Ion Precursors Research Articles

Optimized Tungsten Disulfide via Pyrolytic Deposition for Improved Zn‐Ion Batteries

AbstractThe selection and optimization of cathode materials are crucial for enhancing the performance of aqueous zinc‐ion batteries. In this work, different active materials were created by combining Sulfur powder and polydopamine in four different mass ratios. The novel N‐doped carbon/WS2 is obtained. Thanks to the optimization of the dopamine‐carrying tungsten ion precursor and Sulfur powder (1 : 2, 1 : 4, 1 : 6 and 1 : 8), the four samples exhibited different morphology. The N−C/WS2‐6‐based zinc ion batteries with the highest specific capacity, 120.0 mAh/g in the first discharge at 2.0 A/g, and 78.0 mAh/g after 2500 cycles, with a capacity retention of 65 %, had a relatively good overall performance, according to the results. The reaction kinetics characteristics of the N−C/WS2‐6 cathode reveal that diffusion has a significant impact on the processes in the aqueous zinc ionic material N−C/WS2‐6.

Preparation and Characterization of Materials for Low- to Intermediate-Temperature CO2 Adsorption

Global carbon dioxide emissions are rising and the use of fossil fuels in several sectors are the leading causes. As global population and economies continue to grow significantly, the most practical method of lowering such emissions is to capture CO2. Although other technologies are more developed, adsorption is very promising and has attracted much attention. To ensure this technology’s success, it is essential to have suitable CO2 adsorbent materials. In this work, several new hydrotalcites (HTs) with different initial concentrations of ion precursors were prepared for the first time by the co-precipitation method—it was possible to verify that the ion concentrations influence the characteristics of the materials. The prepared HTs were characterized by thermogravimetric analysis (TG), X-Ray diffraction (XRD), surface area measurements and temperature-programmed desorption of CO2 (TPD-CO2) to relate their CO2 capture capacity to their physicochemical properties; the CO2 adsorption equilibrium isotherms were determined at 35 and 300 °C for the prepared samples, as well as for some commercial materials: magnesium oxide, calcium oxide, aluminium oxide and Zeolite 13X. After determining which materials present the best CO2 adsorption capacity, these were submitted to adsorption-desorption cycles to study their stability. The main objective of the work was to prepare and study different CO2 adsorbents for processes that are carried out at low and intermediate temperatures. From the experimental results, it was possible to conclude that the Zeolite 13X showed the best capacity at 35 °C, 3.38 mmol·g−1 (@ pCO2 = 1 bar), and a prepared calcined HT (c-HT2) was the best at 300 °C, 0.97 mmol·g−1 (@ pCO2 = 1 bar). Moreover, it seems there is an optimum initial concentration of the ions’ solutions for the tested HTs, which depends on the final application—c-HT1 showed a better capacity at 35 °C and c-HT2 at 300 °C. From the adsorption-desorption cycles—performed at 35 and 300 °C with the best materials using a magnetic suspension microbalance at 1 bar of CO2 partial pressure —, a working cyclic capacity of 2.69 mmol∙g−1 was achieved by the Zeolite at 35 °C; in turn, c-HT2 showed a working cyclic capacity of 0.79 mmol∙g−1 at 300 °C.

Selective CO2 Reduction Electrocatalysis Using AgCu Nanoalloys Prepared by a "Host-Guest" Method.

Multimetallic nanoalloy catalysts have attracted considerable interest for enhancing the efficiency and selectivity of many electrochemically driven chemical processes. However, the preparation of homogeneous bimetallic alloy nanoparticles remains a challenge. Here, we present a room-temperature and scalable, host-guest approach for synthesis of dilute Cu in Ag alloy nanoparticles. In this approach, an ionic silver bromide precursor harboring exogenous Cu cations is reduced to yield ∼20 nm diameter AgCu alloy nanoparticles wherein the % Cu loading can be tuned precisely. AgCu nanoparticles with a 5% nominal loading of Cu exhibit peak activity (-0.23 mA/cm2 normalized partial current density) and selectivity (83.2% faradaic efficiency) for CO product formation from electrocatalytic reduction of CO2 at mild overpotentials. These AgCu nanoalloys exhibit a higher mass activity compared to Ag- and Cu-containing nanomaterials used for similar electrocatalytic transformations. Our host-guest synthesis platform holds promise for production of other nanoalloys with relevance in electrocatalysis and optics.

Why Colloidal Syntheses of Bimetallic Nanoparticles Cannot be Generalized.

Introducing one general synthesis to form bimetallic nanoparticles (NPs) could accelerate the discovery of NPs for promising energy applications. Although colloidal syntheses can provide precise structural and morphological control of bimetallic NPs, the complex chemical nature of multicomponent syntheses challenges the realization of such synthetic simplicity. Common synthetic issues are frequently ascribed to the variation in metal ion precursor reactivities and complex chemical interactions between the different metal surfaces and capping agents employed. However, no systematic studies have shown how these factors compete to ultimately assign the factor limiting the mixing and formation of bimetallic NPs. Here, we provide a parametric investigation of how the intrinsic standard reduction potentials (E0red) of the metal ions and cocapping agents influence the formation of bimetallic AuCu, AuPd, and PdCu NPs. Using a combination of in situ X-ray total scattering along with transmission electron microscopy and nuclear magnetic resonance spectroscopy, we illustrate the multifunctional role of the cocapping agents through interactions with both the metal ion precursors and NP surfaces to stabilize metastable structures. Additionally, we demonstrate how system-specific side reactions and the local metal ion coordination environment can be used to selectively tune the formation kinetics, structure, and morphology of bimetallic NPs. Ultimately, these insights show that the chemical interactions rather than the intrinsic E0red are responsible for the formation of bimetallic NPs. Broadly, these insights should aid the synthetic design of tailored multimetallic NPs.

Infiltrated electroless deposition of gold nanoparticles on porous Prussian blue-Fe2O3 hetero-microstructures for environmental remediation applications: A novel infiltration strategy to form 3-D nano-catalytic networks

Metal and metal oxide nanocomposites are promising candidates for heterogeneous catalytic applications. In this regard, most of the metal oxide inner core volume remains as a dead volume, not participating in the catalysis, only the metal/metal oxide hetero-junctions available at the surfaces are involved in the catalysis. Herein, we report a novel strategy for the infiltration of gold nanoparticles into the inner core of 3D-porous Prussian blue/Fe2O3 hetero-microstructures (PBFHM-Au) beyond its outer surface to form an advanced heterogeneous catalyst for the environmental remediation applications. The porosity of the Prussian blue microstructures is thermally tuned for the infiltration of gold ion precursor into the inner core volume of Prussian blue/Fe2O3 hetero-microstructures to facilitate the galvanic displacement reaction between Fe and Au to enlarge the lattice shell and form Au nanoparticle 3D networks throughout the PBFHM. Notably, the resulting PBFHM-Au2 shows enhanced structural stability electron transfer kinetics and catalytic activity in comparison with the only surface-attached Au/Fe2O3 composite. The obtained PBFHM-Au2 catalyst demonstrates remarkable catalytic activity for Rhodamine-B dye degradation with rate constant (k = 3.47 × 10−2 s−1) and p-nitrophenol reduction reactions with rate constant (k = 1.199 × 10−1 s−1).

One-step visible laser writing of Cu-doped graphene hybrid structure for in-plane supercapacitor assembly

High-quality copper-graphene holds great potential for applications in electronics, but fabricating these hybrid structures in a cost-effective route remains challenging. Herein, we propose a one-step writing process for manufacturing copper-doped graphene hybrid structure using low-cost visible laser. The ionic precursor coated on the surface of polymeric substrate not only acts as a copper source for doping, but also can promote near-surface graphenization of the polymer as proved in this study. The interaction between copper and graphene during this in-situ laser processing has been in-deep discussed to reveal the formation mechanism of the hybrid structure. The obtained hybrid structure shows excellent performance that can assemble high-performance devices, such as the in-plane supercapacitor we demonstrated. This study presents a low-cost, rapid, and efficient strategy for structuring the composites to meet the demands for high-performance structures in booming electronics.

Stoichiometric Study on Ion Composition of a Precursor in Chemical Bottom-Up Synthesis for Peroxo-Titanate.

Layered alkali titanates of the lepidocrocite type are gaining enormous interest in various fields owing to their unique properties. These materials are mainly synthesized through a hydrothermal alkali treatment. However, this method uses a highly concentrated alkali solution, which has high environmental impacts and is therefore unsuitable for mass synthesis. Herein, we propose an efficient method for the large-scale synthesis of layered sodium titanate structures (Na2-x H x Ti2O5) using a recently reported bottom-up chemical process. The effects of the Na:Ti molar ratio in the peroxo-titanium complex ion precursor on the products are investigated through stoichiometric calculations for a molar ratio range of 10:1-1:1. The optimal ratio for the complete ionization of TiH2 (which is the starting material) to form the peroxo-titanium complex ion is found to be 1.1:1. The amount of alkali raw material required is 99.6% lower than that required in the traditional hydrothermal method. The crystal structures and morphologies of the samples are almost identical regardless of the Na:Ti molar ratio. The precursor-derived peroxo bonds narrow the energy band gaps of the layered titanates even when the amount of titanium ions dissolved in the precursor increases. The proposed method is not only an efficient synthetic route for mass production but also has potential applications in the development of photofunctional materials.

Pb(II) solid-phase extraction in wastewater samples prior to flame atomic absorption spectrometry analysis using chitosan and alginate modified carbon

ABSTRACT The sustainability concept was kept in view by designing and synthesising a novel adsorbent for Pb(II) ion, using natural and metal-free precursors which are renewable and biodegradable, i.e. alginate, chitosan, and carbon. The study was aimed to introduce the synthesis of Carbon/Alginate/Chitosan composite (CAC) as a beneficial adsorbent tailored for the solid-phase extraction (SPE) of Pb(II) prior to its analysis via flame atomic absorption spectrometry (FAAS). The successful preparation of the CAC material is elucidated, characterised through FTIR for functional group analysis, and evaluated for surface morphology and elemental composition via SEM-EDX. Optimisation of SPE parameters was carefully conducted to enhance adsorption-desorption efficiency across diverse conditions. These optimised factors were a pH level of 6, initial Pb(II) concentration of 20 mg/L, sample flow rate 5 mL/min, elution utilising Na2EDTA at a rate of 5 mL/min, sample volume of 20 mL, Na2EDTA eluent volume of 10 mL, and Na eluent concentration of 0.5 M. Application of CAC-based SPE for Pb(II) analysis in wastewater samples under these optimised conditions yielded exceptional recovery rates of 93–96%, with a limit of detection (LoD) value of 71.4 µg/L. Moreover, a notable preconcentration factor of 4–8 times is achieved for Pb(II) in wastewater samples, facilitating the detection of Pb(II) concentrations as low as 30 µg/L.

Effects of Rapid Heat Treatments on the Properties of Cu2O Thin Films Deposited at Room Temperature Using an Ammonia-Free SILAR Technique

We report herein the analysis of the properties of copper(I) oxide thin films deposited by an optimized ammonium-free successive ion layer adsorption and reaction (SILAR) technique. The Cu2O thin film deposition process was carried out at room temperature using copper acetate monohydrate, sodium citrate as complexing agent, and hydrogen peroxide as precursors of copper and oxygen ions, respectively. The harmless and easy-to-handle sodium citrate replaces the volatile NH4OH commonly employed as complexing agent in the SILAR technique for the deposition of metal oxide thin films. The optical, structural, morphological, and electrical properties of the as-deposited Cu2O thin films were studied as a function of the number of cycles during deposition, as well as their modifications produced by the effect of rapid thermal annealing (RTA) in vacuum in a temperature range of 200–250°C for 1 min, 3 min, and 5 min. The as-deposited thin films had cubic crystalline structure corresponding to the Cu2O phase as determined by x-ray diffraction (XRD), with a direct energy bandgap of 2.43–2.51 eV depending on the number of cycles, and electrical resistivity of the order of 103 Ω cm. The XRD and x-ray photoelectron spectroscopy (XPS) analysis of the Cu2O thin films treated by RTA demonstrated an increase of the crystal size with time and temperature of the RTA and reduction effects from Cu2+ to Cu1+ oxidation states. On the other hand, the RTA treatments also decreased their energy bandgap to 2.38 eV and electrical resistivity to 102 Ω cm. The high energy bandgap values of the Cu2O thin films were attributed to quantum confinement effects produced by their small crystal size in the range of 3.6–8.6 nm.Graphical

Branched polymer grafted graphene oxide (GO) as a 2D template for calcium phosphate growth

HypothesisGraphene Oxide (GO)-templated deposition of inorganic materials through synthesis on dispersed single sheets of GO is often complicated by the loss of the desired 2D morphology owing to the coagulation of GO sheets at high salt concentrations and non-templated homogenous nucleation. Modifying GO with anionic polymer is expected to solve both problems by i) enhancing electrostatic(steric) stabilization upon exposure to high concentrations of the ionic precursors, and ii) offering additional nucleation sites at the grafted anionic moieties to avoid homogeneous secondary nucleation. ExperimentsGO was grafted with branched copolymers of poly(ethylene glycol) methacrylate (PEGMA 500) and diethylene glycol dimethacrylate (DEGDMA) and ω-vinyl terminated methacrylic acid macromonomer (P(MAA)), the latter serving as an addition-fragmentation chain transfer agent. The colloidal stability of GO dispersions in water toward salt was evaluated before and after modification. Precipitation of calcium phosphate (CaP) was performed by incubating modified GO in the precursor solutions. The conditions were optimized to maximize the nucleation selectively onto GO without homogeneous CaP nucleation and coagulation of the GO-sheets. FindingsThe copolymer grafted GO-sheets shows superior colloidal stability when dispersed in water. No aggregation occurs in the incubating ionic CaP precursor solutions. The optimum templated deposition of CaP onto the GO sheets by precipitation is to add a second shot of precursors after the nucleation stage to obtain GO sheets fully decorated with calcium phosphate nanorods without self-nucleation. Via the careful design on the GO modification and incubation process, the growth of calcium phosphate nanorods were confined in the desired 2D order exclusively, hereby achieving the goal of an efficient GO-templated synthesis.

Revisited UV- spectra of chlorohydroxoaurate anions

The most important ionic precursor of gold, [AuCl4]-, is used in aqueous solution leading to chlorohydroxoaurates species, [AuCl4-x(OH)x]- (x = 1–4) due to partial hydrolysis. Their UV spectral signatures are still relatively unknown though very useful in many domains of application. Individual spectra of each of them are determined for the first time thanks to a thorough experimental investigation comprising the range 200–250 nm, surpringly ignored up to now. New isosbestic points useful for species partition analysis are evidenced. Electronic transition attribution is obtained from quantum chemical calculations based on TD-DFT. The prediction of the experimental blueshifted bands of the [AuCl4-x(OH)x]-1 anions was possible only after applying energy corrections calibrated on the full UV range two-band spectrum of the [AuCl4]- complex.

Colorimetric sensor to monitor the temperature with in situ synthesized silver nanoparticles embedded in carboxymethyl cellulose metallogel

A colorimetric sensing platform based on carboxymethyl cellulose-silver nanoparticles (CMC-AgNPs) metallogel was proposed to monitor the temperature history and quality of perishable products stored at low temperature. The carboxymethyl cellulose (CMC) metallogel, fabricated in the presence of Ag+, incorporates ionic crosslinking of biopolymers, complexation between reactants, and subsequent in situ synthesis of AgNPs, which are designed to lead the color transition of metallogel from colorless to dark brown depending on temperature and time. The mechanical and structural properties of metallogels and AgNPs were characterized by rheology, XRD, and FT-IR. Color changes associated with temperature, time, and metal ion precursors were examined by UV–visible spectroscopy and colorimetry. The longer the exposure time to thermal stress condition such as room temperature (25 °C) or high temperature (60 °C), the deeper the color of metallogel. The CMC-AgNPs metallogel-based sensor provides an efficient, safe way to track temperature history and assess perishable products’ quality, crucial for the safe distribution of food, vaccines, and medicines. This cost-effective and reliable visual sensor minimizes spoilage and health risks by enabling accurate temperature monitoring without the need for complicated equipment.

Polypyrrole film formation using DC biasing of substrate in in-solution plasma process

Beyond the existing in-solution plasma (iSP) process used for nanoparticle synthesis, polymer film synthesis has recently been demonstrated via iSP, which occurs at a specific cycle in a substrate with electrical potential. Herein, we propose an iSP reactor designed to tune the characteristics of polypyrrole (PPy) films by applying varied DC biases to the substrate during the solution plasma process. Applying DC bias to the substrate notably enhances the iSP during the negative cycle, thereby generating ionic precursors from pyrrole monomers for PPy film formation. These films demonstrated morphological variances as a function of the applied VDC. At a low voltage (VDC = 0.5 kV), a uniform film was formed via a layer-by-layer growth mechanism, and as the voltage was increased, the film exhibited a structured morphology. Specifically, at VDC = 0.5 kV, the PPy film was successfully coated onto a finely patterned electrode. The proposed iSP process, under specific DC biasing conditions, enables polymer coating without necessitating additional chemicals, catalysts, or masks. This method holds potential for a wide range of applications.

Optimizing the ITER NBI ion source by dedicated RF driver test stand

The experimental fusion reactor ITER will feature two (or three) heating neutral beam injectors (NBI) capable of delivering 33(or 50) MW of power into the plasma. A NBI consists of a plasma source for production of negative ions (extracted negative ion current up to 329 A/m2 in H and 285 A/m2 in D) then accelerated up to 1 MeV for one hour. The negative ion beam is neutralized, and the residual ions are electrostatically removed before injection. The beamline was designed for a beam divergence between 3 and 7 mrad.The ion source in ITER NBIs relies on RF-driven, Inductively-Coupled Plasmas (ICP), based on the prototypes developed at IPP Garching; RF-driven negative-ion beam sources have never been employed in fusion devices up to now. The recent results of SPIDER, the full size ITER NBI ion source operating at NBTF in Consorzio RFX, Padova, measure a beamlet divergence minimum of 12mrad and highlighted beam spatial non-uniformity. SPIDER results confirmed the experimental divergence found in smaller prototype sources, which is larger compared to filament-arc ion sources. Although prototype experiments have shown that the extracted current requirement can be achieved with minor design improvements, the beamlet divergence is expected to marginally achieve the design value of 7 mrad, which in multi-grid long accelerators results in unexpected heat loads over the accelerator grids. A contributor to the beam divergence is the energy/temperature of the extracted negative ions, so it is believed that plasma differences between the two source types play a role. Research is focused on the plasma parameters in the ion source.One RF driver, identical to the ones used in SPIDER, installed in a relatively small-scale experimental set-up, inherently more flexible than large devices, is starting operations devoted to the investigation of the properties of RF-generated plasmas, so as to contribute to the assessment of negative ion precursors, and of their relationship with the plasma parameters, particularly when enhancing plasma confinement. The scientific questions, that have arisen from the preliminary results of SPIDER, guided the design of the test stand, which are described in this contribution, together with the diagnostic systems and related simulation tools. The test stand, which shares with the larger experiment all the geometrical features and constraints, will allow technological developments and optimized engineering solutions related to the ICP design for the ITER NBIs.

Mechanochemical Synthesis of Chromium(III) Complexes Containing Bidentate PN and Tridentate P-NH-P and P-NH-P' Ligands.

Chromium(III) complexes bearing bidentate {NH2(CH2)2PPh2: PN, (S,S)-[NH2(CHPh)2PPh2]: P'N} and tridentate [Ph2P(CH2)2N(H)(CH2)2PPh2: P-NH-P, (S,S)-(iPr)2PCH2CH2N(H)CH(Ph)CH(Ph)PPh2: P-NH-P'] ligands have been synthesized using a mechanochemical approach. The complexes {cis-[Cr(PN)Cl2]Cl (1), cis-[Cr(P'N)Cl2]Cl (2), mer-Cr(P-NH-P)Cl3 (3), and mer-Cr(P-NH-P')Cl3 (4)} were obtained in high yield (95-97%) via the grinding of the respective ligands andthe solid Cr(III) ion precursor [CrCl3(THF)3] with the aid of a pestle and mortar, followed by recrystallization in acetonitrile. The isolated complexes are high spin. A single-crystal X-ray diffraction study of 2 revealed a cationic chromium complex with two P'N ligands in a cis configuration with P' trans to P' with chloride as the counteranion. The X-ray study of 4 shows a neutral Cr(III) complex with the P-NH-P' ligand in a mer configuration. The difference in molecular structures and bulkiness of the ligands influence the electronic, magnetic, and electrochemical properties of the complexes as exhibited by the bathochromic shifts in the electronic absorption peaks of the complexes and the relative increase in the magnetic moment of 3 (4.19 μβ) and 4 (4.15 μβ) above the spin only value (3.88 μβ) for a d3 electronic configuration. Complexes 1-4 were found to be inactive in the hydrogenation of an aldimine [(E)-1-(4-fluorophenyl)-N-phenylmethanimine] under a variety of activating conditions. The addition of magnesium and trimethylsilyl chloride in THF did cause hydrogenation at room temperature, but this occurred even in the absence of the chromium complex. The hydrogen in the amine product came from the THF solvent in this novel reaction, as determined by deuterium incorporation into the product when deuterated THF was used.

The superiority of the photocatalytic and antibacterial performance of mechanochemically synthesized CdS nanoparticles over solvothermal-prepared ones

In this work, we have developed a facile, dry, and environmentally friendly mechanochemical method for the synthesis of cadmium sulfide (m-CdS) nanoparticles in a planetary ball mill using non-toxic precursors. Thiourea was for the first time used as a precursor of sulfide ion in room temperature solid state ball milling synthesis. For comparison of the mechanochemical approach with others, cadmium sulfide nanoparticles were also prepared using the solvothermal method (s-CdS). The crystal structure of cadmium sulfide nanoparticles was studied by XRD, the qualitative chemical band properties were examined by Raman scattering and x-ray photoelectron spectroscopy analysis, and particle morphology and microstructure were investigated by scanning electron microscopy and transmission electron microscopy methods. The sizes of the m-CdS nanoparticles had 5–6 nm in diameter, which is 10 times smaller than the diameter of s-CdS nanorods. The photocatalytic activities of as-prepared cadmium sulfide nanoparticles on the dye degradation and hydrogen production by water splitting were evaluated and the antibacterial activities were also tested. The photocatalytic activity of m-CdS was superior to that of s-CdS in the degradation of Orange II under visible light irradiation. Better results for m-CdS were also evidenced in photocatalytic experiments on hydrogen generation. The maximum rate of hydrogen evolution for m-CdS was 191.9 µmolg−1h−1 at the 120th min,while this indicator for s-CdS was only 58.0 µmolg−1h−1 at the same irradiation time.The better effect of m-CdS was evidenced also in an antibacterial study (namely against gram-positive bacteria).

Flexible Copper-Based Thermistors Fabricated by Laser Direct Writing for Low-Temperature Sensing.

With the flexibilization tendency of traditional electronics, developing sensing devices for the low-temperature field is demanding. Here, we fabricated a flexible copper-based thermistor by a laser direct writing process with Cu ion precursors. The copper-based thermistor performs with excellent temperature sensing ability and high stability under different environments. We discussed the effect of laser power on the temperature sensitivity of the copper-based thermistor, explained the sensing mechanism of the as-written copper-based films, and fabricated a temperature sensor array for realizing temperature management in a specific zone. All of the investigations have demonstrated that such copper-based thermistors can be used as candidate devices for low-temperature sensing fields.

Study on the Influence of UV Light on Selective Antibacterial Activity of Silver Nanoparticle Synthesized Utilizing Protein/Polypeptide-Rich Aqueous Extract from The Common Walkingstick, Diapheromera femorata.

Common walkingstick (Diapheromera femorata) aqueous extract (CWSAE) can induce the synthesis of useful bionanomaterials. CWSAE is rich in water-soluble organic compounds such as proteins and polypeptides that function as reducing/stabilizing agents for nanoparticle formation from Ag+ ion precursors. The synthesized AgNPs exhibited a moderately uniform size, with the majority falling within the range of 20-80 nm. These AgNPs were UV-treated and tested as antibacterial agents to inhibit the growth of four pathogenic bacteria (Burkholderia cenocepacia K-56, Klebsiella pneumoniae ST258, Pseudomonas aeruginosa PAO1, and Staphylococcus aureus USA300), as well as one common bacterium (Escherichia coli BW25113). The disk diffusion test demonstrated that the UV-treated AgNPs significantly and selectively inhibited the growth of Staphylococcus aureus USA300 and P. aeruginosa, while showing a small effect on the other two species. This suggests the potential application of green-chemically synthesized AgNPs as selective antibacterial agents. Furthermore, we studied the effects of short-term (1-2 min) and long-term (5-30 min) UV treatment on the selective cytotoxicity of the AgNPs and found that the cytotoxicity of the AgNPs could depend on the duration of UV exposure against certain bacteria.

Construction of strain responsive Ti-containing carboxymethyl cellulose hydrogel with transitional coordination precursor

Due to marvelous sensitivity and flexibility, conductive hydrogels are popularly used as strain sensors in intelligent skin and wearable electronic devices fields. However, hydrogel tends to be destroyed after long-term use or in accident, leading to performance degradation. Herein, we developed an environmental-friendly Ti-containing conductive hydrogel. The hydrogel network was constructed via a simple two-step method with coordination reaction and amidation reaction based on a metal ion precursor from transitional coordination. The synergies of reversible metal coordination bonds and dynamic hydrogen bonds endowed the hydrogel with excellent self-healing properties (3 h, 93.66 %), tensile properties (136.46 kPa), compression properties (1.122 MPa), and anti-fatigue performance. At the same time, the hydrogel showed excellent self-adhesion, even underwater. Due to Ti4+, electrical conductivity of the hydrogel was visibly enhanced (σ = 25.64 mS·cm−1), which resulted in fast response (TS [time sensitivity] = 24.78 s−1) and short recovery time (153 ms). As a flexible strain sensor, the hydrogel with stable conductivity and high sensitivity could precisely detect and distinguish a series of human motions, even different letter pronunciations. These remarkable features make it a promising application in the fields of intelligent skin and wearable electronic devices.

Facile Hydrogen‐Bonding Assisted Crystallization Modulation for Large‐area High‐quality CsPbI2Br Films and Efficient Solar Cells

AbstractThe thermally stable inorganic cesium‐based perovskites promise efficient and stable photovoltaics. Unfortunately, the strong ionic bonds lead to uncontrollable rapid crystallization, making it difficult in fabricating large‐area black‐phase film for photovoltaics. Herein, we developed a facile hydrogen‐bonding assisted strategy for modulating the crystallization of CsPbI2Br to achieve uniform large‐area phase‐pure films with much‐reduced defects. The simple addition of methylamine acetate in precursors not only promotes the formation of intermediate phase via hydrogen bonding to circumvent the direct crystallization of CsPbI2Br from ionic precursors but also widens the film processing window, thus enabling to fabricate large‐area high‐quality phase‐pure CsPbI2Br film under benign conditions. Combining with stable dopant‐free poly(3‐hexylthiophene), the CsPbI2Br solar cells achieve the record‐high efficiencies of 18.14 % and 16.46 % for 0.1 cm2 and 1 cm2 active area, respectively. The obtained high efficiency of 38.24 % under 1000 lux illumination suggests its potential in indoor photovoltaics for powering the Internet of Things, etc.