Preparation of NIR-II Polymer Nanoprobe Through Twisted Intramolecular Charge Transfer and Förster Resonance Energy Transfer of NIR-I Dye.

Near-infrared-II (NIR-II) fluorescence imaging is pivotal in biomedical research. Organic probes exhibit high potential in clinical translation, due to advantages such as precise structure design, low toxicity, and post-modifications convenience. In related preparation, enhancement of NIR-II tail emission from NIR-I dyes is an efficient method. In particular, the promotion of twisted intramolecular charge transfer (TICT) of relevant NIR-I dyes is a convenient protocol. However, present TICT-type probes still show disadvantages in relatively low emission, large particle sizes, or limited choice of NIR-I dyes, etc. Herein, the synthesis of stable small-sized polymer NIR-II fluoroprobes (e.g., 7.2 nm), integrating TICT and Förster resonance energy transfer process to synergistically enhance the NIR-II emission is reported. Strong enhanced emissions can be obtained from various NIR-I dyes and lanthanide elements (e.g., twelvefold at 1250 nm from Nd-DTPA/IR-808 sample). The fluorophore provides high-resolution angiography, with high-contrast imaging on middle cerebral artery occlusion model mice for distinguishing occlusion. The fluorophore can be rapidly excreted from the kidney (urine ≈65% within 4 h) in normal mice and exhibits long-term renal retention on acute kidney injury mice, showing potential applications in the prognosis of kidney diseases. This development provides an effective strategy to design and synthesize effective NIR-II fluoroprobes.

Formation of compounds with diverse polyelectrolyte morphologies and nonlinear ion conductance in a two-dimensional nanofluidic channel.

Aqueous electrolytes subjected to angstrom-scale confinement have recently attracted increasing interest because of their distinctive structural and transport properties, as well as their promising applicability in bioinspired nanofluidic iontronics and ion batteries. Here, we performed microsecond-scale molecular dynamics simulations, which provided evidence of nonlinear ionic conductance under an external lateral electric field due to the self-assembly of cations and anions with diverse polyelectrolyte morphologies (e.g., extremely large ion clusters) in aqueous solutions within angstrom-scale slits. Specifically, we found that the cations and anions of Li2SO4 and CaSO4 formed chain-like polyelectrolyte structures, whereas those of Na2SO4 and MgSO4 predominantly formed a monolayer of hydrated salt. Additionally, the cations and anions of K2SO4 assembled into a hexagonal anhydrous ionic crystal. These ion-dependent diverse polyelectrolyte morphologies stemmed from the enhanced Coulomb interactions, weakened hydration and steric constraints within the angstrom-scale slits. More importantly, once the monolayer hydrated salt or ionic crystal structure was formed, the field-induced ion current exhibited an intriguing gating effect at a low field strength. This abnormal ion transport was attributed to the concerted movement of cations and anions within the solid polyelectrolytes, leading to the suppression of ion currents. When the electric field exceeded a critical strength, however, the ion current surged rapidly due to the dissolution of many cations and anions within a few nanoseconds in the aqueous solution.

Assisted Self-Assembly of Nanoporous Ices via Carbon Nanomaterial Templates.

Self-assembly is a widely used synthetic method in nanoscience to assemble well-organized structures. Self-assembly processes usually occur in a water solvent environment. However, the self-assembly of water molecules is rarely studied. Herein, we show a strategy to fabricate porous ice via carbon nanomaterial-assisted self-assembly. Diverse frameworks of nanoporous ice are formed by using orthorhombic and tetragonal arrays of carbon nanotubes or carbon-atom chains as templates. In contrast to many bulk ices discovered in nature, nanoporous ices are shown to be stable only under negative pressure. Hence, nanoporous ices cannot be produced through the direct nucleation of water at negative pressure. The template-assisted self-assembly method is shown to be the most effective method to fabricate nanoporous ice in quantity. Several key factors for the self-assembly of nanoporous ices are identified, including proper gap spacings in the carbon nanomaterial template and suitable interactions between water and the carbon nanomaterials.

Enhanced Direct Exchange Interaction and Hybridization by Single-Atom Linkers for High Curie Temperature and Superior Visible-Light Harvesting in Cr3(CN3)2.

Designing two-dimensional (2D) ferromagnetic (FM) semiconductors with elevated Curie temperature, high carrier mobility, and strong light harvesting is challenging but crucial to the development of spintronics with multifunctionalities. Herein, we show first-principles computation evidence of the 2D metal-organic framework Kagome ferromagnet Cr3(CN3)2. Monolayer Cr3(CN3)2 is predicted to be an FM semiconductor with a record-high Curie temperature of 943 K owing to the use of a single-atom linker (N), which results in strong direct d-p exchange interaction and hybridization between dyz/xz and pz of Cr and N, as well as excellent matching characteristics in energy and symmetry. The single-atom linker structural feature also leads to notable band dispersion and a relatively high carrier mobility of 420 cm2 V-1 s-1. Moreover, under the in-plane strain, 2D Cr3(CN3)2 can be tuned to possess a strong visible-light-harvesting functionality. These novel properties render monolayer Cr3(CN3)2 a distinct 2D ferromagnet with high potential for the development of multifunctional spintronics.

High out-of-plane negative Poisson's ratios and strong light harvesting in two-dimensional SiS2 and its derivatives.

Two-dimensional (2D) materials with negative Poisson's ratios (NPRs) hold tremendous potential in diverse electronic devices. However, most 2D auxetic materials exhibit small out-of-plane NPRs and materials with bi-directional NPRs are rare. In this work, the SiS2 monolayer and its derivatives MX2 (M = Si, Ge, Sn and X = S, Se, Te) are systematically studied via first-principles simulation. We demonstrate that a SiS2 monolayer possesses a remarkable out-of-plane NPR with a value of -1.09 and an in-plane NPR (-0.13). Furthermore, a higher out-of-plane NPR (-1.79) can be achieved in a SnS2 monolayer by element substitution. Remarkably, SiS2 and its derivative MX2 monolayers exhibit excellent light harvesting over the ultraviolet and visible range, and the corresponding electronic properties show robustness against strains. Our results confirm that MX2 monolayers provide an ideal platform to explore auxeticity in two-dimensional limits.

mech2d: An Efficient Tool for High-Throughput Calculation of Mechanical Properties for Two-Dimensional Materials.

Two-dimensional (2D) materials have been a research hot topic in the passed decades due to their unique and fascinating properties. Among them, mechanical properties play an important role in their application. However, there lacks an effective tool for high-throughput calculating, analyzing and visualizing the mechanical properties of 2D materials. In this work, we present the mech2d package, a highly automated toolkit for calculating and analyzing the second-order elastic constants (SOECs) tensor and relevant properties of 2D materials by considering their symmetry. In the mech2d, the SOECs can be fitted by both the strain-energy and stress-strain approaches, where the energy or strain can be calculated by a first-principles engine, such as VASP. As a key feature, the mech2d package can automatically submit and collect the tasks from a local or remote machine with robust fault-tolerant ability, making it suitable for high-throughput calculation. The present code has been validated by several common 2D materials, including graphene, black phosphorene, GeSe2 and so on.

Large tunneling magnetoresistance in spin-filtering 1T-MnSe2/h-BN van der Waals magnetic tunnel junction.

The magnetic tunnel junction (MTJ), one of the most prominent spintronic devices, has been widely utilized for memory and computation systems. Electrical writing is considered as a practical method to enhance the performance of MTJs with high circuit integration density and ultralow-power consumption. Meanwhile, a large tunneling magnetoresistance (TMR), especially at the non-equilibrium state, is desirable for the improvement of the sensitivity and stability of MTJ devices. However, achieving both aspects efficiently is still challenging. Here, we propose a two-dimensional (2D) MTJ of 1T-MnSe2/h-BN/1T-MnSe2/h-BN/1T-MnSe2 with efficient electrical writing, reliable reading operations and high potential to work at room temperature. First, for this proposed MTJ with a symmetrical structure and an antiparallel magnetic state, the degeneracy of the energy could be broken by an electric field, resulting in a 180° magnetization reversal. A first principles study confirms that the magnetization of the center 1T-MnSe2 layer could be reversed by changing the direction of the electric field, when the magnetic configurations of the two outer 1T-MnSe2 layers are fixed in the antiparallel state. Furthermore, we report a theoretical spin-related transport investigation of the MTJ at the non-equilibrium state. Thanks to the half-metallicity of 1T-MnSe2, TMR ratios reach very satisfactory values of 2.56 × 103% with the magnetization information written by an electric field at room temperature. In addition, the performance of the TMR effect exhibits good stability even when the bias voltage increases gradually. Our theoretical findings show that this proposed MTJ is a promising high performance spintronic device and could promote the design of ultralow-power spintronic devices.

Strongly Solvating Ether Electrolytes for High-Voltage Lithium Metal Batteries.

Ethers are promising electrolytes for lithium (Li) metal batteries (LMBs) because of their unique stability with Li metal. Although intensive research on designing anion-enriched electrolyte solvation structures has greatly improved their electrochemical stabilities, ether electrolytes are approaching an anodic bottleneck. Herein, we reveal the strong correlation between electrolyte solvation structure and oxidation stability. In contrast to previous designs of weakly solvating solvents for enhanced anion reactivities, the triglyme (G3)-based electrolyte with the largest Li+ solvation energy among different linear ethers demonstrates greatly improved stability on Ni-rich cathodes under an ultrahigh voltage of 4.7 V (93% capacity retention after 100 cycles). Ether electrolytes with a stronger Li+ solvating ability could greatly suppress deleterious oxidation side reactions by decreasing the lifetime of free labile ether molecules. This study provides critical insights into the dynamics of the solvation structure and its significant influence on the interfacial stability for future development of high-efficiency electrolytes for high-energy-density LMBs.

Resolving Interface Barrier Deviation from the Schottky-Mott Rule: A Mitigation Strategy via Engineering MoS2-Metal van der Waals Contact.

The Schottky barrier (SB) in the ultraclean van der Waals contact between two-dimensional (2D) MoS2 and three-dimensional (3D) indium (In) strikingly deviates from the Schottky-Mott limit (SML). Herein, on the basis of first-principles calculation, the origin of the SB deviation is brought to bear, as well as a strategy for mitigating the SB deviation. In light of the good agreement between the SB and the corrected SB by interface potential difference (ΔV) and Fermi -level shift (ΔEF) based on the SML, the SB deviation is attributed to the combined effects of ΔV and ΔEF. Furthermore, when a Au, Sc, or Ti thin film is coated on the back side of In, the SB deviation and the sum of ΔV and ΔEF decrease similarly. Importantly, in the Ti coating situation, the SB is reduced to 0.12 eV, notably smaller than the value of 0.30 eV in the Au coating case. This interface engineering can be generalized to regulate the SB between a 2D semiconductor and a 3D alloy.

Continuous and First-Order Liquid-Solid Phase Transitions in Two-Dimensional Water.

Understanding the phase behaviors of nanoconfined water is of importance in fundamental physical science and nanofluidic applications. Herein, we perform sub-microsecond to microsecond long molecular-dynamics (MD) simulations to show evidence of continuous and first-order phase transitions of water confined between two smooth walls with width of h = 1.0 nm. At either relatively low lateral pressure (PL ≤ 10 MPa) or relatively high lateral pressure (PL ≥ 400 MPa), the freezing of the confined water undergoes a first-order phase transition and gives rise to bilayer low-density amorphous (BL-LDA) ice and the trilayer puckered high-density ice (TL-pHDI), respectively. Very interestingly, within a moderate range of lateral pressures (100 MPa ≤ PL ≤ 300 MPa), the confined water appears to undergo a continuous phase transition in the isobaric condition to form a new phase, namely, the bilayer and puckered high-density amorphous (BL-pHDA) ice. A similar continuous phase transition behavior has been reported previously in tens of nanoseconds MD simulations of the freezing of BL water into the BL flat rhombic ice within a narrower hydrophobic nanoslit (h = 0.8 nm) and in the isochoric condition at high densities of water (Han et al. Nat. Phys. 2010, 6, 685). Our simulation results on the pressure-dependent continuous and first-order phase transitions of the confined water extend the previous study in a different way and thereby provide new insights into the novel thermodynamic phase behavior of low-dimensional water in nanoscale confinement.

Enamel-like Layer of Nanohydroxyapatite Stabilizes Zn Metal Anodes by Ion Exchange Adsorption and Electrolyte pH Regulation.

The instability of Zn anode caused by severe dendrite growth and side reactions has restricted the practical applications of aqueous zinc-ion batteries (AZIBs). Herein, an enamel-like layer of nanohydroxyapatite (Ca5(PO4)3(OH), nano-HAP) is constructed on Zn anode to enhance its stability. Benefiting from the ion exchange between Zn2+ and Ca2+, the adsorption for Zn2+ in enamel-like nano-HAP (E-nHAP) layer can effectively guide Zn deposition, ensuring homogeneous Zn2+ flux and even nucleation sites to suppress Zn dendrites. Meanwhile, the low pH of acidic electrolyte can be regulated by slightly soluble nano-HAP, restraining electrolyte corrosion and hydrogen evolution. Moreover, the E-nHAP layer features high mechanical flexibility due to its enamel-like organic-inorganic composite nanostructure. Hence, symmetric cells assembled by E-nHAP@Zn show superior stability of long-term cycling at different current densities (0.1, 0.5, 1, 5, and 10 mA cm-2). The E-nHAP@Zn∥E-nHAP@Cu cell exhibits an outstanding cycling life with high Coulombic efficiency of 99.8% over 1000 cycles. Notably, the reversibility of full cell based on CNT/MnO2 cathode can be effectively enhanced. This work shows the potential of drawing inspiration from biological nanostructure in nature to develop stable metal electrodes.

Anomalous Phase Behaviors of Monolayer NaCl Aqueous Solutions Induced by Effective Coulombic Interactions within Angstrom-Scale Slits.

Interests in subnanofluidic devices have called for molecular dynamics (MD) simulation studies of the thermodynamic behavior of monolayer salt solution within angstrom-scale slits. However, it still remains a grand challenge to accurately describe the Coulombic interactions by incorporating the effects of charge transfer and electronic dielectric screening. Herein, by using the electronic continuum model, where the effective ion charges are fine-tuned with a scaling factor of λ, we present simulation evidence that the effective Coulombic interactions among Na+/Cl- ions can strongly affect the behavior of monolayer ionic aqueous solution. Our microsecond-scale MD simulations show that only the counterions with moderate effective charges (0.3 ≤ λ ≤ 0.8) can dissolve in monolayer water, whereas the high effective charges (λ ≥ 0.85) induce ions to assemble into monolayer nanocrystals, and ions with the low effective charges (λ ≤ 0.2) exhibit gas-like nanobubble. These findings could provide deeper insights into the physical chemistry behind subnanofluidic iontronic devices.

High-Voltage and Super-Stable Aqueous Sodium-Zinc Hybrid Ion Batteries Enabled by Double Solvation Structures in Concentrated Electrolyte.

Aqueous sodium-zinc hybrid ion batteries are attracting extensive attention due to high energy density, low cost, and environmental friendliness. Unfortunately, there are still some drawbacks associated with the low voltage and cycle performance degradation that limit their practical application. Here, a concentrated aqueous electrolyte with solvation-modulated Zn2+ is reported that reduces the hydrogen evolution reaction on the surface of Zn metal, avoiding the generation of ZnO and uneven deposition. Accordingly, the Zn anode exhibits 1600 h Zn plating/stripping and ≈99.96% Coulombic efficiency after 700 cycles. In addition, solvation-modulated Na+ promotes the excellent structural stability of zinc hexacyanoferrate (ZnHCF) due to the rhombohedral-rhombohedral rather than rhombohedral-cubic phase transition. A ZnHCF//Zn full cell delivers an average voltage of 1.76 V and 98% capacity retention after 2000 cycles at 5 C rates.

An Overcrowded Water-Ion Solvation Structure for a Robust Anode Interphase in Aqueous Lithium-Ion Batteries.

The water-in-salt electrolyte (WISE) features intimate interactions between a cation and anion, which induces the formation of an anion-derived solid electrolyte interphase (SEI) and expands the aqueous electrolyte voltage window to >3.0 V. Although further increasing the salt concentration (even to >60 molality (m)) can gradually improve water stability, issues about cost and practical feasibility are concerned. An alternative approach is to intensify ion-solvent interactions in the inner solvation structure by shielding off outward electrostatic attractions from nearby ions. Here, we design an "overcrowded" electrolyte using the non-polar, hydrogen-bonding 1,4-dioxane (DX) as an overcrowding agent, thereby achieving a robust LiF-enriched SEI and wide electrolyte operation window (3.7 V) with a low salt concentration (<2 m). As a result, the electrochemical performance of aqueous Li4Ti5O12/LiMn2O4 full cells can be substantially improved (88.5% capacity retention after 200 cycles, at 0.57 C). This study points out a promising strategy to develop low-cost and stable high-voltage aqueous batteries.

Two-dimensional monolayer salt nanostructures can spontaneously aggregate rather than dissolve in dilute aqueous solutions.

It is well known that NaCl salt crystals can easily dissolve in dilute aqueous solutions at room temperature. Herein, we reported the first computational evidence of a novel salt nucleation behavior at room temperature, i.e., the spontaneous formation of two-dimensional (2D) alkali chloride crystalline/non-crystalline nanostructures in dilute aqueous solution under nanoscale confinement. Microsecond-scale classical molecular dynamics (MD) simulations showed that NaCl or LiCl, initially fully dissolved in confined water, can spontaneously nucleate into 2D monolayer nanostructures with either ordered or disordered morphologies. Notably, the NaCl nanostructures exhibited a 2D crystalline square-unit pattern, whereas the LiCl nanostructures adopted non-crystalline 2D hexagonal ring and/or zigzag chain patterns. These structural patterns appeared to be quite generic, regardless of the water and ion models used in the MD simulations. The generic patterns formed by 2D monolayer NaCl and LiCl nanostructures were also confirmed by ab initio MD simulations. The formation of 2D salt structures in dilute aqueous solution at room temperature is counterintuitive. Free energy calculations indicated that the unexpected spontaneous salt nucleation behavior can be attributed to the nanoscale confinement and strongly compressed hydration shells of ions.

Formation of porous ice frameworks at room temperature.

Bulk crystalline ices with ultralow densities have been demonstrated to be thermodynamically metastable at negative pressures. However, the direct formation of these bulk porous ices from liquid water at negative pressures is extremely challenging. Inspired by approaches toward porous media based on host-guest chemistry, such as metal-organic frameworks and covalent organic frameworks, we herein demonstrate via molecular dynamics simulations that a class of ultralow-density porous ices with upright channels can be formed spontaneously from liquid water at 300 K with the assistance of carbon nanotube arrays. We refer to these porous ice polymorphs as water oxygen-vertex frameworks (WOFs). Notably, our simulations revealed that the liquid-WOF phase transition is first-order and occurs at room temperature. All the WOFs exhibited the unique structural feature that they can be regarded as assemblies of nanoribbons of hexagonal bilayer ice (2D ice I) at their armchair or zigzag edges. Based on density functional theory calculations, a comprehensive phase diagram of the WOFs was constructed considering both the thermodynamic and thermal stabilities of the porous ices at negative pressures. Like other types of porous media, these WOFs may be applicable to gas storage, purification, and separation. Moreover, these biocompatible porous ice networks may be exploited as medical-related carriers.

First-Principles Molecular Dynamics Simulations of the Spontaneous Freezing Transition of 2D Water in a Nanoslit.

As with bulk ices, two-dimensional (2D) ices exhibit diverse crystalline structures, and the majority of these 2D structures have been predicted based on classical molecular dynamics (MD) simulations. Here, the spontaneous freezing transition of 2D liquid water within hydrophobic nanoslits is demonstrated for the first time using first-principles MD simulations. Various 2D ices are observed under different lateral pressure and temperature conditions. Notably, the liquid water confined to a 6.0 Å-wide nanoslit can spontaneously freeze into a monolayer ice consisting of an array of zigzag water chains at 2.5 GPa and 250 K. Moreover, within an 8.0 Å-wide nanoslit and at 4.0 GPa and 300 K, a previously unreported bilayer ice forms spontaneously that has a structure resembling that of the double surface layers of bulk ice-VII. Both 2D crystalline ices do not obey the ice rule, suggesting first-principles simulation can access a certain phase space that is not easily approached using classical simulations.

Computational Prediction of Novel Ice Phases: A Perspective.

Although computational prediction of new ice phases is a niche field in water science, the scientific subject itself is representative of two important areas in physical chemistry, namely, statistical thermodynamics and molecular simulations. The prediction of a variety of novel ice phases has also attracted general public interest since the 1980s. In particular, the prediction of low-dimensional ice phases has gained momentum since the confirmation of a number of low-dimensional "computer ice" phases in the laboratory over the past decade. In this Perspective, the research advancements in computational prediction of novel ice phases over the past few years are reviewed. Particular attention is placed on new ice phases whose physical properties or dimensional structures are distinctly different from conventional bulk ices. Specific topics include the (i) formation of superionic ices, (ii) electrofreezing of water under high pressure and in a high external electric field, (iii) prediction of low-density porous ice at strongly negative pressure, (iv) ab initio computational study of two-dimensional (2D) ice under nanoscale confinement, and (v) 2D ices formed on a solid surface near ambient temperature without nanoscale confinement. Clearly, the formation of most of these novel ice phases demands certain extreme conditions. Ongoing challenges and new opportunities for predicting new ice phases from either classical molecular dynamics simulation or high-level ab initio computation are discussed.

Direct observation of 2-dimensional ices on different surfaces near room temperature without confinement.

Water-solid interfaces play important roles in a wide range of fields, including atmospheric science, geochemistry, electrochemistry, and food science. Herein, we report simulation evidence of 2-dimensional (2D) ice formation on various surfaces and the dependence of the 2D crystalline structure on the hydrophobicity and morphology of the underlying surface. Contrary to the prevailing view that nanoscale confinement is necessary for the 2D liquid-to-bilayer ice transition, we find that the liquid-to-bilayer hexagonal ice (BHI) transition can occur either on a model smooth surface or on model fcc-crystal surfaces with indices of (100), (110), and (111) near room temperature. We identify a critical parameter that characterizes the water-surface interaction, above which the BHI can form on the surface. This critical parameter increases as the temperature increases. Even at temperatures above the freezing temperature of bulk ice (Ih ), we find that BHI can also form on a superhydrophilic surface due to the strong water-surface interaction. The tendency toward the formation of BHI without confinement reflects a proper water-surface interaction that can compensate for the entropy loss during the freezing transition. Furthermore, phase diagrams of 2D ice formation are described on the plane of the adsorption energy versus the fcc lattice constant (Eads-afcc), where 4 monolayer square-like ices are also identified on the fcc model surfaces with distinct water-surface interactions.

Room temperature electrofreezing of water yields a missing dense ice phase in the phase diagram.

Water can freeze into diverse ice polymorphs depending on the external conditions such as temperature (T) and pressure (P). Herein, molecular dynamics simulations show evidence of a high-density orthorhombic phase, termed ice χ, forming spontaneously from liquid water at room temperature under high-pressure and high external electric field. Using free-energy computations based on the Einstein molecule approach, we show that ice χ is an additional phase introduced to the state-of-the-art T-P phase diagram. The χ phase is the most stable structure in the high-pressure/low-temperature region, located between ice II and ice VI, and next to ice V exhibiting two triple points at 6.06 kbar/131.23 K and 9.45 kbar/144.24 K, respectively. A possible explanation for the missing ice phase in the T-P phase diagram is that ice χ is a rare polarized ferroelectric phase, whose nucleation/growth occurs only under very high electric fields.