A biogenic geodesic dome of the silica skeleton in Phaeodaria.

Unique architectures of microbial skeletons are viewed as a model for the architectural design of artificial structural materials. In particular, the specific geometric arrangement of a spherical skeleton 0.5-1.5 mm in diameter of shell-bearing protists, Phaeodaria (Aulosphaera sp.), is remarkably interesting because of its similarity to a geodesic polyhedron, which is a hollow framework with 6-branched nodes that requires minimal building material for maximal strength. A phaeodarian skeleton composed of silica rods 5-10 µm in diameter was characterized as a distorted dome that is based on an icosahedron sectioned with a 7-frequency subdivision. The major difference of the biogenic architecture from the ideal geodesic dome is the coexistence of 7- and 5-branched nodes with the distortion of the frames and the presence of radial spines. From a microscopic perspective, the frames and radial spines were revealed to be hollow tubes having inner fibers and lamellar walls consisting of silica nanoparticles 4-8 nm in diameter with interlayer organic matter. The high degradability of the silica skeleton in seawater after cell mortality is ascribed to the specific nanometric composite structure. The biological architectonics sheds light on the production of environmentally friendly, lightweight structural materials and microdevices.

High-Sensitive Spatiotemporal Distribution Imaging of Compression Stresses Based on Time-Evolutional Responsiveness.

Mechanoresponsive materials have been studied to visualize and measure stresses in various fields. However, the high-sensitive and spatiotemporal imaging remain a challenging issue. In particular, the time evolutional responsiveness is not easily integrated in mechanoresponsive materials. In the present study, high-sensitive spatiotemporal imaging of weak compression stresses is achieved by time-evolutional controlled diffusion processes using conjugated polymer, capsule, and sponge. Stimuli-responsive polydiacetylene (PDA) is coated inside a sponge. A mechanoresponsive capsule is set on the top face of the sponge. When compression stresses in the range of 6.67-533 kPa are applied to the device, the blue color of PDA is changed to red by the diffusion of the interior liquid containing a guest polymer flowed out of the disrupted capsule. The applied strength (F/N), time (t/s), and impulse (F·t/N s) are visualized and quantified by the red-color intensity. When a guest metal ion is intercalated in the layered structure of PDA to tune the responsivity, the device visualizes the elapsed time (τ/min) after unloading the stresses. PDA, capsule, and sponge play the important roles to achieve the time evolutional responsiveness for the high-sensitive spatiotemporal distribution imaging through the controlled diffusion processes.

The size-dependent valence and conduction band-edge energies of Cu quantum dots.

Ultra-small metal particles having band gaps are regarded as a new class of functional materials. We investigated the size dependencies of the band-edge energies on Cu quantum-dots in the size range of 0.7-2.1 nm. The extremely high conduction band-edge energies owing to the strong quantum-size effects were observed for sizes below 1 nm.

Morphology and size control of an amorphous conjugated polymer network containing quinone and pyrrole moieties via precipitation polymerization.

Morphology and size control of insoluble and infusible conjugated polymers are significant for their applications. Development of a precipitation polymerization route without using a surface stabilizer is preferred to control the reaction, morphology, and size. In the present work, precipitation polymerization for an amorphous conjugated polymer network, a new type of polymerized structure containing functional units, was studied for the size and morphology control in the solution phase at low temperature. The random copolymerization of benzoquinone (BQ) and pyrrole (Py) monomers formed microspheres of the BQ-Py network polymers as the precipitates in the solution phase. The particle diameter was controlled in the range of 70 nm and 1 µm by changing the pH of the solution and concentration of the monomers. The resultant nanoparticles were applied to a metal-free electrocatalyst for the hydrogen evolution reaction (HER). The catalytic activity of the BQ-Py nanoparticles was higher than that of the bulk micrometer-sized particles. The results imply that the morphology and size of amorphous conjugated polymer networks can be controlled by precipitation polymerization.

Imaging of Accumulated Mechanical Stresses Using Self-Assembled Layered Conjugated Polymer.

When mechanical stresses, such as tensile, compressive, and frictional stresses, are applied to objects by various motions, they are accumulated in materials. Conventional mechanoresponsive materials and sensors detect one-time applied stress. However, the accumulated stresses are not visualized or measured in previous works. The present study demonstrated imaging and sensing of not only one-time but also accumulated tensile, compressive, and frictional stresses. Polyurethane (PU) film was combined with 2D layered polydiacetylene (PDA), a stimuli-responsive color-changing polymer. PDA generally exhibits no color changes with the application of tensile and compression stresses because the molecular motion leading to the color change is not induced by such mechanical stresses. Here the versatile mechanoresponsiveness was achieved using a block copolymer guest partially intercalated in the layered PDA. As the interlayer and outerlayer segments interact with PDA and PU, respectively, the applied stresses to the film are transferred from PU to PDA via the block copolymer guest. The color changes of the film imaged and quantified the accumulated work depending on the number and strength of the applied multiple stresses such as tensile, compressive, and frictional stresses. The design strategy of materials and methodology of sensing can be applied to the development of new sensors for accumulated mechanical stresses in a wide range of length and strength scales.

Enhanced and stabilized photoluminescence of perovskite cesium lead bromide nanocubes through ordered assemblies.

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.

A highly sensitive friction-imaging device based on cascading stimuli responsiveness.

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.

Construction of Millimeter-Wide Monolayers of Ordered Nanocubes as a Stain of "Wineglass Tears" Driven by the Marangoni Flow.

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.

Ultraporous, Ultrasmall MgMn2O4 Spinel Cathode for a Room-Temperature Magnesium Rechargeable Battery.

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.

Stimuli-Responsive Sponge for Imaging and Measuring Weak Compression Stresses.

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.

Fabrication process development and basic evaluation of eggshell-based column packing material for reversed-phase preparative separation.

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.

Selective syntheses of thick and thin nanosheets based on correlation between thickness and lateral-size distribution.

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.

Coatable 2D Conjugated Polymers Containing Bulky Macromolecular Guests for Thermal Imaging.

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.

Designed nanostructures created via physicochemical switching of the growth mode between single crystals and mesocrystals.

Most biominerals are composed of mesocrystals, in which individual nanoparticle building units have a defined long-range order on the atomic scale in at least one direction. Although the crystal size and orientation of the mesostructures are spatially designed in biological architectures, it has been difficult to achieve adequate control of the crystal growth to produce modulated mesostructures in artificial aqueous systems. Here, we propose a simple physicochemical approach for the spatial design of nanostructures using an aqueous solution system. The ordered arrays of oriented fluorapatite (FA) rods similar to tooth enamel are produced on a polymer substrate in a supersaturated solution. We succeeded in reversible switching of the growth mode of FA between single-crystalline rods and mesocrystalline grains through the disturbance of the solution. The primary crystal size was tuned between micrometric rods ∼0.5 µm wide and >5 µm long and nanoscale grains ∼10 nm wide and 50 nm long without a drastic change in the c direction. Hierarchical architectures consisting of iso-oriented FA microrods and nanograins were constructed via temporal control of the crystal growth mode by switching a physicochemical parameter, such as the degree of supersaturation at the growth front.

Quantitative evaluation of reversed-phase packing material based on calcium carbonate microspheres modified with an alternating copolymer.

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).

Ultrastructure of setae of a planktonic diatom, Chaetoceros coarctatus.

Silica frustules of most planktonic diatoms have many shallow holes in which the length (L) is smaller than the width (W). The present study focuses on a silica ultrastructure of setae of a planktonic diatom having deep (L/W > 1) holes. Here, we characterized microscopically patterned nanoholes on the silica walls of thick, robust, and hollow setae of a colony of Chaetoceros coarctatus. Basically, tetragonal poroid arrangements with and without a costa pattern are observed on the inner and outer surfaces, respectively, for three kinds of curving hollow setae attached to the anterior, intercalary, and posterior parts of the colony. The seta structures including specific poroid arrangements and continuity of deep nanoholes depend on the location. The deep nanoholes ∼90 nm wide are elongated from 150 to 1500 nm (L/W ∼17) with an increase in the wall thickness of the polygonal tubes of the setae. The inside poroid array, with a period of 190 nm in the extension direction of setae, is lined by parallel plates of the costae. However, the poroid arrangement on the outer surface is disordered, with several holes obstructed with increasing wall thickness of the posterior terminal setae. According to the movement of a colony in a fluid microchannel, the thick curving terminal setae is suggested to involve attitude control and mechanical protection. Using an optical simulation, the patterned deep through-holes on the intercalary setae were suggested to contribute anti-reflection of blue light in the wavelength range of 400 to 500 nm for the promotion of photosynthesis in seawater.

Micro- and nanometric characterization of the celestite skeleton of acantharian species (Radiolaria, Rhizaria).

We clarified the specific micrometric arrangement and nanometric structure of the radiolarian crystalline spines that are not a simple single crystal. A body of the celestite (SrSO4) skeleton of acantharian Acanthometra cf. multispina (Acanthometridae) composed of 20 radial spines having four blades was characterized using microfocus X-ray computed tomography. The regular arrangement of three types of spines was clarified with the connection of the blades around the root of each spine. The surface of the spines was covered with a chitin-based organic membrane to prevent from dissolution in seawater. In the nanometric scale, the mesocrystalline structure that consists of nanoscale grains having distorted single-crystal nature was revealed using scanning- and transmission electron microscopies, electron diffraction, and Raman spectroscopy. The acantharian skeletons have a crystallographically controlled architecture that is covered with a protective organic membrane. These facts are important for penetrating the nature of biogenic minerals.

A Layered Polydiacetylene Containing Hydrogen-Bonding 4,4'-Bipyridyl Guests: Reversible Color Changes with a Wide-Range Temperature Response.

Invited for this month's cover is the group of Prof. Yuya Oaki, Keio University, Japan. The cover picture shows a layered polydiacetylene containing hydrogen-bonding 4,4'-bipyridyl guests formed through self-organization. In classical intercalation chemistry, the interlayer guests are intercalated in the host layers via rigid strong electrostatic interaction. The weaker interlayer interaction via hydrogen bond promotes the dynamic motion directing the thermoresponsive color changes in a wide temperature range. More information can be found in the Full Paper by Yuya Oaki, and co-workers.

Emergence of practical fluorescence in a confined space of nanoporous silica: significantly enhanced quantum yields of a conjugated molecule.

The fluorescence of benzanthrone, which is a conjugated molecule bearing a carbonyl group, is activated by confinement in a pore with a diameter close to the molecular size. An intense emission originating from the aromatic character π-π* transition is achieved through suppression of the nonradiative n-π* transition by strong hydrogen bonding between carbonyl groups and silanol groups with a micropore-filling effect in the nanospace.

A Layered Polydiacetylene Containing Hydrogen-Bonding 4,4'-Bipyridyl Guests: Reversible Color Changes with a Wide-Range Temperature Response.

Layered organic polymers have intercalation capabilities and dynamic properties. In classical intercalation chemistry, the interlayer guests are intercalated in the host layers via electrostatic interaction. The present work shows the organic layered materials with the host-guest interlayer interaction via hydrogen bond. Polydiacetylene (PDA) exhibits color changes from blue to red with the application of external stimuli, such as thermal and mechanical stresses. Here we report on a layered PDA containing 4,4'-bipyridyl in the interlayer space as a hydrogen-bonding guest. Whereas the layered PDA without interlayer guest shows the color transition at 65 °C, gradual color changes with two-stage reversibility are observed in the temperature range of -20-240 °C by the introduction of the hydrogen-bonding guest. The weaker interlayer interaction via the hydrogen bond promotes the dynamic motion directing the thermoresponsive color changes in a wide temperature range.