Zero Linear Compressibility in Nondense Borates with a “Lu‐Ban Stool”‐Like Structure

Discovering materials that exhibit zero linear compressibility (ZLC) behavior under hydrostatic pressure is extremely difficult. To date, only a handful of ZLC materials have been found, and almost all of them are ultrahard materials with densified structures. Here, to explore ZLC in nondense materials, a structural model analogous to the structure of the “Lu‐Ban stool,” a product of traditional Chinese woodworking invented 2500 years ago, is proposed. The application of this model to borates leads to the discovery of ZLC in AEB₂O₄ (AE = Ca and Sr) with the unique “Lu‐Ban stool”‐like structure, which can obtain a subtle mechanical balance between pressure‐induced expansion and contraction effects. Coupled with the very wide ultraviolet transparent windows, the ZLC behavior of AEB₂O₄ may result in some unique but important applications. The applications of the “Lu‐Ban stool” model open a new route for pursuing ZLC materials in nondense structural systems.     

Prüfung der mechanischen Eigenschaften von “Quenching und Partitioning”‐Gefügen mit berührungsloser Dehnungsmessung

The “Quenching and Partitioning” (“Q&P”) concept was designed to fill the gap between the first and second generation of Advanced High Strength Steels (AHSS). It aims at a multiphase microstructure of retained austenite in a matrix of carbon depleted martensite. The martensitic components enhance the strength properties. The ductility is improved by the TRIP effect. This work investigates the “quenching and partitioning” response of a nickel and silicium alloyed TRIP steel. After “quenching and partitioning” processing the mechanical properties are evaluated by tensile testing. An adapted specimen geometry and the contact free measurement of the elongation by a laser speckle system are used. The mechanical properties of the “quenching and partitioning” microstructure are compared to the fully martensitic state and reviewed with respect to published data. Additional tests are stopped after a well defined plastic deformation. Subsequently the retained austenite fraction is measured magnetically in the test length. As a result the TRIP effect can be evaluated. The “quenching and partitioning” processing leads to tensile strengths of around 1300 MPa at elongations of more than 10 %. The martensitic microstructure exhibits a higher tensile strength and lower elongation values. The decreasing fraction of retained austenite with plastic deformation implies the TRIP effect. Comparable mechanical properties are reported in the published literature. The proposed method of annealing and adapted testing shows effective for the investigation of sophisticated heat treatment procedures.     

“Dual Lock‐and‐Key”‐Controlled Nanoprobes for Ultrahigh Specific Fluorescence Imaging in the Second Near‐Infrared Window

Fluorescence imaging in the second near‐infrared window (NIR‐II) is a new technique that permits visualization of deep anatomical features with unprecedented spatial resolution. Although attractive, effectively suppressing the interference signal of the background is still an enormous challenge for obtaining target‐specific NIR‐II imaging in the complex and dynamic physiological environment. Herein, dual‐pathological‐parameter cooperatively activatable NIR‐II fluorescence nanoprobes (HISSNPs) are developed whereby hyaluronic acid chains and disulfide bonds act as the “double locks” to lock the fluorescence‐quenched aggregation state of the NIR‐II fluorescence dyes for performing ultrahigh specific imaging of tumors in vivo. The fluorescence can be lit up only when the “double locks” are opened by reacting with the “dual smart keys” (overexpressed hyaluronidase and thiols in tumor) simultaneously. In vivo NIR‐II imaging shows that they reduce nonspecific activitation and achieve ultralow background fluorescence, which is 10.6‐fold lower than single‐parameter activatable probes (HINPs) in the liver at 15 h postinjection. Consequently, these “dual lock‐and‐key”‐controlled HISSNPs exhibit fivefold higher tumor‐to‐normal tissue ratio than “single lock‐and‐key”‐controlled HINPs at 24 h postinjection, attractively realizing ultrahigh specificity of tumor imaging. This is thought to be the first attempt at implementing ultralow background interference with the participation of multiple pathological parameters in NIR‐II fluorescence imaging.     

“Quasi‐freestanding” Graphene‐on‐Single Walled Carbon Nanotube Electrode for Applications in Organic Light‐emitting Diode

An air‐stable transparent conductive film with “quasi‐freestanding” graphene supported on horizontal single walled carbon nanotubes (SWCNTs) arrays is fabricated. The sheet resistance of graphene films stacked via layer‐by‐layer transfer (LBL) on quartz, and modified by 1‐Pyrenebutyric acid N‐hydroxysuccinimide ester (PBASE), is reduced from 273 Ω/sq to about 76 Ω/sq. The electrical properties are stable to heat treatment (up to 200 ºC) and ambient exposure. Organic light‐emitting diodes (OLEDs) constructed of this carbon anode (T ≈ 89.13% at 550 nm) exhibit ≈88% power efficiency of OLEDs fabricated on an ITO anode (low turn on voltage ≈3.1 eV, high luminance up to ≈29 490 cd/m², current efficiency ≈14.7 cd/A). Most importantly, the entire graphene‐on‐SWCNT hybrid electrodes can be transferred onto plastic (PET) forming a highly‐flexible OLED device, which continues to function without degradation in performance at bending angles >60°.     

“One‐for‐All” Strategy in Fast Energy Storage: Production of Pillared MOF Nanorod‐Templated Positive/Negative Electrodes for the Application of High‐Performance Hybrid Supercapacitor

Currently, metal‐organic frameworks (MOFs) are intensively studied as active materials for electrochemical energy storage applications due to their tunable structure and exceptional porosities. Among them, water stable pillared MOFs with dual ligands have been reported to exhibit high supercapacitor (SC) performance. Herein, the “One‐for‐All” strategy is applied to synthesize both positive and negative electrodes of a hybrid SC (HSC) from a single pillared MOF. Specifically, Ni‐DMOF‐TM ([Ni(TMBDC)(DABCO)_0.5], TMBDC: 2,3,5,6‐tetramethyl‐1,4‐benzenedicarboxylic acid, DABCO: 1,4‐diazabicyclo[2.2.2]‐octane) nanorods are directly grown on carbon fiber paper (CFP) (denoted as CFP@TM‐nanorods) with the help of triethylamine and function as the positive electrode of HSC under alkaline electrolyte. Meanwhile, calcinated N‐doped hierarchical porous carbon nanorods (CFP@TM‐NPCs) are produced and utilized as the negative counter‐electrode from a one‐step heat treatment of CFP@TM‐nanorods. After assembling these two electrodes together to make a hybrid device, the TM‐nanorods//TM‐NPCs exhibit a wide voltage window of 1.5 V with a high sloping discharge plateau between 1‐1.2 V, indicating its great potential for practical applications. This as‐described “One‐for‐All” strategy is widely applicable and highly reproducible in producing MOF‐based electrode materials for HSC applications, which shortens the gap between experimental synthesis and practical application of MOFs in fast energy storage.     

A “Six Sigma”© Black Belt Case Study: G.E.P. Box's Paper Helicopter Experiment Part A

This article presents an application of the “Six Sigma” DMAIC model to G.E.P. Box's famous “paper helicopter” experiment. The define, measure, and analyze phases are presented here, and the improve and control phases are presented in a follow-up article. The intent of this article is to present the reader with a case study for structuring a “Six Sigma” Black Belt project.     

Response to Comment “On the Existence of Excitonic Signatures in the Optical Response of Metal–Organic Frameworks”

This is a response to a comment on the interpretation of the origin of the nonlinear changes of optical properties of van der Waals' metal–organic frameworks (MOFs). The concerns are addressed by clarifying potential pitfalls in density functional theory (DFT) simulations, careful analysis of prior literature, and additionally discussing the previous experimental results to emphasize the applicability of the excitonic concept in molecular crystals, such as MOFs.     

Modeling of creep and stress relaxation of the nickel‐base alloy NiCr20TiAl at isothermal and non‐isothermal loading conditions

The design and dimensioning of new as well as the assessment of operating high‐temperature components in service require a precise prediction of creep and stress relaxation. The increasing share of renewable energies forces fossil‐fired power plants for increasing numbers of start‐ups and shut‐downs. Consequently, transient loading conditions need to be taken into account. In order to meet this demand, non‐isothermal creep equations are necessary, which enables a consistent prediction of creep strain and stress relaxation in a wide range of temperatures and stresses. In this paper, an approach for the visco‐plastic modeling of creep and stress relaxation for non‐isothermal loading conditions is presented. The strain portions creep, “negative creep” and initial plasticity, occurring at elevated temperatures are described by temperature‐dependent phenomenological equations. Within this paper, the adjustment of the parameters is based on a wide database of hot tensile tests, creep and annealing experiments. The nickel‐base alloy NiCr20TiAl has been examined in a temperature range from 450 °C to 650 °C. The developed material models have been successfully validated with isothermal and non‐isothermal relaxation experiments. Further, the recalculation of a staged relaxation test demonstrates the capability of the defined material laws in a wide stress range under isothermal and non‐isothermal loading conditions.