Well-defined Spacing Research Articles

Perception and Knowledge of Rice Value Chain Actors on the Effect of Improved Practices on Yield and Milling Characteristics of Rice in the Sagnarigu and Kumbungu Districts of Ghana

This study presents findings from a comprehensive survey conducted between January and March 2021, aimed at elucidating the agricultural practices and perceptions of rice farmers, processors, and marketers in the Sagnarigu and Kumbungu districts of the Northern Region in Ghana. The research sought to gather essential data on improved techniques employed in rice cultivation, milling, and marketing, as well as understand the perceptions surrounding these practices within the local farming communities. Employing a multi-stage sampling methodology, primary data were collected through face-to-face interviews with 134 rice farmers, 82 processors, and 22 marketers. Key findings revealed that a significant proportion (54.7%) of farmers preferred cultivating local rice varieties such as Moses, Bumbass, Mandii, Bazolgu, Salimasaa, and Assemblyman. Moreover, the survey indicated that 54.5% of farmers adopted the broadcasting method for planting seeds, while only 18% practiced line transplanting with well-defined spacing. Additionally, a majority of transplanting activities occurred when seedlings were at least 4 weeks old, highlighting potential inefficiencies in timing. The study identified several constraints hindering rice production in both lowland and irrigated rice ecosystems across the surveyed districts. These constraints include the prevalence of poor-quality seed varieties, inadequate spacing, suboptimal timing of transplanting, and low soil fertility. Addressing these challenges is imperative for enhancing rice productivity and promoting sustainable agricultural practices in the region.

CO2 electroreduction to multicarbon products from carbonate capture liquid

CO2 electroreduction to multicarbon products from carbonate capture liquid

Modulation on interlayer channels of LDH/polymer hybrid membranes for efficient CO2 separation

Two-dimensional (2D) nanosheets with thickness of one to several atoms serve as ideal building units for separation membranes. Assembling 2D nanosheets into layered stacks with well-defined spacing as molecular separation channels is still a huge challenge. Herein, we report the construction of ultrathin membranes with layered double hydroxides (LDHs) nanosheets, polyacrylic acid (PAA) and polyethyleneimine (PEI) alternately deposited on porous substrates based on layer-by-layer assembly. The chemical tuning of PEI leads to an accurate regulation of interlayer spacing in angstrom scale, resulting in selective nanochannels for CO2 permeation. The laminar membranes with CO2 transport-facilitated channels exhibit excellent gas separation performance and exceed the limit of the state-of-the-art membranes with CO2 permeance of 1068 GPU (1 GPU = 1 × 10-6 cm3 (STP) cm−2 s−1 cmHg−1), CO2/N2 and CO2/CH4 selectivity of 126 and 330 respectively. It is revealed the as-prepared nanofilms with strong adsorption enthalpy overcome the energy barrier of CO2 molecules entering into and diffusing through the nanochannels. The strategy demonstrated in this work would open up new avenues for effective CO2 separation and capture in recycling of carbon resources.

Seaweed and Dendritic Growth in Unsaturated Fatty Acid Monolayers.

The lateral movement in lipid membranes depends on their diffusion constant within the membrane. However, when the flux of the subphase is high, the convective flow beneath the membrane also influences lipid movement. Lipid monolayers of an unsaturated fatty acid at the water–air interface serve as model membranes. The formation of domains in the liquid/condensed coexistence region is investigated. The dimension of the domains is fractal, and they grow with a constant growth velocity. Increasing the compression speed of the monolayer induces a transition from seaweed growth to dendritic growth. Seaweed domains have broad tips and wide and variable side branch spacing. In contrast, dendritic domains have a higher fractal dimension, narrower tips, and small, well-defined side branch spacing. Additionally, the growth velocity is markedly larger for dendritic than seaweed growth. The domains’ growth velocity increases and the tip radius decreases with increasing supersaturation in the liquid/condensed coexistence region. Implications for membranes are discussed.

A tetrahedral DNA nanostructure functionalized paper-based platform for ultrasensitive colorimetric mercury detection

A novel tetrahedral DNA nanostructure (TDN) functionalized paper-based colorimetric sensor was developed for ultrasensitive analysis of mercury ion (Hg2+). On the paper-based platform, TDN was used as scaffold to anchor aptamer to improve the capture efficiency owing to the controllably specific orientation, low steric hindrance effect and well-defined spacing. In the absence of Hg2+, biotinylated aptamer would bind with streptavidin-labeled HRP. Whereas, in the presence of Hg2+, aptamer would preferentially bind to Hg2+ owing to the higher binding constant of T–Hg–T than that of T–A, which consequently leading to the biotinylated aptamer releasing from TDN. After introducing TMB-H2O2 solution, strong variation of color signal could be observed. Therefore, the quantitative analysis of Hg2+ was carried out by using smartphone to monitor the color intensity on paper chip. The proposed strategy exhibits good linearity over a wide range of 10–13–10–7 M with a low detection limit of 30 fM. And this method had been successfully applied in real water samples. Our strategy provided a versatile, low-cost and user-friendly paper-based monitoring platform for rapid and ultrasensitive analysis of heavy metal ions and thus had potential applications in food safety and public health.

Interfacial Ions Sieving for Ultrafast and Complete Desalination through 2D Nanochannel Defined Graphene Composite Membranes.

The layered graphene membrane has high potential for efficient desalination owing to its frictionless surface and hydrophobic nature. However, it has not been demonstrated so far due to the challenges related to controlling membrane microstructure. Herein, we develop a facile and simple thiol-ene click method to prepare a perfluoro-alkyl grafted graphene (fGraphene) membrane on porous ceramic, which features an ultrahigh antiwetting surface, oriented mesoporous surface entrances, and a well-defined interlamellar spacing of ∼1.1 nm. With vacuum membrane distillation, the fGraphene membranes post ∼100% rejections to the small ions of seawater, at least 1 order of magnitude higher water fluxes than those of commercial membranes and graphene-oxide-based membranes, as well as robust stability in the desalination. Fast NaCl desalinations on the fGraphene membrane were also confirmed by the reverse/forward osmosis tests. The complete rejection of ions and high flux are attributed to the interfacial sieving effect over the 2D nanochannels as well as the vapor-phase transport in the mesoscale channels, which is fundamentally different from the solution-diffusion mechanism of dense polymeric membranes and the size-sieving mechanism of microporous membranes. This work not only demonstrates a special separation effect for complete desalination over the layered graphene-based membrane but also offers a reliable method to functionalize and structure graphene membranes for other potential applications.

Transmembrane β-peptide helices as molecular rulers at the membrane surface.

β-Peptides are known to form 14-helices with high conformational rigidity, helical persistence length, and well-defined spacing and orientation regularity of amino acid side chains. Therefore, β-peptides are well suited to serve as backbone structures for molecular rulers. On the one hand, they can be functionalized in a site-specific manner with molecular probes or fluorophores, and on the other hand, the β-peptide helices can be recognized and anchored in a biological environment of interest. In this study, the β-peptide helices were anchored in lipid bilayer membranes, and the helices were elongated in the outer membrane environment. The distances of the covalently bound probes to the membrane surface were determined using graphene-induced energy transfer (GIET) spectroscopy, a method based on the distance-dependent quenching of a fluorescent molecule by a nearby single graphene sheet. As a proof of principle, the predicted distances were determined for two fluorophores bound to the membrane-anchored β-peptide molecular ruler.

Plasmonic Enhancement of Two-Photon Excitation Fluorescence by Colloidal Assemblies of Very Small AuNPs Templated on M13 Phage.

In this study, an engineered M13 bacteriophage was examined as a biological template to create a well-defined spacing between very small gold nanoparticles (AuNPs 3-13 nm). The effect of the AuNP particle size on the enhancement of the nonlinear process of two-photon excitation fluorescence (2PEF) was investigated. Compared to conventional (one-photon) microscopy techniques, such nonlinear processes are less susceptible to scattering given that the density of background-scattered photons is too low to generate a detectable signal. Besides this, the use of very small AuNPs in 2PEF microscopy becomes more advantageous because individual "isolated" AuNPs of this size do not sufficiently enhance 2PEF to produce a detectable signal, resulting in even less background signal. To investigate the 2PEF of the AuNP-M13 assemblies, a variety of sample preparation approaches are tested, and surface-enhanced Raman spectroscopy (SERS) is employed to study the strength of plasmon coupling within the gaps of AuNPs assembled on the M13 template. Results indicate that assemblies prepared with 9-13 nm AuNP were able to clearly label Escherichia coli cells and produce a 2PEF signal that was orders of magnitude higher than the isolated AuNP (below the threshold of detection). This study thus provides a better understanding of the opportunities and limitations relevant to the use of such small AuNPs within colloidal plasmonic assemblies, for applications in biodetection or as imaging contrast agents.

Roles of Cu+ and Cu0 sites in liquid-phase hydrogenation of esters on core-shell CuZnx@C catalysts

Liquid-phase hydrogenolytic reduction of esters on Cu-based catalysts is a promising approach for synthesis of alcohols. Here, core-shell CuZnx@C materials synthesized via pyrolysis of a Zn(NO3)2-loaded metal-organic framework (MOF) were proposed, in which well-defined spacing between Cu species in the parent MOF and the homogeneous loading of a Zn salt leads to an ideal distribution and strong interaction of Cu and Zn after pyrolysis of the precursor. The as-synthesized CuZnx@C showed a much higher catalytic activity than Cu@C. This higher activity is tentatively attributed to the simultaneous presence of Cu0 and Cu+ sites at ZnO crystal domains. The resulting Cu-O-Zn sites have a high tendency to adsorb the ester in the form of a surface bound species that greatly improves the hydrogenolysis, which is the rate controlling step in the reductive pathway. A theoretical study confirms the ability of this site to bind and catalytically convert fatty acid esters.

Anisotropic Two-Dimensional Screening at the Surface of Black Phosphorus.

Electronic screening can have direct consequences for structural arrangements on the nanoscale, such as on the periodic ordering of adatoms on a surface. So far, such ordering phenomena have been explained in terms of isotropic screening of free electronlike systems. Here, we directly illustrate the structural consequences of anisotropic screening, making use of a highly anisotropic two-dimensional electron gas (2DEG) near the surface of black phosphorous. The presence of the 2DEG and its filling is controlled by adsorbed potassium atoms, which simultaneously serve to probe the electronic ordering. Using scanning tunneling microscopy, we show that the anisotropic screening leads to the formation of potassium chains with a well-defined orientation and spacing. We quantify the mean interaction potential utilizing statistical methods and find that the dimensionality and anisotropy of the screening is consistent with the presence of a band bending-induced 2DEG near the surface. The electronic dispersion of the 2DEG inferred by electronic ordering is consistent with that measured by angle-resolved photoemission spectroscopy.

Probing nonlocal spatial correlations in quantum gases with ultra-long-range Rydberg molecules

We present photo-excitation of ultra-long-range Rydberg molecules as a probe of spatial correlations in quantum gases. Rydberg molecules can be created with well-defined internuclear spacing, set by the radius of the outer lobe of the Rydberg electron wavefunction $R_n$. By varying the principal quantum number $n$ of the target Rydberg state, the molecular excitation rate can be used to map the pair-correlation function of the trapped gas $g^{(2)}(R_n)$. We demonstrate this with ultracold Sr gases and probe pair-separation length scales ranging from $R_n = 1400 - 3200$ $a_0$, which are on the order of the thermal de Broglie wavelength for temperatures around 1 $\mu$K. We observe bunching for a single-component Bose gas of $^{84}$Sr and anti-bunching due to Pauli exclusion at short distances for a polarized Fermi gas of $^{87}$Sr, revealing the effects of quantum statistics.

MEMS for biofuel composition measurement based on thermal impedance spectroscopy

Continuous monitoring of the composition of E85 biofuel is essential for a quick start and clean and efficient operation of Flex-Fuel Vehicles. The actual ethanol concentration in E85 fuel is in the range 50%–85% and fuel-line sensors are used for ethanol-gasoline composition measurement. However, also a small amount of water is typically present, which cannot be reliably detected using state-of-the-art capacitive fuel-line sensors. Thermal impedance spectroscopy has been investigated as a non-destructive technique to determine the composition of ternary mixtures of biofuels. The principle of the thermal conductivity detector has been extended for measuring both the thermal conductivity and the thermal capacity of biofuel in the range up to 10 kHz using an AC-operated polysilicon heater for injecting a sinusoidal heat flux, and another polysilicon strip at a well-defined spacing or thermopile sensors for measuring the in-phase and quadrature components of the resulting AC temperature difference. Measurements on the components are in reasonable agreement with simulations, with a −3 dB cut-off frequency at 422.5 Hz and 340.8 Hz for ethanol and gasoline, respectively. However, the cut-off frequency of water was found to be significantly lower than simulations due to its high surface tension, thus limiting access to the detector.

A novel reduced graphene oxide/carbon nanotube hollow fiber membrane with high forward osmosis performance

Forward osmosis (FO)-based water treatment and desalination processes have attracted increasing attention to address the global water crisis, but its practical application is restricted by the lack of FO membranes with high permeability and selectivity. In this work, an all nanocarbon-based FO membrane was successfully fabricated via constructing reduced graphene oxide (RGO) on a carbon nanotube (CNT) hollow fiber substrate via electrophoretic deposition coupling with chemical reduction processes. Due to the ultra-low friction and well-defined interlayer spacing, the RGO active layer provided high water permeability and ion selectivity. Meanwhile, the high porosity and good wettability ensured the CNT hollow fiber substrate with low internal concentration polarization, and thus increasing water flux. During against DI water feed using 0.5 M NaCl draw solution, the prepared RGO/CNT membrane presented an outstanding water flux of 22.6 LMH, which is 3.3 times higher than that of the commercial membrane. Meanwhile, its reverse salt flux was only 1.6 gMH in comparison to 2.2 gMH for the commercial membrane. These results indicate that the all nanocarbon-based membrane is an alternative membrane for providing clean water in the FO process.

Non-swelling graphene oxide-polymer nanocomposite membrane for reverse osmosis desalination

Although pristine graphene oxide (GO)-based membranes have previously demonstrated promising molecular separation due to their well-defined interlayer spacing, their applications in water processing operations remain limited due to the natural swelling tendency of GO in the aqueous phase which decreases separation ability. In this work, pristine GO laminate has been successfully integrated into a highly crosslinked network to produce membranes with anti-swelling behaviour and excellent desalination capability. The process of free-radical polymerisation in aqueous conditions of a GO suspension enables the formation of a GO-polymer network without covalent bonding between GO and polymer, leading to a combination of mechanical robustness, remarkable water transport properties, and an anti-swelling tendency suitable for the high-pressure operation required for reverse osmosis (RO) membrane process. The resulting GO-polymer membrane was not swollen during RO operation while it was stable under a harsh oxidising environment. It also demonstrated water flux of 33.5 L m−2 h−1 with 98.5% NaCl rejection at 10 bar when prepared by high-vacuum filtration and subsequent polymerisation of the precursor solution on to a mesoporous substrate. This methodology makes large-scalable membrane fabrication very feasible.

Selective area epitaxy of AlGaN nanowire arrays across nearly the entire compositional range for deep ultraviolet photonics.

Semiconductor light sources operating in the ultraviolet (UV)-C band (100-280 nm) are in demand for a broad range of applications but suffer from extremely low efficiency. AlGaN nanowire photonic crystals promise to break the efficiency bottleneck of deep UV photonics. We report, for the first time, site-controlled epitaxy of AlGaN nanowire arrays with Al incorporation controllably varied across nearly the entire compositional range. It is also observed that an Al-rich AlGaN shell structure is spontaneously formed, significantly suppressing nonradiative surface recombination. An internal quantum efficiency up to 45% was measured at room-temperature. We have further demonstrated large area AlGaN nanowire LEDs operating in the UV-C band on sapphire substrate, which exhibit excellent optical and electrical performance, including a small turn-on voltage of ~4.4 V and an output power of ~0.93 W/cm2 at a current density of 252 A/cm2. The controlled synthesis of AlGaN subwavelength nanostructures with well-defined size, spacing, and spatial arrangement and tunable emission opens up new opportunities for developing high efficiency LEDs and lasers and promises to break the efficiency bottleneck of deep UV photonics.

Micro-fabricated scaffolds lead to efficient remission of diabetes in mice.

Despite the clinical success of intrahepatic islet transplantation in treating type 1 diabetes, factors specific to this transplantation site hinder long-term insulin independence. The adoption of alternative, extravascular sites likely improve islet survival and function, but few locations are able to sufficiently confine islets in order to facilitate engraftment. This work describes a porous microwell scaffold with a well-defined pore size and spacing designed to guarantee islet retention at an extrahepatic transplantation site and facilitate islet revascularization. Three techniques to introduce pores were characterized: particulate leaching; solvent casting on pillared wafers; and laser drilling. Our criteria of a maximum pore diameter of 40μm were best achieved via laser drilling. Transplantation studies in the epididymal fat of diabetic mice elucidated the potential of this porous scaffold platform to restore blood glucose levels and facilitate islet engraftment. Six out of eight mice reverted to stable normoglycemia with a mean time to remission of 6.2±3.2 days, which was comparable to that of the gold standard of renal subcapsular islet grafts. In contrast, when islets were transplanted in the epididymal fat pad without a microwell scaffold, only two out of seven mice reverted to stable normoglycemia. Detailed histological evaluation four weeks after transplantation found a comparable vascular density in scaffold-seeded islets, renal subcapsular islets and native pancreatic islets. However, the vascularization pattern in scaffold-seeded islets was more inhomogeneous compared to native pancreatic islets with a higher vascular density in the outer shell of the islets compared to the inner core. We also observed a corresponding decrease in the beta-cell density in the islet core. Despite this, our data indicated that islets transplanted in the microwell scaffold platform were able to maintain a viable beta-cell population and restore glycemic control. Furthermore, we demonstrated that the microwell scaffold platform facilitated detailed analysis at a subcellular level to correlate design parameters with functional physiological observations.

Combined quartz crystal microbalance with dissipation (QCM-D) and generalized ellipsometry (GE) to characterize the deposition of titanium dioxide nanoparticles on model rough surfaces

Measuring the interactions between engineered nanoparticles and natural substrates (e.g. soils and sediments) has been very challenging due to highly heterogeneous and rough natural surfaces. In this study, three-dimensional nanostructured slanted columnar thin films (SCTFs), with well-defined roughness height and spacing, have been used to mimic surface roughness. Interactions between titanium dioxide nanoparticles (TiO2NP), the most extensively manufactured engineered nanomaterials, and SCTF coated surfaces were measured using a quartz crystal microbalance with dissipation monitoring (QCM-D). In parallel, in-situ generalized ellipsometry (GE) was coupled with QCM-D to simultaneously measure the amount of TiO2NP deposited on the surface of SCTF. While GE is insensitive to effects of mechanical water entrapment variations in roughness spaces, we found that the viscoelastic model, a typical QCM-D model analysis approach, overestimates the mass of deposited TiO2NP. This overestimation arises from overlaid frequency changes caused by particle deposition as well as additional water entrapment and partial water displacement upon nanoparticle adsorption. Here, we demonstrate a new approach to model QCM-D data, accounting for both viscoelastic effects and the effects of roughness-retained water. Finally, the porosity of attached TiO2NP layer was determined by coupling the areal mass density determined by QCM-D and independent GE measurements.

Positioning colloids at the surfaces of cholesteric liquid crystal droplets.

We report on the internal configurations of aqueous dispersions of droplets of cholesteric liquid crystals (LCs; 5-50 μm-in-diameter; comprised of 4-cyano-4'-pentylbiphenyl and 4-(1-methylheptyloxycarbonyl)phenyl-4-hexyloxybenzoate) and their influence on the positioning of surface-adsorbed colloids (0.2 or 1 μm-in-diameter polystyrene (PS)). When N = 2D/P was less than 4, where D is the droplet diameter and P is the cholesteric pitch, the droplets adopted a twisted bipolar structure (TBS) and colloids were observed to assume positions at either the poles or equator of the droplets. A statistical analysis of the distribution of locations of the colloids revealed a potential well of depth 2.7 kBT near the equator, a conclusion that was supported by computer simulations performed via the minimization of the Landau-de Gennes free energy (well depth of 7 kBT from simulation). In contrast, for N > 4, a majority of the droplets exhibited a radial spherical structure (RSS) characterized by a pair of closely spaced surface defects (angle of separation with respect to the center of the droplet θ < 5°) connected by a disclination winding to/from the droplet center, which led to the positioning of pairs of colloids with well-defined spacing at these surface defects. The separation of the pairs of surface-adsorbed colloids was colloid size-dependent, ranging from 1.11 ± 0.04 μm for 1 μm-in-diameter colloids to 1.7 ± 0.2 μm for 200 nm-in-diameter colloids. We also observed long-lived metastable configurations in which the two surface point defects were separated by much larger distances (corresponding to populations with angles of θ = 20 ± 10° and 85 ± 10° with respect to the center), and observed these pairs of defects to also position pairs of colloids. A third configuration, the diametrical spherical structure (DSS) was also observed. Consistent with the predictions of computer simulations, we found experimentally that the DSS is indeed composed of disconnected defect rings positioned along the diameter of the droplet. Overall, these results reveal that the rich palette of defects exhibited by confined cholesteric LC systems (equilibrium and metastable) provide the basis of a versatile class of templates that enable the surface positioning of colloids in ways that are not possible with achiral LC droplets.

Controlled Self-Assembly of Hexagonal Nanoparticle Patterns on Nanotopographies.

Diblock copolymer micelle nanolithography (BCML) is a versatile and efficient method to cover large surface areas with hexagonally ordered arrays of metal nanoparticles, in which the nanoparticles are equally spaced. However, this method falls short of providing a controlled allocation of such regular nanoparticle arrays with specific spacing into micropatterns. We present here a quick and high-throughput method to generate quasi-hexagonal nanoparticle structures with well-defined interparticle spacing on segments of nanotopographic Si substrates. The topographic height of these segments plays a dominant role in dictating the spacing between the gold nanoparticles, as the nanoparticle arrangement is controlled by immersion forces and by their self-assembly within the segments. Our novel strategy of employing a single-step BCML routine is a highly promising method for the fabrication of regular gold nanopatterns in micropatterns for a wide range of applications.

Directed Self-Assembly of Micron-Sized Gold Nanoplatelets into Oriented Flexible Stacks with Tunable Interplate Distance.

A growing demand for control over the interparticle spacing and the orientation of anisotropic metallic particles into self-assembled structures is fuelled by their use in potential applications such as in plasmonics, catalysis, sensing, and optoelectronics. Here, we present an improved high yield synthesis method to fabricate micron- and submicron-sized gold nanoplatelets with a thickness less than 20 nm using silver nanoplatelets as seeds. By tuning the depth of the secondary minimum in the DLVO interaction potential between these particles, we are able to assemble the platelets into dynamic and flexible stacks containing thousands of platelets arranged face-to-face with well-defined spacing. Moreover, we demonstrate that the length of the stacks, and the interplate distance can be controlled between tens and hundreds of nm with the ionic strength. We use a high frequency external electric field to control the orientation of the stacks and direct the stacks into highly organized 2D and 3D assemblies that strongly polarize light.