論文

Calcitic spines ∼1 μm in diameter are projecting from a trochospiral test of a spinose planktonic foraminifer. According to electron diffraction, Raman spectra, and detailed electron microscope observation, the spines were found to be a single-crystal-like calcite that has a nanogranular texture containing microstrain. An organic envelope protects the biogenic calcite against dissolution in water. Their unique mechanical and chemical properties are ascribed to the specific micro- and nanoscopic structures. This journal is

Development of high-performance organic energy storage is one of the important challenges in recent materials science. Molecular design and synthesis have potential for enhancement of the performances. Efficient exploration and design of the molecules are required in a wide search space. In the present work, a capacity prediction model for organic anodes was constructed on small experimental data by sparse modeling, a method of machine learning, combined with our chemical insights. The straightforward linear regression model facilitated discovery of a high-performance active material for organic anodes in a limited number of experiments. A recommended compound, 5-formylsalicylic acid (SA-CHO), showed one of the highest performances in recent works, i.e., a specific capacity of 873 mA h g-1at 100 mA g-1(sample number: n = 3) with rate performance and cycle stability. The model can be applied to explore organic anode active materials with higher specific capacity.

Imaging and measurement of friction forces are required in a variety of fields. If the friction forces originating from the motions of professionals are quantitatively analyzed, the data can be applied to a motion-copying system by a robot. However, weak friction forces have not been visualized and quantified using conventional sensing materials and devices because of their low sensitivity. Here we present a highly sensitive friction-imaging device based on the cascading responses of stimuli-responsive materials, namely polydiacetylene (PDA) and dry liquid (DL). Weak friction forces disrupt the DL, which is composed of liquid droplets surrounded by solid particles. The outflowing liquid under chemical stress changes the color of PDA. The cascading responses enable colorimetric imaging and measurement of weak friction forces in the range of 0.006-0.080 N. Furthermore, the device visualizes the force distribution of handwriting in calligraphy depending on the individual characteristics of an expert, a practician, and a beginner. A high-sensitivity friction-imaging device can be used to understand various motions.

Biomimetic strained SrSO4 crystals were produced through a nonclassical pathway involving fiber-by-fiber accumulation with poly(acrylic acid) in an aqueous solution system. Polymer-stabilized fibrous hydrate crystals 20-40 nm wide and several micrometers long were formed in the initial stage. Spindle-shaped microrods of SrSO4 were then constructed by oriented attachment of the hydrous fibrils and subsequent dehydration. The strained structure of the anhydrous SrSO4 crystals is similar to biogenic SrSO4 spines of acantharian species, a marine unicellular holoplanktonic protist.

A way to utilize eggshells is desired because most of the eggshell waste is disposed of in landfills. Despite eggshells having attractive features such as a thermodynamically stable porous crystalline structure, their effective utilization as a functional material has yet to be demonstrated. Herein, we developed an alkali-stable column packing material for reversed-phase preparative high-performance liquid chromatography (HPLC) based on eggshells. Nanocrystals and biopolymers present on eggshell powder were removed by surface treatment with buffered ethylenediaminetetraacetic acid (EDTA) and sodium hypochlorite solutions, resulting in bare calcium carbonate with a uniform porous surface. The obtained particles were modified with poly(maleic acid-alt-1-octadecene) (PMAcO) having hydrophobic alkyl chains and anionic carboxylate groups. The prepared PMAcO-modified eggshell-based material was applied to an HPLC column, and its performance is evaluated. The column succeeded in the separation of alkylbenzenes, steroids, and diastereomers. It was also used for the separation of basic tricyclic antidepressants in an alkaline mobile phase, showing excellent retention capacity and alkali stability. This study demonstrates the potential of eggshell utilization, providing not only a practical stationary phase for HPLC but also a solution for recycling calcium carbonate-based biomineral waste.

Dynamic properties are derived from the structural flexibility of 2D polymers. Softening layered structures has the potential for tuning and enhancing the dynamic properties. In the present work, the flexibility of layered polydiacetylene (PDA) is tuned by the interlayer polymeric guests with different branching structures. PDA shows thermoresponsive color-change properties through shortening the effective conjugation length with molecular motion. Whereas the blue-to-red color transition is observed at certain threshold temperatures for the layered PDA without the interlayer guest, the intercalation of the bulky polymer guests lowers the starting temperature and widens the temperature range for the thermoresponsive color changes. The resultant layered composite of PDA and bulky polymer affords the homogeneous coating on substrates on the centimeter scale. The thermoresponsive color-change coating is applied to temperature-distribution imaging. The specific heat of liquids is colorimetrically estimated using the coating on the bottle. The coating on a silk cloth visualizes the temperature distribution on a simulated tissue during surgical operation using an ultrasonic coagulation cutting device. The coating can be applied to thermal imaging in a variety of fields. Moreover, the softening strategy contributes to explore dynamic properties of soft 2D materials.

We constructed millimeter-wide monolayers consisting of tetragonally ordered BaTiO3 (BT) nanocubes through the liquid film formation caused by the Marangoni flow in a toluene-hexane binary liquid containing oleic acid. A thin liquid film containing BT nanocubes was overspread on a standing silicon substrate through the condensation of toluene at the advancing front after the preferential evaporation of hexane. Then, the oscillatory droplet formation like “wineglass tears” occurred on the substrate. Finally, two-dimensionally ordered BT nanocubes were observed as a stain of “wineglass tears” on the substrate after the liquid film receded through evaporation. The presence of a thin liquid film in the binary system is essential for the production of millimeter-wide monolayers on the substrate because multilayer deposition occurs without the formation of a thin liquid film in monocomponent systems. We improved the regularity of the ordered arrays of nanocubes by adjusting the liquid component and evaporation conditions.

Various biological and biomimetic minerals are composed of mesocrystals, in which nanoscale crystalline units are ordered in approximately the same crystallographic direction. However, the variation of the crystallographic regularity of mesocrystals has not been clarified using experimental evidence. This work demonstrated the gradual evolution of disorder in crystalline structures between single crystal and polycrystal by monitoring the crystallographic regularity using electron diffraction patterns. Single-crystal rods of fluorapatite elongated in the c direction are switched to mesocrystals consisting of iso-oriented nanorods by adding a specific molecule having a carboxy group (chemical approach) and to roughly arranged nanograins by increasing the degree of supersaturation at the growth front (physicochemical approach). Lateral and vertical miniaturization of the growth units is achieved through stepwise nucleation and near-epitaxial growth. The crystallographic regularity gradually decreases with deviation of the c axis and rotation of the a axes through reduction of the growth unit size. Here we can tune the disorder in crystalline structures via the chemical and physicochemical approaches.

This work clarified the effects of self-assembly of perovskite cesium lead bromide (CsPbBr3) nanocubes (NCs) covered with didodecyldimethyl ammonium bromide (DDAB) on photoluminescence (PL) properties. Although the PL intensity of isolated NCs was weakened in the solid state even under inert conditions, the quantum yield of PL (PLQY) and the photostability of DDAB-covered NCs were drastically improved by the formation of two-dimensional (2D) ordered arrays on a substrate. The PLQY of the 2D arrays increased to ca. 60% by initial excitation illumination at 468 nm and was maintained for over 4000 h. The improved PL properties are attributable to the fixation of the surface ligand around the NCs in the specific ordered arrays.

Purification of basic drugs in reversed-phase mode is often difficult, mainly due to adsorption of positively charged compounds to the silica gel-based stationary phase. Since this adsorption can be suppressed under alkaline condition, columns with alkali-resistance are required. In addition, compounds with acid-sensitive structures are sometimes degraded during separation on silica gel-based columns which exhibit acidity due to their surface structure. We prepared an alkali-resistant reversed-phase packing material, Eggshell-PMAcO based on eggshells modified with an amphiphilic copolymer, poly(maleic acid-alt-1-octadecene) (PMAcO). The height equivalent to a theoretical plate (HETP) of the Eggshell-PMAcO column was improved by surface treatment with ammonium acetate buffer (900 mM, pH = 3.7), which is an inexpensive reagent, and the retention behavior for hydrophobic compounds was compared to a typical ODS column based on silica gel, resulting in sufficient selectivity of the eggshell-based column for hydrophobic compounds, as indicated by the ratio of retention factors of pentylbenzene and butylbenzene (Eggshell-PMAcO column: 1.55, ODS column: 1.65). Column temperature-dependent retention behavior of naphthalene was investigated in the temperature range from 25 °C to 45 °C, followed by the calculation of thermodynamic parameters. There was little difference in the standard molar enthalpy (Eggshell-PMAcO: −19.6 kJ/mol, ODS: −21.7 kJ/mol). The absolute value of the standard free Gibbs energy for the Eggshell-PMAcO column was much smaller than that of the ODS column (Eggshell-PMAcO: −0.284 kJ/mol, ODS: −13.0 kJ/mol), indicating that the Eggshell-PMAcO column had a weaker retention strength for naphthalene than the ODS column mainly due to the large difference in the standard molar entropy (Eggshell-PMAcO: −64.9 J/mol K, ODS column: −29.2 J/mol K). The retention capacities for imipramine under neutral (water/methanol) and alkaline (0.1% triethylamine water/methanol) conditions were 0.2 mg and 5 mg, respectively, based on injection mass-dependent HETP, retention factor and symmetry factor. Finally, the prepared column was applied to the purification of a building block for nucleic acid drugs. This study demonstrated that reversed-phase columns, which can be fabricated from eggshells and an amphiphilic copolymer in an inexpensive and eco-friendly way, have the ability to purify basic compounds and acid-sensitive compounds.

Anisotropic ultrathin 2D materials are used as building blocks to obtain higher-order structures. Tailoring the size, surface chemistry, and assembly state of exfoliated nanosheets is required for the design of functional materials. However, these factors are not easily controlled during the down-sizing exfoliation process, which is a general route for obtaining 2D materials. In the present work, polydispersed nanosheets of a transition metal oxide are prepared based on prediction model for the size distribution constructed by a combination of machine learning and chemical perspective on small data. Self-assembly of the exfoliated nanosheets results in the uneven thin films exhibiting an angle-independent structural color. As the nanosheets vary in thickness and lateral size, their assembled thin films exhibit structural color independent of the incident angle. The structural color is changed by casting only 20 µL of an aqueous solution containing biogenic amines such as histamine within a sensing time of 5 min. The biogenic amines are intercalated into the interlayer space of the stacked nanosheets and the resulting increase in the thickness changes the color of the thin-film device. The new design strategies can be applied to constructing other thin-film sensing devices based on nanosheets.

We prepared conductive mixtures of Cu1.5Mn1.5O4 and Mn3O4 spinels (CMO–MOs) as positive electrode active materials in rechargeable Mg batteries (RMBs) using a sol–gel complex polymerization method. The CMO–MO spinel mixtures with high specific surface areas above 100 m2 g−1 were obtained with mild calcination in Ar at 300 °C. The conductivity of CMO–MOs was estimated to be approximately 1000 times higher than that of a conventional MgMn2O4 (MMO) spinel powder. The discharge capacities evaluated using 2032-type coin-cell battery with a Mg-alloy negative electrode at room temperature increase with an increase in the specific surface area of the spinel powders. The specific surface area for providing the theoretical capacity of the conductive CMO–MOs was about one-third that of the insulative MMO. High specific surface area and high conductivity are key parameters for the positive active material to realize practical room-temperature operation of RMBs.

Considering the vulnerability of silica gel to alkaline mobile phases, a highly alkaline stable stationary phase for HPLC is required to separate basic compounds with high separation efficiency. To address this issue, we have developed a high alkaline stable packing material (CaCO3-PMAcO) based on mesoporous calcium carbonate microspheres modified with poly(maleic acid-alt-1-octadecene). In this study, we report further investigation of the separation performance of CaCO3-PMAcO column by systematically evaluating the effects of particle size and chromatographic conditions. Based on the theory of the van Deemter equation, the separation efficiency was related to the size of CaCO3-PMAcO particles (2.9 – 5.7 µm). The evaluation of thermodynamics of retention by changing the column temperature from 20 °C to 45 °C implied that the retention mode was dominated by hydrophobic interaction associated with the exothermic enthalpy changes (-11.1 to -12.5 kJ/mol). The results of column selectivity tests revealed that the CaCO3-PMAcO column had hydrophobic selectivity comparable to C18 silica gel columns (αP/B; CaCO3-PMAcO column: 1.53, C18 column: 1.69), and higher shape/steric selectivity (αTri/Ter; CaCO3-PMAcO column: 1.56, C18 column: 0.955). In practice, the CaCO3-PMAcO column could be applied to the separation of not only alkylbenzenes and polycyclic aromatic hydrocarbons, but also to basic tricyclic antidepressants by using an alkaline mobile phase (pH 12).

Exfoliation of layered materials, a typical route to obtain 2D materials, is not easily controlled because of the unpredictable downsizing processes. In particular, the thickness control remains as a complex challenge. Here, we found a correlation between the thickness and lateral size distribution of the exfoliated nanosheets, such as transition metal oxides and graphene oxide. The layered composites of the host metal oxides and interlayer organic guests are delaminated into the surface-modified nanosheets in organic dispersion media. The exfoliation behavior varies by combination of the hosts, guests, and dispersion media. Here, we found that the thick and thin nanosheets were obtained on the monodispersed and polydispersed conditions, respectively. The selective syntheses of the thick and thin nanosheets were achieved using a prediction model of the lateral size distribution. The correlation between the thickness and lateral size distribution can be applied to thickness-selective syntheses of 2D materials.

Imaging and measuring compression stresses secure a safe and healthy life. Compression stresses in kPa range are not easily detected by conventional mechanoresponsive materials because microscopic molecular motion of the chromophores is not induced by such weak stresses. Moreover, imaging of the stress distribution is not achieved so far. The present study shows a sponge device combining two stimuli-responsive materials, a capsule releasing interior liquid and color-changing polymer in responses to compression stress and chemical stimulus, respectively. The stimuli-responsive capsule is dispersed on a melamine sponge comprised of the fibers with coating the layered polydiacetylene (PDA). The application of weak compression stresses induces collapse of the capsules, outflow of the interior liquid, and subsequent irreversible color change of PDA. The cascading response in the sponge device colorimetrically enables imaging of the distribution and measuring the strength of the compression stresses in kPa range. Furthermore, the device demonstrates imaging and measuring unknown weak compression stresses applied by the irregular-shaped objects. A couple of clinical issues in surgical operation of intestine are studied using the stress-imaging sponge device. The device and its design strategy can be applied to stress imaging in a variety of fields.

Magnesium rechargeable batteries (MRBs) promise to be the next post lithium-ion batteries that can help meet the increasing demand for high-energy, cost-effective, high-safety energy storage devices. Early prototype MRBs that use molybdenum-sulfide cathodes have low terminal voltages, requiring the development of oxide-based cathodes capable of overcoming the sulfide’s low Mg2+ conductivity. Here, we fabricate an ultraporous (>500 m2 g-1) and ultrasmall (<2.5 nm) cubic spinel MgMn2O4 (MMO) by a freeze-dry assisted room-temperature alcohol reduction process. While the as-fabricated MMO exhibits a discharge capacity of 160 mAh g-1, the removal of its surface hydroxy groups by heat-treatment activates it without structural change, improving its discharge capacity to 270 mAh g-1─the theoretical capacity at room temperature. These results are made possible by the ultraporous, ultrasmall particles that stabilize the metastable cubic spinel phase, promoting both the Mg2+ insertion/deintercalation in the MMO and the reversible transformation between the cubic spinel and cubic rock-salt phases.

© 2018 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim Stimuli-responsive properties of soft materials originate from dynamic structure changes. Layered polydiacetylene (PDA) shows color-change properties with the application of external stimuli, such as thermal and mechanical stresses. Layered organic materials possessing intercalation capabilities and dynamic properties have potentials for tuning their structures and properties by the intercalated guests. A variety of sensing and imaging devices can be developed by control of the stimuli responsivity. Here, the key structures, processes, and mechanisms for tuning the stimuli-responsive color-change properties of layered PDA are studied by in situ analyses with heating and cooling. The in situ analyses indicate that heating initiates thermal motion of the alkyl side chains of the PDA main chain in the host layers around 60 °C, regardless of the type of intercalated guests. Further heating induces torsion of the PDA main chain leading to color changes at different temperatures, depending on the types of the intercalated guest. Then, the layered structure is irreversibly deformed with lowering the crystallinity. The results indicate that the stimuli-responsive color-change properties are controlled by the rigidity of the layered structures consisting of the host layers and guests. The control strategy based on rigidity tuning can be applied to a variety of soft materials with stimuli responsivity.

© 2018 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim Visualization and quantitative detection of external stimuli are significant challenges in materials science. Quantitative detection of friction force, a mechanical stress, is not easily achieved using conventional stimuli-responsive materials. Here, the quantitative detection of friction force is reported, such as the strength and accumulated ammount, from the visible color of organic layered composites consisting of polydiacetylene (PDA) and organic amines without an excitation light source. The composites of the layered diacetylene monomer crystal and interlayer organic amine are synthesized through self-organization from the precursor solution. After topochemical polymerization, the layered composites based on PDA show tunable temperature-responsive and mechanoresponsive color-change properties depending on the types of interlayer amines. The layered composites are homogeneously coated on a filter paper. The change in color of the paper is quantitatively used to visualize the strength and accumulated amount of the applied friction force. Furthermore, writing pressure is measured by friction force using the paper device.

Two-dimensional nanomaterials have attracted much interest for their anisotropic structures and emergent properties. Whereas a variety of inorganic nanosheets are prepared by exfoliation, design and synthetic strategies of organic nanosheets are still developing. Here we report on crystal-controlled synthesis of conductive and redox-active organic polymer nanosheets with tunable thickness and lateral size. Although the nanosheets consist of classical conductive polymers, such as polypyrrole (PPy) and poly(3,4-ethylenedioxythiophene) (PEDOT), a new crystal-controlled polymerization approach provides 2D nanomaterials with enhanced and characteristic properties. Oxidative polymerization proceeds on the crystal surface of organic oxidants, such as quinone derivatives, with diffusion of the monomer vapor at low temperature under ambient pressure. The present method affords the control of lateral size and thickness of the nanosheets. The resultant nanosheets show the characteristic and enhanced properties originating from a 2D nature, such as the high structure anisotropy with aspect ratio around 104, enhanced conductivity 287 S cm-1, and specific charge-discharge capacitance 523 F g-1 at the current density of 18 A g-1. The organic nanosheets with conductivity and redox activity can be used as a building block for development of functional materials and devices. ©

Measurement of mechanical stresses, such as compression, shear, and tensile stresses, contributes toward achieving a safer and healthier life. In particular, the detection of weak compression stresses is required for healthcare monitoring and biomedical applications. Compression stresses in the order of 106–1010 Pa have been visualized and/or quantified using mechano-responsive materials in previous works. However, in general, it is not easy to detect compression stresses weaker than 103 Pa using conventional mechano-responsive materials because the dynamic motion of the rigid mechano-responsive molecules is not induced by such a weak stress. In the present work, weak compression stresses in the order of 100–103 Pa are visualized and measured via the integration of stimuli-responsive materials, such as layered polydiacetylene (PDA) and dry liquid (DL), through response cascades. DLs consisting of liquid droplets covered by solid particles release the interior liquid and collapse with application of a weak compression stress. The color of the layered PDA is changed by the spilled liquid as a chemical stress. A variety of weak compression stresses, such as expiratory pressure, are visualized and colorimetrically measured using the paper-based device of the integrated stimuli-responsive materials. Diverse mechano-sensing devices can be designed via the integration of stimuli-responsive materials.