This article presents a comprehensive overview of currently available research on bioimplantable energy harvesters, with a specific focus on their fabrication and issue of biocompatibility. Both the achievements and limitations of the field are pointed out from the standpoint of materials science and engineering as directions for future research. Particular attention is paid to the controversy over the use of lead-based or lead-free piezoelectric ceramics in biomedical applications, which is closely related to different temporalities of research on biological conditions. This report is intended to serve as a reference guide for developing the next generation of piezoelectric biomedical devices.

The deeper comprehension of biological phenomena has led to the pursuit of designing and architecting complex biological systems. This has been incorporated through the advances in bioprinting of artificial organs and implants even at the microscale. In addition, tissue modeling has been employed to understand and prevent malfunctional and detrimental mechanisms that lead to fatal diseases. Furthermore, the endeavor to convey the mechanical properties of both scaffolds and cells has enabled the unveiling of disease modeling and regenerative medicine. This paper aims to provide a brief review of the design, modeling and characterization of conventional and architected structures employed in bioengineering.

Unconventional techniques to benefit from the low-cost and high-efficiency monocrystalline silicon solar cells can lead to new device capabilities and engineering prospects. Here, a nature-inspired spherical solar cell is demonstrated, which is capable of capturing light three-dimensionally. The proposed cell architecture is based on monocrystalline silicon and is fabricated using a corrugation technique. The spherical cell shows an increase in power output by up to 101% with respect to a traditional flat cell with the same projection area using different reflective materials. Finally, the spherical cell shows advantages in terms of enhanced heat dissipation and reduced dust accumulation over conventional cells.

Bioelectronics aims to design electronic devices which can be fully integrated within tissues to monitor or stimulate specific cell functions. The main challenge is the engineering of the cell–chip interface and diverse materials, and devices have been developed to recapitulate biological architectures and functionalities. In this Prospective article, the authors give an overview on how the bioelectronics community has exploited biomimetic approaches to emulate cell morphologies, interactions, and functions to design optimal electrical platforms to be coupled to living cells.

The current COVID-19 pandemic has caused the shortage of personal protective equipment (PPE) where improvised manufacturing in particular 3D printing has addressed many needs. This prospective discusses the current global crisis, then follows the wide interest in addressing the shortage of medical devices and PPEs used for treatment and protection against pathogens. An overview of the 3D printing process with polymer materials is given followed by the different 3D printing projects of PPEs and medical devices that emerged for the pandemic (including validation/testing). The potential for rapid prototyping with different polymer materials and eventual high-throughput production is emphasized.

Inspired by the recently reported translucency of monolayer graphene (GE) to wetting, atomistic simulations are employed to evaluate water flow enhancement induced by GE deposited on the inner surfaces of hydrophilic nanochannels. The flow in the coated channels exhibits a slip length of approximately 3.0 nm. Moreover, by contrasting the flow rates in channels with coated walls against flow rates in the corresponding uncoated channels, an “effective” flow enhancement from 3.2 to 3.7 is computed. The probability density function of the water dipole orientation indicates that the flow enhancement is related to a thinner structured water layer at the solid–liquid interface. This study provides quantitative evidence that GE employed as coating reduces substantially hydraulic losses in hydrophilic nanoconfinement.

Sample geometry effects on mechanical strengths of gold micro-cantilevers are evaluated by a micro-bending test. Six micro-cantilevers with the same length of 50 μm are prepared, and the width and the thickness are varied to examine individual effects on the yield stress. The yield stress increases from 428 to 519 MPa when the thickness decreases from 11.1 to 6.0 μm. No obvious dependency is observed when varying the width. The results reveal that the thickness and the width each has a different influence on the yield stresses of micro-cantilevers evaluated by the bending test, which is the sample geometry effect.

The photothermal experiments on the incident light angle dependence are carried out using simulated solar light on thin films of both iron oxides (Fe3O4 and Fe3O4@Cu2-xS) and porphyrin compounds (chlorophyll and chlorophyllin). Fe3O4 and Fe3O4@Cu2-xS are synthesized using various solution methods that produce mono-dispersed nanoparticles on the order of 10 nm. Chlorophyll is extracted from fresh spinach and chlorophyllin sodium copper is a commercial product. These photothermal (PT) materials are dispersed in polymethyl methacrylate (PMMA) solutions and deposited on glass substrates via spin coating that result in clear and transparent thin films. The iron-oxide based thin films show distinctive absorption spectra; Fe3O4 exhibits a strong peak near UV and gradually decreases into the visible and NIR regions; the absorption of Fe3O4@Cu2-xS is similar in the UV region but shows a broad absorption in the NIR region. Both chlorophyll and chlorophyllin are characterized with absorption peaks near UV and NIR showing a “U”-shaped spectrum, ideally required for efficient solar harvest and high transparency in energy-efficient single-pane window applications. Upon coating of the transparent PT films on the window inner surfaces, solar irradiation induces the photothermal effect, consequently raising the film temperature. In this fashion, the thermal loss through the window can be significantly lowered by reducing the temperature difference between the window inner surface and the room interior, based on a new concept of so-called optical thermal insulation (OTI) without any intervention medium, such as air/argon, as required in the glazing technologies. Single-panes are therefore possible to replace double- or triple panes. As OTI is inevitably affected by seasonal and daily sunlight changes, an incident light angle dependence of the photothermal effect is crucial in both thin film and window designs. It is found that the heating curves reach their maxima at small angles of incidence while the photothermal effect is considerably reduced at large angles. This angle dependence is well explained by light reflection by the thin film surface, however, deviated from what is predicted by the Fresnel's law, attributable to non-ideal surfaces of the substrates. The angle dependence data provide an important reference for OTI that window exposure to the sun is greater at winter solstice while that is considerably reduced in the summer. This conclusion indicates much enhanced solar harvesting and heat conversion via optically insulated windows in the winter season, resulting in much lower U-factors.

Gravity is commonly considered negligible when the surface tension is dominant; i.e., the Bond number is less than 1. In this paper, however, the authors present a technique in which drops slide over surfaces with zero effective gravity. Our study compared the sliding motion of water drops on hydrophilic and hydrophobic surfaces in scenarios: one in which effective gravity = 1 (1 g) and one in which it = 0 (0 g). The authors found that the lateral retention force was greater under 1 g than it was under 0 g. Also, the results showed that retention forces calculated by Furmidge equation are higher than the measured forces.

Material changes in yttrium-doped barium zirconate, BaZr0.8Y0.2O3–x, were studied using in situ Raman spectroscopy and ex situ x-ray photoelectron spectroscopy analysis. During in situ Raman analysis, samples were heated to temperatures of 300–600 °C and exposed to both dry and humidified H2 atmospheres. At the lower temperatures (300–450 °C), a new vibrational peak appears in the Raman spectra during exposure to humidified H2. The appearance of this feature is reversible, dependent on previous sample history, and possibly results from new, secondary phase formation or lattice distortion.

The dendrite morphologies of the cast nickel-based superalloy CMSX-4® (CMSX-4® is registered trademarks of the Cannon-Muskegon Corporation) and the austenitic stainless steel HP microalloy have been obtained via an automated serial-sectioning process which allows three-dimensional (3D) microstructural characterization. The dendrite arm spacing, volume fraction of segregation, and fraction of porosity have been determined. This technique not only increases the depth, scope, and level of detailed microstructural characterization but also delivers microstructural data for modeling and simulation.

Our recent exploration into the use of biodegradable metals and surface treatments resulting in sufficient strength for skeletal reconstruction applications has led to the need to test these devices’ cytotoxicity. More specifically, our group has developed a resorbable magnesium alloy, Mg–1.2Zn–0.5Ca–0.5Mn, that can be strengthened by heat treatment and coated with a ceramic layer offering time-certain resorption of a medical device. This in vitro study shows that these treatments do not result in cytotoxicity. Both heat-treated (HT) and HT + ceramic-coated (sol–gel) coupons demonstrated more than 70% viability. Thus, these processing steps are likely to be useful in producing biocompatible, resorbable implants that incorporate our Mg–1.2Zn–0.5Ca–0.5Mn alloy.

This research investigates a novel composite of encapsulated paraffin in boron nitride nanotube (BNNT) which is more thermally and chemically stable than carbon nanotube. This composite can achieve high thermal conductivity and, meanwhile, have thermal energy storage capability for efficient thermal management under extreme conditions. Equilibrium molecular dynamics simulations were conducted to study self-diffusion coefficient, thermal conductivity, and specific heat of encapsulated paraffin. The simulation results indicated that the self-diffusion coefficient and thermal conductivity of paraffin could be increased by up to 10 and 7 times, respectively, while specific heat was reduced after encapsulating into BNNT.

In this paper, the Lewis base character of 3-aminopropyltrimethoxysilane (3-APTMS), an imine derivative of siloxane, and an indole monomer were shown to enable the reduction of gold cations in acetone. The Lewis acid–base adduct of indole monomers and gold formed a polyindole–gold nanoparticle sol. Similarly, the Lewis acid–base adduct of 3-APTMS and gold enabled the formation of gold nanoparticles in the presence of acetone. The polyindole–gold nanoparticle sol and siloxane–gold nanoparticles underwent self-assembly into a polymeric nanofluid that was suitable for casting membranes. The use of these membranes as a potentiometric ion sensor for both cations and anions was considered; a common nonspecific ion exchange molecule, sodium tetraphenylborate, and the polymeric nanofluid were used to prepare an anion sensor and a cation sensor.

To overcome the steric effect of norbornene (NB), first-generation Grubbs’ catalyst (GC1) was used as the catalyst to graft NB onto the polypropylene (PP) chain by reactive extrusion. Instead of harsh reaction conditions, such as anhydrous, which was the general method to synthesize NB polymers, this convenient method would be easier to industrialize. The mechanism of grafting was studied by using Fourier Transform InfraRed spectra and differential scanning calorimetry. It was found that GC1 could initiate the ring-opening metathesis polymerization of NB to obtain short NB chain-grafted PP-g-NB. The rheological behavior showed that the grafted NB short chains on PP-g-NB increase the shear thinning of the polymers and decrease the system viscosity.

This study compares the investigated water vapor diffusion coefficient in the neat polyurethane (PU) membrane, the silica–PU nanocomposite membrane, and two surface-modified silica–PU nanocomposite membranes. The silane first surface modifier is with an amine functional group known as N-[3-(trimethoxysilyl)propyl]ethylenediamine, while the second one is with an aniline functional group known as N-[3-(trimethoxysilyl)propyl]aniline. The enhancement of water vapor diffusivity values through the polymer nanocomposite is desirable for the membrane air dehumidification application. The diffusivities were calculated via molecular dynamics simulations at the temperature of 298.15 K. The Einstein's relationship known as the mean square displacement method was used to obtain the diffusivity for the membranes. The results showed a significant effect on the diffusivity of water vapor for the surface-modified silica–PU nanocomposite membrane as compared with the neat PU and the unmodified silica–PU nanocomposite membranes. For the amine-modified silica, the diffusion coefficient increased by 80.3% compared with the unmodified silica–PU nanocomposite membrane. On the other hand, the aniline-modified silica outperformed the amine-modified one in terms of the diffusion coefficient by 22.4%.

The advancement of lead-free piezoelectric nanogenerators (PENGs) for flexible electronics necessitates designing more efficient systems for improved energy storage capacity. In this light, the effects of patterning BaTiO3 nanotubes within PENG on the electromechanical properties of the device were investigated. The PENGs comprised a sandwich structure of Ti–BaTiO3–graphite–Ti encapsulated in polydimethylsiloxane. Four patterns of vertically aligned BaTiO3 nanotubes were synthesized via the hydrothermal conversion of selectively-anodized TiO2 nanotubes. The highest output voltage reached up to 1.9 V. Decreasing the nanotube array spacing and pattern diameter increased the lateral displacement of BaTiO3 therefore, increasing the output voltage of the device.

This research focuses toward calculating the thermal conductivity of pillared-graphene structures (PGS). PGS consists of graphene and carbon nanotubes (CNTs). These two materials have great potential to manage heat generated by nano- and microelectronic devices because of their superior thermal conductivities. However, the high anisotropy limits their performance when it comes to three-dimensional heat transfer. Nonequilibrium molecular dynamics (NEMD) simulations were conducted to study thermal transport of PGS. The simulation results suggest that the thermal conductivity along the graphene plane can reach up to 284 W/m K depending on PGS’ parameters while along the CNT direction, the thermal conductivity can reach 20 W/m K.

This work investigates the influence of poly(dimethylsiloxane) (PDMS) within a nanocomposite coating solution constituted by silica nanoparticles and toluene on mechanical properties, surface wettability, and surface morphology. The developed coating's hardness and elastic modulus were studied in detail. A variation in mechanical properties was observed as the amount of PDMS was varied. Also, the average surface roughness, skewness, and kurtosis values show the influence of the amount of PDMS on the surface roughness characteristics of the coating. Furthermore, it was observed that the water contact angles were linked with the proportion of PDMS.

The development of new metalloplastic material from the combination of an alkaline-fused dehydrated glucose–copper (II) chloride, carbon soot, and polysulfone and the evaluation of its potential for the electrochemical detection of a pro-carcinogenic humic acid in water is reported. Excellent detection limit greater than 1 pico-part-per-million (order of 10–13 mg/L) was achieved, a value that proved to be first-of-its-kind till date. Transfer coefficients between 0.8 and 1.0 were realized. The new material showed some potential for splitting hydrogen peroxide to oxygen and thus may be explored for energy application in addition to its use as a water quality monitoring probe.