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This study investigates the formation of duplex electroless Ni-P/Ni-B and Ni-P/Ni-B-W alloys through electroless plating process coatings on mild steel using hypophosphite and sodium borohydride as a reducing agent, employing heat-treated. Electroless plating is affordable and suitable for coating convoluted structures. Duplex electroless on mild steel was characterized by X-ray diffraction (XRD), Energy-dispersive X-ray spectrometry (EDS), scanning electron microscopy (SEM) were used to examine the surface and cross-sectional morphologies of the duplex coating, and finally study electrochemical corrosion properties. The analysis reveals that duplex coating yields a thicker, more homogeneous coating with a characteristic cauliflower morphology and spherical nodular structures. The coating was initially amorphous, but finally crystallized when heated to 400 °C. More corrosion resistance was found in the Ni-P/Ni-B and Ni-P/Ni-B-W layers when Ni-B served as the outer covering. This study focuses on the important effects of varying tungsten concentrations and heat treatment on the corrosion resistance, surface quality, and microstructural characteristics of duplex coatings. Showed improved corrosion resistance when exposed to 0.5 g/L of Na 2 WO 4 ., (© 2024. The Author(s).)

Filtration membranes coated in metals such as copper have dramatically improved biofouling resistance and pathogen destruction. However, existing coating methods on polymer membranes impair membrane performance, lack uniformity, and may detach from their substrate, thus contaminating the permeate. To solve these challenges, we developed the first electroless deposition protocol to immobilize copper nanoparticles on electrospun polyacrylonitrile (PAN) fibers for the design of antimicrobial membranes. The deposition was facilitated by prior silver seeding. Distinct mats with average fiber diameters of 232 ± 36 nm, 727 ± 148 nm and 1017 ± 80 nm were evaluated for filtration performance. Well-dispersed copper nanoparticles were conformal to the fibers, preserving the open-cell architecture of the membranes. The copper particle sizes ranged from 20 to 140 nm. Infrared spectroscopy revealed the PAN fiber mats' relative chemical stability/resistance to the copper metallization process. In addition, the classical cyclization of the cyano functional group in PAN was observed. For model polystyrene beads with average sizes of 3 μm, Cu NP-PAN fiber mats had high water flux and separation efficiency with negligible loss of Cu NP from the fibers during flow testing. Fiber size increased flux and somewhat decreased separation efficiency, though the efficiency values were still high.

Hypothesis: Magnetic particles are widely used in many adsorption and removal processes. Among the many types of magnetic colloids, magnetic Janus particles offer significant possibilities for the effective removal of several components from aqueous solutions. Nevertheless, the synthesis of structures integrating different types of materials requires scalable fabrication processes to overcome the limitations of the available methodologies. Herein, we hypothesized a fabrication process for dual-surface functionalized magnetic Janus particles., Experiments: The primary silica particles with surface-attached amine groups are further asymmetrically modified by iron oxide nanoparticles, exploiting Pickering emulsion and electroless deposition techniques. The dual surface functionality of the particles is designed for its versatility and demonstrated in two wastewater-related applications., Findings: We show that our design can simultaneously remove chromium (VI) and phenol from aqueous solution. The fabricated magnetic-responsive Janus particles are also an effective adsorbent for genomic Deoxyribonucleic acid (DNA) and show superior performance to commercial magnetic beads. Thus, this study provides a novel platform for designing magnetic Janus particles with multifunctional surfaces for wastewater treatment applications., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 The Author(s). Published by Elsevier Inc. All rights reserved.)

This study explores MgB 2 as a reinforcing agent in electroless deposition on AZ91 magnesium alloy substrates, evaluating its impact on coating properties. X-ray diffraction (XRD) analysis shows that the amorphous Ni-B coating masks initial magnesium peaks, while MgB 2 enhances MgB 2 O(OH) 6 , MgB 2 O 5 , MgO, and MgB 2x Oy oxide phases. SEM images illustrate morphological shifts from cauliflower-like Ni-B structures to dendritic and fibrous MgB 2 forms, with higher MgB 2 concentrations leading to granular structures with randomly oriented crystallites resembling platelets, indicating increased magnesium content. MgB 2 -reinforced Ni-B coatings exhibited higher hardness than the substrate but lower than as-deposited Ni-B. Friction coefficients initially decreased with Ni-B, increased significantly with 0.1 g MgB 2 , and decreased with higher reinforcements, remaining higher than substrate and as-deposited Ni-B. MgB 2 reinforcement increased surface roughness, causing local agglomerations in 0.5 g MgB 2 coatings. Contact angle measurements demonstrated enhanced hydrophilicity due to MgB 2 's superhydrophilic properties influenced by surface roughness. Antibacterial tests revealed superior properties with 0.1 g MgB 2 , suggesting a transition to MgB 2 -enriched structures and influencing material properties. While Ni-B/MgB 2 coatings improved over substrate, further research is needed to optimize parameters and understand stabilizer effects. These coatings also exhibited superhydrophilicity and promising antibacterial properties, suggesting potential in advanced surface engineering applications., Competing Interests: The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (© 2024 The Authors. Published by Elsevier Ltd.)

Tailoring a material's surface with hierarchical structures from the micro- to the nanoscale is key for fabricating highly sensitive detection platforms. To achieve this, the fabrication method should be simple, inexpensive, and yield materials with a high density of surface features. Here, using benchtop fabrication techniques, gold surfaces with hierarchically structured roughness are generated for sensing applications. Hierarchical gold electrodes are prepared on pre-stressed polystyrene substrates via electroless deposition and amperometric pulsing. Electrodes fabricated using 1 mm H[AuCl₄] and roughened with 80 pulses revealed the highest electroactive surface area. These electrodes are used for enzyme-free detection of glucose in the presence of bovine serum albumin and achieved a limit of detection of 0.36 mm, below glucose concentrations in human blood. The surfaces nanoroughened with 100 pulses also showed excellent surface-enhanced Raman scattering (SERS) response for the detection of rhodamine 6G, with an enhancement factor of ≈2 × 10 6 compared to detection in solution, and for the detection of a self-assembled monolayer of thiophenol, with an enhancement factor of ≈30 compared to the response from microstructured gold surfaces. It is envisioned that the simplicity and low fabrication cost of these gold-roughened structures will expedite the development of electrochemical and SERS sensing devices., (© 2024 The Authors. Small Methods published by Wiley‐VCH GmbH.)

The emergence of defects during the early production phases of ferrous-alloy additively manufactured (AM) parts poses a serious threat to their versatility and adversely impacts their overall mechanical performance in industries ranging from aerospace engineering to medicine. Lack of fusion and gas entrapment during the manufacturing stages leads to increased surface roughness and porosities in the finished part. In this study, the efficacy of employing electroless nickel-boron (Ni-B) deposition to fill and level simulated AM defects was evaluated. The approach to levelling was inspired by the electrochemical deposition techniques used to fill vias in the electronics industry that (to some extent) resemble the size and shape of AM-type defects. This work investigated the use of surfactants to attenuate surface roughness in electroless nickel coatings, thereby achieving the preferential inhibition of the coating thickness on the surface and promoting the filling of the simulated defects. A cationic surfactant molecule, CTAB (cetyltrimethyl ammonium bromide), and a nonpolar surfactant, PEG (polyethylene glycol), at different concentrations were tested using a Ni-B electrolyte for the levelling study. It was found that the use of electroless Ni-B to fill simulated defects on ferrous alloys was strongly influenced by the concentration and nature of the surfactant. The highest levelling percentages were obtained for the heavy-molecular-weight PEG-mediated coatings at 1.2 g/L. The results suggest that electroless Ni-B deposition could be a novel and facile approach to filling defects in ferrous-based AM parts.

Flexible copper conductors have been extensively utilized in flexible and wearable electronics. They can be fabricated by using a variety of patterning techniques such as vacuum deposition, photolithography, and various printing techniques. However, vacuum deposition and photolithography are costly and result in material wastage. Moreover, traditional printing inks require posttreatment, which can damage flexible substrates, or grafting polymers, which involve complex processes to adhere to flexible substrates. Therefore, this study proposes a facile method of fabricating flexible metal patterns with high electrical conductivities and remarkable bonding forces on a diverse range of flexible substrates. Catalytic ink was prepared by using a mixture of epoxy resin, copper nanopowder, and nanosilica. The ink was applied to a variety of flexible substrates, including a poly(ethylene terephthalate) (PET) film, polyimide film, and filter paper, using screen printing to establish a bridge layer for subsequent electroless deposition (ELD). The catalytic efficiency was significantly improved by treating the cured ink patterns with air plasma. The fabricated flexible metals exhibited excellent adhesion and desirable electrical conductivity. The sheet resistance of the copper layer on the PET substrate decreased to 9.2 mΩ/□ after 150 min of ELD. The resistance of the flexible metal on the PET substrate increased by only 3.125% after 5000 bending cycles. The flexible metals prepared in this study demonstrated good foldability, and the samples with filter paper and PET substrates failed after 40 and 70 folds, respectively. A pressure sensor with a bottom electrode consisting of a copper interdigital electrode on a PET substrate displayed favorable sensing performance.

Electroless noble metal deposition on the conducting substrate is widely used to obtain the desired film or coating on the substrate of interest. Wire-gauge-based Pt/Pd/Pt-Pd (individually, sequentially, and simultaneously deposited) catalysts have been developed using formaldehyde and sodium formate as reducing agents. Various surface pretreatment methods like SnCl 2 + PdCl 2 seeding, oxalic acid etching, and HCl activation (etching) have been employed to obtain the desired noble metal coating. Minimum time duration was observed for simultaneously deposited catalysts using formaldehyde as a reducing agent. Prepared catalysts were characterized for noble metal deposition, coating kinetics, surface morphology, and binding energy. The catalyst was found to be active for H 2 and O 2 recombination reactions for hydrogen mitigation applications in nuclear reactors.

A Pt-coated Ni layer supported on a Ni foam catalyst (denoted PtNi/Ni foam ) was investigated for the electro-oxidation of the formic acid (FAO) in acidic media. The prepared PtNi/Ni foam catalyst was studied as a function of the formic acid (FA) concentration at bare Pt and PtNi/Ni foam catalysts. The catalytic activity of the PtNi/Ni foam catalysts, studied on the basis of the ratio of the direct and indirect current peaks ( j d )/( j nd ) for the FAO reaction, showed values approximately 10 times higher compared to those on bare Pt, particularly at low FA concentrations, reflecting the superiority of the former catalysts for the electro-oxidation of FA to CO 2 . Ni foams provide a large surface area for the FAO, while synergistic effects between Pt nanoparticles and Ni-oxy species layer on Ni foams contribute significantly to the enhanced electro-oxidation of FA via the direct pathway, making it almost equal to the indirect pathway, particularly at low FA concentrations.

This paper reports the synthesis of composite track-etched membranes (TeMs) modified with electrolessly deposited copper microtubules using copper deposition baths based on environmentally friendly and non-toxic reducing agents (ascorbic acid (Asc), glyoxylic acid (Gly), and dimethylamine borane (DMAB)), and comparative testing of their lead(II) ion removal capacity via batch adsorption experiments. The structure and composition of the composites were investigated by X-ray diffraction technique and scanning electron and atomic force microscopies. The optimal conditions for copper electroless plating were determined. The adsorption kinetics followed a pseudo-second-order kinetic model, which indicates that adsorption is controlled by the chemisorption process. A comparative study was conducted on the applicability of the Langmuir, Freundlich, and Dubinin-Radushkevich adsorption models to define the equilibrium isotherms and the isotherm constants for the prepared composite TeMs. Based on the regression coefficients R 2 , it has been shown that the Freundlich model better describes the experimental data of the composite TeMs on the adsorption of lead(II) ions.

Triboelectric nanogenerators (TENGs) are devices that can harvest energy from mechanical motions; such devices can be used to power wearable sensors and various low-power electronics. To increase the lifetime of the device, scientists mainly use the method of making TENG in a hard skeleton to simplify the complex possible relative movements between two triboelectric parts. However, the hard skeletons cannot be embedded in soft and lightweight clothing. To make matters worse, the materials used in the garments must be able to withstand high mechanical forces when worn, such as the pressure of more than 100 KPa exerted by body pressure or everyday knocks. Notably, the TENGs are usually made of fragile materials, such as vacuum-evaporated metal electrodes and nano-sized coatings, on the contact interface; these electrodes and coatings often chip or wear off under the action of external loads. In this work, we succeeded in creating a thin, light-weight, but extremely robust garment-integrated triboelectric nanogenerator (G-TENG) that can be embedded in clothing and pass the water wash test. First, we chemically deposited a durable electrode with flexible properties for G-TENG using a novel technique called polymer-assisted metal deposition (PAMD). The as-formed metal electrodes are firmly bonded to the plastic substrate by a sub-10 nm adhesive polymer brush and can withstand a pressure of 22.5 MPa and a tear force of 0.7 MPa. We then removed the traditionally used fragile nanoparticle materials and the non-durable poly-dimethylsiloxane (PDMS) layer at the triboelectric interface, and then used a cost-effective, durable and slightly flowable pressure-sensitive adhesive to form a plastic contact interface. Such a soft plastic interface can ensure full contact of the triboelectric materials, which is excellent in complex environments and ultimately improves the power generation efficiency of the devices. The as-formed low-cost energy harvesting device could become an industry standard for future smart clothing.

Recent developments in embedded electronics require the development of micro sources of energy. In this paper, the fabrication of an on-chip interdigitated all-solid-state supercapacitor, using porous gold electrodes and a PVA/KOH quasisolid electrolyte, is demonstrated. The fabrication of the interdigitated porous gold electrode is performed using an original bottom-up approach. A templating method is used for porosity, using a wet chemistry process followed by microfabrication techniques. This paper reports the first example of an all-gold electrode micro-supercapacitor. The supercapacitor exhibits a specific capacitance equal to 0.28 mF·cm -2 and a specific energy of 0.14 mJ·cm -2 . The capacitance value remains stable up to more than 8000 cycles.

Zinc oxide, as a commonly used photocatalytic degradation of organic pollutants, typically shows limitations in wastewater treatment, such as aggregation and recycling problems caused by nanoscale dimensions and inappropriate substrates. Anchoring ZnO on substrates is a strategy to obtain stable catalytic performance. Particularly, natural fibers with hollow structures are an attractive alternative for ecological and economical ZnO loading templates, but depositing ZnO onto hollowed fiber surfaces presents a challenge. Here, a straightforward in situ growth method for producing nanostructured zinc oxide on cotton fibers from recycled garments is reported. The modified polydopamine on the fiber surface captures the catalyst required for in situ growth of ZnO and serves as a platform for spontaneous catalytic crystal growth on the fiber surface. The ZnO nanocrystals are uniformly dispersed on the outer and inner walls of cotton fibers, demonstrating excellent durability in wastewater treatments. Moreover, the photocatalytic performance of functional fibers is optimized by doping Ag nanoparticles to improve degradation efficiency. This can extend the prospect of further applications of developed ZnO/fibers in optoelectronics, spintronics, and provide inspiration for recycling and upgrading of used garments., Competing Interests: The authors declare no conflict of interest., (© 2022 The Authors. Global Challenges published by Wiley‐VCH GmbH.)

Hierarchical functionalization of flax fibers with ZnO nanostructures was achieved by electroless deposition to improve the interfacial adhesion between the natural fibers and synthetic matrix in composite materials. The structural, morphological, thermal and wetting properties of the pristine and ZnO-coated flax fibers were investigated. Thus, the ZnO-coated flax fabric discloses an apparent contact angle of ~140° immediately after the placement of a water droplet on its surface. An assessment of the interfacial adhesion at the yarn scale was also carried out on the flax yarns coated with ZnO nanostructures. Thus, after the ZnO functionalization process, no significant degradation of the tensile properties of the flax yarns occurs. Furthermore, the single yarn fragmentation tests revealed a notable increase in the interfacial adhesion with an epoxy matrix, reductions of 36% and 9% in debonding and critical length values being measured compared to those of the pristine flax yarns, respectively. The analysis of the fracture morphology by scanning electron microscopy and X-ray microtomography highlighted the positive role of ZnO nanostructures in restraining debonding phenomena at the flax fibers/epoxy resin matrix interphase.

Gold nanowires have great potential use as interconnects in electronic, photonic, and optoelectronic devices. To date, there are various fabrication strategies for gold nanowires, each one associated with particular drawbacks as they utilize high temperatures, toxic chemicals, or expensive compounds to produce nanowires of suboptimal quality. Inspired by nanowire fabrication strategies that used higher-order biopolymer structures as molds for electroless deposition of gold, we here report a strategy for the growth of gold nanowires from seed nanoparticles within the lumen of microtubules. Luminal targeting of seed particles occurs through covalently linked Fab fragments of an antibody recognizing the acetylated lysine 40 on the luminal side of α-tubulin. Gold nanowires grown by electroless deposition within the microtubule lumen exhibit a homogeneous morphology and high aspect ratios with a mean diameter of 20 nm. Our approach is fast, simple, and inexpensive and does not require toxic chemicals or other harsh conditions.

Zinc oxide (ZnO), a widely used ultraviolet (UV) degrading substance, offers high selectivity for wastewater treatment, but the leaching of ZnO into water could cause secondary contamination. Using porous substrates to fix and load ZnO is a promising technical method to improve the water purification efficiency and recycling durability of ZnO. However, limited by the slow kinetics and shielding effects, it is challenging to use traditional techniques to introduce ZnO into the interior of a hollow structure. Here, inspired by an ancient dyeing procedure, we formed a unique single-molecule bio-interfacial entanglement as an absorption layer to capture the catalyst for ZnO electroless deposition (ELD) on the surface of natural ultrathin hollow-structured Kapok fibers. With curcumin serving as a linking bridge, ELD allowed the spontaneous formation of intensive ZnO nanocrystals on both the outer and inner walls. ZnO-kapok as the catalyst for ultraviolet photodecomposition of organic pollutants (methylene blue (MB) and phenol as model pollutants) delivered a decomposition efficiency of 80% and outstanding durability. Further modification of the ZnO-kapok catalyst by doping with reduced graphene oxide (rGO) showed an improvement in photodegradation performance of 90% degradation under 2-h irradiation with 21.85 W/dm 2 light power. Moreover, to the best of our knowledge, this is the first report featuring ZnO loading on both the outer and inner walls of a fiber-structured hollow kapok material, which provides inspiration for immobilization of metallic oxides on hollow-structured materials for further applications in renewable catalysis, chemical engineering, and energy storage fields.

Electronic transport through molecular-scale devices has been studied extensively for its extraordinary dimension superiority. Assembling such devices into large-scale functional circuits is crucial since the molecular tunnel junctions must be reliable, stable and reproducible during technological applications. In ideal circumstances, the device architecture should be designed such that the metal-molecule-metal (MMM) junctions can be analyzed by the more sensitive four point probe system. In this paper, we expound a delicate method to manufacture molecular junctions, which show excellent stability and reproducibility with high yields ( > 91 per cent). We form self-assembled monolayers (SAMs) on conductive Au thin film by microcontact printing and then generate robust covalently bound metal thin film electrodes on top of the SAMs by selective electroless deposition. Following MMM junction formation, a photoresist is coated and wells are opened on each feature by lithography. Then, Au thin film, as a permanent top electrode, is deposited into the photolithographically defined well. Conductivity analyzations were carried out on the 50 μm square junctions by the four point probe measurement, and the results showed reproducible tunneling I - V characteristics. This method reveals an approach not only offering a unique vehicle to investigate the electrical properties of molecule ensembles in MMMs, but also making a significant step toward MMM applications at the device level.

In this study, sodium borohydride oxidation has been investigated on the platinum nanoparticles modified copper/titanium catalysts (PtNPsCu/Ti), which were fabricated by employing the electroless copper plating and galvanic displacement technique. ICP-OES, XRD, FESEM, and EDX have been used to characterize PtNPsCu/Ti catalysts' composition, structure, and surface morphology. The oxidation of sodium borohydride was examined on the PtNPsCu/Ti catalysts using cyclic voltammetry and chrono-techniques.

Paper and textile are two ideal carriers in wearable and printed electronics because of their flexibility and low price. However, the porous and fibrous structures restrain their use in printed electronics because the capillary effect results in ink diffusion. Especially, conventional metal ink needs to be post-treated at high temperatures (>150 °C), which is not compatible with paper and textile. To address problems involved in ink diffusion and avoid high-temperature treatment, herein, a new strategy is proposed: screen-printing of high-viscosity catalytic inks combined with electroless deposition of metal layers on paper and textile substrates. The ink consists of Ag nanoparticles, a polydimethylsiloxane (PDMS) prepolymer, and a curing agent. PDMS as a viscoelastic matrix of catalysts plays key roles in limiting ink diffusion, enhancing interfacial adhesion between the substrate and metal layer, keeping metal flexible. As a demonstration, metal Cu and Ni are printed, respectively. The printed precision (diffusion < 1% on filter paper) can be controlled by adjusting the Ag content in the PDMS matrix; interfacial adhesion can be enhanced by ink coating on substrate microfibers and metal embedding into the PDMS matrix. In addition, Cu on paper shows extremely low sheet resistance (0.29 mΩ/□), and Cu on nylon shows outstanding foldability with a resistance of less than five times of initial resistance during 5000 folding cycles.

Over the past few years, metal nanowire networks have attracted attention as an alternative to transparent conducting oxide materials such as indium tin oxide for transparent conducting electrode applications. Recently, electrodeposition of metal on nanoscale template is widely used for formation of metal network. In the present work, junctionless Cu nanowire networks were simply fabricated on a substrate by forming a nanostructured Ru with 80 nm width as a seed layer, followed by direct electroless deposition of Cu. By controlling the density of Ru nanowires or the electroless deposition time, we readily achieve desired transmittance and sheet resistance values ranging from ∼1 kΩ sq -1 at 99% to 9 Ω sq -1 at 89%. After being transferred to flexible substrates, the nanowire networks exhibited no obvious increase in resistance during 8000 cycles of a bending test to a radius of 2.5 mm. The durability was verified by evaluation of its heating performance. The maximum temperature was greater than 180 °C at 3 V and remained constant after three repeated cycles and for 10 min. Transmission electron microscopy and x-ray diffraction studies revealed that the adhesion between the electrolessly deposited Cu and the seed Ru nanowires strongly influenced the durability of the core-shell structured nanowire-based heaters., (Creative Commons Attribution license.)

The low efficiency of water electrolysis mostly arises from the thermodynamic uphill oxygen evolution reaction. The efficiency can be greatly improved by rationally designing low-cost and efficient oxygen evolution anode materials. Herein, we report the synthesis of Ni-P alloys adopting a facile electroless plating method under mild conditions on nickel substrates. The relationship between the Ni-P properties and catalytic activity allowed us to define the best conditions for the electroless synthesis of highperformance Ni-P catalysts. Indeed, the electrochemical investigations indicated an increased catalytic response by reducing the thickness and Ni/P ratio in the alloy. Furthermore, the Ni-P catalysts with optimized size and composition deposited on Ni foam exposed more active sites for the oxygen evolution reaction, yielding a current density of 10 mA cm -2 at an overpotential as low as 335 mV, exhibiting charge transfer resistances of only a few ohms and a remarkable turnover frequency (TOF) value of 0.62 s -1 at 350 mV. The present study provides an advancement in the control of the electroless synthetic approach for the design and large-scale application of high-performance metal phosphide catalysts for electrochemical water splitting.

The development of new composites with improved functional properties is the important task of modern materials science. The composites must be structurally organized to provide improved properties. For metal-ceramic composites, there is a need for a uniform distribution of the dispersed ceramic phase in the bulk metallic matrix The modification of the dispersed ceramic phase surface with a metal coating is one of the more effective ways to accomplish this. Particularly, in this work, the conditions of Ni nanolayer deposition on titanium carbide (TiC) particles were studied. The goal was to create core-shell particles with a thickness of the Ni coating on TiC not exceeding 90 nm. Preliminary work was also carried out to study the effect of the dispersed phase composition on the mechanical properties of the composite with an Al matrix.

In this study, the surface-initiated atom transfer radical polymerization (SI-ATRP) technique and electroless deposition of silver (Ag) were used to prepare a novel multi-functional cotton (Cotton-Ag), possessing both conductive and antibacterial behaviors. It was found that the optimal electroless deposition time was 20 min for a weight gain of 40.4%. The physical and chemical properties of Cotton-Ag were investigated. It was found that Cotton-Ag was conductive and showed much lower electrical resistance, compared to the pristine cotton. The antibacterial properties of Cotton-Ag were also explored, and high antibacterial activity against both Escherichia coli and Staphylococcus aureus was observed.

As an important basic material of electronic equipment, copper (Cu) foils should have a small thickness, good mechanical properties, and excellent thermal conductivity. However, preparing an ultrathin Cu foil with good properties remains challenging. Herein, we report an electroless deposition (ELD) strategy for the facile and scalable preparation of an ultrathin freestanding nickel-coated graphene (NCG)/Cu composite foil in a short time of 25 min. The NCG can significantly improve the mechanical and physical properties of composite foils. Experimental results reveal that the NCG/Cu composite foil manifests the best performance when the NCG concentration in an ELD bath was 30 mg/L. The composite foil evidenced a thickness of 1.1 μm, a high tensile strength of 338.7 MPa, and a high thermal conductivity of 431.2 W/mK. Compared with the pure Cu foil, both bending times and elastic modulus are increased by 298.1 and 737.3%, respectively. Remarkably, the composite foil has excellent heat dissipation performance, showing enormous potential as a heat sink material. This work proposes a new method for manufacturing the ultrathin graphene-reinforced Cu composite foil with high performance for numerous applications.

Researchers have been committed to reducing the hazardous pollutants by developing efficient catalysts while ignoring the pollution caused by the use of toxic surface capping agents, reductants and/or organic solvents in the catalyst preparation process. To alleviate such problems, we here report a novel one-step oxygenated functional group-driven electroless deposition strategy to synthesize clean and uniformly distributed Pd nanoparticles (NPs) using porous carbon nanosheets (PCN) as both substrates and reducing agents. It is observed that the oxygenated functional groups enriched PCN possesses a low work function and allows the spontaneous reduction of PdCl 4 2- ions to Pd NPs deposited on the PCN support (Pd/PCN). The particle size of Pd NPs can be flexibly modulated by simply controlling the immersing time and thereby their maximum catalytic performances can be achieved. Specifically, the optimal Pd/PCN-08 with a Pd loading of 3.0 wt% shows an excellent activity with a turnover frequency of 0.38 min -1 for electrocatalytic hydrodechlorination (ECH) of 4-chlorophenol (4-CP), superior to the previously reported materials. The stability of Pd/PCN-08 for 4-CP ECH is impressive in repetitive cycles. This work proposes a facile and efficient strategy to synthesize high-performance catalysts for detoxifying the hazardous organic pollutants., (Copyright © 2020 Elsevier B.V. All rights reserved.)

In the present work, the kinetics of electroless deposition of Pt, using a cobalt ion redox system (Co 3+ /Co 2+ ) as a reducing agent, has been investigated. The deposition rate of Pt depends on the pH, concentration of reactants, and temperature. The deaeration and bubbling of the plating solution with argon play an essential role. It was found that 0.11 mg cm -2 of Pt films could be deposited on the surface of a roughed glass sheet in one hour without replenishing the solution. Additional data have been obtained on the grounds of electrochemical quartz crystal microbalance experiments. The bubbling (agitation) of the electroless Pt plating solution with argon during the deposition of Pt results in a higher deposition rate and is ca. 3 µg cm -2 min -1 . The Pt deposition rate is far less, and is as low as 0.14 µg cm -2 min -1 when the electroless Pt plating solution is not bubbled with argon during the deposition of Pt.

Controlled deposition of metals is essential for the creation of bimetallic catalysts having predictable composition and character. Continuous co-electroless deposition (co-ED) permits the creation of bimetallic catalysts with predictive control over composition. This method was applied to create a suite of Cu-Pt mixed-metal shell catalysts for use in methanol electrooxidation in direct methanol fuel cell applications (DMFCs). Enhanced performance of Cu-Pt compositions over Pt alone was predicted by existing computational studies in the literature. Experimental evidence from this study supports the bifunctional catalyst explanation for enhanced activity and confirms the optimum Cu:Pt ratio as Cu 3 Pt for this methanol electrooxidation. This ability to control the composition of a bimetallic shell can be extended to other systems where the ratio of two metals is critical for catalytic performance.

Plastic bottles are generally recycled by remolding them into numerous products. In this study, waste from plastic bottles was used to fabricate recycled polyethylene terephthalate (r-PET) nanofibers via the electrospinning technique, and high-performance conductive polyethylene terephthalate nanofibers (r-PET nanofibers) were prepared followed by copper deposition using the electroless deposition (ELD) method. Firstly, the electrospun r-PET nanofibers were chemically modified with silane molecules and polymerized with 2-(methacryloyloxy) ethyl trimethylammonium chloride (METAC) solution. Finally, the copper deposition was achieved on the surface of chemically modified r-PET nanofibers by simple chemical/ion attraction. The water contact angle of r-PET nanofibers, chemically modified r-PET nanofibers, and copper deposited nanofibers were 140°, 80°, and 138°, respectively. The r-PET nanofibers retained their fibrous morphology after copper deposition, and EDX results confirmed the presence of copper on the surface of r-PET nanofibers. XPS was performed to analyze chemical changes before and after copper deposition on r-PET nanofibers. The successful deposition of copper one r-PET nanofibers showed an excellent electrical resistance of 0.1 ohms/cm and good mechanical strength according to ASTM D-638.

Electroless deposition on zinc and its alloys is challenging because of the negative standard potential of zinc, the formation of poor surface layers during oxidation in aqueous solutions, and extensive hydrogen evolution. Therefore, there are only few reports of electroless deposition on Zn and its alloys, neither of them on micro/nano powders. Here, we propose a two-step process that allows the formation of compact, uniform, and conformal Ni/NiP shell on Zn-based alloy microparticles without agglomeration. The process utilizes controlled galvanic displacement of Ni deposition in ethanol-based bath, followed by NiP autocatalytic deposition in an alkaline aqueous solution. The mechanism and effect of deposition conditions on the shell formation are discussed. Thermal stability and functional analysis of core-shell powder reveal a thermal storage capability of 98.5% with an encapsulation ratio of 66.5%. No significant morphological change of the core-shell powder and no apparent leakage of the ZnAl alloy through the Ni shell are evident following differential scanning calorimetry tests. Our two-step process paves the way to utilize electroless deposition for depositing metallic-based functional coatings on Zn-based bulk and powder materials.

Herein, a novel, facile, and versatile approach to fabricate highly flexible and conductive paper is proposed by electroless deposition (ELD) with the assistance of aminocellulose as the interface layer. The obtained Cu nanoparticles (NPs)-coated cellulose paper is highly conductive with a significant low resistance of 0.38 Ω sq -1 after only 10 min of ELD treatment. This conductive cellulose paper shows excellent stability when it suffers from bending, folding, and tape adhesion cycles. With the same method, the Cu NPs can also be successfully deposited on the polypropylene (PP)-filled hybrid paper. The conductive paper exhibits very smooth and hydrophobic surface with high reflection, which can be used for special electronic devices. In a word, the fabrication of aminocellulose interface permits a controlled ELD of metal nanoparticles on paper substrate, and this mild and low-cost method opens up new opportunities for large-scale production of flexible and wearable electronics., (© 2020 Wiley-VCH GmbH.)

96-Well technology is associated with automated sample preparation and simultaneous analysis based on the low-cost well plate format. To explore the potential applications of 96-well technology in SERS detection, we examined the surface-bound electroless deposition procedure for the preparation of uniform and stable Ag mirror films on polydopamine (PDA)-coated well plates as active-SERS substrates. In the presented procedure, small Ag seeds assembled on PDA coating were employed as the surface-bound catalyst and provided the active sites for electroless Ag deposition. The high-quality Ag mirror films showed high performance in terms of sensitivity, uniformity, reproducibility and stability using rhodamine 6G (R6G) as the probe molecule. A remarkable enhancement factor of 3.41 × 10 8 was obtained. The relative standard deviations against well-by-well and batch-by-batch reproducibility were less than 5%. The SERS films on well plates were successfully used to quantify the amounts of organic dyes (R6G and malachite green) in environmental water samples and small biological molecules (adenosine triphosphate and adenine) in urine matrix, displaying satisfactory sensitivity, selectivity and recovery. Their limit of detection values were at nanomolar, even picomolar concentration., (Copyright © 2020 Elsevier B.V. All rights reserved.)

Bimetallic cobalt (Co)-based coatings were prepared by a facile, fast, and low-cost electroless deposition on a copper substrate (CoFe, CoMn, CoMo) and characterized by scanning electron microscopy with energy dispersive X-ray spectroscopy and X-ray diffraction analysis. Prepared coatings were thoroughly examined for hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) in alkaline solution (1 M potassium hydroxide, KOH) and their activity compared to that of Co and Ni coatings. All five coatings showed activity for both reactions, where CoMo and Co showed the highest activity for HER and OER, respectively. Namely, the highest HER current density was recorded at CoMo coating with low overpotential (61 mV) to reach a current density of 10 mA·cm -2 . The highest OER current density was recorded at Co coating with a low Tafel slope of 60 mV·dec -1 . Furthermore, these coatings proved to be stable under HER and OER polarization conditions.

High-efficient electromagnetic interference (EMI) shielding films were successfully fabricated by electroless deposition of silver nanoparticles (AgNPs) on polydopamine (PDA) functionalized cellulose nanofibrils (CNFs) as building blocks according to a pressured-extrusion film-forming process. PDA was first functionalized on CNFs by oxidative self-polymerization of dopamine (DA) to synthesize CNFs@PDA, on which AgNPs were electrolessly deposited. The obtained CNFs@PDA@AgNPs composite films served as tightly-connected conductive network, so as to significantly improve the whole electrical conductivity of the EMI shielding films. Utilizing CNFs as green and soft matrix, the fabricated CNFs@PDA@AgNPs EMI films show an outstanding mechanical enduring performance. The CNFs@PDA@AgNPs films with weight ratios of CNFs:AgNO 3 = 1:24 exhibited superb electrical conductivity of 1,000,000 S m -1 and remarkable EMI shielding effectiveness of 93.8 dB at 8.2 GHz in X band. This work provides a simple methodology to achieve surface metallization of insulating fibers to supersede traditional metals for highly efficient EMI shielding applications., (Copyright © 2020 Elsevier Ltd. All rights reserved.)

Intelligent human-machine interfaces (HMIs) integrated wearable electronics are essential to promote the Internet of Things (IoT). Herein, a curcumin-assisted electroless deposition technology is developed for the first time to achieve stretchable strain sensing yarns (SSSYs) with high conductivity (0.2 Ω cm -1 ) and ultralight weight (1.5 mg cm -1 ). The isotropically deposited structural yarns can bear high uniaxial elongation (>>1100%) and still retain low resistivity after 5000 continuous stretching-releasing cycles under 50% strain. Apart from the high flexibility enabled by helical loaded structure, a precise strain sensing function can be facilitated under external forces with metal-coated conductive layers. Based on the mechanics analysis, the strain sensing responses are scaled with the dependences on structural variables and show good agreements with the experimental results. The application of interfacial enhanced yarns as wearable logic HMIs to remotely control the robotic hand and manipulate the color switching of light on the basis of gesture recognition is demonstrated. It is hoped that the SSSYs strategy can shed an extra light in future HMIs development and incoming IoT and artificial intelligence technologies., Competing Interests: The authors declare no conflict of interest., (© 2020 The Authors. Published by Wiley‐VCH GmbH.)

3D magnetic nanostructures are of great interest due to the possibility to design novel properties and the benefits for both technological applications such as high-density data storage, as well as more fundamental studies. One of the main challenges facing the realization of these three-dimensional systems is their fabrication, which includes the deposition of magnetic materials on 3D surfaces. In this work, the electroless deposition of Ni-Fe on a 3D-printed, non-conductive microstructure is presented. The deposited films exhibit low coercivity, with the saturation magnetization and composition corresponding to the archetypal soft magnetic material permalloy. For fundamental studies of 3D micromagnetism, this new development in fabrication offers the possibility to combine the flexibility of 3D nanofabrication techniques such as two-photon lithography for the fabrication of 3D scaffolds with a homogeneous soft ferromagnetic thin film, and thus represents an important step toward exploring the rich physics of complex 3D magnetic architectures with tailored properties and the development of advanced applications., (© 2020 Wiley-VCH GmbH.)

An electroless deposition method is reported for the fabrication of gold nanoparticles (Au NPs) modified carbon nanopipette electrode (CNPE) for sensitive electrochemical detection of dopamine (DA) in aqueous solution and catecholamines released from PC12 cells. A CNPE is fabricated by chemical vapor deposition with a carbon layer onto nanocapillary and then contacted with copper (Cu) wire. Cu wire of CNPE is able to serve as reducing agent for electroless deposition of Au NPs on the CNPE because the potential of Cu 2+ /Cu is more negative than that of AuCl 4 /Au. The method is simple, time-saving, and environmentally friendly. Field emission scanning electron microscopy, energy-dispersive X-ray analysis, and electrochemical techniques confirm the successful fabrication of the Au NPs/CNPE. Furthermore, Au NPs/CNPE exhibits a good sensing activity for DA oxidation with a wide linear determination range of 0.1-8 μmol/L and a low detection limit of 6 nmol/L. The Au NPs/CNPE can be potentially applied for measurement of catecholamines released from PC12 cells. This present work is believed to be beneficial to the design and development of active metal catalysts onto nanoelectrodes for the detection of electroactive biological molecules in living cells.Graphical abstract An electroless deposition method was developed for the fabrication of gold nanoparticles onto the carbon nanopipette electrode, which was served as an enhanced electrochemical sensing platform for highly sensitive detection of dopamine with a linear range of 0.1-8 μmol/L and a detection limit of 6 nmol/L, and was also applied in the detection of catecholamines released from PC12 cells.- /Au. The method is simple, time-saving, and environmentally friendly. Field emission scanning electron microscopy, energy-dispersive X-ray analysis, and electrochemical techniques confirm the successful fabrication of the Au NPs/CNPE. Furthermore, Au NPs/CNPE exhibits a good sensing activity for DA oxidation with a wide linear determination range of 0.1-8 μmol/L and a low detection limit of 6 nmol/L. The Au NPs/CNPE can be potentially applied for measurement of catecholamines released from PC12 cells. This present work is believed to be beneficial to the design and development of active metal catalysts onto nanoelectrodes for the detection of electroactive biological molecules in living cells.Graphical abstract An electroless deposition method was developed for the fabrication of gold nanoparticles onto the carbon nanopipette electrode, which was served as an enhanced electrochemical sensing platform for highly sensitive detection of dopamine with a linear range of 0.1-8 μmol/L and a detection limit of 6 nmol/L, and was also applied in the detection of catecholamines released from PC12 cells.

Corrosion and heat treatment studies are essential to predict the performance and sustainability of the coatings in harsh environments, such as the oil and gas industries. In this study, nickel phosphorus (NiP)-titanium (Ti) nanocomposite coatings (NiP-Ti nanoparticles (TNPs)), containing various concentrations of Ti nanoparticles (TNPs) were deposited on high strength low alloy (HSLA) steel through electroless deposition processing. The concentrations of 0.25, 0.50 and 1.0 g/L TNPs were dispersed in the electroless bath, to obtain NiP-TNPs nanocomposite coatings comprising different Ti contents. Further, the effect of TNPs on the structural, mechanical, corrosion, and heat treatment performance of NiP coatings was thoroughly studied to illustrate the role of TNPs into the NiP matrix. Field emission scanning electron microscope (FESEM) and energy dispersive spectroscopy (EDX) results confirm the successful incorporation of TNPs into the NiP matrix. A substantial improvement in the mechanical response of the NiP matrix was noticed with an increasing amount of TNPs, which reached to its ultimate values (hardness 675 Hv, modulus of elasticity 18.26 GPa, and stiffness 9.02 kN/m) at NiP-0.5TNPs coatings composition. Likewise, the electrochemical impedance spectroscopy measurements confirmed a tremendous increase in the corrosion inhibition efficiency of the NiP coatings with an increasing amount of TNPs, reaching ~96.4% at a composition of NiP-0.5TNPs. In addition, the NiP-TNPs nanocomposite coatings also unveiled better performance after heat treatment than NiP coatings, due to the presence of TNPs into the NiP matrix and the formation of more stable (heat resistant) phases, such as Ni 3 P, Ni 3 Ti, NiO, etc., during the subsequent processing.

Wearable sensor technologies, especially continuous monitoring of various human health conditions, are attracting increased attention. However, current rigid sensors present obvious drawbacks, like lower durability and poor comfort. Here, a strategy is proposed to efficiently yield wearable sensors using cotton fabric as an essential component, and conductive materials conformally coat onto the cotton fibers, leading to a highly electrically conductive interconnecting network. To improve the conductivity and durability of conductive coatings, a topographical modification approach is developed with genus-3 and genus-5 structures, and topological genus structures enable cage metallic seeds on the surface of substrates. A textile-based capacitive sensor with flexible, comfortable, and durable properties has been demonstrated. High sensitivity and convenience of signal collection have been achieved by the excellent electrical conductivity of this sensor. Based on results of deep investigation on capacitance, effects of distance and angles between two conductive fabrics contribute to the capacitive sensitivity. In addition, the textile-based capacitive sensor has successfully been used for real-time monitoring human breathing, speaking, blinking, and joint motions during physical rehabilitation exercises.

Electroless deposition (ELD) is a process widely used for the production of thin metal films, but stripping the films from the substrate remains challenging. Here, we report a low-cost ELD method for the large-scale production of freestanding copper (Cu) foils in a short time of 25-55 min. By atomizing a thin (<100 nm) sacrificial layer of chitosan with weak glycosyl bonds and a high degree of deacetylation on the glass substrate, the chitosan is completely decomposed in the process of Cu-deposition, producing automatically shedded Cu foils with varied thicknesses from 746 nm to 8.33 μm and high elastic modulus. When used as battery current collectors, the thin Cu foils with enhanced adhesive fastness and contact areas greatly enhance the capacity and rate capability of graphite anodes. Compared with the commercial Cu current collectors, both the battery capacity and energy density are increased by 429.6 and 484.1%, respectively. The reported approach can be extended for fabricating other metal foils such as nickel with properties appealing for applications.

The corrosion behavior of duplex Ni-P coatings deposited on AZ91 magnesium alloy was studied. The electroless deposition process of duplex Ni-P coating consisted in the preparation of low-phosphorus Ni-P coating (5.7 wt.% of P), which served as a bond coating and high-phosphorus Ni-P coating (11.5 wt.% of P) deposited on it. The duplex Ni-P coatings with the thickness of 25, 50, 75 and 100 µm were deposited on AZ91 magnesium alloy. The electrochemical corrosion behavior of coated AZ91 magnesium alloy was investigated by electrochemical impedance spectroscopy and potentiodynamic polarization method in 0.1 M NaCl. Obtained results showed a significant improvement in the corrosion resistance of coated specimens when compared to uncoated AZ91 magnesium alloy. From the results of the immersion tests in 3.5 wt.% NaCl, 10% solution of HCl and NaOH and 5% neutral salt spray, a noticeable increase in the corrosion resistance with the increasing thickness of the Ni-P coating was observed.

Zone plates are diffractive optics commonly used in X-ray microscopes. Here, we present a wet-chemical approach for fabricating high aspect ratio Pd/Si zone plate optics aimed at the hard X-ray regime. A Si zone plate mold is fabricated via metal-assisted chemical etching (MACE) and further metalized with Pd via electroless deposition (ELD). MACE results in vertical Si zones with high aspect ratios. The observed MACE rate with our zone plate design is 700 nm/min. The ELD metallization yields a Pd density of 10.7 g/cm 3 , a value slightly lower than the theoretical density of 12 g/cm 3 . Fabricated zone plates have a grid design, 1:1 line-to-space-ratio, 30 nm outermost zone width, and an aspect ratio of 30:1. At 9 keV X-ray energy, the zone plate device shows a first order diffraction efficiency of 1.9%, measured at the MAX IV NanoMAX beamline. With this work, the possibility is opened to fabricate X-ray zone plates with low-cost etching and metallization methods.

Electroless deposition via a spontaneous redox reaction between the metal precursor and support is believed to be a promising approach for the syntheses of supported metal nanoparticles (SMNPs). However, its widespread applications are significantly prohibited by the low reductivity and high cost of support. To overcome these shortcomings, a porous carbon (PC) is herein developed as a promising matrix for the electroless deposition of metal NPs. Benefiting from abundant oxygen-based surface functional groups, the PC shows stronger reducibility (low redox potential) than conventional carbon substrate such as carbon nanotubes or graphene oxide, enabling a facile electroless deposition of Ir, Rh, and Ru NPs on its surface. These SMNPs exhibit an impressive electrocatalytic activity for the hydrogen evolution reaction (HER) or hydrogen oxidation reaction (HOR). For example, the Rh NP/PC can deliver an HER current density of 10 mA cm -2 with a small overpotential of 21 mV in 0.5 m H 2 SO 4 , while the Ru NP/PC exhibits excellent HOR activity in 0.1 m KOH in terms of high mass and surface specific exchange current density of 263 A g -1 Ru and 0.227 mA cm -2 Ru . The present strategy may open up opportunities for mass production of efficient supported NPs for diverse applications., (© 2019 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.)

We designed the flexible chloride ion selective sensor that directly monitors electrochemical reactions of chloride ions without using a reference electrode. A flexible polytetrafluoroethylene (PTFE) substrate was utilized to provide bendability to the fabricated sensor. As an ion selective material, Ag nanoparticles were employed on the MWCNTs loaded on the PTFE substrate. Enhanced adsorption property of the fabricated sensor toward the chloride ions was given by incorporation of hydrophilic copper benzene-1,3,5-tricarboxylate (Cu-BTC) with great flexibility and stability. Accordingly, compared to the bare sensor the sensing performance of the Cu-BTC treated Ag NPs/AgCl electrode sensor was improved by indicating the decrease in response and recovery time about 4 times. It elucidated that the Cu-BTC layer could work as an effective medium between the Ag-NPs surface and electrolyte containing chloride ions. As a result of contact angle measurement, the hydrophilicity much increased in the Cu-BTC treated sensor because the exposed surface of the sensor not treated by the Cu-BTC largely consisted of hydrophobic MWCNTs. Furthermore, the Cu-BTC layer could hold the electrolyte for effective adsorption of analytes with large specific surface area., (Copyright © 2019 Kwak, Park, Lee, Kim and Yoo.)

The rapid development of flexible and wearable electronics favors low-cost, solution-processing, and high-throughput techniques for fabricating metal contacts, interconnects, and electrodes on flexible substrates of different natures. Conventional top-down printing strategies with metal-nanoparticle-formulated inks based on the thermal sintering mechanism often suffer from overheating, rough film surface, low adhesion, and poor metal quality, which are not desirable for most flexible electronic applications. In recent years, a bottom-up strategy termed as polymer-assisted metal deposition (PAMD) shows great promise in addressing the abovementioned challenges. Here, a detailed review of the development of PAMD in the past decade is provided, covering the fundamental chemical mechanism, the preparation of various soft and conductive metallic materials, the compatibility to different printing technologies, and the applications for a wide variety of flexible and wearable electronic devices. Finally, the attributes of PAMD in comparison with conventional nanoparticle strategies are summarized and future technological and application potentials are elaborated., (© 2019 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.)

In this study, carbon nanotube-reinforced silver composites (CNT/Ag) were prepared by the powder metallurgy process via spark plasma sintering (SPS) and hot pressing sintering (HP) with composite powders through an improved electroless plating method assisted by ultrasonic spray atomization. The dispersion of CNTs was effectively improved by ultrasonic spray atomization, and uniform silver layers were deposited on the surface of CNTs by electroless deposition. The property testing results showed significant improvements of the electrical conductivity, hardness, and tensile strength in the samples prepared by SPS, as compared to their HP sintered counterparts. When the volume fraction of CNTs reached 2.5%, the tensile strength reached a maximum value of 221 MPa, which was more than twice that of the pure silver samples. The structural analysis indicated different degrees of CNT agglomeration and matrix mean grain sizes in the composites prepared by SPS and HP, which are responsible for the differences in properties.

For the stretchable electrode, strong interface adhesion is the primary guarantee for long service life, and the maximization of the tensile limit with remarkable electrical stability can expand the scope of its use. Here, a cost-effective strategy is proposed to fabricate a high-adhesion stretchable electrode. By modifying dopamine and functionalized silane on a polydimethylsiloxane (PDMS) substrate in sequence before the electroless deposition process, super-high adhesion up to 3.1 MPa is achieved between the PDMS substrate and silver layer, and the electrode exhibits extraordinary conductivity of 4.0 × 10 7 S/m. This process is also suitable for other common flexible substrates and metals. Moreover, inspired by the micro-/nanostructure on the surface of lotus leaf, a biomimetic elastomeric micropore film with a uniformly distributed micropore is fabricated by the one-step soft lithography replication process. The electrode exhibits a large tensile limit exceeding 70% uniaxial tensile and superior electrical stability from 6.3 to 11.5 Ω under 20% uniaxial tensile for more than 10 000 cycles. This study seeks a promising method to manufacture stretchable electrodes with high adhesion, large tensile limit, and excellent electrical stability, showing great potential to detect various biological signals including joint movement, surface electromyography, and so forth.

Integration of sensors in textile garments requires the development of flexible conductive structures. In this work, cellulose-based woven lyocell fabrics were coated with copper during an electroless step, produced at 0.0284 M copper sulfate pentahydrate, 0.079 M potassium hydrogen L-tartrate, and 0.94 M formaldehyde concentrations. High concentrations led to high homogeneous copper reaction rates and the heterogeneous copper deposition process was diffusion controlled. Thus, the rate of copper deposition did not increase on the cellulose surface. Conductivity of copper coatings was investigated by the resistance with a four probe technique during fabric deformation. In cyclic tensile tests, the resistance of coated fabric (19 × 1.5 cm 2 ) decreased from 13.2-3.7 Ω at 2.2 % elongation. In flex tests, the resistance increased from 5.2-6.6 Ω after 5000 bending cycles. After repeated wetting and drying cycles, the resistance increased by 2.6×10 5 . The resistance raised from 11-23 Ω/square with increasing relative humidity from 20%-80%, which is likely due to hygroscopic expansion of fibers. This work improves the understanding of conductive copper coating on textiles and shows their applicability in flexible strain sensors., Competing Interests: The authors declare no conflict of interest.

In an effort to develop a cost-efficient technology for wireless high-temperature surface acoustic wave sensors, this study presents an evaluation of a combined method that integrates physical vapor deposition with electroless deposition for the fabrication of platinum-based planar antennas. The proposed manufacturing process becomes attractive for narrow, thick, and sparse metallizations for antennas in the MHz to GHz frequency range. In detail, narrow platinum-based lines of a width down to 40 μm were electroless-deposited on γ-Al 2O 3 substrates using different seed layers. At first, the electrolyte chemistry was optimized to obtain the highest deposition rate. Films with various thickness were prepared and the electrical resistivity, microstructure, and chemical composition in the as-prepared state and after annealing at temperatures up to 1100 ∘C were evaluated. Using these material parameters, the antenna was simulated with an electromagnetic full-wave simulation tool and then fabricated. The electrical parameters, including the S-parameters of the antenna, were measured. The agreement between the simulated and the realized antenna is then discussed.

Developing functional materials via electroless deposition, without the need of external energy is a fascinating concept. Electroless deposition can be subcategorized into galvanic displacement reaction, disproportionation reaction, and deposition in presence of reducing agents. Galvanic displacement reaction is a spontaneous reduction process wherein the redox potentials of the metal/metal ion in the electrolyte govern the thermodynamic feasibility of the process. In aqueous solutions, the galvanic displacement reaction takes place according to the redox potentials of the standard electrochemical series. In comparison, in the case of ionic liquids, galvanic displacement reaction can be triggered by forming metal ion complexes with the anions of the ionic liquids. Therefore, the redox potentials in ILs can be different to those of metal complexes in aqueous solutions. In this review, we highlight the progress in the electroless deposition of metals and semiconductors nanostructures, from ionic liquids and their application toward lithium/sodium batteries, and in catalysis.

Three-dimensional (3D) printing is a next-generation free-form manufacturing technology for structural electronics. The realization of structural electronic devices necessitates the direct integration of electronic circuits into 3D objects. However, creating highly conductive, high-resolution patterns in 3D remains a major challenge. Here, we report on a metallic 3D printing method that incorporates electroless deposition (ELD) into the direct ink writing method. Our approach consists of two steps: (1) direct ink writing of catalyst microstructures with a functional catalyst ink containing Ag ions and (2) ELD of Cu onto the printed catalyst structures. High-quality, stable Cu 3D printing is achieved through the design of the Ag catalyst ink; hydroxypropyl cellulose is added as both a rheological modifier (printing) and dissolution inhibitor (ELD). As a result, various two-dimensional (2D) and 3D Cu micro circuitries with high conductivity (∼65% of bulk) can be directly integrated onto 3D plastic substrates without the need for high-temperature annealing. A hybrid strategy that combines ELD-assisted 3D printing and conventional fused deposition modeling enables full fabrication of structural electronic devices. This 3D printing strategy can be a low-cost and facile method for obtaining highly conductive metallic 2D and 3D microstructures in structural electronics.