Solvent Water Molecules Research Articles

Chasing weakly-bound biological water in aqueous environment near the peptide backbone by ultrafast 2D infrared spectroscopy

There has been a long-standing debate as to how many hydrogen bonds a peptide backbone amide can form in aqueous solution. Hydrogen-bonding structural dynamics of N-ethylpropionamide (a β-peptide model) in water was examined using infrared (IR) spectroscopy. Two amide-I sub bands arise mainly from amide C=O group that forms strong H-bonds with solvent water molecules (SHB state), and minorly from that involving one weak H-bond with water (WHB state). This picture is supported by molecular dynamics simulations and ab-initio calculations. Further, thermodynamics and kinetics of the SHB and WHB species were examined mainly by chemical-exchange two-dimensional IR spectroscopy, yielding an activation energy for the SHB-to-WHB exchange of 13.25 ± 0.52 kJ mol‒1, which occurs in half picosecond at room temperature. Our results provided experimental evidence of an unstable water molecule near peptide backbone, allowing us to gain more insights into the dynamics of the protein backbone hydration.

Exploring Cu-Doped Co3O4 Bifunctional Oxygen Electrocatalysts for Aqueous Zn-Air Batteries.

The efficiency of oxygen electrocatalysis is a key factor in diverse energy domain applications, including the performance of metal-air batteries, such as aqueous Zinc (Zn)-air batteries. We demonstrate here that the doping of cobalt oxide with optimal amounts of copper (abbreviated as Cu-doped Co3O4) results in a stable and efficient bifunctional electrocatalyst for oxygen reduction (ORR) and evolution (OER) reactions in aqueous Zn-air batteries. At high Cu-doping concentrations (≥5%), phase segregation occurs with the simultaneous presence of Co3O4 and copper oxide (CuO). At Cu-doping concentrations ≤5%, the Cu ion resides in the octahedral (Oh) site of Co3O4, as revealed by X-ray diffraction (XRD)/Raman spectroscopy investigations and molecular dynamics (MD) calculations. The residence of Cu@Oh sites leads to an increased concentration of surface Co3+-ions (at catalytically active planes) and oxygen vacancies, which is beneficial for the OER. Temperature-dependent magnetization measurements reveal favorable d-orbital configuration (high eg occupancy ≈ 1) and a low → high spin-state transition of the Co3+-ions, which are beneficial for the ORR in the alkaline medium. The influence of Cu-doping on the ORR activity of Co3O4 is additionally accounted in DFT calculations via interactions between solvent water molecules and oxygen vacancies. The application of the bifunctional Cu-doped (≤5%) Co3O4 electrocatalyst resulted in an aqueous Zn-air battery with promising power density (=84 mW/cm2), stable cyclability (over 210 cycles), and low charge/discharge overpotential (=0.92 V).

Syntheses, characterizations and crystal structures of two Ni(II) complexes [Ni2(neoc)4(H2O)(CO3)](NO3)2·3H2O and [Ni(bapa)2](NO3)2·H2O and magnetic properties of the carbonato complex

By the reaction of nickel(II) nitrate hexahydrate with 2,9-dimethyl-1,10-phenanthroline (neoc) and bis(3-aminopropyl)amine (bapa) two novel complexes were isolated, namely [Ni2(neoc)4(H2O)(CO3)](NO3)2·3H2O (1) and [Ni(bapa)2](NO3)2·H2O (2). Both structures are ionic and comprise hexacoordinated Ni(II) central atoms. Complex 1 is built up of dinuclear [Ni2(neoc)4(H2O)(CO3)]2+ complex cation, nitrate anions and water solvate molecules. The dinuclear complex cation is centrosymmetric and the two Ni(II) atoms are linked by a μ3-bridging-chelating carbonato ligand which, due to the presence of an inversion centre, exhibits two orientations with equal probability. The coordination sphere of Ni(II) atom is heteroleptic with an N4O2 donor set formed by two chelating neoc ligands and two O-donor atoms from bridging carbonato and aqua ligands. The carbonato ligand was formed by transformation of absorbed carbon dioxide from air (single crystals) or from dry ice (bulk sample). The crystal structure of 2 is formed by [Ni(bapa)2]2+ complex cation, nitrate anions and water solvate molecule. The coordination sphere of Ni(II) atom in 2 is homoleptic with N6 donor set. Both bapa ligands act as double chelating 3 N-donor ligands and are coordinated in mer-fashion. The study of the magnetic response of 1 in the temperature range 1.8–300 K revealed that the system can be considered as a system of antiferromagnetic S = 1 spin dimers with exchange interaction J/hc = -13.86 cm−1 (J/kB = -19.96 K) and axial single-ion anisotropy D/hc = -4.94 cm−1 (D/kB = -7.12 K). The experimental magnetic results were corroborated by ab initio and DFT calculations.

In-situ constructed solvated carbon quantum dot clusters to achieve uniform Zn plating in aqueous zinc ion batteries

Zinc ion batteries (ZIBs) have become the most competitive candidates for the next-generation energy storage systems due to its low-price, good safety and high theoretical capacity. However, the uncontrollable dendrite growth and parasitic side reactions still hinder the practical application of the zinc ion batteries. Herein, a hybrid functionalized carbon quantum dots (FCQDs)/ZnSO4 electrolyte is in-situ synthesized via a simple one-pot hydrothermal method with glucose as precursor. The created FCQDs possess abundant anionic groups like hydroxyl, carboxyl and sulfonic acid groups, and those anionic groups can strongly absorb Zn2+ ions and then the FCQDs, Zn2+ and water molecules together generate a special solvation structure of solvated carbon quantum dot clusters [FCQDsZnx(H2O)y]2x+. The solvated FCQDs clusters can help to in-situ induce the uniform Zn deposition through a co-plating of Zn atoms and the functionalized FCQDs. Additionally, this unique solvation structure promotes easier dissociation of solvation water molecules, thus decreasing the de-solvation energy. The lower de-solvation energy barrier can help to restrain the water decomposition and the related by-products. Benefiting from the construction of this unique solvated FCQDs clusters, the hybrid electrolyte with FCQDs endows a better performance of both Zn||Zn symmetric cells and full ZIBs.

The Effective Fragment Molecular Orbital Method: Achieving High Scalability and Accuracy for Large Systems.

The effective fragment molecular orbital (EFMO) method has been developed to predict the total energy of a very large molecular system accurately (with respect to the underlying quantum mechanical method) and efficiently by taking advantage of the locality of strong chemical interactions and employing a two-level hierarchical parallelism. The accuracy of the EFMO method is partly attributed to the accurate and robust intermolecular interaction prediction between distant fragments, in particular, the many-body polarization and dispersion effects, which require the generation of static and dynamic polarizability tensors by solving the coupled perturbed Hartree-Fock (CPHF) and time-dependent HF (TDHF) equations, respectively. Solving the CPHF and TDHF equations is the main EFMO computational bottleneck due to the inefficient (serial) and I/O-intensive implementation of the CPHF and TDHF solvers. In this work, the efficiency and scalability of the EFMO method are significantly improved with a new CPU memory-based implementation for solving the CPHF and TDHF equations that are parallelized by either message passing interface (MPI) or hybrid MPI/OpenMP. The accuracy of the EFMO method is demonstrated for both covalently bonded systems and noncovalently bound molecular clusters by systematically examining the effects of basis sets and a key distance-related cutoff parameter, Rcut. Rcut determines whether a fragment pair (dimer) is treated by the chosen ab initio method or calculated using the effective fragment potential (EFP) method (separated dimers). Decreasing the value of Rcut increases the number of separated (EFP) dimers, thereby decreasing the computational effort. It is demonstrated that excellent accuracy (<1 kcal/mol error per fragment) can be achieved when using a sufficiently large basis set with diffuse functions coupled with a small Rcut value. With the new parallel implementation, the total EFMO wall time is substantially reduced, especially with a high number of MPI ranks. Given a sufficient workload, nearly ideal strong scaling is achieved for the CPHF and TDHF parts of the calculation. For the first time, EFMO calculations with the inclusion of long-range polarization and dispersion interactions on a hydrated mesoporous silica nanoparticle with explicit water solvent molecules (more than 15k atoms) are achieved on a massively parallel supercomputer using nearly 1000 physical nodes. In addition, EFMO calculations on the carbinolamine formation step of an amine-catalyzed aldol reaction at the nanoscale with explicit solvent effects are presented.

STUDY OF THE MECHANISM OF SORPTION OF Cu2+, Co2+, AND Mn2+ IONS ON A MODIFIED NATURAL POLYMER – PECTIN

Sorption materials based on apple pectin modified with biologically active organic acids (salicylic, anthranilic, 5-aminosalicylic, nicotinic) capable of effectively extracting Cu2+, Co2+ and Mn2+ ions from aqueous solutions of their salts have been obtained. The regularities of the sorption kinetics of Cu2+, Co2+ and Mn2+ ions by modified pectin samples were studied. An increase in the efficiency of extraction of d-metal ions by modified pectin sorbents compared to the original polysaccharide was revealed. Sorption isotherms of Cu2+, Co2+, Mn2+ ions by modified pectins have been obtained and analyzed for compliance with known theoretical models. Integral kinetic curves have been obtained, and the values of the experimental sorption capacity of biosorbents have been calculated. It was found that the process of sorption of Cu2+, Co2+ and Mn2+ ions on the studied biosorbents proceeds in the diffusion mode. The predominance of the external diffusion nature of the limiting stage of the process of extracting transition metal ions with modified pectins was established. The rate constants of sorption processes are calculated. The values of the apparent activation energy of the sorption process are determined. The thermodynamic parameters of the extraction of Cu2+, Co2+ and Mn2+ ions by pectin sorbents have been calculated. It has been established that the sorption of Cu2+, Co2+, and Mn2+ ions by modified polysaccharide materials is an exothermic process, which can be considered as physical adsorption of metal ions due to solvation and complex formation with the participation of sorbent sorption centers and solvent (water) molecules. The obtained new highly active biosorbents can be recommended as enterosorbents for detoxification of the human body.&#x0D; Keywords: sorption, d-metal ions, pectin, modification, kinetic curves, thermodynamic parameters.

Synthesis, self-assembly and surface-active properties of alkyl halide mediated imidazolium monomeric surfactants

Two imidazolium monomeric surfactants, that is, 1-tetradecyl-1H-imidazole [14IM] and 1-hexadecyl-1H-imidazole [16IM] has been synthesized and characterized by 1H NMR,13C NMR, FTIR, HRMS spectroscopies and thermogravimetric analysis (TGA) for number and types of protons and carbon, functional groups, estimation of molecular weight and thermal stability of these compounds. The conductivity was measured in double distilled water at four different temperatures, 288, 293, 298, and 303 K. The results showed that these surfactants behave as weak electrolytes. The density and viscosity data have shown the existence of strong interactions between imidazolium surfactants and solvent (water) molecules. The results obtained from Root’s equation indicate that surfactant–solvent interactions are important than surfactant–surfactant interactions in dilute solutions, that is, below critical micellar concentration. The values of constants obtained from Einstein and Moulik equations have revealed that there was stronger and significant interaction between imidazolium surfactants and water molecules below critical micellar region. The surface tension parameters have indicated that these surfactants are good contenders to lower the surface tension of air/water interface. The results obtained from surface tension data have shown that standard change in free energy of micellization (ΔG°mic) and adsorption (ΔG°ads) were negative, indicating that these surfactants molecules have spontaneous tendencies to form micelles in solution at higher concentration and to get adsorb at the air/water interface at lower concentration. The TGA has indicated good thermally stability and activation energy for thermal decomposition was found in the range of 37.26.26–98.20.20 kJ/mol.

Enticing a Proton using Single Ammonia Molecule as Bait.

In microhydrated acid-solvent clusters, deprotonation of an acid is assisted by a critical number of solvent molecules and a solvent electric field. Born-Oppenheimer molecular dynamics simulations reveal that trifluoroacetic acid undergoes spontaneous proton transfer in water clusters, with the critical number being five. Acetic acid and phenol, on the other hand, do not dissociate even in the presence of a large number of water molecules (in excess of 40). The addition of a single ammonia molecule to the water cluster, which interacts directly with the protic group, lowers the critical number of solvent water molecules required for proton transfer to three and seven in the case of acetic acid and phenol, respectively. The population of the undissociated and the proton-transferred structures get dispersed to form separate islands on the electric field versus the O-H distance representation with the cusp representing the critical values. The critical electric fields for the spontaneous proton transfer are around 254, 237, and 318 MV cm-1 for trifluoroacetic acid, acetic acid, and phenol, respectively. In the case of phenol, the free energy profiles suggest that proton transfer to the ammonia moiety embedded in water promotes proton transfer efficiently due to the higher basicity of ammonia and enhanced hydrogen bonding network of solvent water, vis-à-vis phenol-ammonia clusters.

Detangling Solvatochromic Effects by the Effective Fragment Potential Method.

Understanding molecular interactions in complex systems opens avenues for the efficient design of new materials with target properties. Energy decomposition methods provide a means to obtain a detailed picture of intermolecular interactions. This work introduces a molecular modeling approach for decomposing the solvatochromic shifts of the electronic excited states into the contributions of the individual molecular fragments of the environment surrounding the chromophore. The developed approach is implemented for the QM/EFP (quantum mechanics/effective fragment potential) model that provides a rigorous first-principles-based description of the electronic states of the chromophores in complex polarizable environments. On the example of two model systems, water pentamer and hydrated uracil, we show how the decomposition of the solvatochromic shifts into the contributions of individual solvent water molecules provides a detailed picture of the intermolecular interactions in the ground and excited states of these systems. The analysis also demonstrates the nonadditivity of solute-solvent interactions and the significant contribution of solute polarization to the total values of solvatochromic shifts.

Two-component Supramolecular Adduct based on Hydroxyl Substituted Triptycene with 4,4’-bipyridine: Crystal Structure Analysis

A new cocrystal solvate possessing 2,7,14-trihydroxytriptycene (THT) and 4,4′-bipyridine (bpy) was grown from a MeOH solution by solvent evaporation to form THT·0.5bpy·MeOH·H2O (1).The crystal structure of 1 was determined by single-crystal X-ray diffraction in the monoclinic space group C2/c. In the new cocrystal solvate (1), the asymmetric unit consists of one unit of THT, a half unit of disordered bpy, one unit of a water molecule and one MeOH molecule. A 2D supramolecular architecture is observed in (1) linking THT, bpy and solvent water molecules via classical O-H···N and O-H···O hydrogen bonds. The MeOH and water molecules entrapped in (1) form stabilizing hydrogen bondswith the surrounding “trimeric cocrystals.” Furthermore, we investigated whether these hydrogen bonds stabilize the crystal packing. The calculations were carried out using Hydrogen Bond Statistics and Full Interaction Maps packages, and the results exhibit common bonding behaviour in terms of bond distances and strength.

Room temperature spin crossover properties in a series of mixed-anion Fe(NH2trz)3(BF4)2-x(SiF6)x/2 complexes.

A series of mixed-anion Fe(NH2trz)3(BF4)2-x(SiF6)x/2 spin crossover complexes is obtained modifying the reaction time but also using an increase amount of tetraethyl orthosilicate as the source for the production and the incorporation of SiF62- competing with the BF42- anions present in the mother solution. The increase of the SiF62- anion inclusion to the detriment of the BF4- counterpart induces a shift of the temperature transition toward high temperatures leading to interesting bistability properties around room temperature with T1/2 spanning from 300 K to 325 K. Moreover, the implementation of a solid-liquid post synthetic modification approach from the Fe(NH2trz)3(BF4)2 parent complex with identical TEOS proportions and under certain experimental conditions lead systematically to the same Fe(NH2trz)3(BF4)1.2(SiF6)0.4 composition. This compound presents an abrupt spin crossover behaviour with a narrow hysteresis loop just above room temperature (320 K), which is stable under thermal cycling and along time with no specific storage conditions. Such crystalline powder sample incorporates homogeneous rod-shaped particles whose formation and physical properties can be followed simultaneously using infra-red spectroscopy, dynamic light scattering (DLS), transmission electronic microscopy (TEM) and optical reflectance. The observation of a stabilized single ca. 800 nm population of mixed-anion particles starting from insoluble various sizes (from nano- to microscale) Fe(NH2trz)3(BF4)2 particles supports the key role of the solvent (water molecules) on the separation, the reactivity and the reorganization of the 1D iron-triazole chains forming the packing of the structure.

Mixed-ligand complex [Cu4(bpy)4(PO4)2(CO3)(H2O)2]: synthesis, crystal structure and biological properties

The interaction in the system {Сu(OAc)2·H2O–phytic acid–2,2`-bipyridine (bpy)} in an aqueous-methanol solution led to the formation of a molecular mixed-ligand tetranuclear complex [(Cu4(bpy)4(PO4)2(CO3 )(H2O)2]13H2O (I), the structure of which was established based on the results of an X-ray diffraction experiment (CCDC 2262998). According to X-ray diffraction data, the molecule contains four nonequivalent Cu2+ cations, which coordinate two phosphate anions (PO43-, remaining as a result transformation of the phytate cycle), four neutral bpy, two water molecules and one carbonate anion fragment (CO32-). The presence of a large number of solvate water molecules in the outer coordination sphere created a hydrogen-bonded framework involved in the stabilization of the crystal packing. Study of antimycobacterial activity of I in against the non-pathogenic strain Mycolicibacterium smegmatis showed its high bioeffectiveness.

The cooperative effects of ligand substituent positions and solvents on spin crossover in Mn(III) complexes based on hexadentate Schiff-base ligands

Spin crossover (SCO), as a molecular bistable phenomenon, has attracted extensive interest. In this paper, the syntheses, crystal structures and magnetic properties of three Mn(III) hexadentate Schiff-base complexes [Mn(3-OMe-sal-N-1,5,8,12)]AsF6·H2O (1), [Mn(4-OMe-sal-N-1,5,8,12)]AsF6·H2O (2) and [Mn(5-OMe-sal-N-1,5,8,12)]AsF6(3) have been reported. The substituent positions of ligands and solvent molecules have a cooperative effect on SCO behavior. Complex 1 shows a complete SCO between the high-spin (HS, S = 2) and low-spin (LS, S = 1) states without thermal hysteresis, and complex 2 shows a gradual incomplete SCO behavior. The transition temperatures of 2 (T1/2 = 241 K) is 98 K higher than that of 1 (T1/2 = 143 K), which indicates that the ligand field strength of (4-OMe-sal-N-1,5,8,12)2– is stronger than that of (3-OMe-sal-N-1,5,8,12)2–. Due to the absence of crystallizing solvent water molecule, complex 3 maintains a HS state in the test temperature range.

A Hydrophobic and Zincophilic Interfacial Nanofilm as a Protective Layer for Stable Zn Anodes

AbstractThe Zn metal anode has emerged as a promising contender for aqueous batteries. However, challenges such as H2 evolution and Zn dendrite formation have hindered the attainment of satisfactory cycling longevity. In this context, a hydrophobic and zincophilic interfacial nanofilm (HZF) is successfully developed and demonstrated as a protective layer for stabilizing Zn anodes. The HZF nanofilm, characterized by its uniformly distributed zincophilic groups, actively participates in the interfacial solvated structure of Zn2+ ions, thereby modulating the uniform deposition of Zn2+ flux onto Zn anodes and curtailing the deprotonation of solvated water molecules. Concurrently, the exposed hydrophobic surfactant within the nanofilm effectively acts as a barrier, preventing direct contact between water and the Zn anode. As a result, the Zn anode coated with the HZF nanofilm achieves stable and reversible Zn plating/stripping behavior. This is evidenced by the extended cycling lifespan of over 300 h at a discharge capacity of 10 mAh cm−2, with a deep discharge of 67% Zn utilization.

SPANA: Spatial decomposition analysis for cellular-scale molecular dynamics simulations.

The rapid increase in computational power with the latest supercomputers has enabled atomistic molecular dynamics (MDs) simulations of biomolecules in biological membrane, cytoplasm, and other cellular environments. These environments often contain a million or more atoms to be simulated simultaneously. Therefore, their trajectory analyses involve heavy computations that can become a bottleneck in the computational studies. Spatial decomposition analysis (SPANA) is a set of analysis tools in the Generalized-Ensemble Simulation System (GENESIS) software package that can carry out MD trajectory analyses of large-scale biological simulations using multiple CPU cores in parallel. SPANA applies the spatial decomposition of a large biological system to distribute structural and dynamical analyses into individual CPU cores, which reduces the computational time and the memory size, significantly. SPANA opens new possibilities for detailed atomistic analyses of biomacromolecules as well as solvent water molecules, ions, and metabolites in MD simulation trajectories of very large biological systems containing more than millions of atoms in cellular environments.

Stabilization of Guest Molecules inside Cation-Lidded Cucurbiturils Reveals that Hydration of Receptor Sites Can Impede Binding.

Docking of alkali metal ions to water-soluble macrocyclic receptors generally reduces the affinity of guest molecules due to competitive binding. The idea that solvation water molecules could display a larger steric hindrance towards guest binding than cations has not been considered to date. We show that the docking of large cations to cucurbit[5]uril (CB5) unexpectedly increases (by a factor of 5-8) the binding of hydrophobic guests, methane and ethane. This is due to the removal of water molecules from the carbonyl portals of CB5 during cation binding, which frees up space for hydrophobe encapsulation. In contrast, smaller cations like sodium protrude deeply into the cavity of CB5 and cause the expected decrease in binding, such that the rational selection of alkali cations allows for a variation of up to a factor of 20 in binding of methane and ethane. The statistical analysis of crystallographic data shows that the cavity volume of CB5 can be enlarged by placing large alkali ions (Rb+ and Cs+ ) centro-symmetrically at the portals. The results reveal a hitherto elusive steric hindrance of solvation water molecules near receptor binding sites, which is pertinent for the design of supramolecular catalysts and the understanding of biological receptors.

Stabilization of Guest Molecules inside Cation‐Lidded Cucurbiturils Reveals that Hydration of Receptor Sites Can Impede Binding

AbstractDocking of alkali metal ions to water‐soluble macrocyclic receptors generally reduces the affinity of guest molecules due to competitive binding. The idea that solvation water molecules could display a larger steric hindrance towards guest binding than cations has not been considered to date. We show that the docking of large cations to cucurbit[5]uril (CB5) unexpectedly increases (by a factor of 5–8) the binding of hydrophobic guests, methane and ethane. This is due to the removal of water molecules from the carbonyl portals of CB5 during cation binding, which frees up space for hydrophobe encapsulation. In contrast, smaller cations like sodium protrude deeply into the cavity of CB5 and cause the expected decrease in binding, such that the rational selection of alkali cations allows for a variation of up to a factor of 20 in binding of methane and ethane. The statistical analysis of crystallographic data shows that the cavity volume of CB5 can be enlarged by placing large alkali ions (Rb+ and Cs+) centro‐symmetrically at the portals. The results reveal a hitherto elusive steric hindrance of solvation water molecules near receptor binding sites, which is pertinent for the design of supramolecular catalysts and the understanding of biological receptors.

Competition between Solvent···Solvent and Solvent···Solute Interactions in the Microhydration of the Tetrafluoroborate Anion, BF4-(H2O)n=1,2,3,4.

This study systematically examines the interactions of the tetrafluoroborate anion (BF4-) with up to four water molecules (BF4-(H2O)n=1,2,3,4). Full geometry optimizations and subsequent harmonic vibrational frequency computations are performed using a variety of density functional theory (DFT) methods (B3LYP, B3LYP-D3BJ, and M06-2X) and the MP2 ab initio method with a triple-ζ correlation consistent basis set augmented with diffuse functions on all non-hydrogen atoms (cc-pVTZ for H and aug-cc-pVTZ for B, O, and F; denoted as haTZ). Optimized structures and harmonic vibrational frequencies were also obtained with the CCSD(T) ab initio method and the haTZ basis set for the mono- and dihydrate (n = 1, 2) structures. The 2-body:Many-body (2b:Mb) technique, in which CCSD(T) computations capture the 1- and 2-body contributions to the interactions and MP2 computations recover all higher-order contributions, was used to extend these demanding computations to the tri- and tetrahydrate (n = 3, 4) systems. Four, five, and eight new stationary points have been identified for the di-, tri-, and tetrahydrate systems, respectively. The global minimum of the monohydrate adopts a symmetric double ionic hydrogen bond motif with C2v symmetry and an electronic dissociation energy of 13.17 kcal mol-1 at the CCSD(T)/haTZ level of theory. This strong solvent···solute interaction, however, competes with solute···solute interactions in the lowest-energy BF4-(H2O)n=2,3,4 minima that are not seen in the other di-, tri-, or tetrahydrate minima. The latter interactions help increase the 2b:Mb dissociation energies to more than 26, 41, and 51 kcal mol-1 for n = 2, 3, and 4, respectively. Structures that form hydrogen bonds between the solvating water molecules also exhibit the largest shifts in the harmonic OH stretching frequencies for the waters of hydration. These shifts can exceed -280 cm-1 relative to an isolated H2O molecule at the 2b:Mb/haTZ level of theory.

Inhibiting zinc dendrites and side reactions enabled by solvation structure regulation and facile de-solvation process

Rechargeable aqueous zinc-ion batteries show great promise as next-generation energy storage devices given their advantages of low cost and high safety. However, dendrite growth and detrimental side reactions result in poor reversibility of Zn anodes. Here, TEG molecules were introduced as additives to regulate the solvation structure through occupying the position of water molecules in the solvation shell, which also further decreasing the de-solvation energy barrier. The lower de-solvation energy barrier is beneficial for the dissociation of solvation water molecules and help to restrain the water decomposition and the related by-products. Theoretical studies also reveal that TEG is more easily adsorbed on the surface of zinc than water molecules, electrons are more easily transferred from the TEG molecule to the zinc foil, thus promoting the uniform deposition of zinc atoms. Benefiting from the solvation structure regulation and facile de-solvation process of Zn2+, Zn/Zn symmetric cell achieve a long cycling life of 2000 h at the current density and capacity of 1 mA cm−2 and 1mAh cm−2, and a MnO2-Zn full cell reach a superior stability of 3000 cycles at the current density of 1000 mA g−1.

The stability of oxygen-centered radicals and its response to hydrogen bonding interactions.

The stability of various alkoxy/aryloxy/peroxy radicals, as well as TEMPO and triplet dioxygen (3 O2 ) has been explored at a variety of theoretical levels. Good correlations between RSEtheor and RSEexp are found for hybrid DFT methods, for compound schemes such as G3B3-D3, and also for DLPNO-CCSD(T) calculations. The effects of hydrogen bonding interactions on the stability of oxygen-centered radicals have been probed by addition of a single solvating water molecule. While this water molecule always acts as a H-bond donor to the oxygen-centered radical itself, it can act as a H-bond donor or acceptor to the respective closed-shell parent.