RESUMEN
Taking into account the electron-rich and visible light response of thiophene, first-principles calculations have been carried out to explore the photocatalytic activity of donor-acceptor polymers incorporating thiophene and boron. Honeycomb-kagome boron-thiophene (BTP) polymers with varying numbers of thiophene units and fixed B center atoms are direct bandgap semiconductors with tunable bandgaps ranging from 2.41 to 1.88 eV and show high absorption coefficients under the ultraviolet and visible regions of the solar spectrum. Fine-tuning the band edges of the BTP polymer is efficiently achieved by adjusting the pore size through the manipulation of thiophene units between the B centers. This manipulation, achieved without excessive chemical functionalization, facilitates the generation of an appropriate quantity of photoexcited electrons and/or holes to straddle the redox potential of the water. Our study demonstrates that two units between B centers of thiophene in BTP polymers enable overall photocatalytic water splitting, whereas BTP polymers with larger pores solely promote photocatalytic hydrogen reduction. Moreover, the thermodynamics of hydrogen and oxygen reduction reactions either proceed spontaneously or need small additional external biases. Our findings provide the rationale for designing metal-free and single-material polymer photocatalysts based on thiophene, specifically for achieving efficient overall water splitting.
RESUMEN
The anion-intercalation chemistries of graphite have the potential to construct batteries with promising energy and power breakthroughs. Here, we report the use of an ultrathin, positively charged two-dimensional poly(pyridinium salt) membrane (C2DP) as the graphite electrode skin to overcome the critical durability problem. Large-area C2DP enables the conformal coating on the graphite electrode, remarkably alleviating the electrolyte. Meanwhile, the dense face-on oriented single crystals with ultrathin thickness and cationic backbones allow C2DP with high anion-transport capability and selectivity. Such desirable anion-transport properties of C2DP prevent the cation/solvent co-intercalation into the graphite electrode and suppress the consequent structure collapse. An impressive PF6--intercalation durability is demonstrated for the C2DP-covered graphite electrode, with capacity retention of 92.8% after 1000 cycles at 1 C and Coulombic efficiencies of > 99%. The feasibility of constructing artificial ion-regulating electrode skins with precisely customized two-dimensional polymers offers viable means to promote problematic battery chemistries.
RESUMEN
The chelating ability of quinoxaline cores and the redox activity of organosulfide bridges in layered covalent organic frameworks (COFs) offer dual active sites for reversible lithium (Li)-storage. The designed COFs combining these properties feature disulfide and polysulfide-bridged networks showcasing an intriguing Li-storage mechanism, which can be considered as a lithium-organosulfide (Li-OrS) battery. The experimental-computational elucidation of three quinoxaline COFs containing systematically enhanced sulfur atoms in sulfide bridging demonstrates fast kinetics during Li interactions with the quinoxaline core. Meanwhile, bilateral covalent bonding of sulfide bridges to the quinoxaline core enables a redox-mediated reversible cleavage of the sulfursulfur bond and the formation of covalently anchored lithium-sulfide chains or clusters during Li-interactions, accompanied by a marked reduction of Li-polysulfide (Li-PS) dissolution into the electrolyte, a frequent drawback of lithium-sulfur (Li-S) batteries. The electrochemical behavior of model compounds mimicking the sulfide linkages of the COFs and operando Raman studies on the framework structure unravels the reversibility of the profound Li-ion-organosulfide interactions. Thus, integrating redox-active organic-framework materials with covalently anchored sulfides enables a stable Li-OrS battery mechanism which shows benefits over a typical Li-S battery.
RESUMEN
Two-dimensional (2D) membranes are emerging candidates for osmotic energy conversion. However, the trade-off between ion selectivity and conductivity remains the key bottleneck. Here we demonstrate a fully crystalline imine-based 2D polymer (2DPI) membrane capable of combining excellent ionic conductivity and high selectivity for osmotic energy conversion. The 2DPI can preferentially transport cations with Na+ selectivity coefficient of 0.98 (Na+/Cl- selectivity ratio ~84) and K+ selectivity coefficient of 0.93 (K+/Cl- ratio ~29). Moreover, the nanometer-scale thickness (~70 nm) generates a substantially high ionic flux, contributing to a record power density of up to ~53 W m-2, which is superior to most of nanoporous 2D membranes (0.8~35 W m-2). Density functional theory unveils that the oxygen and imine nitrogen can both function as the active sites depending on the ionization state of hydroxyl groups, and the enhanced interaction of Na+ versus K+ with 2DPI plays a significant role in directing the ion selectivity.
RESUMEN
Dithiine linkage formation via a dynamic and self-correcting nucleophilic aromatic substitution reaction enables the de novo synthesis of a porous thianthrene-based two-dimensional covalent organic framework (COF). For the first time, this organo-sulfur moiety is integrated as a structural building block into a crystalline layered COF. The structure of the new material deviates from the typical planar interlayer π-stacking of the COF to form undulated layers caused by bending along the C-S-C bridge, without loss of aromaticity and crystallinity of the overall COF structure. Comprehensive experimental and theoretical investigations of the COF and a model compound, featuring the thianthrene moiety, suggest partial delocalization of sulfur lone pair electrons over the aromatic backbone of the COF decreasing the band gap and promoting redox activity. Postsynthetic sulfurization allows for direct covalent attachment of polysulfides to the carbon backbone of the framework to afford a molecular-designed cathode material for lithium-sulfur (Li-S) batteries with a minimized polysulfide shuttle. The fabricated coin cell delivers nearly 77% of the initial capacity even after 500 charge-discharge cycles at 500 mA/g current density. This novel sulfur linkage in COF chemistry is an ideal structural motif for designing model materials for studying advanced electrode materials for Li-S batteries on a molecular level.
RESUMEN
In the present era of growing energy demands, low-dimensional materials are emerging as the suitable choices for energy storage due to their excellent ion transport properties, improved reversible capacity, fine rate performance and good cycling stability. In this context, we have investigated the applicability of black and blue phosphorene monolayers as potential cathodes for Al batteries. Both black and blue phosphorene monolayers show similar electrochemical behavior as that of experimentally reported graphite with a charge transfer from the surface in order to bind the tetrahedral geometry of AlCl4 during the charging process. The adsorption of AlCl4 drives semiconductor-to-metallic transformation of black/blue phosphorene, which ensures constant conductivity in Al batteries. Following the systematic adsorption of AlCl4 , the voltage for black and blue phosphorene is calculated to be ≈1.50â V and ≈1.80â V with storage capacities of 144â mAh g-1 and 108â mAh g-1 , respectively. Besides, low diffusion barriers of 0.11â eV and 0.14â eV are predicted for AlCl4 on the respective systems of black and blue phosphorene monolayers. Our work suggests that both black and blue phosphorene monolayers can be potential cathodes for Al batteries with delivery of high storage capacity and high voltage, respectively.
RESUMEN
Using state-of-the-art density functional theoretical calculations, we have modelled a facetted CdS nanotube (NT) catalyst for photocatalytic water splitting. The overall photocatalytic activity of the CdS photocatalyst has been predicted based on the electronic structures, band edge alignment, and overpotential calculations. For comparisons, we have also investigated the water splitting process over bulk CdS. The band edge alignment along with the oxygen evolution reaction/hydrogen evolution reaction (OER/HER) mechanism studies help us find out the effective overpotential for the overall water splitting on these surfaces. Our study shows that the CdS NT has a highly stabilized valence band edge compared to that of bulk CdS owing to strong p-d mixing. The highly stabilized valence band edge is important for the hole-transfer process and reduces the risk of electron-hole recombination. CdS nanotube requires less overpotential for water oxidation reaction than the bulk CdS. Our findings suggest that the efficiency of the water oxidation/reduction process further improves in CdS as we reduce its dimensionality, that is going from bulk CdS to one-dimensional nanotube. Furthermore, the stabilized valence band edge of CdS nanotube also improves the photostability of CdS, which is a problem for bulk CdS.
RESUMEN
The primary research target of the rapidly evolving spintronic industry is to design highly efficient novel materials that consume very low power and operate with high speed. Main group based ferromagnetic half-metallic materials are very promising due to their long spin-relaxation time. In recent years, the discovery of superconducting state with high critical temperature in a magnesium based system (MgB2) invigorated researchers due to its simple crystal structure and intriguing results, leading to its use as a good material for large scale application in electronic devices. Here, we report ferromagnetism and strong half-metallicity in another Mg-based system, which can be a promising material for spintronics based devices rather than for electronic devices (such as MgB2). Based on the first principle calculations, we report here a series of magnetic half-metallic magnesium chloride based monolayers [Mg0.89δ0.11Cl2, Mg0.78δ0.22Cl2, and Mg0.67δ0.33Cl2 (MgCl3)]. This MgCl3 phase has a similar pattern as that in CrI3, which has drawn remarkable attention worldwide as the first intrinsic 2D magnet. These magnesium chloride monolayer based systems are 100% spin-polarized, and promising for scattering-less transport due to strong half-metallicity and large spin-up gap (â¼6.135-6.431 eV). The unusually large spin-up gap in our proposed system may shield spin current leakage even in nanoscale device. Further investigation explores a ferromagnetic ordering in Mg0.89δ0.11Cl2 with a Curie temperature of 250 K, which makes the system viable for operation at temperatures slightly lower than the room temperature. High magnetic anisotropy energy (MAE) in Mg0.89δ0.11Cl2 (452.84 µeV) indicates that the energy required to flip the spin is high, and therefore inhibits spin fluctuation. These results suggest a promising way to discover MgCl2-based 2D spin valves, GMR, TMR and other spintronics devices.
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Graphite dual-ion batteries represent a potential battery concept for large-scale stationary storage of electricity, especially when constructed free of lithium and other chemical elements with limited natural reserves. Owing to their non-rocking-chair operation mechanism, however, the practical deployment of graphite dual-ion batteries is inherently limited by the need for large quantities of electrolyte solutions as reservoirs of all ions that are needed for complete charge and discharge of the electrodes. Thus far, lithium-free graphite dual-ion batteries have employed moderately concentrated electrolyte solutions (0.3-1 M), resulting in rather low cell-level energy densities of 20-70 Wh kg-1. In this work, we present a lithium-free graphite dual-ion battery utilizing a highly concentrated electrolyte solution of 5 M potassium bis(fluorosulfonyl)imide in alkyl carbonates. The resultant battery offers an energy density of 207 Wh kg-1, along with a high energy efficiency of 89% and an average discharge voltage of 4.7 V.
RESUMEN
Recently, rechargeable non-aqueous Mg-air batteries have gained a lot of interest as the next-generation energy storage device due to the high theoretical volumetric density (3832â Ah L-1 for Mg anode vs. 2062â Ah L-1 for Li), low cost and safety. The field of Mg-air batteries is in the initial stage of development having a limited number of experimental and theoretical reports, in which mainly a carbon cathode is used; however, the information regarding the structural form of carbon is still missing. In this work, using first-principles density functional theory (DFT) calculations, we demonstrate the possibility of graphene and graphite as a cathode material towards Mg-air batteries by studying the initial MgO and MgO2 nucleation processes on the surfaces of graphene and graphite. The calculated free energy diagrams for the redox reactions of oxygen are used to identify the rate-determining step controlling the overpotentials for initial nucleation of MgO and MgO2 . We observe that graphene and graphite surfaces show similar reactivity towards the nucleation of MgO or MgO2 , and the overpotential of the controlling steps for MgO2 nucleation is comparatively less than that of MgO nucleation, which is supported by a recent experimental study, where a higher discharge voltage was observed in a cell having a mixed MgO/MgO2 discharge product than MgO-based cells. Furthermore, the preferable formation of MgO2 cluster compared to MgO on the graphene surface during the ab initio molecular dynamic (AIMD) simulations confirms the selectivity of MgO2 formation over MgO as the final discharge product. We believe that our study will be helpful in understanding the initial nucleation processes during the oxygen reduction reaction (ORR) mechanism and development of suitable cathodes for the future Mg-air batteries.
RESUMEN
Exploring suitable electrode materials is a fundamental step toward developing Al batteries with enhanced performance. In this work, we explore using density functional theory calculations the feasibility of single-walled carbon nanotubes (SWNTs) as a cathode material for Al batteries. Carbon nanotubes with hollow structures and large surface area are able to overcome the difficulty of activating the opening of interlayer spaces as observed in graphite electrode during the first intercalation cycle. Our results show that AlCl4 binds strongly with the SWNT to result in an energetically and thermally stable AlCl4 -adsorbed SWNT system. Diffusion calculations show that the SWNT system allows ultrafast diffusion of AlCl4 with a more favorable inner surface diffusion than outer surface diffusion. Our charge-density difference and Bader atomic charge analysis confirm the oxidation of SWNT upon adsorption of AlCl4 , which shows a similar behavior to the previously studied graphite cathode. The average open-circuit voltage and AlCl4 storage capacity increases with increasing SWNT diameter and can be as high as 1.96â V and 275â mA h g-1 in (25,25) SWNT relative to graphite (70â mA h g-1 ). All of these properties show that SWNTs are a potential cathode material for high-performance Al batteries and should be explored further.
RESUMEN
Identifying a suitable electrode material with desirable electrochemical properties remains a primary challenge for rechargeable Al-ion batteries. Recently an ultrafast rechargeable Al-ion battery was reported with high charge/discharge rate, (relatively) high discharge voltage and high capacity that uses a graphite-based cathode. Using calculations from first-principles, we have investigated the staging mechanism of AlCl4 intercalation into bulk graphite and evaluated the stability, specific capacity and voltage profile of AlCl4 intercalated compounds. Ab initio molecular dynamics is performed to investigate the thermal stability of AlCl4 intercalated graphite structures. Our voltage profiles show that the first AlCl4 intercalation step could be a more sluggish step than the successive intercalation steps. However, the diffusion of AlCl4 is very fast in the expanded graphite host layers with a diffusion barrier of â¼0.01 eV, which justifies the ultrafast charging rate of a graphite based Al-ion battery. And such an AlCl4 intercalated battery provides an average voltage of 2.01-2.3 V with a maximum specific capacity of 69.62 mA h g-1, which is excellent for anion intercalated batteries. Our density of states and Bader charge analysis shows that the AlCl4 intercalation into the bulk graphite is a charging process. Hence, we believe that our present study will be helpful in understanding the staging mechanism of AlCl4 intercalation into graphite-like layered electrodes for Al-ion batteries, thus encouraging further experimental work.