Search

Abstract Atomically‐dispersed copper sites coordinated with nitrogen‐doped carbon (Cu–N–C) can provide novel possibilities to enable highly selective and active electrochemical CO2 reduction reactions. However, the construction of optimal local electronic structures for nitrogen‐coordinated Cu sites (Cu–N4) on carbon remains challenging. Here, we synthesized the Cu–N–C catalysts with atomically‐dispersed edge‐hosted Cu–N4 sites (Cu–N4C8) located in a micropore between two graphitic sheets via a facile method to control the concentration of metal precursor. Edge‐hosted Cu–N4C8 catalysts outperformed the previously reported M–N–C catalysts for CO2‐to‐CO conversion, achieving a maximum CO Faradaic efficiency (FECO) of 96%, a CO current density of –8.97 mA cm–2 at –0.8 V versus reversible hydrogen electrode (RHE), and over FECO of 90% from –0.6 to –1.0 V versus RHE. Computational studies revealed that the micropore of the graphitic layer in edge‐hosted Cu–N4C8 sites causes the d‐orbital energy level of the Cu atom to shift upward, which in return decreases the occupancy of antibonding states in the *COOH binding. This research suggests new insights into tailoring the locally coordinated structure of the electrocatalyst at the atomic scale to achieve highly selective electrocatalytic reactions.

Abstract Phase engineering is an efficient strategy for enhancing the kinetics of electrocatalytic reactions. Herein, phase engineering was employed to prepare high‐performance phosphorous‐doped biphase (1T/2H) MoS2 (P‐BMS) nanoflakes for hydrogen evolution reaction (HER). The doping of MoS2 with P atoms modifies its electronic structure and optimizes its electrocatalytic reaction kinetics, which significantly enhances its electrical conductivity and structural stability, which are verified by various characterization tools, including X‐ray photoelectron spectroscopy, high‐resolution transmission electron microscopy, X‐ray absorption near‐edge spectroscopy, and extended X‐ray absorption fine structure. Moreover, the hierarchically formed flakes of P‐BMS provide numerous catalytic surface‐active sites, which remarkably enhance its HER activity. The optimized P‐BMS electrocatalysts exhibit low overpotentials (60 and 72 mV at 10 mA cm−2) in H2SO4 (0.5 M) and KOH (1.0 M), respectively. The mechanism of improving the HER activity of the material was systematically studied using density functional theory calculations and various electrochemical characterization techniques. This study has shown that phase engineering is a promising strategy for enhancing the H* adsorption of metal sulfides.

Abstract Understanding the adsorption interactions between carbon materials and sulfur compounds has far‐reaching impacts, in addition to their well‐known important role in energy storage and conversion, such as lithium‐ion batteries. In this paper, properties of intrinsic B or Si single‐atom doped, and B–Si codoped graphene (GR) and graphdiyne (GDY) were investigated by using density functional theory‐based calculations, in which the optimal doping configurations were explored for potential applications in adsorbing sulfur compounds. Results showed that both B or Si single‐atom doping and B–Si codoping could substantially enhance the electron transport properties of GR and GDY, improving their surface activity. Notably, B and Si atoms displayed synergistic effects for the codoped configurations, where B–Si codoped GR/GDY exhibited much better performance in the adsorption of sulfur‐containing chemicals than single‐atom doped systems. In addition, results demonstrated that, after B–Si codoping, the adsorption energy and charge transfer amounts of GDY with sulfur compounds were much larger than those of GR, indicating that B–Si codoped GDY might be a favorable material for more effectively interacting with sulfur reagents.

Abstract Blueberry juice is one of deep‐processed products of blueberries, anthocyanins are main bioactive substance in blueberry juice. However, anthocyanins have poor stability. Thermal, high pressure, electric field, magnetic field and cobalt source irradiation were used to treat blueberry juice, and then the treated blueberry juice composition and antioxidant capacity were determined to explore ways to better protect anthocyanins. Metabolomics was used to qualitatively and quantitatively analyze the anthocyanins in blueberry juice, a total of 54 anthocyanins were identified. Different processing methods of treatment did not significantly change the types of anthocyanins in blueberry juice. Their effects were mainly focused on the changes in content. By determining the antioxidant capacity of blueberry juice, it was found that there is more than a simple linear relationship between the total anthocyanin content of blueberry juice and its antioxidant capacity. Therefore, the structural parameters of the four main anthocyanin monomers of blueberry juice were calculated using density functional theory to predict the antioxidant capacity and the antioxidant capacity of the monomers was determined for validation. The effect of different treatments on the change of antioxidant activity of blueberry juice due to anthocyanin occupancy was explained using equivalent antioxidant. The results showed that the 1 kGy irradiation treatment had a better protective effect on the anthocyanins, whereas the change in the percentage of anthocyanins due to this treatment was the key factor for the change in their antioxidant capacity.

Abstract Vitrimers are an innovative class of polymers that boast a remarkable fusion of mechanical and dynamic features, complemented by the added benefit of end‐of‐life recyclability. This extraordinary blend of properties makes them highly attractive for a variety of applications, such as the automotive sector, soft robotics, and the aerospace industry. At their core, vitrimer materials consist of crosslinked covalent networks that have the ability to dynamically reorganize in response to external factors, including temperature changes, pressure variations, or shifts in pH levels. In this review, the aim is to delve into the latest advancements in the theoretical understanding and computational design of vitrimers. The review begins by offering an overview of the fundamental principles that underlie the behavior of these materials, encompassing their structures, dynamic behavior, and reaction mechanisms. Subsequently, recent progress in the computational design of vitrimers is explored, with a focus on the employment of molecular dynamics (MD)/Monte Carlo (MC) simulations and density functional theory (DFT) calculations. Last, the existing challenges and prospective directions for this field are critically analyzed, emphasizing the necessity for additional theoretical and computational advancements, coupled with experimental validation.

Abstract Decreasing particle size (like thickness) is a common strategy to enhance the activities of catalysts. In this work, we have synthesized two coppers, which are bismuth‐based metal‐organic framework (CuBi‐MOF) catalysts with different thicknesses (134.8 and 2.0 nm). In contrast to common expectations, large thickness CuBi‐MOF has exhibited superior activities as a comparison to its small‐thickness counterpart in terms of carbon dioxide electroreduction to produce formate, characteristic of high selectivity (Faraday efficiency > 90%), a wide window of potential (−0.6 to −1.6 V vs. reversible hydrogen electrode), and large current densities (up to −380 mA cm−2). The mechanism study has been performed by using density functional theory calculations, which highlight the strong synergic effect between Cu and Bi sites in large‐thickness CuBi‐MOF for activating CO2 molecules. Consequently, large‐thickness CuBi‐MOF could show smaller Gibbs free energies compared to its small counterpart for binding with reaction intermediate (*COOH, 1.1 vs. 1.8 eV). The result of this work could provide new insights into catalyst design toward a number of electrochemical systems.

Abstract Finding effective strategies to design efficient photocatalysts and decompose refractory organic compounds in wastewater is a challenging problem. Herein, by coupling element doping and constructing heterostructures, S‐scheme CdS QDs/La‐Bi2WO6 (CS/LBWO) photocatalysts are designed and synthesized by a simple hydrothermal method. As a result, the RhB degradation efficiency of the optimized 5% CS/LBWO reached 99% within 70 min of illumination with excellent stability and recyclability. CS/LBWO shows improvement in the adsorption range of visible light and promotes electron–hole pair generation/migration/separation, attributing the superior degradation performance. The degradation RhB mechanism is proposed by a free radical capture experiment, electron paramagnetic resonance, and high‐performance liquid chromatography‐mass spectrometry results, indicating that h+ and •O2– play a significant role during four degradation processes: de‐ethylation, chromophore cleavage, ring opening, and mineralization. Based on in situ irradiated X‐ray photoelectron spectroscopy, Mulliken electronegativity theory, and the work function results, the S‐scheme heterojunction of CS/LBWO promotes the transfer of photogenerated electron–hole pairs and promotes the generation of reactive radicals. This work not only reports that 5% CS/LBWO is a promising photocatalyst for degradation experiments but also provides an approach to design advanced photocatalysts by coupling element doping and constructing heterostructures.

Abstract The reviving of the “Holy Grail” lithium metal batteries (LMBs) is greatly hindered by severe parasitic reactions between Li anode and electrolytes. Herein, first, we comprehensively summarize the failure mechanisms and protection principles of the Li anode. Wherein, despite being in dispute, the formation of lithium hydride (LiH) is demonstrated to be one of the most critical factors for Li anode pulverization. Secondly, we trace the research history of LiH at electrodes of lithium batteries. In LMBs, LiH formation is suggested to be greatly associated with the generation of H2 from Li/electrolyte intrinsic parasitic reactions, and these intrinsic reactions are still not fully understood. Finally, density functional theory calculations reveal that H2 adsorption ability of representative Li anode protective species (such as LiF, Li3N, BN, Li2O, and graphene) is much higher than that of Li and LiH. Therefore, as an important supplement of well‐known lithiophilicity theory/high interfacial energy theory and three key principles (mechanical stability, uniform ion transport, and chemical passivation), we propose that constructing an artificial solid electrolyte interphase layer enriched of components with much higher H2 adsorption ability than Li will serve as an effective principle for Li anode protection. In summary, suppressing formation of LiH and H2 will be very important for cycle life enhancement of practical LMBs.

Abstract Carbonate melts have been proposed to exist in the lower mantle, but their interaction with other lower mantle melt compositions is poorly understood. To understand miscibility in the carbonate‐silicate‐metal melt system, we simulate endmember, binary, and ternary melt mixtures and study how their Gibbs free energies of mixing evolve with pressure. We find that carbonate‐metal and carbonate‐silicate melts have miscibility gaps that close with increasing pressure, while silicate‐metal melts are immiscible at all lower‐mantle pressures. Extending this analysis to the core‐mantle boundary, we suggest three miscible melt fields near the endmember carbonate, silicate, and iron melt compositions. Analysis of the densities of these miscible melt compositions indicates that some carbonate‐rich and some silicate‐rich melt compositions are gravitationally stable at the core‐mantle boundary and could be candidate compositions to explain ultra‐low velocity zones. Additionally, we evaluate the speciation of an example immiscible melt composition at various pressures throughout the mantle and identify reduced carbon species that would be expected to form in the melt. Our analysis reveals that a majority of Earth's carbon could have been transported to the core during core‐mantle differentiation and that much of Earth's carbon may be stored in the deep interior today.

Abstract A main challenge for the development of two‐dimensional devices based on atomically thin transition‐metal dichalcogenides (TMDs) is the realization of metal–semiconductor junctions (MSJs) with low contact resistance and high charge transport capability. However, traditional metal–TMD junctions usually suffer from strong Fermi‐level pinning (FLP) and chemical disorder at the interfaces, resulting in weak device performance and high energy consumption. By means of high‐throughput first‐principles calculations, we report an attractive solution via the formation of van der Waals (vdW) contacts between metallic and semiconducting TMDs. We apply a phase‐engineering strategy to create a monolayer TMD database for achieving a wide range of work functions and band gaps, hence offering a large degree of freedom to construct TMD vdW MSJs with desired contact types. The Schottky barrier heights and contact types of 728 MSJs have been identified and they exhibit weak FLP (−0.62 to −0.90) as compared with the traditional metal–TMD junctions. We find that the interfacial interactions of the MSJs bring a delicate competition between the FLP strength and carrier tunneling efficiency, which can be utilized to screen high‐performance MSJs. Based on a set of screening criteria, four potential TMD vdW MSJs (e.g., NiTe2/ZrSe2, NiTe2/PdSe2, HfTe2/PdTe2, TaSe2/MoTe2) with Ohmic contact, weak FLP, and high carrier tunneling probability have been predicted. This work not only provides a fundamental understanding of contact properties of TMD vdW MSJs but also renders their huge potential for electronics and optoelectronics.

The application of explainable artificial intelligence in nanomaterial research has emerged in the past few years, which has facilitated the discovery of novel physical findings. However, a fundamental question arises concerning the physical insights presented by deep neural networks; the model interpretation results have not been carefully evaluated. Herein, explainable artificial intelligence and quantum mechanical calculations is bridged to investigate the correlation between light scattering and emission in a WSe2 monolayer. Convolutional neural networks using light scattering and emission data are first trained, while expecting the networks to determine the relationships between them. The trained models are interpreted and the specific phonon contribution during the exciton relaxation process is derived. Finally, the findings are independently evaluated through quantum mechanical calculations, such as the Born–Oppenheimer molecular dynamics simulation and density functional perturbation theory. The study provides reliable fundamental physical insight by evaluating the results of neural networks and suggests a novel methodology that can be applied in materials science.

Abstract The scarcity of high electrocatalysis composite electrode materials has long been suppressing the redox reaction of V(II)/V(III) and V(IV)/V(V) couples in high performance vanadium redox flow batteries (VRFBs). Herein, through ingeniously regulating the growth of Aspergillus Niger, a wrinkle‐like carbon (WLC) material that possesses edge‐rich carbon, abundant heteroatoms, and nature wrinkle‐like structure is obtained, which is subsequently successfully introduced and uniform dispersed on the surface of carbon fiber of graphite felt (GF). This composite electrode presents a lower overpotential and higher charge transfer ability, as the codoped multiheteroatoms increase the electrocatalysis activity and the wrinkled structure affords more abundant reaction area for vanadium ions in the electrolyte when compared with the pristine GF electrode, which is also supported by the density functional theory (DFT) calculations. Hence, the assembled battery using WLC electrodes achieves a high energy efficiency of 74.5% for 300 cycles at a high current density of 200 mA cm−2, as well as the highest current density of 450 mA cm−2. The WLC material not only uncovers huge potential in promoting the application of VRFBs, but also offers referential solution to synthesis microorganism‐based high‐performance electrode in other energy storage systems.

Abstract Plumbene, with a structure similar to graphene, is expected to possess a strong spin–orbit coupling and thus enhances its superconducting critical temperature (Tc). In this work, a buckled plumbene‐Au Kagome superstructure grown by depositing Au on Pb(111) is investigated. The superconducting gap monitored by temperature‐dependent scanning tunneling microscopy/spectroscopy shows that the buckled plumbene‐Au Kagome superstructure not only has an enhanced Tc with respect to that of a monolayer Pb but also possesses a higher value than what owned by a bulk Pb substrate. By combining angle‐resolved photoemission spectroscopy with density functional theory, the monolayer Au‐intercalated low‐buckled plumbene sandwiched between the top Au Kagome layer and the bottom Pb(111) substrate is confirmed and the electron–phonon coupling‐enhanced superconductivity is revealed. This work demonstrates that a buckled plumbene‐Au Kagome superstructure can enhance superconducting Tc and Rashba effect, effectively triggering the novel properties of a plumbene.

Abstract Doping of foreign atoms and construction of unique structures are considered as effective approaches to design high‐activity and strong‐durability electrocatalysts. Herein, we report Fe‐doped nickel hydroxide carbonate hierarchical microtubes with Ag nanoparticles (denoted Ag/NiFeHC HMTs) through hydrolysis precipitation process. Experimental tests and density functional theory calculations reveal that Fe doping can tune the electron configuration to enhance the conductivity, markedly improve the electrochemical surface area to expose more active sites, and act as reactive centers to lower the free energy of the rate determination step. In addition, the unique hierarchical structure can also offer active sites and excellent cycling stability. Benefitting from these advantages, the as‐obtained Ag/NiFeHC HMTs show excellent oxygen evolution reaction activity, with an overpotential of 208 mV at 10 mA cm−2 in 1.0 M KOH. Also, it could achieve long‐term stability at a current density of 20 mA cm−2 for 24 h.

Abstract Flexible carbon fiber cloth (CFC) is an important scaffold and/or current collector for active materials in the development of flexible self‐supportive electrode materials (SSEMs), especially in lithium‐ion batteries. However, during the intercalation of Li ions into the matrix of CFC (below 0.5 V vs. Li/Li+), the incompatibility in the capacity of the CFC, when used directly as an anode material or as a current collector for active materials, leads to difficulty in the estimation of its actual contribution. To address this issue, we prepared Ni5P4 nanosheets on CFC (denoted CFC@Ni5P4) and investigated the contribution of CFC in the CFC@Ni5P4 by comparing to the powder Ni5P4 nanosheets traditionally coated on a copper foil (CuF) (denoted P‐Ni5P4). At a current density of 0.4 mA cm−2, the as‐prepared CFC@Ni5P4 showed an areal capacity of 7.38 mAh cm−2, which is significantly higher than that of the P‐Ni5P4 electrode. More importantly, theoretical studies revealed that the CFC has a high Li adsorption energy that contributes to the low Li‐ion diffusion energy barrier of the Ni5P4 due to the strong interaction between the CFC and Ni5P4, leading to the superior Li‐ion storage performance of the CFC@Ni5P4 over the pristine Ni5P4 sample. This present work unveils the underlying mechanism leading to the achievement of high performance in SSEMs.

Abstract Gallium nitride (GaN) single crystal, as the representative of wide‐band semiconductors, has great prospects for high‐temperature energy storage, of its splendid power output, robust temperature stability, and superior carrier mobility. Nonetheless, it is an essential challenge for GaN‐based devices to improve energy storage. Herein, an innovative strategy is proposed by constructing GaN/Nickel cobalt oxygen (NiCoO2 ）heterostructure for enhanced supercapacitors (SCs). Benefiting from the synergy effect between the porous GaN network as a highly conductive skeleton and the NiCoO2 with massive active sites. The GaN/NiCoO2 heterostructure‐based SCs with ion liquids electrolyte are assembled and delivered an impressive energy density of 15.2 µWh cm−2 and power density, as well as superior service life at 130 °C. The theoretical calculation further explains that the reason for the energy storage enhancement of the GaN/NiCoO2 is due to the presence of the built‐in electric fields. This work offers a novel perspective for meeting the practical application of GaN‐based energy storage devices with exceptional performance capable of operation under high‐temperature environments.

Abstract The rational synergy of chemical composition and spatial nanostructures of electrode materials play important roles in high‐performance energy storage devices. Here, we designed pea‐like MoS2@NiS1.03–carbon hollow nanofibers using a simple electrospinning and thermal treatment method. The hierarchical hollow nanofiber is composed of a nitrogen‐doped carbon‐coated NiS1.03 tube wall, in which pea‐like uniformly discrete MoS2 nanoparticles are enclosed. As a sodium‐ion battery electrode material, the MoS2@NiS1.03–carbon hollow nanofibers have abundant diphasic heterointerfaces, a conductive network, and appropriate volume variation‐buffering spaces, which can facilitate ion diffusion kinetics, shorten the diffusion path of electrons/ion, and buffer volume expansion during Na+ insertion/extraction. It shows outstanding rate capacity and long‐cycle performance in a sodium‐ion battery. This heterogeneous hollow nanoarchitectures designing enlightens an efficacious strategy to boost the capacity and long‐life stability of sodium storage performance of electrode materials.

Abstract A new concentrated ternary salt ether‐based electrolyte enables stable cycling of lithium metal battery (LMB) cells with high‐mass‐loading (13.8 mg cm−2, 2.5 mAh cm−2) NMC622 (LiNi0.6Co0.2Mn0.2O2) cathodes and 50 μm Li anodes. Termed “CETHER‐3,” this electrolyte is based on LiTFSI, LiDFOB, and LiBF4 with 5 vol% fluorinated ethylene carbonate in 1,2‐dimethoxyethane. Commercial carbonate and state‐of‐the‐art binary salt ether electrolytes were also tested as baselines. With CETHER‐3, the electrochemical performance of the full‐cell battery is among the most favorably reported in terms of high‐voltage cycling stability. For example, LiNixMnyCo1–x–yO2 (NMC)‐Li metal cells retain 80% capacity at 430 cycles with a 4.4 V cut‐off and 83% capacity at 100 cycles with a 4.5 V cut‐off (charge at C/5, discharge at C/2). According to simulation by density functional theory and molecular dynamics, this favorable performance is an outcome of enhanced coordination between Li+ and the solvent/salt molecules. Combining advanced microscopy (high‐resolution transmission electron microscopy, scanning electron microscopy) and surface science (X‐ray photoelectron spectroscopy, time‐of‐fight secondary ion mass spectroscopy, Fourier‐transform infrared spectroscopy, Raman spectroscopy), it is demonstrated that a thinner and more stable cathode electrolyte interphase (CEI) and solid electrolyte interphase (SEI) are formed. The CEI is rich in lithium sulfide (Li2SO3), while the SEI is rich in Li3N and LiF. During cycling, the CEI/SEI suppresses both the deleterious transformation of the cathode R‐3m layered near‐surface structure into disordered rock salt and the growth of lithium metal dendrites.

Abstract Transition‐metal dichalcogenides exhibit strong light–matter interactions and unique multifunctional logic behavior. Here, the strong interlayer transition and excellent broadband photodetection of GeSe/MoTe2 van der Waals (vdW) heterojunction are demonstrated. Differential charge density and photoluminescence quenching analyses reveal a strong interlayer transition between GeSe and MoTe2. In addition, density functional theory analysis predicts the formation of staggered band alignment, which contributed to the spatial segregation of photogenerated electron–hole pairs. The diode exhibited excellent optoelectronic characteristics in the visible and near‐infrared region. A high responsivity of ~1.0 × 104 A/W, an excellent detectivity of ~8.4 × 1012 jones, and a fast rise and fall time of 458 and 498 μs, respectively. Finally, a two‐dimensional complementary inverter consisting of p‐channel GeSe and n‐channel MoTe2 is examined to analyze its application for a logic inverter. The findings of this study will play a crucial role in the stimulation and fabrication of multifunctional vdW heterostructure devices.

Abstract Ruthenium has been hailed as a competitive alternative for platinum toward hydrogen evolution reaction (HER), a critical process in electrochemical water splitting. In this study, we successfully prepare metallic Ru nanoparticles supported on carbon paper by utilizing a novel magnetic induction heating (MIH) method. The samples are obtained within seconds, featuring a Cl‐enriched surface that is unattainable via conventional thermal annealing. The best sample within the series shows a remarkable HER activity in both acidic and alkaline media with an overpotential of only ‐23 and ‐12 mV to reach the current density of 10 mA/cm2, highly comparable to that of the Pt/C benchmark. Theoretical studies based on density functional theory show that the excellent electrocatalytic activity is accounted by the surface metal‐Cl species that facilitate charge transfer and downshift the d‐band center. Results from this study highlight the unique advantages of MIH in rapid sample preparation, where residual anion ligands play a critical role in manipulating the electronic properties of the metal surfaces and the eventual electrocatalytic activity.

Abstract The electrochemical CO2 reduction reaction (CO2RR) has been regarded as a promising technique for converting CO2 into high‐value fuels and chemicals. Powered by renewable electricity, the CO2RR provides a viable strategy to mitigate the CO2 concentration in the atmosphere and close the anthropogenic carbon cycle. Recent studies exhibit that copper‐based catalysts are capable of reducing CO2 to C2+ products, such as ethylene and ethanol, which are of higher value compared with C1 products. The reaction process toward C2+ products involves the formation of key intermediate *CO, the C–C bonding, and the post‐C–C bonding to final products. This perspective is focusing on the mechanism leading to C2+ products, examining the evidence from in situ/operando spectroscopy and density functional theory calculations. The effects of Cu facet and electrolyte on catalytic performance are reviewed. An in depth discussion of mechanistic aspects of Cu catalyst is presented, shedding light on the intrinsic features of catalyst and electrode‐electrolyte interface, therefore moving towards an understanding of CO2RR at the atomic level.

Abstract Metal–organic frameworks (MOFs) are recognized as promising electrocatalysts for the oxygen evolution reaction (OER) because of their permanent porosity and rich architectural diversity; however, ionic MOFs enabling fast ions exchange during OER are rarely explored. Here, an ionic MOF (Ni‐btz) constructed with an azolate ligand is selected, and continuous 3D bimetallic MOF (NiFe‐btz) films deriving from high‐degree intergrowth of microsized MOFs particles are fabricated. The as‐prepared NiFe‐btz/NF‐OH electrode exhibits excellent OER performance with a low overpotential of 239 mV at 10 mA cm−2 under alkaline condition. The OER charge transfer process and bimetallic coupling effect in ionic NiFe‐btz are probed by density functional theory calculations and confirmed via X‐ray photoelectron spectroscopy and in situ Raman measurements. The partial density of states of NiFe‐btz indicates that the main contribution for electron density around the Fermi level is from Cl ions clarifying the profitable impact of ionic MOF framework. This work systematically demonstrates the relationship of electronic structure and OER activity in ionic, bimetallic MOFs and expands the scope of 3D MOF films for efficient OER.

Abstract Calcite surface was modified with stearic acids, and the interaction between them was investigated both experimentally and theoretically. Stearic‐acid‐modified calcite powders were investigated with Fourier transform infrared spectroscopy, X‐ray diffraction, zeta potential analyser and contact angle measurement. Then, the density functional theory calculations were performed to explore the interaction at the atomic scale. The experimental results and simulation indicated that stearic acids interact with calcite surface via chelation between the double‐bond O atom of –COOH and the Ca atom on calcite surface. The terminal methyl group of the stearic acids decreases the hydrophilicity of the calcite surface, and the interaction between different crystal faces of calcite is different.

Abstract Water, as a ubiquitous and relatively inert medium, plays a vital role in nature. The interactions between water and organic molecules or inorganic salts are of fundamental interest in understanding hydration processes in chemistry. The combination of scanning probe microscopy and theoretical calculations provides a versatile tool to directly visualize and further rationalize such interactions as well as influences of water on organic molecules and inorganic salts. In this review, we provide a brief overview of the recent exciting progress in revealing the interactions between water and organic molecules as well as inorganic salts (including ions) on surfaces. Herein, we describe first steps of hydration of organic molecules followed by a microsolvation process on surfaces. Subsequently, water‐induced tautomerization and chiral separation of small biomolecules on surfaces are discussed for understanding the roles of water in driving biological self‐assembly processes. Moreover, water is also able to assist structural transformation globally by selectively interrupting the relatively weak hydrogen bonds within nanostructures. Based on the water‐incorporated molecular nanostructures, dissolution of sodium halides on wet surfaces is achievable using confined water, while hydrates of halide ions desorb from the surface. More interestingly, ion hydrates are also demonstrated to be artificially accessible, which enables atomic‐scale investigation into local ion hydration and transport at interfaces. This review provides new insights into the role of water in the hydration‐related molecular and ionic systems, with implications for hydration and solvent effects down to the single‐molecule level.

Abstract Rational design hybrid nanostructure photocatalysts with efficient charge separation and transfer, and good solar light harvesting ability have critical significance for achieving high solar‐to‐chemical conversion efficiency. Here a highly active and stable composite photocatalyst is reported by integrating ultrathin ZnIn2S4 nanosheets on surface of hollow CdS cube to form the cube‐in‐cube structure. Experimental results combined with density functional theory calculations confirm that the Z‐scheme ZnIn2S4/CdS heterojunction is formed, which highly boosts the charge separation and transfer under the local‐electric‐field at semiconductor/semiconductor interface, and thus prolongs their lifetimes. Moreover, such a structure affords the highly enhanced light‐harvesting property. The optimized ZnIn2S4/CdS nanohybrids exhibit superior H2 generation rate under visible‐light irradiation (λ ≥ 420 nm) with excellent photochemical stability during 20 h continuous operation.

Abstract Inorganic perovskites exhibit impressive optoelectronic properties through experimental doping or composition modification. However, the underlying mechanism of the atomic substitution effect needs to be elucidated to guide future device optimizations. In this work, we have carried out systematic research on a series of inorganic perovskites regarding their electronic, optical, and vibrational properties. The band structures are strongly affected by the B‐sites. Meanwhile, phonon dispersions have revealed that the peculiar energy band offset is determined by the varied orbital and bonding characteristics. In addition, optical properties are directly influenced by the bond lengths between B‐sites and halogens, which are regulated by atomic substitutions. In addition, the infrared active spectrum and corresponding vibration modes indicate that the metal‐halogen octahedrons were confirmed to be the main source of these vibration modes. This work reveals the atomic substation effects of inorganic perovskites, which offer significant guidance for the design of next‐generation optoelectronic devices.

A series of pentagonal bipyramidal anionic germanium clusters doped with heavy rare earth elements, REGe 6 - (RE = Gd, Tb, Dy, Ho, Er, Tm, Yb, and Lu), have been identified at the PBE0/def2-TZVP level using density functional theory (DFT). Our findings reveal that the centrally doped pentagonal ring structure demonstrates enhanced stability and heightened aromaticity due to its uniform bonding characteristics and a larger charge transfer region. Through natural population analysis and spin density diagrams, we observed a monotonic decrease in the magnetic moment from Gd to Yb. This is attributed to the decreasing number of unpaired electrons in the 4f orbitals of the heavy rare earth atoms. Interestingly, the system doped with Er atoms showed lower stability and anti-aromaticity, likely due to the involvement of the 4f orbitals in bonding. Conversely, the systems doped with Gd and Tb atoms stood out for their high magnetism and stability, making them potential building blocks for rare earth-doped semiconductor materials., (© 2024 Wiley Periodicals LLC.)

The reactivity of 22 unsaturated molecules undergoing attack by a methyl radical (⋅CH 3 ) have been elucidated using the condensed radical general-purpose reactivity indicator (condensed radical GPRI) appropriate for relatively nucleophilic or electrophilic molecules. Using the appropriate radical GPRI equation for electrophilic attack or nucleophilic radical attack, seven different population schemes were used to assign the most reactive atoms in each of the 22 molecules. The results show that the condensed radical GPRI is sensitive to the population scheme chosen, but less sensitive than the radical Fukui function. Therefore, the reliability of these methods depends on the population scheme. Our investigation indicates that the condensed radical GPRI is most accurate in predicting the dominant products of the methyl radical addition reactions on a variety of unsaturated molecules when the Hirshfeld, Merz-Singh-Kollman, or Voronoi deformation density population schemes are used. Furthermore, for all populations schemes in the majority of instances where the radical Fukui function failed the radical GPRI was able to identify the most reactive atom under certain reactivity conditions., (© 2024 Wiley Periodicals LLC.)

In this article, we explore the construction of Hamiltonians with long-range interactions and their corrections using the short-range behavior of the wave function. A key aspect of our investigation is the examination of the one-particle potential, kept constant in our previous work, and the effects of its optimization on the adiabatic connection. Our methodology involves the use of a parameter-dependent potential dependent on a single parameter to facilitate practical computations. We analyze the energy errors and densities in a two-electron system (harmonium) under various conditions, employing different confinement potentials and interaction parameters. The study reveals that while the mean-field potential improves the expectation value of the physical Hamiltonian, it does not necessarily improve the energy of the system within the bounds of chemical accuracy. We also delve into the impact of density variations in adiabatic connections, challenging the common assumption that a mean field improves results. Our findings indicate that as long as energy errors remain within chemical accuracy, the mean field does not significantly outperform a bare potential. This observation is attributed to the effectiveness of corrections based on the short-range behavior of the wave function, a universal characteristic that diminishes the distinction between using a mean field or not., (© 2024 Wiley Periodicals LLC.)

The effective calculation of static nonlinear optical properties requires a considerably high accuracy at a reasonable computational cost, to tackle challenging organic and inorganic systems acting as precursors and/or active layers of materials in (nano-)devices. That trade-off implies to obtain very accurate electronic energies in the presence of externally applied electric fields to consequently obtain static polarizabilities ( α i j ) and hyper-polarizabilities ( β i j k and γ i j k l ). Density functional theory is known to provide an excellent compromise between accuracy and computational cost, which is however largely impeded for these properties without introducing range-separation techniques. We thus explore here the ability of a modern (double-hybrid and range-separated) Range-Separated eXchange Quadratic Integrand Double-Hybrid exchange-correlation functional to compete in accuracy with more costly and/or tuned methods, thanks to its robust and parameter-free nature., (© 2024 The Authors. Journal of Computational Chemistry published by Wiley Periodicals LLC.)

The structural, optoelectronics, and transport properties of TlTaO 3 compounds were determined utilizing the full potential augmented plane wave approach using first-principle method. We have considered the generalized gradient approximation for structural optimization and modified Becke-Johnson for electronic properties. The electronic properties reveal that the studied TlTaO 3 possesses direct bandgap of magnitude 1.52 eV. Between 0 and 12 eV, optical spectra calculations are made, taking into account the real and imaginary parts of the dielectric function, refractive index, and loss function. The transport properties are estimated considering Boltzmann transport theory. The Seebeck coefficient, electrical conductivity, thermal conductivity, and power factor are all assessed using the Boltzmann transport theory. The optimized thermoelectric response of the examined TlTaO 3 is produced by the improved carrier mobility, which also improves the thermoelectric efficiency of the TlTaO 3 . The obtained results will act as a theoretical road map for upcoming experimental and commercial TlTaO 3 applications., (© 2024 Wiley Periodicals LLC.)

Partial charges are a central concept in general chemistry and chemical biology, yet dozens of different computational definitions exist. In prior work [Cho et al., ChemPhysChem 21, 688-696 (2020)], we showed that these can be reduced to at most three 'principal components of ionicity'. The present study addressed the dependence of computed partial charges q on 1-particle basis set and (for WFT methods) n -particle correlation treatment or (for DFT methods) exchange-correlation functional, for several representative partial charge definitions such as QTAIM, Hirshfeld, Hirshfeld-I, HLY (electrostatic), NPA, and GAPT. Our findings show that semi-empirical double hybrids can closely approach the CCSD(T) 'gold standard' for this property. In fact, owing to an error compensation in MP2, CCSD partial charges are further away from CCSD(T) than is MP2. The nonlocal correlation is important, especially when there is a substantial amount of nonlocal exchange. Employing range separation proves to be "mostly" not advantageous, while global hybrids perform optimally for 20%-30% Hartree-Fock exchange across all charge types. Basis set convergence analysis shows that an augmented triple-zeta heavy-aug-cc-pV(T+d)Z basis set or a partially augmented jun-cc-pV(T+d)Z basis set is sufficient for Hirshfeld, Hirshfeld-I, HLY, and GAPT charges. In contrast, QTAIM and NPA display slower basis set convergence. It is noteworthy that for both NPA and QTAIM, HF exhibits markedly slower basis set convergence than the correlation components of MP2 and CCSD. Triples corrections in CCSD(T), denoted as CCSD(T)-CCSD, exhibit even faster basis set convergence., (© 2024 The Authors. Journal of Computational Chemistry published by Wiley Periodicals LLC.)

In recent years, the demand for electronic materials has significantly increased, driven by industrial needs and the pursuit of cost-efficient alternatives. This comprehensive study investigates the effects of Mn substitution on LaFeO 3 through the implementation of the GGA approach in density functional theory. The research findings demonstrate remarkable consistency with the experimental outcomes reported in the existing literature pertaining to the studied compounds. However, this study unveils novel insights into the mechanical and optical characteristics of the doped structures, which have not been previously reported. The structural stability is rigorously examined through multiple stability criteria, encompassing structural optimization, tests of elastic stability, and enthalpy of formation calculations. Furthermore, the electronic and optical properties of the compounds exhibit exceptional improvements in conductivity and reflectivity as a result of the doping process. The band structure analysis reveals the presence of a Moss-Burstein shift. Investigation of the magnetic properties indicates an increase in the magnetic moment value due to the Fe-Mn degeneracy resulting from increased Mn content. Mechanical analysis of the elastic moduli B, G, and Y demonstrates an enhanced strength and metal-like conductivity, attributed to the induced anharmonicity. Moreover, the internal strain factor suggests a higher degree of bond flexibility, implying potential applications of these compounds in flexible electronics., (© 2023 Wiley Periodicals LLC.)

A recent work (arXiv:2401.04685) has merged N-centered ensembles of neutral and charged electronic ground states with ensembles of neutral ground and excited states, thus providing a general and in-principle exact (so-called extended N-centered) ensemble density functional theory of neutral and charged electronic excitations. This formalism made it possible to revisit the concept of density-functional derivative discontinuity, in the particular case of single excitations from the highest occupied Kohn-Sham (KS) molecular orbital, without invoking the usual "asymptotic behavior of the density" argument. In this work, we address a broader class of excitations, with a particular focus on double excitations. An exact implementation of the theory is presented for the two-electron Hubbard dimer model. A thorough comparison of the true physical ground- and excited-state electronic structures with that of the fictitious ensemble density-functional KS system is also presented. Depending on the choice of the density-functional ensemble as well as the asymmetry of the dimer and the correlation strength, an inversion of states can be observed. In some other cases, the strong mixture of KS states within the true physical system makes the assignment "single excitation" or "double excitation" irrelevant., (© 2024 The Authors. Journal of Computational Chemistry published by Wiley Periodicals LLC.)

This study describes the interaction of human serum albumin (HSA) with the binol derivative (R)-(+)-3,3'-dibromo-1,1'-bi-2-naphthol (R-BrB), which has its optical activity based on the prohibitive energetic barrier for conversion into the enantiomer (S)-(+)-3,3'-dibromo-1,1'-bi-2-naphthol (S-BrB). The objective was to assess the ability of HSA to differentiate axial enantiomers based on their binding efficiency and their impact on the CD spectra. We discovered that both enantiomers were effective ligands, and the CD signal disappeared when equimolar amounts of R-BrB and S-BrB were simultaneously added, indicating no preference for either enantiomer. The complexation resulted in a significant signal increase at 250 nm and a bathochromic effect at 370 nm. Molecular docking simulations were performed, and the lower energy pose of R-BrB was selected for DFT calculations. The theoretical CD spectra of free and complexed R-BrB were obtained and showed alterations corroborating the experimental results. By comparing the difference spectrum (HSA:R-BrB minus HSA) with the spectrum of free RBrB in water or ethyl alcohol, we concluded that the CD signal intensification was due to the increased solubilization of R-BrB upon binding to HSA., (© 2024 Wiley Periodicals LLC.)

We developed a method for evaluating the accuracies of the local properties of DFT functionals in detail using a clustering method based on machine learning and structural/electronic descriptors. We generated 36 clusters consistent with human intuition using 30,436 carbon atoms from the QM9 dataset. The results were used to evaluate 13 C NMR chemical shifts calculated using 84 DFT functionals. Carbon atoms were grouped based on their similar environments, reducing errors within these groups. This enables more accurate assessment of the accuracy using a specific DFT functional. Therefore, the present atomic clustering provides more detailed insight into accuracy verification., (© 2024 Wiley Periodicals LLC.)

Machine learning techniques have found their way into computational chemistry as indispensable tools to accelerate atomistic simulations and materials design. In addition, machine learning approaches hold the potential to boost the predictive power of computationally efficient electronic structure methods, such as density functional theory, to chemical accuracy and to correct for fundamental errors in density functional approaches. Here, recent progress in applying machine learning to improve the accuracy of density functional and related approximations is reviewed. Promises and challenges in devising machine learning models transferable between different chemistries and materials classes are discussed with the help of examples applying promising models to systems far outside their training sets., (© 2024 Wiley Periodicals LLC.)

We present a comprehensive investigation of the electronic properties of fluorinated monolayer violet phosphorus using first-principles calculations. Our results reveal a strong dependence of the electronic properties on the different fluorine coverages of fluorination. As the fluorine coverage increases, monolayer violet phosphorus undergoes a significant transition from a wide direct bandgap semiconductor to a narrow indirect bandgap semiconductor. Moreover, both semi-fluorinated and fully fluorinated monolayer violet phosphorus exhibit advantageous semiconducting characteristics, with a tunable bandgap of 0.50 ~ 1.04 eV under biaxial strain ranging from -6% to 6%. Notably, the fully fluorinated monolayer violet phosphorus demonstrates a higher coefficient of light absorption within the visible range. Therefore, our findings highlight the tunability of monolayer violet phosphorus properties through the absorption of various fluorine coverages, providing valuable insights for the design and development of novel semiconductor devices based on this material., (© 2024 Wiley Periodicals LLC.)

Herein, the structural evolution, electronic and magnetic properties of silicon clusters with two different dopants, CrMnSi n (n = 4-20) clusters were investigated at density functional theory (DFT) level. Small-sized CrMnSi n (n = 4-9) clusters tend to adopt bipyramid-based geometries, while clusters with sizes n = 10 and 11 prefer to opening cage-like structures. For sizes n = 12 to 14, the half-encapsulated structures gradually transform into closed-cage Cr@Si n structures, with the Mn atom exposed outside. Starting from size 15, both the Cr and Mn atoms are completely encapsulated by silicon atoms. Meanwhile, the Cr and Mn atoms in smaller-sized CrMnSi n (n = 4-7) clusters tend to be separated, while they prefer to stay together for larger sizes. Cr atom always acts as electron donor, but not for Mn atom. From the average binding energies, one can conclude that it is easier to form larger size clusters. Smaller and larger sized CrMnSi n (n = 4-9 and 19-20) clusters prefer to exhibit ferromagnetic Cr-Mn coupling, while sizes n = 10-18 always exhibit ferrimagnetic state. To our knowledge, the CrMnSi n clusters is the first kind of neutral transition-metal doped semiconductor clusters that show ferrimagnetic state within a wide size range., (© 2023 Wiley Periodicals LLC.)

The concept of chemical bonding is a crucial aspect of chemistry that aids in understanding the complexity and reactivity of molecules and materials. However, the interpretation of chemical bonds can be hindered by the choice of the theoretical approach and the specific method utilized. This study aims to investigate the effect of choosing different density functionals on the interpretation of bonding achieved through energy decomposition analysis (EDA). To achieve this goal, a data set was created, representing four bonding groups and various combinations of functionals and dispersion correction schemes. The calculations showed significant variation among the different functionals for the EDA terms, with the dispersion correction terms exhibiting the highest variability. More information was extracted by using machine learning in combination with dimensionality reduction on the data set. Results indicate that, despite the differences in the EDA terms obtained from different functionals, the functional has the least significant impact, suggesting minimal influence on the bonding interpretation., (© 2023 The Authors. Journal of Computational Chemistry published by Wiley Periodicals LLC.)

Metalloenzymes catalyze a wide range of chemical transformations, with the active site residues playing a key role in modulating chemical reactivity and selectivity. Unlike smaller synthetic catalysts, a metalloenzyme active site is embedded in a larger protein, which makes interrogation of electronic properties and geometric features with quantum mechanical calculations challenging. Here we implement the ability to fetch crystallographic structures from the Protein Data Bank and analyze the metal binding sites in the program molSimplify. We show the usefulness of the newly created protein3D class to extract the local environment around non-heme iron enzymes containing a two histidine motif and prepare 372 structures for quantum mechanical calculations. Our implementation of protein3D serves to expand the range of systems molSimplify can be used to analyze and will enable high-throughput study of metal-containing active sites in proteins., (© 2023 The Authors. Journal of Computational Chemistry published by Wiley Periodicals LLC.)

Benzophenone and related derivatives are widely used as photoinitiators for food packaging to cure inks or lacquers with ultraviolet (UV) light on cardboard and paper. However, there are concerns about the potential health risks of their migration into food. Knowing the physical and chemical properties of benzophenone and its derivatives could play a significant role in their quantification and analysis using chemical ionization mass spectrometry (CI-MS) methods. These parameters are evaluated using B3LYP/6-311++** density functional theory (DFT) implemented on Gaussian code. Ion-molecule chemistry through the selection of reagent ions, reaction energetics and kinetics, thermodynamic stability, and reactivity of molecules deemed to foster VOC identification and quantification via CI-MS techniques. The VOCs under study are expected to undergo exothermic reactions from H 3 O + , NH 4 + , NO + , and O 2 + ions, except endothermic proton transfer from NH 4 + to 2-hydroxy-4-methoxybenzophenone and 2,3,4-trihydroxy benzophenone. These compounds possess less proton affinities than NH 3 and are least stable in their protonated forms. The DFT computed properties provide the basis for developing reliable and accurate methods to detect and measure the presence of benzophenone and its derivatives in packaging materials and food products., (© 2024 John Wiley & Sons Ltd.)

Abstract Lithium–sulfur batteries (Li‐S batteries) are promising next‐generation energy storage systems because of their high‐theoretical energy density. However, the commercialization of Li‐S batteries is still impeded by the aggregation of sulfur, low‐sulfur utilization, shuttling of dissolved polysulfides and sluggish reaction kinetics. Herein, we designed a hierarchically maple leaf‐like structured sulfur electrodes by in‐situ growth of ultrathin sulfur microcrystal on two‐dimensional MXene‐graphene‐cellulose nanofiber (MGN) matrice (denoted as IS‐MGN@S). The sulfur microcrystal as cathode can achieve improved kinetics than bulk sulfur due to its few layers of sulfur atoms, which is proved by the density functional theory calculations. The MXene not only confines polysulfides through strong chemisorption but also promotes the catalytic conversion of polysulfides. The introduction of graphene improves the conductivity and boosts the immobilization and conversion of polysulfides. As a result, the IS‐MGN@S cathode demonstrates remarkable electrochemical properties with a high‐initial capacity (1229 mAh g−1 at 0.2C), substantial improvement in rate capability (770 mAh g−1 at 2C), and stable long‐term cycling capacity. Moreover, the pouch cells with IS‐MGN@S cathode and gel electrolyte demonstrate excellent mechanical properties under mechanical damage (nail & cut tests, severe deformations), suggesting their promising applications for wearable electronic devices.

Abstract This study examines the use of an aggregation‐induced enhanced emission fluorophore (TPE‐MRh) to prepare red‐emitting luminescent solar concentrators (LSCs) based on poly(methyl methacrylate) (PMMA) and poly(cyclohexyl methacrylate) (PCMA). TPE‐MRh is a tetraphenylethylene (TPE) derivative bearing two dimethylamino push groups and a 3‐methyl‐rhodanine pull moiety, with absorption maxima at around 500 nm and fluorescence peak at 700 nm that strongly increases in solid‐state. TPE‐MRh displays a typical crystallization‐induced enhanced emission that has been rationalized by modeling the compound behavior in solution and solid‐state via density functional theory calculations with the inclusion of the environment. TPE‐MRh dispersed into 5 × 5 cm2 polymer films with a thickness of 25 ± 5 μm has revealed a partial fluorescence quenching with fluorophore content. Quantum yields (QYs) below 10% for the 2 wt.% of doping have been addressed to the formation of less emissive micro‐sized clusters of fluorophores. PMMA slabs with the same surface size but 3 mm of thickness and 200 ppm of TPE‐MRh have provided QY of 36.5% thanks to the attenuation of the detrimental effects of fluorophore aggregation. This feature is reflected in the LSCs performance, with devices achieving the largest power collected by the photovoltaic cell.

Abstract Indium antimonide (InSb) nanowires are used as building blocks for quantum devices because of their unique properties, that is, strong spin‐orbit interaction and large Landé g‐factor. Integrating InSb nanowires with other materials could potentially unfold novel devices with distinctive functionality. A prominent example is the combination of InSb nanowires with superconductors for the emerging topological particles research. Here, the combination of the II–VI cadmium telluride (CdTe) with the III–V InSb in the form of core–shell (InSb–CdTe) nanowires is investigated and potential applications based on the electronic structure of the InSb–CdTe interface and the epitaxy of CdTe on the InSb nanowires are explored. The electronic structure of the InSb–CdTe interface using density functional theory is determined and a type‐I band alignment is extracted with a small conduction band offset ( ⩽0.3 eV). These results indicate the potential application of these shells for surface passivation or as tunnel barriers in combination with superconductors. In terms of structural quality, it is demonstrated that the lattice‐matched CdTe can be grown epitaxially on the InSb nanowires without interfacial strain or defects. These shells do not introduce disorder to the InSb nanowires as indicated by the comparable field‐effect mobility measured for both uncapped and CdTe‐capped nanowires.

Abstract Carbon group element‐based materials are the most widely used anode materials for Li‐ion batteries (LIBs). However, their performance is limited by the low capacity (eg, graphite) or high‐volume changes (eg, Si and Sn). Therefore, exploring high‐performance anode materials is quite appealing and promising. By first‐principle calculations in this study, we found that distorted T‐carbon (DTC) as a desired LIB anode shows properties of the enhanced capacity, decreased volume change, and the increased ion migration. The origin of such improved properties is attributed to the interconnected tunnels and large cavities of the carbon skeleton. The theoretical specific capacity of DTC is found to be 558 mAh/g, which is 1.5 times higher than that of commercial graphite anodes. Interestingly, the volume change of the DTC anode is only 3% at the full‐lithiation state (one‐fifth of that of the commercial graphite anode), which can overcome the pulverization problem in most high‐capacity anode materials and attain a longer cycling lifetime. Both transition state calculations and molecular dynamics simulations demonstrate that the Li‐ion migration barrier is less than 0.1 eV and the Li‐ion vacancy is only 0.2 eV, enabling its promising rate performance. This study provides a new and effective strategy to improve the anode properties of LIBs.

Abstract Polarization of ionic and electronic defects in response to high electric fields plays an essential role in determining properties of materials in applications such as memristive devices. However, isolating the polarization response of individual defects has been challenging for both models and measurements. Here the authors quantify the nonlinear dielectric response of neutral oxygen vacancies, comprised of strongly localized electrons at an oxygen vacancy site, in perovskite oxides of the form ABO3. Their approach implements a computationally efficient local Hubbard U correction in density functional theory simulations. These calculations indicate that the electric dipole moment of this defect is correlated positively with the lattice volume, which they varied by elastic strain and by A‐site cation species. In addition, the dipole of the neutral oxygen vacancy under electric field increases with increasing reducibility of the B‐site cation. The predicted relationship among point defect polarization, mechanical strain, and transition metal chemistry provides insights for the properties of memristive materials and devices under high electric fields.

Abstract Hitherto, there are almost no reports on the complete reconstruction in hydrogen evolution reaction (HER). Herein, the authors develop a new type of reconfigurable fluoride (such as CoF2) pre‐catalysts, with ultra‐fast and in‐depth self‐reconstruction, substantially promoting HER activity. By experiments and density functional theory (DFT) calculations, the unique surface structure of fluorides, alkaline electrolyte and bias voltage are identified as key factors for complete reconstruction during HER. The enrichment of F atoms on surface of fluorides provides the feasibility of spontaneous and continuous reconstruction. The alkaline electrolyte triggers rapid F− leaching and supplies an immediate complement of OH− to form amorphous α‐Co(OH)2 which rapidly transforms into β‐Co(OH)2. The bias voltage promotes amorphous crystallization and accelerates the reconstruction process. These endow the generation of mono‐component and crystalline β‐Co(OH)2 with a loose and defective structure, leading to an ultra‐low overpotential of 54 mV at 10 mA cm−2 and super long‐term stability exceeding that of Pt/C. Moreover, DFT calculations confirm that F− leaching optimizes hydrogen and water adsorption energies, boosting HER kinetics. Impressively, the self‐reconstruction is also applicable to other non‐noble transition metal fluorides. The work builds the fundamental comprehension of complete self‐reconstruction during HER and provides a new perspective to conceive advanced catalysts.

Abstract The sulfur redox kinetics critically matters to superior lithium–sulfur (Li–S) batteries, for which single atom catalysts (SACs) take effect on promoting Li2S redox process and mitigating the shuttle behavior of lithium polysulfide (LiPs). However, conventional trial‐and‐error strategy significantly slows down the development of SACs in Li–S batteries. Here, the Li2S oxidation processes over MN4@G catalysts are fully explored and energy barrier of Li2S decomposition (Eb) is identified to correlate strongly with three parameters of energy difference between initial and final states of Li2S decomposition, reaction energy of Li2S oxidation and LiS bond strength. These three parameters can serve as efficient descriptors by which two excellent SACs of MoN4@G and WN4@G are screened which give rise to Eb values of 0.58 and 0.55 eV, respectively, outperforming other analogues in adsorbing LiPs and accelerating the redox kinetics of Li2S. This method can be extended to a wider range of SACs by coupling MN4 moiety with heterostructures and heteroatoms beyond N where WN4@G/TiS2 heterointerface is predicted to exhibit enhanced catalytic performance for Li2S decomposition with Eb of 0.40 eV. This work will help accelerate the process of designing a wider range of efficient catalysts in Li–S batteries and even beyond, e.g. alkali‐ion‐Chalcogen batteries.

Abstract Preciously tuning the surface composition of noble metal nanoparticles with the particle size of only 2 nm or less by alloying with other metals represents a powerful strategy to boost their electrocatalytic selectivity. However, the synthesis of ultrafine nanoalloys and tuning their surface composition remain challenging. In this report, ultrafine CuPd nanoalloys with the particle size of ca. 2 nm are synthesized based on the galvanic replacement reaction between presynthesized Cu nanoparticles and Pd2+ precursors, and the tuning of their surface compositions is also achieved by changing the atom ratios of Cu/Pd. For the electrocatalytic reduction of CO2, Cu5Pd5 nanoalloys show the CO Faradaic efficiency (FE) of 88% at −0.87 V, and the corresponding mass activity reaches 56 A/g that is much higher than those of Cu8Pd2 nanoalloys, Cu3Pd7 nanoalloys and most of previously reported catalysts. Density functional theory uncovers that with the increase of Pd on the surface of the ultrafine CuPd nanoalloys, the adsorbed energy of both of intermediate COOH* and CO* to the Pd sites is strengthened. The Cu5Pd5 nanoalloys with the optimal surface composition better balance the adsorption of COOH* and desorption of CO*, achieving the highest selectivity and activity. The difficult liberation of absorbed CO* on the surface of Cu3Pd7 nanoalloys provides carbon source to favor the production of ethylene, endowing the Cu3Pd7 nanoalloys with the highest selectivity for ethylene among these ultrafine CuPd nanoalloys.