Evidence for root adaptation to a spatially discontinuous water availability in the absence of external water potential gradients.

We hereby show that root systems adapt to a spatially discontinuous pattern of water availability even when the gradients of water potential across them are vanishingly small. A paper microfluidic approach allowed us to expose the entire root system of Brassica rapa plants to a square array of water sources, separated by dry areas. Gradients in the concentration of water vapor across the root system were as small as 10-4⋅mM⋅m-1 (∼4 orders of magnitude smaller than in conventional hydrotropism assays). Despite such minuscule gradients (which greatly limit the possible influence of the well-understood gradient-driven hydrotropic response), our results show that 1) individual roots as well as the root system as a whole adapt to the pattern of water availability to maximize access to water, and that 2) this adaptation increases as water sources become more rare. These results suggest that either plant roots are more sensitive to water gradients than humanmade water sensors by 3-5 orders of magnitude, or they might have developed, like other organisms, mechanisms for water foraging that allow them to find water in the absence of an external gradient in water potential.

How Can Materials Chemists Contribute to Food Supply Security in the Age of AI and Robotics?

Global factors are compromising the security of the food supply. Many of us in our community might be unsure about how to help with our seemingly inapplicable expertise. In this piece, I describe how materials chemistry and materials chemists will be essential in addressing this problem, but not only in the way we might think. There is a gigantic and largely unexplored opportunity for real societal impact if we accept a broader view of what academic materials chemistry can be.

Hydrogel-based transparent soils for root phenotyping in vivo.

Root phenotypes are increasingly explored as predictors of crop performance but are still challenging to characterize. Media that mimic field conditions (e.g., soil, sand) are opaque to most forms of radiation, while transparent media do not provide field-relevant growing conditions and phenotypes. We describe here a "transparent soil" formed by the spherification of hydrogels of biopolymers. It is specifically designed to support root growth in the presence of air, water, and nutrients, and allows the time-resolved phenotyping of roots in vivo by both photography and microscopy. The roots developed by soybean plants in this medium are significantly more similar to those developed in real soil than those developed in hydroponic conditions and do not show signs of hypoxia. Lastly, we show that the granular nature and tunable properties of these hydrogel beads can be leveraged to investigate the response of roots to gradients in water availability and soil stiffness.

Growth of Colloidal Nanocrystals by Liquid-Like Coalescence*.

We here describe, model, and predict the growth kinetics of amine-capped PbS colloidal nanoparticles in the absence of supersaturation. The particles grow by coalescence rather than by Ostwald ripening. A comparison of different models indicates that the effective activation energy of coalescence (67.65 kJ mol-1 ) is associated with two terms: a term proportional to the contact area between the ligand shells of two colliding particles, and a constant term. Our Brownian dynamics simulations show (i) how the remarkably low activation energy (or large rate constants) are most likely due to the large difference in size between the particles and their mean free path of diffusion, and (ii) how the low polydispersity is the likely result of the suppression of collision rates between rare populations due to crowding. The model successfully predicts the growth kinetics of nanoparticles, therefore enabling the precise control of the average particle size without the need of supersaturation.

Suppressing Evaporative Loss in Slippery Liquid-Infused Porous Surfaces (SLIPS) with Self-Suspended Perfluorinated Nanoparticles.

This article describes an approach to resolving the issue of evaporative loss from slippery liquid-infused porous surfaces (SLIPS). Hydrophobic and oleophobic fluids with significantly reduced evaporative loss rates at temperatures of up to 90 °C were obtained by the one-step mixing of commercially available perfluorinated lubricants with colloidal nanoparticles to form self-suspended nanoparticle fluids (i.e., suspensions nearly devoid of solvent). No evaporative loss was detected at temperatures of as high as 50 °C for over 3 months. Furthermore, the approach allows us to combine the function of the nanoparticles with the slippery characteristic of SLIPS.

On the kinetics of the removal of ligands from films of colloidal nanocrystals by plasmas.

This paper describes the kinetic limitations of etching ligands from colloidal nanocrystal assemblies (CNAs) by plasma processing. We measured the etching kinetics of ligands from a CNA model system (spherical ZrO2 nanocrystals, 2.5-3.5 nm diameter, capped with trioctylphosphine oxide) with inductively coupled plasmas (He and O2 feed gases, powers ranging from 7 to 30 W, at pressures ranging from 100 to 2000 mTorr and exposure times ranging between 6 and 168 h). The etching rate slows down by about one order of magnitude in the first minutes of etching, after which the rate of carbon removal becomes proportional to the third power of the carbon concentration in the CNA. Pressure oscillations in the plasma chamber significantly accelerate the overall rate of etching. These results indicate that the rate of etching is mostly affected by two main factors: (i) the crosslinking of the ligands in the first stage of plasma exposure, and (ii) the formation of a boundary layer at the surface of the CNA. Optimized conditions of plasma processing allow for a 60-fold improvement in etching rates compared to the previous state of the art and make the timeframes of plasma processing comparable to those of calcination.

Plasma-based post-processing of colloidal nanocrystals for applications in heterogeneous catalysis.

This review summarizes the work on the use of plasmas to post-process nanostructures, in particular colloidal nanocrystals, as promising candidates for applications of heterogeneous catalysis. Using plasma to clean or modify the surface of nanostructures is a more precisely controlled method compared to other conventional methods, which is preferable when strict requirements for nanostructure morphology or chemical composition are necessary. The ability of plasma post-processing to create mesoporous materials with high surface areas and controlled microstructure, surfaces, and interfaces has transformational potential in catalysis and other applications that leverage surface/interface processes.

Colloidal TiO2 nanocrystals with engineered defectivity and optical properties.

Partially reduced forms of titanium dioxide (sometimes called "black" titania) have attracted widespread interest as promising photocatalysts of oxidation due to their absorption in the visible region. The main approaches to produce it rely on postprocessing at high temperatures (up to 800 °C) and high pressures (up to 40 bar) or on highly reactive precursors (e.g., TiH2), and yield powders with poorly controlled sizes, shapes, defect concentrations and distributions. We describe an approach for the one-step synthesis of TiO2 colloidal nanocrystals at atmospheric pressure and temperatures as low as 280 °C. The temperature of the reaction allows the density of oxygen vacancies to be controlled by nearly two orders of magnitude independently of their size, shape, or colloidal stability. This synthetic pathway appears to produce vacancies that are homogeneously distributed in the nanocrystals, rather than being concentrated in an amorphous shell. As a result, the defects are protected from oxidation and result in stable optical properties in oxidizing environments.

Polymer-like conformation and growth kinetics of Bi2S3 nanowires.

One-dimensional inorganic crystals (i.e., crystalline nanowires) are one of the most intensely investigated classes of materials of the past two decades. Despite this intense effort, an important question has yet to be answered: do nanowires display some of the unique characteristics of polymers as their diameter is progressively decreased? This work addresses this question with three remarkable findings on the growth and form of ultrathin Bi(2)S(3) nanowires. (i) Their crystallization in solution is quantitatively describable as a form of living step-growth polymerization: an apparently exclusive combination of addition of "monomer" to the ends of the nanowires and coupling of fully formed nanowires "end-to-end", with negligible termination and initiation. (ii) The rate constants of these two main processes are comparable to those of analogous processes found in polymerization. (iii) The conformation of these nanowires is quantitatively described as a worm-like conformation analytically analogous to that of semiflexible polymers and characterized by a persistence length of 17.5 nm (shorter than that of double-stranded DNA) and contour lengths of hundreds of micrometers (longer than those of most synthetic polymers). These findings do not prove a chemical analogy between crystals and polymers (it is unclear if the monomer is a molecular entity tout court) but demonstrate a physical analogy between crystallization and polymerization. Specifically, they (i) show that the crystallization of ensembles of nanoscale inorganic crystals can be conceptually analogous to polymerization and can be described quantitatively with the same experimental and mathematical tools, (ii) demonstrate that one-dimensional nanocrystals can display topological characteristics of polymers (e.g., worm-like conformation in solution), (iii) establish a unique experimental model system for the investigation of polymer-like topological properties in inorganic crystals, and (iv) provide new heuristic guidelines for the synthesis of polymer-like nanowires.

Ultrathin Bi2S3 nanowires: surface and core structure at the cluster-nanocrystal transition.

Herein, we present the structural characterization of the core and surface of colloidally stable ultrathin bismuth sulfide (Bi(2)S(3)) nanowires using X-ray Absorption Spectroscopy (EXAFS and XANES), X-ray Photoelectron Spectroscopy (XPS), and Nuclear Magnetic Resonance (NMR). These three techniques allowed the conclusive structural characterization of the inorganic core as well as the coordination chemistry of the surface ligands of these structures, despite the absence of significant translational periodicity dictated by their ultrathin diameter (1.6 nm) and their polycrystallinity. The atomic structure of the inorganic core is analogous to bulk bismuthinite, but Bi atoms display a remarkably higher coordination number than in the bulk. This can be only explained by a model in which each bismuth atom at the surface (or in close proximity to it) is bound to at least one ligand at any time.

Cross-linking Bi2S3 ultrathin nanowires: a platform for nanostructure formation and biomolecule detection.

This paper describes the use of chemical cross-linking of ultrathin inorganic nanowires as a bottom-up strategy for nanostructure fabrication as well as a chemical detection platform. Nanowire microfibers are produced by spinning a nanowire dispersion into a cross-linker solution at room temperature. Nanomembranes with thicknesses down to 50 nm were obtained by injecting the nanowire dispersion at the cross-linker-solution/air interface. Furthermore, the sensitivity of the nanowire to amine cross-linkers allowed development of a novel sensing platform for small molecules, like the neurotransmitter serotonin, with detection limits in the picomolar regime.

Nanocrystal plasma polymerization: from colloidal nanocrystals to inorganic architectures.

Nanocrystal superstructures are increasingly becoming a subject of intense study. Such materials could constitute a new class of nanocomposites of designed structure, of homogeneous composition, and with unique properties. New phenomena are observed in these materials because of the interaction at such diminutive length scales. A common problem in the development of devices relying on colloidal nanocrystal assemblies is that the individual nanocrystal building blocks require organic molecules to control their size. These ligands are responsible for the colloidal stability of the individual nanocrystal building blocks and are thus necessary for their solution processibility. Because of the ligands' incompatibility with many solid state applications, it is important to develop post-processing techniques that mildly remove them from these nanocomposites, while maintaining the size-dependent properties of the building blocks. This Account highlights a new strategy, nanocrystal plasma polymerization (NPP), for processing colloidal nanocrystal assemblies. This technique exposes the nanocomposite to a mild air plasma and allows for the removal of the nanocrystals' capping ligands while preserving their size-dependent and material properties. As a result, the process yields a nearly all-inorganic flexible solid-state material with unprecedented characteristics. We describe early experiments, in which NPP was used to create arbitrarily complex 1D, 2D, and 3D inorganic free-standing architectures entirely composed of nanocrystals, as well as future directions and challenges. We expect this platform will be useful for the design of new materials and will be a valuable new addition to the nanoscientist's toolbox.

Self-Limiting Processes in the Flame-Based Fabrication of Superhydrophobic Surfaces from Silicones.

Outdoor applications of superhydrophobic coatings require synthetic approaches that allow their simple, fast, scalable, and environmentally benign deployment on large, heterogeneous surfaces and their rapid regeneration in situ. We recently showed that the thermal degradation of silicones by flames fulfills these characteristics by spontaneously structuring silicone surfaces into a hierarchical, textured structure that provides wear-resistant, healable superhydrophobicity. This paper elucidates how flame processing-a simple, rapid, and out-of-equilibrium process-can be so counterintuitively reliable and robust in producing such a complex structure. A comprehensive study of the effect of the processing speed and flame temperature on the chemical and physical properties of the coatings yielded three surprising results. (i) Three thermal degradation mechanisms drive the surface texturing: depolymerization (in the O2-rich conditions of the surface), decomposition (in the O2-poor conditions found a few micrometers from the surface), and pyrolysis at excessive temperatures. (ii) The operational condition is delimited by the onset of the depolymerization at low temperatures and the onset of pyrolysis at high temperatures. (iii) The remarkably wide operational conditions and robustness of this approach result from self-limiting growth and oxidation of the silicone particles that are responsible for the surface texturing and in the extent of their deposition. As a result of this analysis we show that superhydrophobic surfaces can be produced or regenerated with this approach at a speed of 15 cm s-1 (i.e., the length of an airport runway in ∼4.5 h).

Stress response to CO2 deprivation by Arabidopsis thaliana in plant cultures.

After being the standard plant propagation protocol for decades, cultures of Arabidopsis thaliana sealed with Parafilm remain common today out of practicality, habit, or necessity (as in co-cultures with microorganisms). Regardless of concerns over the aeration of these cultures, no investigation has explored the CO2 transport inside these cultures and its effect on the plants. Thereby, it was impossible to assess whether Parafilm-seals used today or in thousands of older papers in the literature constitute a treatment, and whether this treatment could potentially affect the study of other treatments.For the first time we report the CO2 concentrations in Parafilm-sealed cultures of A. thaliana with a 1 minute temporal resolution, and the transcriptome comparison with aerated cultures. The data show significant CO2 deprivation to the plants, a drastic suppression of photosynthesis, respiration, starch accumulation, chlorophyll biosynthesis, and an increased accumulation of reactive oxygen species. Most importantly, CO2 deprivation occurs as soon as the cotyledons emerge. Gene expression analysis indicates a significant alteration of 35% of the pathways when compared to aerated cultures, especially in stress response and secondary metabolism processes. On the other hand, the observed increase in the production of glucosinolates and flavonoids suggests intriguing possibilities for CO2 deprivation as an organic biofortification treatment in high-value crops.

Sustainable scalable synthesis of sulfide nanocrystals at low cost with an ionic liquid sulfur precursor.

Increasing the sustainability of nanocrystals is crucial to their application and the protection of the environment. Sulfur precursors for their synthesis are commonly obtained through multiple steps from H2S, only to be converted back to H2S during the synthesis of the nanocrystals. This convoluted process requires energy, reduces yields, increases waste and auxiliaries, and complicates recycling. Using H2S directly could drastically improve sustainability, but is prevented by toxicity and handling. We here show that H2S is stabilized by reaction with oleylamine (the most common and versatile ligand in nanoparticle synthesis) to form an ionic liquid precursor that addresses all major principles of green chemistry: it is made in one exothermic step, it leaves the reaction yielding a safer product and allowing the separate recycling of the precursors, and it produces high quality nanocrystals with high yields (sulfur yield > 70%) and concentrations (90 g L-1) in ambient conditions.

HOMEs for plants and microbes - a phenotyping approach with quantitative control of signaling between organisms and their individual environments.

We describe a simple, scalable, modular, and frugal approach to create model ecosystems as millifluidic networks of interconnected habitats (hosting microbes or plants), which offers (i) quantitative and dynamic control over the exchange of chemicals between habitats, and (ii) independent control over their environment. Oscillatory laminar flows produce regions of vortex mixing around obstacles. When these overlap, rapid mass transport by dispersion occurs, which is quantitatively describable as diffusion, but is directional and tunable in rate over 3 orders of magnitude. This acceleration in the rate of diffusion is equivalent to reducing the distance between the habitats, and therefore, the organisms, down to the length scales characteristic of signaling in soil (<2 mm).

Large-Scale Synthesis of Colloidal Si Nanocrystals and Their Helium Plasma Processing into Spin-On, Carbon-Free Nanocrystalline Si Films.

This paper describes a simple approach to the large-scale synthesis of colloidal Si nanocrystals and their processing into spin-on carbon-free nanocrystalline Si films. The synthesized silicon nanoparticles are capped with decene, dispersed in hexane, and deposited on silicon substrates. The deposited films are exposed to nonoxidizing room-temperature He plasma to remove the organic ligands without adversely affecting the silicon nanoparticles to form crack-free thin films. We further show that the reactive ion etching rate in these films is 1.87 times faster than that for single-crystalline Si, consistent with a simple geometric argument that accounts for the nanoscale roughness caused by the nanoparticle shape.

From Petri Dishes to Model Ecosystems.

Model ecosystems could provide significant insight into the evolution and behavior of real ecosystems. We discuss the advantages and limitations of common approaches like mesocosms. In this context, we highlight recent breakthroughs that allow for the creation of networks of organisms with independently controlled environments and rates of chemical exchange.