We devise a unique heteronanostructure array to overcome a persistent issue of simultaneously utilizing the surface-enhanced Raman scattering, inexpensive, Earth-abundant materials, large surface areas, and multifunctionality to demonstrate near single-molecule detection. Room-temperature plasma-enhanced chemical vapor deposition and thermal evaporation provide high-density arrays of vertical TiO2 nanotubes decorated with Ag nanoparticles. The role of the TiO2 nanotubes is 3-fold: (i) providing a high surface area for the homogeneous distribution of supported Ag nanoparticles, (ii) increasing the water contact angle to achieve superhydrophobic limits, and (iii) enhancing the Raman signal by synergizing the localized electromagnetic field enhancement (Ag plasmons) and charge transfer chemical enhancement mechanisms (amorphous TiO2) and by increasing the light scattering because of the formation of vertically aligned nanoarchitectures. As a result, we reach a Raman enhancement factor of up to 9.4 × 107, satisfying the key practical device requirements. The enhancement mechanism is optimized through the interplay of the optimum microstructure, nanotube/shell thickness, Ag nanoparticles size distribution, and density. Vertically aligned amorphous TiO2 nanotubes decorated with Ag nanoparticles with a mean diameter of 10–12 nm provide enough sensitivity for near-instant concentration analysis with an ultralow few-molecule detection limit of 10–12 M (Rh6G in water) and the possibility to scale up device fabrication.

In this work, the flexure strength and fracture propagation mechanisms in yttria tetragonal zirconia (3YTZP) dense composites with 1 and 5 vol.% exfoliated graphene nanoplatelets (e-GNP) were assessed. The composite powders were processed by dry planetary ball milling to exfoliate the as-received GNP, and then densified by spark plasma sintering (SPS). The hardness and Young’s modulus were measured by Vickers indentation and the impulse-echo technique, respectively. Flexural strength and modulus were estimated by four-point bending tests. Finally, cracks originated by Vickers indentations were analyzed by scanning electron microscopy (SEM). The Raman spectra and SEM observations showed a reduction in the number of graphene layers and most remarkably in the lateral size of the e-GNP, achieving a very homogeneous distribution in the ceramic matrix. The hardness, elastic modulus, and flexural strength of the 3YTZP matrix did not vary significantly with the addition of 1 vol.% e-GNP, but they decreased when the content increased to 5 vol.%. The addition of e-GNP to 3YTZP increased its reliability under bending, and the small lateral size of the e-GNP produced isotropic fracture propagation. However, the energy dissipation mechanisms conventionally attributed to the larger GNP such as fracture deflection or blocking were limited.

Despite the youthfulness of hybrid halide perovskite solar cells, their efficiencies are currently comparable to commercial silicon and have surpassed quantum‐dots solar cells. Yet, the scalability of these devices is a challenge due to their low reproducibility and stability under environmental conditions. However, the techniques reported to date to tackle such issues recurrently involve the use of solvent methods that would further complicate their transfer to industry. Herein a reliable alternative relaying in the implementation of an ultrathin plasma polymer as a passivation interface between the electron transport layer and the hybrid perovskite layer is presented. Such a nanoengineered interface provides solar devices with increased long‐term stability under ambient conditions. Thus, without involving any additional encapsulation step, the cells retain more than 80% of their efficiency after being exposed to the ambient atmosphere for more than 1000 h. Moreover, this plasma polymer passivation strategy significantly improves the coverage of the mesoporous scaffold by the perovskite layer, providing the solar cells with enhanced performance, with a champion efficiency of 19.2%, a remarkable value for Li‐free standard mesoporous n‐i‐p architectures, as well as significantly improved reproducibility.

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The eventual exploitation of one-dimensional nanomaterials yet needs the development of scalable, high yield, homogeneous and environmentally friendly methods able to meet the requirements for the fabrication of under design...

Fabrication of tunable wetting surfaces is sought for the last years given its importance on energy, biomaterials and antimicrobials, water purification, microfluidics, and smart surfaces. Liquid management on surfaces mainly depends on the control at the micro‐ and nanoscale of both roughness and chemical composition. Herein, the combination of a soft‐template method and plasma‐enhanced chemical vapor deposition is presented for the synthesis of TiO2 nanofibers on porous substrates such as cellulose and stainless‐steel membranes. The protocol, carried out under mild conditions, produces 3D nanomembranes with superhydrophobicity and oleophilicity that are tested as microliter water/oil filters. Photoactivation of TiO2 by UV illumination provides a straightforward approach for wetting tunability that converts the surface into amphiphilic. A final chemical modification of the TiO2 nanofibers by embedding them in an elastomeric polymeric shell and by fluorine‐based grafting opens the path toward the formation of superomniphobic and self‐cleaning surfaces with long‐lasting lifetimes. Thus, a reliable procedure is demonstrated for the fabrication of TiO2 nanofibers, which allows the modification of porous supports and provides an innovative route for the development of 3D nanomembranes with under design wetting. This protocol is extendable to alternative metal oxides, metals, and core@shell nanoarchitectures with potential multifunctionalities.

optoelectronic properties, finding applications as solar cells, [1,2] light-emitting devices, [3,4] and photodetectors. [5][6][7] Within these applications, the synthesis by vacuum deposition arises as an industrial scalable, low cost, and environmentally friendly methodology to fabricate efficient, stable, and durable optoelectronic devices. [8][9][10][11] Moreover, the anisotropic nanostructuration of OMHP such as nanorods, nanowires, or nanoplatelets has been achieved by different routes, [6,[12][13][14] which can be divided into template-and chemical-assisted growth: [15] the first makes use of template structures such as electrospun fibers [16] or nanostructures such as pillars or grooves [17,18] to grow the OMHP in its interior, while the second, the most used, employs solution synthetic approaches to control the growth such as surfactants or anion-exchange reactions, among others. [12,19] One crucial characteristic of these semiconductor anisotropic nanostructures is their polarizationsensitive optoelectronic response. [15,[20][21][22] Although many of our current devices make use of polarizers to produce polarized light, there are several drawbacks, such as the reduced intensity of the generated beam and/or their integration in micro-and nanoscale devices, limiting the overall efficiency of the optoelectronic systems. [15,23] Polarizers are ubiquitous components in current optoelectronic devices as displays or photographic cameras. Yet, control over light polarization is an unsolved challenge, since the main drawback of the existing display technologies is the significant optical losses. In such a context, organometal halide perovskites (OMHP) can play a decisive role given their flexible synthesis with tunable optical properties such as bandgap and photoluminescence, and excellent light emission with a low non-radiative recombination rate. Therefore, along with their outstanding electrical properties have elevated hybrid perovskites as the material of choice in photovoltaics and optoelectronics. Among the different OMHP nanostructures, nanowires and nanorods have lately arisen as key players in the control of light polarization for lighting or detector applications. Herein, the fabrication of highly aligned and anisotropic methylammonium lead iodide perovskite nanowalls by glancing-angle deposition, which is compatible with most substrates, is presented. Their high alignment degree provides the samples with anisotropic optical properties such as light absorption and photoluminescence. Furthermore, their implementation in photovoltaic devices provides them with a polarization-sensitive response. This facile vacuum-based approach embodies a milestone in the development of last-generation polarization-sensitive perovskite-based optoelectronic devices such as lighting appliances or self-powered photodetectors.

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