2D-Mn2C12: An Optimal Electrocatalyst with Nonbonding Multiple Single Centers for CO2-to-CH4 Conversion.

The CO2 reduction reaction (CO2RR) is a promising method that can both mitigate the greenhouse effect and generate valuable chemicals. The 2D-M2C12 with high-density transition metal single atoms is a potential catalyst for various catalytic reactions. Using an effective strategy, we screened 1s-Mn2C12 as the most promising electrocatalyst for the CO2RR in the newly reported 2D-M2C12 family. A low applied potential of -0.17 V was reported for the CO2-to-CH4 conversion. The relative weak adsorption of H atom and H2O in the potential range of -0.2 to -0.8 V, ensures the preferential adsorption of CO2 and the following production of CH4. The different loading amounts of Mn atoms on γ-graphyne (GY) were also investigated. The Mn atoms prefer doping in the nonadjacent triangular pores instead of the adjacent ones due to the repulsive forces between d-orbitals when the Mn loading is less than 32.3 wt % (5Mn). As the Mn concentration further increases, adjacent Mn atoms begin to appear, and the Mn@GY becomes metallic or half-metallic. The presence of four adjacent Mn atoms increases the d-band center of Mn@GY, particularly the dz2 center involved in CO2 adsorption, thereby enhancing the adsorption capacity for CO2. These findings indicate that 1s-Mn2C12 with high Mn atomic loadings is an excellent CO2RR electrocatalyst, and it provides new insights for designing efficient CO2RR electrocatalyst.

Influence of Zr aggregation on Li-ion conductivity of amorphous solid-state electrolyte Li-La-Zr-O.

In our study, we investigated the influence of the local structure of amorphous Li-La-Zr-O (a-LLZO) on Li-ion conductivity using ab initio molecular dynamics (AIMD). A-LLZO has shown promising properties in inhibiting the growth of lithium dendrites, making it a potential candidate for solid electrolytes in all-solid-state lithium batteries. The low Li-ion conductivity of a-LLZO is currently limiting its practical applications. Our findings revealed that the homogeneous distribution of Zr-O polyhedra within the pristine structure of a-LLZO contributes to enhanced Li-ion conductivity. By reducing the interconnections among Zr-O polyhedra, the AIMD-simulated a-LLZO sample achieved a Li-ion conductivity of 5.78 × 10-4 S/cm at room temperature, which is slightly lower than that of cubic LLZO (c-LLZO) with a Li-ion conductivity of 1.63 × 10-3 S/cm. Furthermore, we discovered that Li-ion conductivity can be influenced by adjusting the elemental ratios within a-LLZO. This suggests that fine-tuning the composition of a-LLZO can potentially further enhance its Li-ion conductivity and optimize its performance as a solid electrolyte in lithium batteries.

First-Principles Studies on the Structural and Electronic Properties of α-Na2FePO4F with Strong Antisite Disorder.

Polyanionic Na2FePO4F is one of the most important cathode materials for sodium-ion batteries. The orthorhombic ß-Na2FePO4F material has been studied extensively and intensively since it was proposed. In this article, a novel monoclinic sodium phosphate fluoride α-Na2FePO4F is concerned. Kirsanova's experiment showed that Na and Fe ions in α-Na2FePO4F are prone to antisite, leading to strong antisite disorder. Through first-principle calculations, we show that the steric effect, the magnetic exchange and superexchange interactions between transition-metal cations are shown to be the main driving forces for Na+/Fe2+ antisite disorder. We first calculated the crystal structures, electronic properties, and cohesive energies of all the 10 antisite phases of α-Na2FePO4F and ß-Na2FePO4F. Then, we compared the difference charge densities, magnetism, binding energies, and electrostatic potentials of α-Na2FePO4F and ß-Na2FePO4F materials in the antisite and pristine phases. In α-Na2FePO4F, the binding energy of the antisite phase with the lowest binding energy is almost degenerate with that of the pristine phase. Moreover, only small differences of the electrostatic potential and the charge density distribution are found between the antisite (with lowest energy) and the pristine phases of α-Na2FePO4F, which also helped elaborate the facile formation of Na+/Fe2+ antisite in the α-Na2FePO4F material. Our research contributes to the understanding of the mechanism of Na+/Fe2+ antisite and the development of high-performance polyanionic cathode materials.

Generating waxy rice starch with target type of amylopectin fine structure and gelatinization temperature by waxy gene editing.

Waxy rice, which lacks amylose, is an important variant in rice, and its starches have been widely used. New waxy rice varieties generated via the CRISPR/Cas9 gene-editing system is described. Herein, four waxy rice starches with different physicochemical properties were successfully obtained by the CRISPR/Cas9 editing Waxy (Wx) gene. The results showed that the amylose content (AC) of wx mutant starches ranged from 0.26 to 1.78 %, and CZBwx1 starches had the best gel consistency and highest water solubility among all wx mutants. Mutations of Wxb allele produced more short-chains (degree of chain polymerization (DP) 6-11), and less medium- and long-chains (DP12-70) than that of Wxa, while the AC of Wxa allele mutants was higher than the mutations of Wxb allele. The gelatinization temperature (GT) of wxa mutant starches was higher than that of wxb mutant starches. Moreover, we found that the GT and amylopectin fine structure type of waxy rice starch did not change after Wx gene editing. Based on these findings, it is possible to produce waxy rice starch with different physicochemical properties, containing target GT and chain length distributions of amylopectin.

Assessment of the Characteristics of Waxy Rice Mutants Generated by CRISPR/Cas9.

The cooking and eating quality of rice grains is a major focus from a consumer's perspective and is mainly determined by the apparent amylose content (AAC) of the starch. Waxy rice, a type of rice with an AAC of less than 2%, is an important goal for the breeding of high-quality rice. In recent years, the cloning of the Waxy (Wx) gene has revealed the molecular mechanism of the formation of waxy traits in rice. However, there have been limited studies on the physicochemical properties, such as gelatinization temperature, rapid viscosity analyzer profile, and amylopectin fine structure of wx mutants. In the current study, a rapid and highly efficient strategy was developed through the CRISPR/Cas9 gene-editing system for generating wx mutants in the background of five different rice varieties. The wx mutation significantly reduced the AAC and starch viscosity but did not affect the major agronomic traits (such as plant height, panicle number per plant, grain number per panicle, and seed-setting frequency). Incorporation of the wx mutation into varieties with low initial AAC levels resulted in further reduction in AAC, but without significantly affecting the original, desirable gelatinization traits and amylopectin structure types, suggesting that parents with low initial AAC should be preferred in breeding programs.

In Situ Induced Lattice-Matched Interfacial Oxygen-Passivation-Layer Endowing Li-Rich and Mn-Based Cathodes with Ultralong Life.

The high capacity of Li-rich and Mn-based (LRM) cathode materials is originally due to the unique hybrid anion- and cation redox, which also induces detrimental oxygen escape. Furthermore, the counter diffusion of released oxygen (into electrolyte) and induced oxygen vacancies (into the interior bulk phase) that occurs at the interface will cause uncontrolled phase collapse and other issues. Therefore, due to its higher working voltage (>4.7 V) than the activation voltage of lattice oxygen in LRM (≈4.5 V), the anion-redox-free and structurally consistent cobalt-free LiNi0.5 Mn1.5 O4 (LNMO) is selected to in situ construct a robust, crystal-dense and lattice-matched oxygen-passivation-layer (OPL) on the surface of LRM particles by the electrochemical delithiation to protect the core layered components. As expected, the modified sample displays continuously decreasing interfacial impedance and high specific capacity of 135.5 mAh g-1 with a very small voltage decay of 0.67 mV per cycle after 1000 cycles at 2 C rate. Moreover, the stress accumulation during cycling is mitigated effectively. This semicoherent OPL strengthens the surface stability and interrupts the counter diffusion of oxygen and oxygen vacancies in LRM cathode materials, which would provide guidance for designing high-energy-density layered cathode materials.

Charge Compensation Mechanisms and Oxygen Vacancy Formations in LiNi1/3Co1/3Mn1/3O2: First-Principles Calculations.

Charge compensation mechanisms in the delithiation processes of LiNi1/3Co1/3Mn1/3O2 (NCM111) are compared in detail by the first-principles calculations with GGA and GGA+U methods under different U values reported in the literature. The calculations suggested that different sets of U values lead to different charge compensation mechanisms in the delithiation process. Co3+/Co4+ couples were shown to dominate the redox reaction for 1 ≥ x ≥ 2/3 by using the GGA+U 1 method (U 1 = 6.0 3.4 3.9 for Ni, Co, and Mn, respectively). However, by using the GGA+U 2 (U 2 = 6.0 5.5 4.2) method, the results indicated that the redox reaction of Ni2+/Ni3+ took place in the range of 1 ≥ x ≥ 2/3. Therefore, according to our study, experimental charge compensation processes during delithiation are of great importance to evaluate the theoretical calculations. The results also indicated that all the GGA+U i (i = 1, 2, 3) schemes predicted better voltage platforms than the GGA method. The oxygen anionic redox reactions during delithiation are also compared with GGA+U calculations under different U values. The electronic density of states and magnetic moments of transition metals have been employed to illustrate the redox reactions during the lithium extractions in NCM111. We have also investigated the formation energies of an oxygen vacancy in NCM111 under different values of U, which is important in understanding the possible occurrence of oxygen release. The formation energy of an O vacancy is essentially dependent on the experimental conditions. As expected, the decreased temperature and increased oxygen partial pressure can suppress the formation of the oxygen vacancy. The calculations can help improve the stability of the lattice oxygen.

Quantum spin Hall effect in tilted penta silicene and its isoelectronic substitutions.

Silicene, a competitive two-dimensional (2D) material for future electronic devices, has attracted intensive attention in condensed matter physics. Utilizing an adaptive genetic algorithm (AGA), we identify a topological allotrope of silicene, named tilted penta (tPenta) silicene. Based on first-principles calculations, the geometric and electronic properties of tPenta silicene and its isoelectronic substitutions (Ge, Sn) are investigated. Our results indicate that tPenta silicene exhibits a semimetallic state with distorted Dirac cones in the absence of spin-orbit coupling (SOC). When SOC is considered, it shows semiconducting behavior with a gap opening of 2.4 meV at the Dirac point. Based on the results of invariant ( = 1) and the helical edge states, we demonstrate that tPenta silicene is a topological insulator. Furthermore, the effect of isoelectronic substitutions on tPenta silicene is studied. Two stoichiometric phases, i.e., tPenta Si0.333Ge0.667 and tPenta Si0.333Sn0.667 are found to retain the geometric framework of tPenta silicene and exhibit high stabilities. Our calculations show that both tPenta Si0.333Ge0.667 and tPenta Si0.333Sn0.667 are QSH insulators with enlarged band gaps of 32.5 meV and 94.3 meV, respectively, at the HSE06 level, offering great potential for practical applications at room temperature.

Formation of oxygen vacancies in Li2FeSiO4: first-principles calculations.

The formation of oxygen vacancies could affect various properties of oxides. Herein we have investigated the formation energies of an oxygen vacancy (VO) with the relevant charge states in bulk Pnma-Li2FeSiO4 using first-principles calculations. The formation energies of the VO are essentially dependent on the atomic chemical potentials that represent the experimental conditions. The calculated formation energies of an oxygen vacancy in different charge states indicate that it would be energetically favorable to fully ionize the oxygen vacancy in Li2FeSiO4. The presence of VO is accompanied by a distinct redistribution of the electronic charge densities only around the Fe and Si ions next to the O-vacancy site, which shows a very local influence on the host material arising from VO. This local characteristic is also confirmed by the calculated partial densities of states (PDOS). We also studied the influence of substitutional (MnFe and CoFe) and cation vacancy defects (i.e., VFe and VLi) in the vicinity of an O-vacancy on the formation of an O-vacancy, respectively. We find that the calculated interaction energies between these defects and the oxygen vacancy are all negative, which implies that the formation of an oxygen vacancy becomes easier when the above defects are introduced. Compared to the substitutional defects, the interaction energies between the vacancy defects and the oxygen vacancy are significantly larger. Among them, the interaction energy between VFe and VO is the largest.

First-Principles Observation of Bonded 2D B4C3 Bilayers.

Two-dimensional (2D) B-C compounds possess rich allotropic structures with many applications. Obtaining new 2D B4C3 structures is highly desirable due to the novel applications of three-dimensional (3D) B4C3 in protections. In this work, we proposed a new family of 2D B4C3 from the first-principles calculations. Distinct from previous observations, this family of 2D B4C3 consists of bonded 2D B4C3 bilayers. Six different types of bilayers with distinct bonded structures are found. The phonon spectrum calculations and ab initio molecular dynamics simulations at room temperature demonstrate their dynamic and thermal stabilities. Low formation energies suggest the high possibility of realizing such structures in experiments. Rich electronic structures are found, and the predicted Young's moduli are even higher than those of the previous ones. It is revealed that the unique electronic and mechanical properties are rooted in the bonding structures, indicating the prompting applications of this family of 2D B4C3 materials in photovoltaics, nanoelectronics, and nanomechanics.

Significant second-harmonic generation and bulk photovoltaic effect in trigonal selenium and tellurium chains.

One-dimensional (1D) selenium and tellurium crystalize in helical chainlike structures and thus exhibit fascinating properties. By performing first-principles calculations, we have researched the linear and nonlinear optical (NLO) properties of 1D Se and Te, and find that both systems exhibit pronounced NLO responses. In particular, 1D Se is found to possess a large second-harmonic generation coefficient with the χ value being up to 7 times larger than that of GaN, and is even several times larger than that of the bulk counterpart. On the other hand, 1D Te also produces significant NLO susceptibility χ which exceeds that of bulk GaN by 5 times. Furthermore, 1D Te is shown to possess a prominent linear electro-optic coefficient rxxx(0). In particular, the Te chain exhibits a large shift current response and the maximum is twice as large as the maximal photovoltaic responses obtained from BaTiO3. Therefore, 1D Se and Te may find potential applications in solar energy conversion, electro-optical switches, and so on. Finally, the much stronger NLO effects of 1D Se and Te are attributed to their one-dimensional structures with high anisotropy, strong covalent bonding and lone-pair electrons. These findings will contribute further to experimental studies and the search for excellent materials with large NLO effects.

Identifying a Li-rich superionic conductor from charge-discharge structural evolution study: Li2MnO3.

Li2MnO3 is a critical member of the Li-rich Mn-based layered material. To understand the process of electrochemical reaction in the monoclinic Li2MnO3, the structural evolution is investigated through the first-principles calculations based on density functional theory. During the delithiation process, a phase transformation together with a new trigonal phase at x = 0.5 (LixMnO3) has been reported, which belongs to the space group P3[combining macron]1m. Lithium ions are embedded in Li0.5MnO3 until the trigonal Li2MnO3 phase is formed with the P3[combining macron]1m symmetry preserved. Phonon and molecular dynamics simulations verify that this trigonal Li2MnO3 is dynamically and thermodynamicaly stable. Furthermore, our calculated results reveal that it has high conductivity of 0.36 S cm-1 in the ab plane, which proves that this trigonal Li2MnO3 is a promising lithium superionic conductor.

Luminescence and energy transfer of warm white-emitting phosphor Mg2Y2Al2Si2O12:Dy3+,Eu3+ for white LEDs.

A series of Mg2Y2Al2Si2O12:Dy3+,Eu3+ phosphors were synthesized by the solid-state method. The luminescent properties and crystal structures of the Mg2Y2Al2Si2O12:Dy3+,Eu3+ phosphors were analyzed. The XRD results show that the synthesized Mg2Y2Al2Si2O12:Dy3+,Eu3+ phosphors are of pure phase. Mg2Y2Al2Si2O12:Dy3+ can emit blue and yellow light under 367 nm light excitation; when doped with Eu3+, there is an obvious energy transfer from Dy3+ to Eu3+, and warm white light can be realized by adjusting the concentrations of Dy3+ and Eu3+ in Mg2Y2Al2Si2O12. A warm white LED device was fabricated by combining Mg2Y1.88Al2Si2O12:0.05Dy3+,0.07Eu3+ and a UV LED chip (370 nm) under a voltage of 3.2 V and current of 5 mA, the characteristics of the white LED being CIE = (0.4071, 0.3944), CCT = 3500 K and CRI = 91.3.

Anionic Redox Processes in Maricite- and Triphylite-NaFePO4 of Sodium-Ion Batteries.

In recent years, NaFePO4 has been regarded as one of the most promising cathode materials for next-generation rechargeable sodium-ion batteries. There is significant interest in the redox processes of rechargeable batteries for high capacity applications. In this paper, the redox processes of triphylite-NaFePO4 and maricite-NaFePO4 materials have been analyzed based on first-principles calculations and analysis of Bader charges. Different from LiFePO4, anionic (O2-) redox reactions are evidently visible in NaFePO4. Electronic structures and density of states are calculated to elaborate the charge transfer and redox reactions during the desodiation processes. Furthermore, we also calculate the formation energies of sodium extraction, convex hull, average voltage plateaus, and volume changes of Na1-x/12FePO4 with different sodium compositions. Deformation charge density plots and magnetization for NaFePO4 are also calculated to help understand the redox reaction processes.

HOT Graphene and HOT Graphene Nanotubes: New Low Dimensional Semimetals and Semiconductors.

We report a new graphene allotrope named HOT graphene containing carbon hexagons, octagons, and tetragons. A corresponding series of nanotubes are also constructed by rolling up the HOT graphene sheet. Ab initio calculations are performed on geometric and electronic structures of the HOT graphene and the HOT graphene nanotubes. Dirac cone and high Fermi velocity are achieved in a non-hexagonal structure of HOT graphene, implying that the honeycomb structure is not an indispensable condition for Dirac fermions to exist. HOT graphene nanotubes show distinctive electronic structures depending on their topology. The (0,1) n (n ≥ 3) HOT graphene nanotubes reveal the characteristics of semimetals, while the other set of nanotubes (1,0) n shows continuously adjustable band gaps (0~ 0.51 eV) with tube size. A competition between the curvature effect and the zone-folding approximation determines the band gaps of the (1,0) n nanotubes. Novel conversion between semimetallicity and semiconductivity arises in ultra-small tubes (radius < 4 Å, i.e., n < 3).

Manipulating External Electric Field and Tensile Strain toward High Energy Density Stability in Fast-Charging Li-Rich Cathode Materials.

Li-rich layered oxides (LLOs) are promising cathodes for lithium-ion batteries because of their high energy density provided by anionic redox. Although great improvements have been achieved in electrochemical performance, little attention has been paid to the energy density stability during fast charging. Indeed, LLOs have severe capacity fading and voltage decay especially at a high state of charge (SOC), disabling the application of the frequently used constant-current-constant-voltage mode for fast charging. Herein, we address this problem by manipulating the external electric field and tensile strain induced by lattice expansion effect in nanomaterials under the guidance of theoretical calculations, which indicate that LLOs at high SOC have almost a zero band gap and a low oxygen formation energy. This strategy will weaken polarization, stabilize lattice oxygen, and restrict phase transition simultaneously. Thus, the energy density during fast charging can be highly stabilized. Therefore, it may be of great value for the practical application of layered cathodes.

Dependence of Electronic and Optical Properties of MoS2 Multilayers on the Interlayer Coupling and Van Hove Singularity.

In this paper, the structural, electronic, and optical properties of MoS2 multilayers are investigated by employing the first-principles method. Up to six-layers of MoS2 have been comparatively studied. The covalency and ionicity in the MoS2 monolayer are shown to be stronger than those in the bulk. As the layer number is increased to two or above two, band splitting is significant due to the interlayer coupling. We found that long plateaus emerged in the imaginary parts of the dielectric function [Formula: see text] and the joint density of states (JDOS) of MoS2 multilayers, due to the Van Hove singularities in a two-dimensional material. One, two and three small steps appear at the thresholds of both the long plateau of [Formula: see text] and JDOS, for monolayer, bilayer, and trilayer, respectively. As the number of layers further increased, the number of small steps increases and the width of the small steps decreases accordingly. Due to interlayer coupling, the longest plateau and shortest plateau of JDOS are from the monolayer and bulk, respectively.

Lithium Deficiencies Engineering in Li-Rich Layered Oxide Li1.098Mn0.533Ni0.113Co0.138O2 for High-Stability Cathode.

Li-rich layered oxides have been in focus because of their high specific capacity. However, they usually suffer from poor kinetics, severe voltage decay, and capacity fading. Herein, a long-neglected Li-deficient method is demonstrated to address these problems by simply reducing the lithium content. Appropriate lithium vacancies can improve dynamics features and induce in situ surface spinel coating and nickel doping in the bulk. Therefore, the elaborately designed Li1.098Mn0.533Ni0.113Co0.138O2 cathode possesses improved initial Coulombic efficiency, excellent rate capability, largely suppressed voltage decay, and outstanding long-term cycling stability. Specifically, it shows a superior capacity retention of 93.1% after 500 cycles at 1 C (250 mA g-1) with respect to the initial discharge capacity (193.9 mA h g-1), and the average voltage still exceeds 3.1 V. In addition, the discharge capacity at 10 C can be as high as 132.9 mA h g-1. More importantly, a Li-deficient cathode can also serve as a prototype for further performance enhancement, as there are plenty of vacancies.

A Guideline for Tailoring Lattice Oxygen Activity in Lithium-Rich Layered Cathodes by Strain.

Lattice oxygen activity plays a dominant role in balancing discharge capacity and performance decay of lithium-rich layered oxide cathodes (LLOs). On the basis of density functional theory (DFT) and tight-binding theory, the activity of lattice oxygen can be improved by tensile strain and suppressed by compressive strain. To verify this conclusion, LLOs with large lattice parameters (L-LLOs) were synthesized taking advantage of the lattice expansion effect in nanomaterials. Compared with conventional LLOs with small lattice parameters (S-LLOs), particles in L-LLOs are imposed by tensile strain. L-LLOs show a larger initial discharge capacity and decay faster in the prolonged cycles than S-LLOs. Actually, most of the modified methods in LLOs can come down to strain-induced changes in lattice parameters. We believe this conclusion is a useful guideline to understand and tailor the lattice oxygen activity and may be generalized to other layered oxide cathodes involving anionic redox.

Comparative study on the electronic structures and redox reactions in LiCrX2 and NaCrX2 (X = O and S).

LiCrO2 and NaCrO2 have been well-studied as cathode materials in lithium and sodium ion batteries, while the studies on LiCrS2 and NaCrS2 are relatively rare. In this work, a comparative study on the electronic structures and redox reactions in oxides (LiCrO2, NaCrO2) and sulfides (LiCrS2, NaCrS2) is performed. A first-principles method has been used to calculate the Bader charge transfer, the electronic structures and the magnetic moments during the entire delithiation or desodiation process. The Bader charge analysis suggests that all the S, O and Cr ions in LiCrX2 and NaCrX2 participate in the redox reactions, where the loss of electrons of S ions is clearly larger than that of O ions. Besides, the redox processes of Cr ions are of much less significance. It is noted that, in the sulfides, Cr ions even gain a small portion of electrons rather than losing electrons during the extraction of Li/Na ions. All the charge transfer happens between the S-3p/O-2p and the Cr-3d bands. The redox reactions of O or S ions originate from the energy levels of O/S being pushed towards/across the Fermi surface due to the strong p-d hybridization.