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Prevailing Li‐rich layered oxide cathodes (LLOs) possessing with polycrystalline morphology suffer from unsatisfactory cyclic stability due to serious structural failures including irreversible oxygen release, phase transformation, and microcrack, further limiting its commercial application for high‐energy‐density lithium‐ion batteries. Herein, single‐crystallization combining with a simple boric acid treatment strategy is applied to robust the stability of lattice structure for achieving the reversible oxygen anionic redox of LLOs. The obtained single‐crystal LLOs display less grain boundaries and excellent mechanical stability, contributing to suppress the accumulation of lattice strain and microcracks. Additionally, the induced surface Li2B4O7 with spinel phase coating and bulk gradient B doping after boric acid treatment significantly inhibit the irreversible oxygen release and enhance the stability of lattice structure. Besides, lattice structure regulation also boosts the Li+ diffusion kinetics due to the existence of oxygen defects, fast Li‐ion conductive coating, and enlarged Li+ layer spacing. As a result, the modified SC‐LLOs showcase superior cyclic stability with a capacity retention of 87.42% after 300 cycles at 1 C and excellent rate performance with a high capacity of 144.9 mAh g−1 at 5 C. This work provides some significant references to strengthen the structural stability of single‐crystal LLOs with long‐term cyclic capability via lattice engineering. [ABSTRACT FROM AUTHOR]

In this study, single-crystalline and poly-crystalline CrCoNi alloys are utilized as model systems to analyze the distinct roles of each GB and interstitial lattice sites. To effectively reveal hydrogen behavior, both electrochemical and gaseous hydrogen pre-charging methods are applied. Hydrogen content, diffusivity, and trap behaviors are quantified using thermal desorption analysis and hydrogen permeation tests, which determines (1) changes in hydrogen behavior depending on the presence of GB and (2) alterations in hydrogen behavior depending on lattice crystallographic orientation. The results indicate that GB and interstitial lattice sites exhibit comparable binding energies for hydrogen trapping. However, the introduction of GB alters the primary trapping sites from interstitial lattice sites to GB. In this case, the hydrogen content in the poly-crystalline alloy is determined by the trap site density of the primary trapping site. On the other hand, in the single-crystalline alloy, where only interstitial lattice sites exist, the crystallographic orientation of the hydrogen-charged plane is an important variable that determines hydrogen content and hydrogen diffusivity. Such insights contribute to a deeper understanding of hydrogen behavior within a more intricate microstructure, suggesting the alloy design approach to enhance resistance to HE.

[Display omitted] The voltage decay of Li-rich layered oxide cathode materials results in the deterioration of cycling performance and continuous energy loss, which seriously hinders their application in the high-energy–density lithium-ion battery (LIB) market. However, the origin of the voltage decay mechanism remains controversial due to the complex influences of transition metal (TM) migration, oxygen release, indistinguishable surface/bulk reactions and the easy intra/inter-crystalline cracking during cycling. We investigated the direct cause of voltage decay in micrometer-scale single-crystal Li 1.2 Mn 0.54 Ni 0.13 Co 0.13 O 2 (SC-LNCM) cathode materials by regulating the cut-off voltage. The redox of TM and O2− ions can be precisely controlled by setting different voltage windows, while the cracking can be restrained, and surface/bulk structural evaluation can be monitored because of the large single crystal size. The results show that the voltage decay of SC-LNCM is related to the combined effect of cation rearrangement and oxygen release. Maintaining the discharge cutoff voltage at 3 V or the charging cutoff voltage at 4.5 V effectively mitigates the voltage decay, which provides a solution for suppressing the voltage decay of Li-rich and Mn-based layered oxide cathode materials. Our work provides significant insights into the origin of the voltage decay mechanism and an easily achievable strategy to restrain the voltage decay for Li-rich and Mn-based cathode materials. [ABSTRACT FROM AUTHOR]

Benefited from its high process feasibility and controllable costs, binary-metal layered structured LiNi0.8Mn0.2O2 (NM) can effectively alleviate the cobalt supply crisis under the surge of global electric vehicles (EVs) sales, which is considered as the most promising next-generation cathode material for lithium-ion batteries (LIBs). However, the lack of deep understanding on the failure mechanism of NM has seriously hindered its application, especially under the harsh condition of high-voltage without sacrifices of reversible capacity. Herein, single-crystal LiNi0.8Mn0.2O2 is selected and compared with traditional LiNi0.8Co0.1Mn0.1O2 (NCM), mainly focusing on the failure mechanism of Co-free cathode and illuminating the significant effect of Co element on the Li/Ni antisite defect and dynamic characteristic. Specifically, the presence of high Li/Ni antisite defect in NM cathode easily results in the extremely dramatic H2/H3 phase transition, which exacerbates the distortion of the lattice, mechanical strain changes and exhibits poor electrochemical performance, especially under the high cutoff voltage. Furthermore, the reaction kinetic of NM is impaired due to the absence of Co element, especially at the single-crystal architecture. Whereas, the negative influence of Li/Ni antisite defect is controllable at low current densities, owing to the attenuated polarization. Notably, Co-free NM can exhibit better safety performance than that of NCM cathode. These findings are beneficial for understanding the fundamental reaction mechanism of single-crystal Ni-rich Co-free cathode materials, providing new insights and great encouragements to design and develop the next generation of LIBs with low-cost and high-safety performances.

For the development of optical technologies aimed at research, diagnostics and operation in a wide spectral range, the creation of new materials capable of being highly transparent and effective for transmitting electromagnetic waves in the visible, IR and THz regions is required. This article studies the properties of single crystals and two-phase ceramics based on solid solutions of the AgCl 0.25 Br 0.75 – TlCl 0.74 Br 0.26 and AgCl 0.25 Br 0.75 – TlBr 0.46 I 0.54 systems. The materials showed transparency in the range of 0.4–60.0 and 350–1500 μm (0.20–0.86 THz). With an increase in the proportion of thallium halides in the AgCl 0.25 Br 0.75 solid solutions, a shift and the transmission spectrum broadening to longer wavelengths was observed. These effects are typical for compounds with both Fm3m and Pm3 m type cubic crystal lattice. The refractive indices of the developed materials have normal wavelength dispersion and vary from 2.107 to 2.539 depending on the system and composition. The indicators for solid solutions with an intermediate composition of homogeneity regions lie within the values characteristic of boundary compositions. Based on this data a description of the index dependence by the Sellmeier equation, adapted by Fleming, was obtained. The refractive indices imaginary parts of all developed materials were 0.11*10−4–3.55*10−4, which was 2–4 times lower in comparison with other substances based on silver and thallium halides. The materials were characterized by a photostability improvement with an increase in the part of thallium halides in the solid solution, as well as with a growth in the amount of the orthorhombic phase in the case of two-phase ceramics. The materials showed low values of optical losses, as well as high functional properties. This makes single crystals and ceramics promising for transmission and fiber optics designed to operate in a wide spectral range. [ABSTRACT FROM AUTHOR]

Contact resistance has become one of the main bottlenecks that hinder further improvement of mobility and integration density of organic field‐effect transistors (OFETs). Much progress has been made in reducing contact resistance by modifying the electrode/semiconductor interface and decreasing the crystal thickness, however, the development of new organic semiconductor materials with low contact resistance still faces many challenges. Here, 2,6‐bis‐phenylethynyl‐anthracene (BPEA) is found, which is a material that combines high mobility with low contact resistance. Single‐crystal BEPA OFETs with a thickness of ≈20 nm demonstrated high mobility of 4.52 cm2 V−1 s−1, contact resistance as low as 335 Ω cm, and band‐like charge transport behavior. The calculated compatibility of the EHOMO of BPEA with the work function of the Au electrode, and the decreased |EHOMO‐ΦAu| with the increase of external electric field intensity from source to gate both contributed to the efficient charge injection and small contact resistance. More intriguingly, p‐type BPEA as a buffer layer can effectively reduce the contact resistance, improve the mobility, and meanwhile inhibit the double‐slope electrical behavior of p‐channel 2,6‐diphenyl anthracene (DPA) single‐crystal OFETs. [ABSTRACT FROM AUTHOR]

Se‐functionalized small molecule acceptors (SMAs) exhibit unique advantages in constructing materials with near‐infrared absorption, but their photovoltaic performance lags behind that of S‐containing analogs in organic solar cells (OSCs). Herein, two new Se‐containing SMAs, namely Se‐EH and Se‐EHp, are designed and synthesized by regulating bifurcation site of outer alkyl chain, which enables Se‐EH and Se‐EHp to form different 3D crystal frameworks from CH1007. Se‐EH displays tighter π–π stacking and denser packing framework with smaller‐sized pore structure induced by larger steric hindrance effect of outer alkyl chain branched at 2‐position, and a higher dielectric constant of PM6:Se‐EH active layer can be obtained. OSCs based on PM6:Se‐EH achieved very high PCEs of 18.58% in binary and 19.03% in ternary devices with a high FF approaching 80% for Se‐containing SMAs. A more significant alkyl chain steric hindrance effect in Se‐EH adjusts the molecular crystallization to form a favorable nanofiber interpenetrating network with an appropriate domain size to reduce rate of sub‐ns recombination and promote balanced transport of carriers. This work provides references for further design and development of highly efficient Se‐functionalized SMAs. [ABSTRACT FROM AUTHOR]

Sulfide all-solid-state lithium batteries (SASSLBs) with a single-crystal nickel-rich layered oxide cathode (LiNixCoyMn1-x-yO2, x ​≥ ​0.8) are highly desirable for advanced power batteries owing to their excellent energy density and safety. Nevertheless, the cathode material's cracking issue and its severe interfacial problem with sulfide solid electrolytes have hindered the further development. This study proposes to employ surface modification engineering to produce B-NCM cathode materials coated with boride nanostructure stabilizer in situ by utilizing NCM encapsulated with residual lithium. This approach enhances the electrochemical performance of SASSLBs by effectively inhibiting electrochemical-mechanical degradation of the NCM cathode material on cycling and reducing deleterious side reactions with the solid sulfide electrolyte. The B-NCM/LPSCl/Gr SASSLBs demonstrate impressive cycling stability, retaining 84.19 ​% of its capacity after 500 cycles at 0.2 ​C, which represents a 30.13 ​% increase vs. NCM/LPSCl/Gr. It also exhibits a specific capacity of 170.4 mAh/g during its first discharge at 0.1 ​C. This work demonstrates an effective surface engineering strategy for enhancing capacity and cycle life, providing valuable insights into solving interfacial problems in SASSLBs.

Nickel‐rich layered oxides are a class of promising cathodes for high‐energy‐density lithium‐ion batteries (LIBs). However, their structural instability derived from crystallographic planar gliding and microcracking under high voltages has significantly hindered their practical applications. Herein, resurfacing engineering for single‐crystalline LiNi0.83Co0.07Mn0.1O2 (SNCM) cathode is undertaken. A passivation shell, comprising a surface fast ion conductor Li1.25Al0.25Ti1.5O4 (LATO) layer and a near‐surface confined cation hybridization region, is established through co‐infiltrating Al and Ti into SNCM, which can profoundly improve structural stability. Compelling evidences show that high‐conductivity LATO‐overcoat facilitates Li+ conduction and resists electrolyte attack. The introduction of strong Al─O bonds and resurfacing regions stabilize bulk and near‐surface lattice oxygen respectively during cycling, thus hindering the formation of oxygen vacancies and the occurrence of detrimental phase transformations, ultimately suppressing the crystallographic planar gliding and nanocracking. Subsequently, the modified SNCM drastically outperforms the baseline SNCM, exhibiting an ultrahigh 88.9% retention rate of original capacity at 1.0C after 400 cycles, and a discharge capacity of 146.8 mAh g−1 with a 92.6% capacity retention rate after 200 cycles at 5.0C within a voltage window of 2.7–4.3 V. The promising performance demonstrated by the multifunctional surface coating highlights a new way to stabilize Ni‐rich cathodes for LIBs. [ABSTRACT FROM AUTHOR]

Single‐crystal Ni‐rich LiNi1−x−yCoxMnyO2 (NCM) cathodes have garnered widespread attention in the lithium‐ion battery community due to their unique advantages in mechanical performance and their ability to minimize interfacial electrochemical side reactions. The synthesis of single‐crystal materials with monodisperse and appropriate size, minimal lattice defects, and highly ordered structures is the key for high‐performance batteries. However, achieving this goal poses challenges due to the lack of in‐depth understanding regarding specific experimental parameters and the solid reaction mechanism during the synthesis process. In this review, the aim is to provide an in‐depth analysis of the critical process parameters involved in the synthesis and their impact on crystal morphology, structure, and electrochemical performance. Consequently, the first section focuses on the effect of the precursor morphology, lithium salt, atmosphere, and sintering procedure. In the second section, the study delves into an in‐depth discussion of the solid reaction and crystal growth mechanism. Lastly, it is concluded by highlighting the prospects and challenges associated with the synthesis and application of single‐crystal Ni‐rich NCM cathodes. [ABSTRACT FROM AUTHOR]

Ni‐rich layered oxides are promising lithium‐ion batteries (LIBs) cathode materials for their high reversible capacity, but they suffer from fast structural degradation during cycling. Here, we report the Ce/Gd incorporated single‐crystalline LiNi0.83Co0.07Mn0.10O2 (SC‐NCM) cathode materials with significantly enhanced cycling stability. The Gd ions are adequately incorporated in SC‐NCM while Ce ions are prone to aggregate in the outer surface, resulting in the formation of a high‐entropy zone in the near‐surface of SC‐NCM, including a Gd doped LiCeO2 (LCGO) shell and Ce/Gd dopant‐concentrated layer. The high‐entropy zone can effectively inhibit the oxygen evolution and prevent the formation of oxygen vacancies. Meanwhile, it leads to a greatly improved H2‐H3 phase transformation reversibility and mitigated stress/strain caused by Li‐ion extraction/insertion during (de)lithiation process. The synergetic effects of reduced oxygen vacancies concentration and mitigated stress/strain can effectively prevent the in‐plane migration of TM ions, lattice planar gliding as well as the formation of intragranular nanocracks. Consequently, Ce/Gd incorporated SC‐NCM (SC‐NCM@CG2) delivers a high initial discharge specific capacity of 219.7 mAh g−1 at 0.1 C and an excellent cycling stability with a capacity retention of 90.2 % after 100 cycles at 1.0 C. [ABSTRACT FROM AUTHOR]

Abstract Contact resistance has become one of the main bottlenecks that hinder further improvement of mobility and integration density of organic field‐effect transistors (OFETs). Much progress has been made in reducing contact resistance by modifying the electrode/semiconductor interface and decreasing the crystal thickness, however, the development of new organic semiconductor materials with low contact resistance still faces many challenges. Here, 2,6‐bis‐phenylethynyl‐anthracene (BPEA) is found, which is a material that combines high mobility with low contact resistance. Single‐crystal BEPA OFETs with a thickness of ≈20 nm demonstrated high mobility of 4.52 cm2 V−1 s−1, contact resistance as low as 335 Ω cm, and band‐like charge transport behavior. The calculated compatibility of the EHOMO of BPEA with the work function of the Au electrode, and the decreased |EHOMO‐ΦAu| with the increase of external electric field intensity from source to gate both contributed to the efficient charge injection and small contact resistance. More intriguingly, p‐type BPEA as a buffer layer can effectively reduce the contact resistance, improve the mobility, and meanwhile inhibit the double‐slope electrical behavior of p‐channel 2,6‐diphenyl anthracene (DPA) single‐crystal OFETs.

Vanadium (IV) chalcogenide materials are of increasing interest for use in catalysis and energy conversion-related applications. Since no ternary compounds are yet known in the V–Se–Te system, we studied ternary VwSeyTe2−y (w = 1.10, 1.13; y = 0.42, 0.72) phases crystallizing in space group P 3 ¯ m1 (no. 164). Two single-crystal specimens with differing compositions of a solid solution were obtained using the ceramic method. All products were characterized by either single-crystal or powder X-ray diffraction. The lattice parameters increase with rising tellurium content in accordance with the larger ionic radius of the tellurium anion compared to selenium. The chemical compositions were confirmed by energy-dispersive X-ray spectroscopy. Furthermore, magnetic measurements mostly revealed antiferromagnetic properties. Simultaneous differential scanning calorimetry/thermogravimetric analyses in a nitrogen atmosphere showed endothermic decomposition accompanied by the formation of VN. The decomposition of VSe and VTe was observed in an argon atmosphere. The results of this work can serve as a basis for the synthesis of new phases in the V–Se–Te and related vanadium chalcogenide systems. [ABSTRACT FROM AUTHOR]

Organic solar cells (OSCs) have garnered significant attention as a novel photovoltaic technology and have been extensively investigated. In recent years, OSCs have made rapid strides in power conversion efficiency (PCE), demonstrating their significant potential in practical applications. In addition to high PCE, the practical application of OSCs demands a prolonged operating lifespan. The rational design of materials and devices to achieve efficient and stable OSCs is pivotal. This feature article presents a thorough analysis of our group's studies on enhancing efficiency and stability through material and device design. We introduce a range of exceptional chlorine-mediated organic photovoltaic materials and systematically summarize chlorine atom (Cl) induced effects on energy levels, molecular stacking, active layer film morphology and photovoltaic performance. Furthermore, the use of single-crystal diffraction technology allows for a comprehensive understanding of inter-molecular packing and interaction at the molecular level. A series of highly efficient non-fullerene acceptors (NFAs) with three-dimensional (3D) network packing structures are developed and discussed. Subsequently, based on efficient 3D network brominated NFAs, the studies on polymer and oligomer acceptor materials are carried out and achieve efficient and stable OSCs. In addition to materials design, the development of the "quasiplanar heterojunction" (Q-PHJ) based OSC device also plays an important role in achieving superior efficiency and stability. These design experiences of materials and devices hope to provide valuable guidance for the development of efficient and stable OSCs. [ABSTRACT FROM AUTHOR]

Semiconductor metal oxides are widely used in the field of wave absorption because of their easily tunable dielectric properties. Doping or modulating the morphology has been demonstrated to be an effective method to improve the microwave (MW) absorbing performance of semiconductor metal oxides. In this study, Ce-doped SnO 2 was prepared by a simple and effective coprecipitation method. Single-crystal SnO 2 nanorods were generated during the doping process and the size of the nanorods could be controlled by modifying the concentration of Ce. The presence of nanorods greatly enhances the MW absorbing performance: when the doping molar ratio is 3%, the minimum reflection loss of the absorber is −77.91 dB at a frequency of 13.79 GHz with a thickness of 1.6 mm and the maximum effective absorbing bandwidth is 4.47 GHz at a thickness of 1.5 mm. Excellent MW absorbing performance of Ce-doped SnO 2 is attributed to its excellent impedance matching and interfacial polarization. [ABSTRACT FROM AUTHOR]

Coating modification of single-crystal materials was studied to improve the electrochemical properties of the materials by suppressing the electrode/electrolyte side reactions. The commercial LiNi 0·6 Co 0·1 Mn 0·3 O 2 was used as the base material and Sm 2 O 3 coating was applied on its surface. The Sm 2 O 3 -coated NCM613 single-crystal material was synthesized. The structure and morphology of the electrode materials were characterized by XRD, FESEM, and TEM. The results showed that Sm 2 O 3 was successfully coated on the surface of the particles without damaging the original structure of the material. Meanwhile, the lithium ions diffusion kinetics of the material was analyzed by cyclic voltammetry. The results show that the coated cathode material has a more excellent lithium ions diffusion coefficient, which provides a kinetic basis for charging and discharging the battery at high voltage. At 25 °C, 3.0−4.5 V, and 1 C current density, the capacity retention of the coated cathode material after 100 cycles was 87.5% (182.8−159.9 mAh g−1), which was much higher than that of the original material at 77% (177−136.3 mAh g−1). SEM and other characterizations of the electrode sheets after cycling showed that the Sm 2 O 3 coating layer effectively prevented the direct contact between the cathode material and the electrolyte, which played a positive role in suppressing the occurrence of side reactions, and inhibits the formation of microcracks during the cycling process. In general, this method contributed to the stability of the electrode/electrolyte interface and electrochemical performance. [ABSTRACT FROM AUTHOR]

Narrow-band photodetectors based on halide perovskite have recently attracted significant attention due to their exceptional narrow-band detection performance and tunable absorption peaks covering a wide optical range. In this work, we report mixed-halide CH3NH3PbCl x Br3– x single crystal-based photodetectors have been fabricated, where the Cl/Br ratios were varied (3:0, 10:1, 5:1, 1:1, 1:7, 1:14 and 0:3). Vertical and parallel structures devices were fabricated which exhibited ultranarrow spectral responses under bottom illumination, with a full-width at half-maximum less than 16 nm. The observed performance can be ascribed to the unique carrier generation and extraction mechanisms within the single crystal under short and long wavelength of illumination. These findings offer valuable insights into the development of narrow-band photodetectors that do not necessitate the use of filters and hold tremendous potential for a diverse array of applications. [ABSTRACT FROM AUTHOR]

Diamond-based transistors have been considered as one of the best choices due to the numerous advantages of diamond. However, difficulty in the growth and fabrication of diamond needs to be addressed. In this paper, high quality diamond film with an atomically flat surface was grown by microwave plasma chemical vapor deposition. High growth rate, as much as 7 μm/h, has been acquired without nitrogen doping, and the root mean square (RMS) of the surface roughness was reduced from 0.92 nm to 0.18 nm by using a pre-etched process. H-terminated diamond MOSFETs were fabricated on a high-quality epitaxial diamond layer, of which the saturated current density was enhanced. The hysteresis of the transfer curve and the shift of the threshold voltage were significantly reduced as well. [ABSTRACT FROM AUTHOR]

[Display omitted] Transition metal-based selenides (TMSe) are considered as efficient pre-electrocatalysts towards oxygen evolution reaction (OER). However, the key factor in determining the surface reconstruction of TMSe under OER condition is not yet clear. Herein, we uncover that the crystallinity of TMSe will obviously impact the conversion degree from TMSe to transition metal oxyhydroxides (TMOOH) during OER. A novel single-crystal (NiFe) 3 Se 4 nano-pyramid array grown on NiFe foam is fabricated by a facile one-step polyol process, which exhibits an excellent OER activity and stability, only requiring 170 mV to reach a current density of 10 mA cm−2 and can sustain for more than 300 h. In situ Raman spectrum studies reveals that the single-crystal (NiFe) 3 Se 4 is partially oxidized on its surface during OER, generating a dense heterostructure of (NiFe)OOH/(NiFe) 3 Se 4. Benefiting from the in situ formed heterointerface, the adsorption of OER intermediates on Ni active sites calculated by density functional theory (DFT) analysis is optimized, leading to the reduced energy barrier, which accounts for the enhanced intrinsic activity. This work not only reports a novel single-crystal (NiFe) 3 Se 4 nano-pyramid array electrocatalyst with high-efficient OER performance, but also gains a deep insight into the role of the crystallinity of TMSe on the surface reconstruction during OER. [ABSTRACT FROM AUTHOR]

It is well known that sulfonamide derivatives, through exchange of different functional groups without modification of the –S(O)2N(H)– function, can exhibit a wide variety of pharmacological activities. In addition, some metal complexes of these ligands have been prepared to promote rapid healing of burns in humans and animals, for example, the complex of Zn(ii) sulfadiazine. Their effectiveness does not depend solely on the slow release of the metal ion, but rather strongly on the nature of the material to which the metal is bound. Given the ability of sulfonamide derivatives to coordinate with metal atoms in different ways, considerable interest in the synthesis and structural aspects of new complexes has arisen. These results confirm that the significant chemical capacity of sulfonamides to act as ligands is based on the acidity of its –S(O)2N(H)– function, which gives a donor anionic ligand, allied to the presence of atoms vicinal to nitrogen, sulfur or oxygen of the heterocyclic ring, which provide the stereochemical requirements for the realization of complexes with monodentate ligand, chelating agent or bridging ligand, providing monomeric structures, dimeric arrangements and polymers. In addition, the aromatic amino group is responsible for the chemical versatility of the sulfonamides, since it can act as a coordination site, as well as a reactive site for chemical modifications of sulfonamide complexes with very interesting biological purposes. In the present work, the synthesis and structure of a novel sulfanilamide complex: nitro (4-aminobenzenesulfonamide) zirconium was presented. Characterization of the complex was performed by infrared spectroscopic, thermogravimetric and X-ray diffraction analysis.

In this paper, single-crystal GePb films were obtained by magnetron sputtering with high substrate temperature and rapid deposition rate. The GePb films have high crystalline qualities and smooth surface. The Pb content reached 1.29% and no segregation was observed. Based on this, a GePb based p–i–n photodetector was successfully prepared. The device showed a RT dark current density of 5.83 mA cm ^−2 at −1.0 V and a cutoff wavelength of 1990 nm, which covers all communication windows. At the wavelength of 1625 nm, responsivity of the photodetector reached 0.132 A W ^−1 at −1.0 V. The device demonstrates potential application in optical communications.

With the scarcity of cobalt resources and soaring prices, the removal of cobalt from nickel-rich layered cathodes is now a priority to reduce the material costs and develop the sustainability of lithium-ion batteries (LIBs). In this work, we report a single-crystal cobalt-free LiNi0.6Mn0.4O2 (NM64) layered oxide cathode and compare it with single-crystal LiNi0.6Co0.1Mn0.3O2 (NCM613) cathode. On the one hand, NM64 exhibits competitive energy density to NCM613 and better long-term cycle stability under a high cutoff voltage of 4.5 V. Impressively, single-crystal NM64 not only could effectively suppress the microcrack formation, resulting in the excellent structural stability and long cycling lifespan even at the full delithiated state, but also, it has superior thermal stability to single-crystal NCM613, which is beneficial to achieve high operational safety of LIBs. On the other hand, due to the removal of expensive cobalt, the material cost of NM64 is only 2/3 of NCM613, which is conducive to significantly reducing the cost of LIBs. As a result, NM64 exhibits high energy density (765.27 Wh kg−1) and remarkable cycle stability (93.21 mA h g−1 after 200 cycles at a high charging voltage of 4.5 V). Considering the cost and electrochemical performance advantages, the NM64 cathode is highly expected to stand out in the next generation of cobalt-free LIBs. [ABSTRACT FROM AUTHOR]

Non‐equilibrium kinetic intermediates are usually preferentially generated instead of thermodynamic stable phases in the solid‐state synthesis of layered oxides. Understanding the inherent complexity between thermodynamics and kinetics is important for designing high cationic ordering cathodes. Single‐crystal strategy is an effective way to solve the intrinsic chemo‐mechanical problems of Ni‐rich cathodes. However, the synthesis of high‐performance single‐crystal is very challenging. Herein, the kinetic reaction path and the formation mechanism of non‐equilibrium intermediates in the synthesis of single‐crystal Co‐free Ni‐rich were explored. We demonstrate that the formation of non‐equilibrium intermediate and the electrochemical‐thermo‐mechanical failure can be effectively inhibited by driving low‐temperature topotactic lithiation. This work provides a basis for designing high‐performance single‐crystal Ni‐rich layered oxides by regulating the defective structures. [ABSTRACT FROM AUTHOR]

In this study, synthesis of CsPbBr3 perovskite single-crystals in a hydrobromic solution was investigated. Single-crystal growth experiments were conducted at the solution-nucleation border at a constant temperature or controlled cooling conditions. Working at the solutionnucleation border poses some practical difficulties such as fast precipitation. Often researchers opt to oversaturate the solution and use the supernatant after filtration. However, for conditions where the A to B ratio in the precursor solution for the formation of ABX3 is not 1, oversaturation is a waste of resources. In this work, precursor solutions were prepared for a particular working temperature and either held at a constant temperature or were gradually cooled to a predetermined temperature. The constant temperature method resulted in large and clear crystals as it reached saturation more slowly. Crystals prepared at high temperatures appeared to be more transparent with clear facets. Crystals prepared at low temperatures appeared to be opaque with multiple nuclei growth on a single-crystal. Seeding of the saturated solution resulted in larger single-crystals. The procedure adapted in this work made possible the production of clear CsPbBr3 perovskite single-crystals in a hydrobromic acid solution with sizes of up to 5 mm in only 10 days. [ABSTRACT FROM AUTHOR]

Single-crystalline transition metal dichalcogenides (TMD) films are of potential application in future electronics and optoelectronics. In this work, a halide vapor phase epitaxy (HVPE) strategy was proposed and demonstrated for the epitaxy of molybdenum diselenide (MoSe2) single crystals, in which metal halide vapors were in-situ produced by the chlorination of molybdenum as sources for the TMD growth. Combined with the epitaxial sapphire substrate, unidirectional domain alignment was successfully achieved and monolayer single-crystal MoSe2 films have been demonstrated on a 2-inch wafer for the first time. A series of characterizations ranging from centimeter to nanometer scales have been implemented to demonstrate the high quality and uniformity of the MoSe2. This work provides a universal strategy for the growth of TMD single-crystal films.

Abstract Ultrathin two‐dimensional transition‐metal dichalcogenides (TMDs) have been pursued extensively in recent years for interesting physics and application potentials. For the latter, it is essential to synthesize crystalline TMD monolayers at wafer‐scale. Here, we report growth of single‐crystalline MSe2 (M = Mo, W) monolayers at wafer‐scale by molecular‐beam epitaxy at low temperatures (200–400°C) on nominally flat Au(1 1 1) substrates. The epifilms have low intrinsic defect densities of low 1012 cm−2. The grown films have then been exfoliated and transferred onto SiO2/Si by a wet chemical process, on which some optical measurements are performed, revealing high spatial uniformity of the samples. We also establish that MSe2 grows on Au via the van der Waals epitaxy mechanism, where a continuous film extends across the whole surface, overhangs atomic‐layer steps on substrate. We identify that the growth of highly crystalline MSe2 is promoted by an enhanced interaction between Au substrate and MSe2 islands rather than by the guidance of surface steps on substrate. The latter only arrests MSe2 lateral growth if they are multilayer high. Key points MBE growth of wafer‐scale highly crystalline TMD monolayers at low‐temperature is achieved. Island‐substrate interaction is found to play a critical role in vdW epitaxy of single‐crystalline TMDs on on‐axis substates. The TMD monolayers are of high uniformity and low intrinsic defect density.

Vanadium (IV) chalcogenide materials are of increasing interest for use in catalysis and energy conversion-related applications. Since no ternary compounds are yet known in the V–Se–Te system, we studied ternary VwSeyTe2−y (w = 1.10, 1.13; y = 0.42, 0.72) phases crystallizing in space group P3¯m1 (no. 164). Two single-crystal specimens with differing compositions of a solid solution were obtained using the ceramic method. All products were characterized by either single-crystal or powder X-ray diffraction. The lattice parameters increase with rising tellurium content in accordance with the larger ionic radius of the tellurium anion compared to selenium. The chemical compositions were confirmed by energy-dispersive X-ray spectroscopy. Furthermore, magnetic measurements mostly revealed antiferromagnetic properties. Simultaneous differential scanning calorimetry/thermogravimetric analyses in a nitrogen atmosphere showed endothermic decomposition accompanied by the formation of VN. The decomposition of VSe and VTe was observed in an argon atmosphere. The results of this work can serve as a basis for the synthesis of new phases in the V–Se–Te and related vanadium chalcogenide systems.

In practical pouch cell, LiNi0.5Mn0.3Co0.2O2/artificial graphite lithium ion battery using single-crystal LiNi0.5Mn0.3Co0.2O2 (S-NMC532) as cathode can have excellent cycle performance. However, single-crystal LiNi0.5Mn0.3Co0.2O2 inevitably suffers poor rate capability compared to the polycrystalline materials. Here, we systematically studied the relationship between microstructural characteristics and the practical rate performance, as well as explored the impedance change during the cycling process in the pouch cell. This work shows that the (001) plane microtexture of the electrode surface structure is a critical barrier for rate capability. Electron backscatter diffraction (EBSD), electrochemical impedance spectroscopy (EIS) and distribution of relaxation times (DRT) are conducted on the cathodes. These analyses allow to conclude on the influence of the (001) plane microtexture on the electrode surface, which illustrates a diffusion resistance of lithium ions, and then, leading a high interfacial resistance. Thus, this work confirms the main cause of the inferior rate capability of S-NMC532 and offers guidance for developing a battery with high rate and ultralong cycling life.

Mn-based oxides are promising cathode materials for potassium-ion batteries due to their high theoretical capacity and abundant raw materials. However, the anisotropic properties of their conventional polycrystalline structures lead to insufficient rate capability and cycle life. Here, a single-crystal Mn-based layered oxide, P3′-type K0.35Mn0.8Fe0.1Cu0.1O2 (KMFCO), is designed and synthesized through a bimetallic co-induction effect and used as a cathode for potassium-ion battery. Benefiting from a unique single-crystal structure that is devoid of grain boundaries, it achieves a higher K+ transport rate and a reduced volume change during the K+ intercalation/deintercalation process. Accordingly, the single-crystal P3′-type KMFCO delivers superior rate capability (52.9 ​mAh ​g−1 at 1000 ​mA ​g−1) and excellent cycling stability (91.1% capacity retention after 500 cycles at 500 ​mA ​g−1). A full cell assembled with the P3′-type KMFCO cathode and a graphite anode also exhibits a high reversible capacity (81.2 ​mAh ​g−1 at 100 ​mA ​g−1) and excellent cycling performance (97% capacity retention after 300 cycles). The strategy of developing single-crystal materials may offer a new pathway for maintaining structural stability and improving the rate capability of layered manganese oxide cathodes and beyond.

To drive electrical vehicles for long‐range, the energy density of Li‐ion batteries must be further enhanced, which requires high‐energy cathode materials. Among them, Ni‐rich LiNixMnyCo1−x–yO2 (x > 0.5, NMC) is one of the most promising candidates. However, traditional poly‐crystal (PC) NMC materials, whose particles are secondary clusters consisting of many primary crystalline particles, are susceptible to pulverization along the inter grain/particle boundaries, resulting in poor cycle stability. Recently, single crystal (SC)‐NMC cathodes are proposed as they are believed to have several merits such as high structural integrity, lower interface with electrolyte, and potentially better energy storage performance. Nevertheless, several queries, such as the merits of SC structure and the mechanism for their structure degradation, are still controversial and required to be addressed. Herein, the synthesis parameters, properties, energy storage as well as safety of SC‐ and PC‐NMC cathodes with various Ni contents are critically reviewed, for clarifying the merits and drawbacks of SC. Furthermore, the study focuses on the recent advances of insight mechanisms and strategies for stabilizing the structure/interface by doping, morphology engineering, surface coating, and composition tailoring. The remaining challenges, safety concerns, and perspectives to enhance the electrochemical performance of SC‐NMC cathodes for electric vehicle application are followed. [ABSTRACT FROM AUTHOR]

The booming electric vehicle industry continues to place higher requirements on power batteries related to economic-cost, power density and safety. The positive electrode materials play an important role in the energy storage performance of the battery. The nickel-rich NCM (LiNixCoyMnzO2 with x + y + z = 1) materials have received increasing attention due to their high energy density, which can satisfy the demand of commercial-grade power batteries. Prominently, single-crystal nickel-rich electrodes with s unique micron-scale single-crystal structure possess excellent electrochemical and mechanical performance, even when tested at high rates, high cut-off voltages and high temperatures. In this review, we outline in brief the characteristics, problems faced and countermeasures of nickel-rich NCM materials. Then the distinguishing features and main synthesis methods of single-crystal nickel-rich NCM materials are summarized. Some existing issues and modification methods are also discussed in detail, especially the optimization strategies under harsh conditions. Finally, an outlook on the future development of single-crystal nickel-rich materials is provided. This work is expected to provide some reference for research on single-crystal nickel-rich ternary materials with high energy density, high safety levels, long-life, and their contribution to sustainable development. [ABSTRACT FROM AUTHOR]

Due to their exceptional properties, the study of hybrid perovskite (HyP) structures and applications dominate current photovoltaic prospects. Methylammonium lead tri-iodide perovskite (MAPI) is the model compound of the HyP class of materials that, in a few years, achieved, in photovoltaics, a power conversion efficiency of 25%. The attention on HyP has recently moved to large single crystals as emerging candidates for photovoltaic application because of their improved stability and optoelectronic properties compared to polycrystalline films. To control the quality and symmetry of the large MAPI single crystals, we proposed an original method that consisted of adding short-chain carboxylic acids to the inverse temperature crystallization (ICT) of MAPI in γ-butyrolactone (GBL). The crystals were characterized by single-crystal X-ray diffraction (SC-XRD), X-ray powder diffraction (XRPD) and Raman spectroscopy. Based on SC-XRD analysis, MAPI crystals grown using acetic and trifluoroacetic acids adopt a tetragonal symmetry "I4cm". MAPI grown in the presence of formic acid turned out to crystallize in the orthorhombic "Fmmm" space group demonstrating the acid's effect on the crystallization of MAPI. [ABSTRACT FROM AUTHOR]

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Compared with the polycrystal (PC) Ni‐rich cathode materials, the single‐crystal (SC) counterpart displayed excellent structural stability, high reversible capacity and limited voltage decay during cycling, which received great attention from academics and industry. However, the origin of fascinating high‐voltage stability within SC is poorly understood yet. Herein, we tracked the evolution of phase transitions, in which the destructive volume change and H3 phase formation presented in PC, are effectively suppressed in SC when cycling at a high cut‐off voltage of 4.6 V, further clarifying the origin of high‐voltage stability in SC cathode. Moreover, SC electrode displayed crack‐free morphology, and excellent electrochemical stability during long‐term cycling, whereas PC suffered severe capacity and voltage fade because of the spinel‐like phase, decoding the failure mechanisms of PC and SC during cycling at high cut‐off voltages. This finding provides universal insights into high‐voltage stability and failure mechanisms of layered Ni‐rich cathode materials. [ABSTRACT FROM AUTHOR]

Single crystals of a novel sodium–magnesium boride silicide, Na3MgB37Si9 [a = 10.1630 (3) Å, c = 16.5742 (6) Å, space group R\overline{3}m (No. 166)], were synthesized by heating a mixture of Na, Si and crystalline B with B2O3 flux in Mg vapor at 1373 K. The Mg atoms in the title compound are located at an interstitial site of the Dy2.1B37Si9-type structure with an occupancy of 0.5. The (001) layers of B12 icosahedra stack along the c-axis direction with shifting in the [–a/3, b/3, c/3] direction. A three-dimensional framework structure of the layers is formed via B—Si bonds and {Si8} units of [Si]3—Si—Si—[Si]3.

Obtaining large ingots of refractory metals with a single-crystal structure is still a difficult technical task. Large-sized tungsten ingots up to 15 cm cross-section can be obtained at rates of 17...70 mm/min using the technology of additive plasma-induction layer-by-layer growth. The most single-crystalline repeated structure of the tungsten ingot was obtained at 26 mm/min. Some deterioration in the structure of the ingot is associated with a technological change in the rate of surfacing and technical pauses. Volumetric single-crystallinity in the layers of the tungsten ingot is confirmed by research with such analytical criteria as the misorientation angle of the subgrain structure is less than 2°, the deviations in growth directions specified by the primary single-crystal base (seed) not exceeding 0,053° according to reflection Laue, and the volumetric repeatability of physical and mechanical properties. • Single-crystal tungsten ingots of unique-sized 15 cm diameter can be obtained using an additive plasma-induction growth. • Technology includes the primary seed forming, which provides repeatability in the next layers during an additive process. • <2° sub grain misorientation angle and the volumetric repeatability of the mechanical properties confirm layers similarity. • Obtaining refractory metal ingots with single-crystal layers is a difficult task but are in demand by high-tech industries. [ABSTRACT FROM AUTHOR]

We studied the orientation-dependent dynamic properties and plastic deformation mechanisms in single-crystal austenitic FeCr18Ni12.5 stainless steel shocked to peak stresses ranging 3.8-12.0 GPa. The 〈 110 〉 and 〈 111 〉 principal Hugoniots generally match that of polycrystalline 304L stainless steel, but the 〈 100 〉 Hugoniot exhibits lower shock velocities and comprises two distinct regions. The Hugoniot elastic limits (HELs) and spallation strengths range 0.5-1.2 GPa and 2.2-3.8 GPa, respectively, and exhibit trends previously observed in polycrystalline steels. We generally observed the largest HELs along 〈 100 〉 and the largest spallation strengths along 〈 111 〉. Microscopy revealed larger twin and martensite fractions in the 〈 100 〉 samples, correlations in twinning and martensite prevalence with dynamic response, and orientation-dependent differences in dislocation behavior near the spallation plane. [Display omitted] [ABSTRACT FROM AUTHOR]

Single-crystal materials have high structural stability and low parasitic side reactions for nickel-rich cathodes due to the absence of grain boundaries. However, they suffer challenges such as the complex synthesis route, sluggish lithium-ion diffusion kinetics, and microcracking evolution at high voltage. Bulk co-doping of Al and Mg into the precursors is first employed by a co-precipitation method, and then the Al-Mg dual-doped single-crystal NCM811 cathode is successfully prepared using a straightforward one-step method to reduce production cost. The cycle retention of the corresponding optimized single-crystal material is notably increased by 24.36% compared to the commercial counterpart at 1 C and a high voltage of 4.5 V. Additionally, the discharge capacity at 0.1 C is improved by 4.64% compared to the commercial one with an appropriate annealing temperature and lithium salt ratio. Some advances in the synthesis approach and modification strategy for developing commercial single-crystal material are provided. [Display omitted] • One-step method is proposed to synthesize Mg-Al doped single-crystal NCM811. • Bulk Mg-Al doped precursor is first prepared using the co-precipitation method. • Dispersed single-crystal particle is obtained by an optimal sintering temperature. • Annealing procedure affects morphology and performance of single-crystal cathodes. [ABSTRACT FROM AUTHOR]

Diamond-based transistors have been considered as one of the best choices due to the numerous advantages of diamond. However, difficulty in the growth and fabrication of diamond needs to be addressed. In this paper, high quality diamond film with an atomically flat surface was grown by microwave plasma chemical vapor deposition. High growth rate, as much as 7 μm/h, has been acquired without nitrogen doping, and the root mean square (RMS) of the surface roughness was reduced from 0.92 nm to 0.18 nm by using a pre-etched process. H-terminated diamond MOSFETs were fabricated on a high-quality epitaxial diamond layer, of which the saturated current density was enhanced. The hysteresis of the transfer curve and the shift of the threshold voltage were significantly reduced as well.

[Display omitted] As an important heterogeneous catalyst, Titanium Silicalite-1 (TS-1) zeolite has been widely applied in various catalytic processes. Here, hierarchical TS-1 single-crystals were successfully synthesized by a steam-assisted crystallization strategy using hierarchically porous titanium-containing silica (Ti-NKM-5) as a precursor. Due to the presence of large mesopores (10–40 nm)， the microporous structure-directing agents penetrated the interstitial structure of silica particles, inducing the dissolution and crystallization process. During crystallization, the generated nanocrystals grew together to form a hierarchical structure. Titanium was fully incorporated into the zeolite framework, and no extra-framework anatase was formed. Compared with the traditional microporous TS-1 zeolite, the synthesized hierarchical TS-1 single-crystal exhibited superior catalytic performance in oxidative desulfurization (ODS) of dibenzothiophene (DBT) and 4, 6-dimethyl dibenzothiophene (4, 6-DMDBT) owing to the hierarchically porous and anatase-free structure. The recycling test revealed the durability of the obtained hierarchical TS-1 catalyst under moderate reaction conditions. [ABSTRACT FROM AUTHOR]

Single crystal superalloys are prone to severe plastic deformation during the precision finishing process, resulting in the recrystallization generated on the surface layer and thus weakening the high-temperature service performance. In view of the characteristics of small cutting depth and high processing consistency of stacking abrasive belt, a new-type structural hollow-sphere abrasive belt is expected to be employed in the precision machining of single crystal superalloy. Scratching tests were performed on DD6 with the specially structured hollow-sphere grain, aiming to reveal the effects of progressive abrasive wear on the recrystallization behavior of the DD6 surface. The three-dimensional fractal dimension was introduced to evaluate the wear morphology of hollow-sphere grain, and the novel evaluating indicators of recrystallization depth and area were defined to represent the recrystallization degree of DD6 under unit self-sharpness conditions. The experiment results indicated that the normal force and the wear of hollow-sphere grain were the critical factors for recrystallization. The recrystallization damage is positively correlated with the normal force, but the increase of the normal force will aggravate the wear of the abrasive grain. The degree of recrystallization damage of DD6 scratched by hollow-sphere abrasive grains at different wear stages is quite different. Moreover, when the wear morphology of the hollow-sphere grain was hemispherical, the recrystallization depth and area were controlled within 7.23 μm and 2.16 μm2 for the 20 N normal force. [ABSTRACT FROM AUTHOR]

Constructing nanoreactors with multiple active sites in well-defined crystalline mesoporous frameworks is an effective strategy for tailoring photocatalysts to address the challenging of CO 2 reduction. Herein, one-dimensional (1-D) mesoporous single-crystal TiO 2 nanorod (MS-TiO 2 -NRs, ≈110 nm in length, high surface area of 117 m 2 g -1 , and uniform mesopores of ≈7.0 nm) based nanoreactors are prepared via a droplet interface directed-assembly strategy under mild condition. By regulating the interfacial energy, the 1-D mesoporous single-crystal TiO 2 can be further tuned to polycrystalline fan- and flower-like morphologies with different oxygen vacancies (O v ). The integration of single-crystal nature and mesopores with exposed oxygen vacancies make the rod-like TiO 2 nanoreactors exhibit a high-photocatalytic CO 2 reduction selectivity to CO (95.1%). Furthermore, photocatalytic cascade nanoreactors by in situ incorporation of CuW 6 O 24 (W-Cu) clusters onto MS-TiO 2 -NRs via O v are designed and synthesized, which improved the CO 2 adsorption capacity and achieved two-step CO 2 -CO-CH 4 photoreduction. The second step CO-to-CH 4 reaction induced by W-Cu sites ensures a high generation rate of CH 4 (420.4 µmol g -1 h -1 ), along with an enhanced CH 4 selectivity (≈94.3% electron selectivity). This research provides a platform for the design of mesoporous single-crystal materials, which potentially extends to a range of functional ceramics and semiconductors for various applications., (© 2024 Wiley‐VCH GmbH.)

A hitherto unknown modification of I2O5 was obtained from high-pressure/high-temperature syntheses in a Walker-type multianvil device at 8 GPa and 250 °C. HP-I2O5 crystallizes in the monoclinic crystal system in the space group P21/c (no. 14) with the unit cell parameters a = 12.0612(3) Å, b = 4.8613(2) Å, c = 6.9585(2) Å, β = 100.10(1)° (at 173 K), and four formula units per cell. The single-crystal structure data are accompanied by powder X-ray diffraction data at ambient and elevated temperatures. Furthermore, DFT calculations were carried out to investigate the phase transition between the ambient-pressure polymorph NP-I2O5 to the newly synthesized high-pressure phase., (© 2024 Wiley‐VCH GmbH.)

Single-crystal metal foils with high-index facets are currently being investigated owing to their potential application in the epitaxial growth of high-quality van der Waals film materials, electrochemical catalysis, gas sensing, and other fields. However, the controllable synthesis of large single-crystal metal foils with high-index facets remains a great challenge because high-index facets with high surface energy are not preferentially formed thermodynamically and kinetically. Herein, single-crystal nickel foils with a series of high-index facets are efficiently prepared by applying prestrain energy engineering technique, with the largest single-crystal foil exceeding 5×8 cm 2 in size. In terms of thermodynamics, the internal mechanism of prestrain regulation on the formation of high-index facets is proposed. Molecular dynamics simulation is utilized to replicate and explain the phenomenon of multiple crystallographic orientations resulting from prestrain regulation. Additionally, large-sized and high-quality graphite films are successfully fabricated on single-crystal Ni(012) foils. Compared to the polycrystalline nickel, the graphite/single-crystal Ni(012) foil composites show more than five-fold increase in thermal conductivity, thereby showing great potential applications in thermal management. This study hence presents a novel approach for the preparation of single-crystal nickel foils with high-index facets, which is beneficial for the epitaxial growth of certain two-dimensional materials., (© 2024 Wiley‐VCH GmbH.)

Compounds of the solid solution series SnTe1–xSex, derived from pristine SnSe and SnTe, are considered as thermoelectric lead-free materials. The crystal structure re-refinement of NaCl-type SnTe0.73 (2)Se0.27 (2) is based on single-crystal X-ray diffraction data and results in higher precision of the bond length [Sn—(Te,Se) = 3.0798 (3) Å] compared to a previous report on basis of powder X-ray data [Krebs & Langner (1964). Z. Anorg. Allg. Chem. 334, 37–49].

Single-crystal precursor of hybrid oxides NiO–MnCo2O4–Ni6MnO8 (SCNCM) is synthesized via an improved continuous two-step spray pyrolysis system (CTSP). This kind of mixed oxide is to be regarded as an ideal precursor for the single-crystal Ni-rich Li[Ni 0. 6 Co 0. 2 Mn 0. 2 ]O2 cathode materials (SCLNCM). The new pilot plant (30 t/a), method, and chlorate in this work could extremely improve the lengthy process, reducing segregation of metal element, excessive sintering temperature, high water consumption, non-polluting, and production efficiency of the SCLNCM. The resulting SCLNCM powders have a type of fine particle size and porous structure with a typical α -NaFeO2 lamellar structure. It also has a type of better cyclic stability, safety, rate capability, crystallinity, and surface area than polycrystalline cathode materials. It delivers an initial discharge capacity of 184 mAh/g at 0.1 C (18 mA/g) with a capacity retention of 91% after 100 cycles in the voltage window of 2.8–4.3 V. [ABSTRACT FROM AUTHOR]