above-mentioned molecular indicators─which can be considered as PET global indices─was explored on the basis of a partitioning of the electron density. Relevant insight was gained on the relation these global indices have with the evolution of (local) features characterizing either chemical bond or electron delocalization upon vertical excitations.

Boosting Rechargeable Batteries R&D by Multiscale Modeling: Myth or Reality?

This review addresses concepts, approaches, tools, and outcomes of multiscale modeling used to design and optimize the current and next generation rechargeable battery cells. Different kinds of multiscale models are discussed and demystified with a particular emphasis on methodological aspects. The outcome is compared both to results of other modeling strategies as well as to the vast pool of experimental data available. Finally, the main challenges remaining and future developments are discussed.

A tool for deciphering the redox potential ranking of organic compounds: a case study of biomass-extracted quinones for sustainable energy.

Carbonyl compounds have emerged as promising organic electrodes for sustainable energy storage. Accelerating the process of performant materials discovery relies on the possibility of developing methodologies to enable scanning of various sets of candidates. The genesis of this educated guess strategy must be privileged to reduce the search space of experiments, accelerate this research area and contribute to sustainable effort. To address this challenge, we built a quantitative structure-activity relationship to unveil the origin of the redox potential magnitude as a function of both structural features and complexation effects. The potential of this prediction model was demonstrated on various ortho-quinones directly derived from naturally occurring catechols. In addition to the modulation provided by substituent changes, the possibility of applying various types of alkaline(-earth)-ion electrochemistry was examined thoroughly. The power of partitioning the total molecular energy into additive atomic group contributions is highlighted, and the construction of this robust strategy provides guidance towards rational selection of the most suitable compound/metal-ion couples. An upshift/downshift of the redox potential by switching from Li to Mg/Na is revealed, while the identification of the relative role played by the various components of the systems as well as electrostatic interactions is clearly identified. These results, particularly the evidence of the different substituent effects on the single/double reduction potentials and as a function of the type of electrochemistry (Li/Na/Mg), have important implications for designing new electroactive compounds with tailored redox properties.

Robotic Nipple-Sparing Mastectomy and Immediate Breast Reconstruction With Robotic Latissimus Dorsi Flap Harvest: Technique and Results.

Introduction. Only few cases of robotic latissimus dorsi flap reconstruction (RLDFR) have been reported in indication of reconstruction for breast cancer (BC). We report our experience of combined robotic nipple-sparing mastectomy (R-NSM) and RLDFR, and analyze technique, indications, and reproducibility. Methods. All patients with R-NSM and RLDFR from November 2016 to August 2, 2018, were analyzed, and technics have been described. Complication rate with Clavien-Dindo grading and postoperative hospitalization length (days) are reported. Results. Thirty-five R-NSM with RLDFR were performed in 22 cases for primitive BC and 13 for local recurrence. In 12 patients, another surgical procedure was performed during the same time (axillary lymph node dissection or contralateral breast surgery). R-NSM was realized through a short axillar incision, with inside-only installation for 12 patients (34.3%): 18 nonautologous and 17 autologous RLDFR associated with implant in 9 patients. In logistic regression, mastectomy weight >330 g was significantly associated with the use of implant (odds ratio [OR] = 17, P = .015), and significant factor of the time of anesthesia ≥380 minutes was 2 installations (OR = 10.4, P = .049). The median duration of hospitalization stay was 4 days. Complications rates were 51.4% (18/35; 9 grade-1, 2 grade-2, and 7 grade-3). In logistic regression, associated other surgical procedure was predictive of grade-3 complications (OR = 6.87, P = .053). Conclusion. We confirmed the reproducibility and safety of R-NSM and RLDFR with a decreased complication rate. NSM was performed in 42.8% of our patients after previous radiotherapy. We observed an increase of grade-3 complications when R-NSM and RLDFR was combined to another surgical procedure.

Playing with isomerism and N substitution in pentalenedione derivatives for organic electrode batteries: how high are the stakes?

New concepts to design innovating and top-performing redox-active organic molecules based electrodes should push forward and promote an eco-friendly alternative to classical Li-ion batteries. In this promising research area, density functional theory calculations lend support to experiments through the prediction of redox voltage and give promise to rationalize the trends, thus providing a general approach for engineering advanced materials. In this study in which we analysed spin density/net atomic charges distribution along with global energy decomposition thanks to Bader's partitioning of the molecular space, a vision for designing pentalenedione derivatives by fine tuning of the redox potential properties is presented. The concept relies on combined effects of isomerism and N single/double substitution for CH on the parent backbone. Such dual nature modification is able to provide a series of compounds within the range of 2.2-3.6 V vs. Li(+)/Li (against a more restricted range of 2.2-2.8 V vs. Li(+)/Li for the sole effect of isomerism on the unsubstituted parent compounds). The incidence of double N substitution alone generally follows an almost additive rule based on the combined actions of the composing single N substitutions. Few exceptions to the rule were, however, also observed and rationalized. Beyond learning gained for this peculiar family, these results may have exciting implications for future design strategies.

High-potential reversible Li deintercalation in a substituted tetrahydroxy-p-benzoquinone dilithium salt: an experimental and theoretical study.

Efficient organic Li-ion batteries require air-stable lithiated organic structures that can reversibly deintercalate Li at sufficiently high potentials. To date, most of the cathode materials reported in the literature are typically synthesized in their fully oxidized form, which restricts the operating potential of such materials and requires use of an anode material in its lithiated state. Reduced forms of quinonic structures could represent examples of lithiated organic-based cathodes that can deintercalate Li(+) at potentials higher than 3 V thanks to substituent effects. Having previously recognized the unique electrochemical properties of the C(6)O(6)-type ring, we have now designed and then elaborated, through a simple three-step method, lithiated 3,6-dihydroxy-2,5-dimethoxy-p-benzoquinone, a new redox amphoteric system derived from the tetralithium salt of tetrahydroxy-p-benzoquinone. Electrochemical investigations revealed that such an air-stable salt can reversibly deintercalate one Li(+) ion on charging with a practical capacity of about 100 mAh g(-1) at about 3 V, albeit with a polarization effect. Better capacity retention was obtained by simply adding an adsorbing additive. A tetrahydrated form of the studied salt was also characterized by XRD and first-principles calculations. Various levels of theory were probed, including DFT with classical functionals (LDA, GGA, PBEsol, revPBE) and models for dispersion corrections to DFT. One of the modified dispersion-corrected DFT schemes, related to a rescaling of both van der Waals radii and s(6) parameter, provides significant improvements to the description of this kind of crystal over other treatments. We then applied this optimized approach to the screening of hypothetical frameworks for the delithiated phases and to search for the anhydrous structure.

Electrochemical properties of crystallized dilithium squarate: insight from dispersion-corrected density functional theory.

The stacking parameters, lattice constants, and bond lengths of solvent-free dilithium squarate (Li(2)C(4)O(4)) crystals were investigated using density functional theory with and without dispersion corrections. The shortcoming of the GGA (PBE) calculation with respect to the dispersive forces appears in the form of an overestimation of the unit cell volume up to 5.8%. The original Grimme method for dispersion corrections has been tested together with modified versions of this scheme by changing the damping function. One of the modified dispersion-corrected DFT schemes, related to a rescaling of van der Waals radii, provides significant improvements for the description of intermolecular interactions in Li(2)C(4)O(4) crystals: the predicted unit cell volume lies then within 0.9% from experimental data. We applied this optimised approach to the screening of hypothetical framework structures for the delithiated (LiC(4)O(4)) and lithiated (Li(3)C(4)O(4)) phases, i.e. oxidized and reduced squarate forms. Their relative energies have been analysed in terms of dispersion and electrostatic contributions. The most stable phases among the hypothetical models for a given lithiation rate were selected in order to calculate the corresponding average voltages (either upon lithiation or delithiation of Li(2)C(4)O(4)). A first step towards energy partitioning in view of interpretating crystal phases relative stability in link with (de)-intercalation processes has been performed through the explicit evaluation of electrostatic components of lattice energy from atomic charges gained with the Atoms in Molecules (AIM) method.

LiMSO(4)F (M = Fe, Co and Ni): promising new positive electrode materials through the DFT microscope.

A theoretical study of the lithium intercalated LiMSO(4)F and deintercalated MSO(4)F systems, where M = Fe, Co and Ni has been performed within the framework of density functional theory. Beyond predictions of structural evolution and average voltages versus a lithium electrode, we have applied partial density of states and Bader's topological analysis of the electron density to the study of lithium deintercalation. Upon lithium extraction, charge rearrangement occurs for nickel between different d-orbitals, but with little net positive charge gain, while cobalt and iron atoms end up with a clear oxidized state. The participation of oxygen ions in accepting the electron of the lithium is thus enhanced for LiNiSO(4)F. However, this effect does not affect the long-range electrostatic interactions a lot in the lithiated phase, since the valence of all transition metals is very close due to initial lower oxidized state for the Ni atom in the host. It is found that this is not essentially a long-range electrostatic interaction within the lithiated phase but within the host which explains, at least partly, the increase in voltage by passing from Fe to Ni. Our results also shed light upon the possibility of getting an approximate evaluation of the local strain associated with delithiation from the atomic volume evolutions, which are also likely to affect the electrochemical potential.

Photochromic Behavior of ZnO/MoO3 Interfaces.

ZnO/MoO3 powder mixture exhibits a huge photochromic effect in comparison with the corresponding single oxides. The coloring efficiency of such combined material after UV-light irradiation was studied in terms of intensity, kinetics, and ZnO/MoO3 powder ratio. Additionally, the incidence of the pretreatment step of the ZnO and MoO3 powders under different atmospheres (air, Ar or Ar/H2 flow) was analyzed. The huge photochromic effect discovered herein was interpreted as the creation of "self-closed Schottky barrier" at the solid/solid interfaces between the two oxides, associated with the full redox reaction which can be pictured by the equation ZnO1-ε + MoO3 → ZnO + MoO3-ε. Remarkable optical contrast between virgin and color states as well as self-bleaching in dark allowing the reversibility of the photochromism is emphasized. From this first discovery, deeper characterization of the self-bleaching process shows that the photochromic mechanism is complex with a bleaching efficiency (possibility to come back to the virgin material optical properties without any deterioration) and a bleaching kinetics, which are both dependent on the coloring irradiation time. This demonstrates that the oxygen exchange through the Schottky interface proceeds in at least two convoluted steps: an anionic surface exchange allowing a reversibility of the redox reaction followed by bulk diffusion of the exchanged anions which are then definitively trapped. An emergent "negative photochromism effect" (i.e., photochromism associated with a self-bleaching instead of a darkening under irradiation) is observed after a long irradiation time.