Conductive Substrate Research Articles

Maximizing Oxygen Evolution Performance of NiFeOx Semitransparent Electrocatalysts Applicable to Photoelectrochemical Water Splitting Device

In photoelectrochemical (PEC) water splitting, semiconductor‐based photoelectrodes can improve reaction rates and durability by incorporating cocatalysts that serve as active sites for the water splitting process. However, achieving both high light transmittance and efficient catalytic activity is essential for these cocatalysts. This study aimed to optimize the surface loading of semitransparent NiFeOx thin‐film electrocatalysts to enhance the oxygen evolution reaction (OER) rates while maintaining high light transmittance. NiFeOx thin films were deposited on fluorine‐doped SnO2 (FTO) transparent conductive substrates, and the relationship between the NiFeOx loading amount (Γ) and the OER rate was examined using electrochemical techniques. The OER rate of NiFeOx on FTO (NiFeOx/FTO) was the highest at a Γ value of 0.20 μmol cm‐2. To further explore the connection between this optimized Γ and PEC activity, the impact of Γ on the PEC OER performance of visible‐light‐absorbing α‐Fe2O3 semitransparent photoanodes was evaluated as a model system. Applying the optimized Γ of NiFeOx to modify the α‐Fe2O3 surface also led to enhanced PEC OER performance. These findings highlight the critical role of surface design, specifically the optimization of cocatalyst loading and electrocatalytic activity, in improving PEC water splitting efficiency, providing valuable guidelines for future semitransparent photoelectrode development.

Silk Nanofibers/Carbon Nanotube Conductive Aerogel.

Natural silk nanofibers (SNF) are attractive conductive substrates due to their high aspect ratio, outstanding mechanical strength, excellent biocompatibility, and controllable degradability. However, the inherently non-conductivity severely restricts the potential sensor application of SNF-based aerogels. In this work, the conductive nanofibrous aerogels with low-density achieved through freeze-drying by dispersing carbon nanotubes (CNT) into SNF suspension. The addition of CNT significantly increases the conductivity with improved mechanical properties of composite aerogels. SEM results reveal that the distinct hierarchical structure comprising micropores and nanofibrous networks within the pores is formed when CNT content reached 30%. Furthermore, increased cell viability suggested the excellent biocompatibility of SNF-CNT-based conductive aerogel for tissue-engineering applications. Subsequently, the elastic water-borne polyurethane (WPU) is incorporated to SNF-CNT system to construct aerogel with good sensing properties. The introduction of WPU demonstrates enhanced compressive performances and an exceptionally high elastic recovery ratio of 99.8%, thereby exhibiting a stable and lossless strain-sensing signal output at 5% strain. This study provides a feasible choice and strategy for exploring the potential application of SNF in functional aerogels.

A Polymeric Hole Transporter with Dual-Interfacial Interactions Enables 25%-Efficiency Blade-Coated Perovskite Solar Cells.

Self-assembly monolayer (SAM) hole transporters, consisting of anchoring, spacer, and terminal groups, have played a significant role in the development of inverted perovskite solar cells (PSCs). However, the weak interaction between perovskite and hydrophobic terminal group of SAMs limits surface wettability and interface stability. To address this issue, two novel hole transporters (named DBPP and Poly-DBPP) with centrosymmetric biphosphonic acid groups are developed. Unlike conventional SAM hole transporters, the biphosphonic acid groups in DBPP and Poly-DBPP can anchor to the underlying conductive substrate and interact with the perovskite layer simultaneously, improving surface wettability and suppressing interface recombination. Furthermore, compared to the small-molecular DBPP, Poly-DBPP exhibits higher conductance and excellent uniformity. This translates to a remarkable power conversion efficiency of 25.1% for blade-coated PSCs and 22.0% for large-area modules, respectively. Additionally, the PSCs based on Poly-DBPP demonstrate impressive operational stability, retaining 92% of their initial PCE after 1,600 h of light soaking. This work presents a promising strategy for designing multifunctional hole transporters, paving the way for highly efficient and stable PSCs.

Enabling Efficient Oxygen Evolution via Anchoring Carbon-Layer-Confined RuOx on a Well-Matched Substrate.

Oxygen evolution reaction (OER) is a multistep proton-coupled four-electron process with sluggish kinetics, which seriously limits the hydrogen production efficiency, thus it is of great importance to develop an efficient and stable OER catalyst. In this study, a two-step differential pyrolysis strategy is employed to design a three-dimensional porous microstructured material consisting of RuOx nanoparticles coated by a thin-layer carbon, where the active particles were isolated in separate chambers and the RuOx nanoparticles mainly existed in the form of a heterogeneous interface between RuO2 and partial metallic Ru. The preparation parameters of the catalysts are optimized via combining transient and steady-state polarization properties, and the target catalyst Cat-500-1.5t shows the best OER catalytic performance after ca. 60 h of a chronopotentiometry test in an acidic medium with a much smaller performance change than other samples. The unique design of adopting a carbon layer to form separate reaction chambers largely mitigates the excessive oxidation loss of the active components under strong oxidation potential. The suitability of the catalyst with the loaded substrate and test media is explored, and in an acidic medium, the carbon paper is much better than the titanium fiber, while in an alkaline medium, the titanium fiber is obviously superior to the carbon paper. On both carbon paper and titanium fiber, the performance in an alkaline medium outperforms that in an acidic medium, and the possible reasons for the performance difference are analyzed. Herein, to obtain the actual electrocatalytic performance, the optimal design of the catalyst structure and matching suitable conductive substrate in a specific medium are quite necessary, which provides a feasible strategy for the acquisition of efficient and stable electrocatalysts and the desirable presentation of performance.

Enhancing the conductivity and crystallinity of (111) platinum films via a two-temperature deposition and substrate annealing

Developing routes to deposit highly conductive (111) oriented platinum films with sub-nanometer roughness will provide a platform to develop unique hexagonal and (111) oriented cubic materials. A two-temperature e-beam deposition process is proposed for the growth of (111) oriented platinum films on Al2O3 to simultaneously induce crystallographic texturing, improve conductivity, and reduce surface roughness. Depositing an initial platinum layer at 700 °C induces texturing then subsequently depositing at 500 °C promotes planar growth. The resulting (111) platinum films exhibit a narrow rocking curve full width at half maximum of 0.004°, a surface roughness of 0.20 nm, and conductivity of 8.99 × 106 S/m simultaneously—reaching metrics that are not currently available by other deposition methods. The e-beam deposition methodology developed in this study provides a route to increase the performance of platinum as a conductive substrate.

Fabrication of Flexible Organic Field Effect Transistor Using Patterned Electrospray Deposition

ABSTRACTThe electrospray deposition (ESD) method is a wet process that uses the solution spray formed by an electric field between the needle of a syringe containing the solution and a conductive substrate or an insulated electrode. In this study, we fabricated thin films based on 6,13‐bis(triisopropyl‐silylethynyl) pentacene (TIPS‐pentacene) formed by a new direct patterning ESD method. This method utilizes an electric field applied between the nozzle and patterned electrodes on the substrate. It enables the formation of patterns on materials such as plastic films. Moreover, this ESD method allows for the control of patterned film width using the voltage on a counter‐patterned electrode. These results demonstrate that the patterned TIPS‐pentacene film width can be controlled by controlling voltage. We fabricated a flexible organic field‐effect transistor (OFET) using this method and measured its static electrical characteristics.

Coherent Epitaxy of HfxZr1-xO2 Thin Films by High-pressure Magnetron Sputtering

Due to remarkable high-k and ferroelectric properties in CMOS devices, the study of crystalline HfxZr1-xO2 (HZO) thin films has attracted tremendous interest recently. However, up to now, the epitaxial growth of HZO films has only been achieved by pulse laser deposition, a technique scarcely utilized in CMOS devices. Therefore, developing appropriate epitaxial methods of HZO films (such as sputtering) is fairly necessary, but a challenge at present. In this work, high-quality single-crystalline HZO films were synthesized by high-pressure magnetron sputtering. The epitaxial growth of HZO films on yttria-stabilized zirconia (YSZ) substrate was demonstrated by a combination of high-resolution X-ray diffraction, atom force microscope, and scanning transmission electron microscope. In addition, good insulating characteristics were obtained by replacing insulating substrates with conductive substrates as electrodes. Our results provide a novel way for the epitaxial growth of the single-crystalline structure of HZO thin films towards the high performance of high-k and ferroelectric devices.

Breaking the Limitations of Activity and Stability in Powdered Materials for Oxygen Evolution Reaction: The Critical Role of Catalyst-Inducing Seeds

Powdered catalysts are extensively employed in industrial-scale energy conversion devices but struggle with weak powder-substrate adhesion and inherent instability in gas-evolving and highly oxidative oxygen evolution reactions (OER). This work introduces an innovative strategy in which powdered materials serve a critical role as catalyst-inducing seeds to break these limitations. Specifically, powdered Ti2CTx MXene with anchored cobalt single atoms (Co-SAs) shows negligible catalytic activity on its own but serves as catalyst-inducing seeds, significantly enhancing the catalytic activity of the conductive FeNi substrate. Mechanistic studies demonstrate that Co-SAs accelerate the oxidation rate of Ti2CTx, leading to the micro-battery corrosion behavior between oxidized Co/Ti2CTx and FeNi alloy, which generates highly OER-active corrosion products tightly bonded to FeNi alloy, thereby enhancing catalytic activity and ensuring stability. The prepared porous electrode shows a low overpotential of 303mV to deliver an ultra-high current density of 1000mAcm-2 and maintains activity for 1200hours under high current density conditions, rivaling advanced self-supporting electrodes. Moreover, replacing Co in Co/Ti2CTx with metals like Fe, Ni or Mn, yields comparable effects, suggesting the scalability of catalyst-inducing seeds. This approach breaks traditional limitations of powdered materials in OER, offering an effective pathway to engineer advanced catalytic electrodes.

Role of Sulfur in Enhancing UV‐Light Absorption and Photoelectrochemical Performance of ZnO/N,S‐doped CQDs Nanocomposite

AbstractThe modification of ZnO, such as transforming it from 1‐D to 3‐D nanostructures or compositing it with carbon‐based materials, has been extensively explored to enhance light energy harvesting and reduce electron‐hole recombination‐key limitations of ZnO. Herein, the effect of different composite materials, specifically nitrogen‐doped carbon quantum dots (N‐CQDs) and nitrogen, sulfur‐doped carbon quantum dots (N,S‐CQDs), on ZnO's morphology and photocurrent response was studied. Various morphologies were synthesized on conductive glass substrate using a one‐pot hydrothermal method, including flower‐like structure for ZnO/N‐CQDs (∼d = 0.9 µm) and multilayered microspheres for ZnO/N,S‐CQDs (∼d = 1.1 µm). The inclusion of sulfur atoms in the composite resulted in a reduced bandgap value from 3.22 to 3.11 eV, along with enhanced light absorption efficiency and improved separation of photogenerated electron‐hole pairs. Furthermore, the crystallinity of ZnO/N,S‐CQDs was significantly enhanced compared to ZnO without sulfur doping. These improvements were reflected in the photoelectrochemical (PEC) measurements, where ZnO/N,S‐CQDs showed a current density of 21.8 µA/cm2 at 0.5 V (vs. Ag/AgCl), which is 5.5 times higher than that of ZnO/N‐CQDs (4.0 µA/cm2). These findings demonstrate that sulfur doping improves photocatalytic efficiency, making 3D ZnO/N,S‐CQDs a promising candidate for various UV‐driven PEC applications.

Electrochemical activation and characterization of carbon cloth

Here, carbon cloth (CC), which is a disposable, inexpensive, conductive substrate, was electrochemically activated for the formation of function al groups on the electrode surface. The electrochemical activation of commercial CC was achieved in various acidic solutions such as 0.1 M H2SO4, 0.1 M HCl and 0.1 M HNO3 to create functional groups on the surface of the gas diffusion layer by applying a constant 100 mA current (galvanostatic) for 10 s, 20 s, and 30 s, respectively. The electrochemical measurements were conducted using a 3-electrode system, including disposable carbon cloth as a working electrode, saturated Ag/AgCl as a reference electrode and Pt wire as a counter electrode. The modified CCs were tested via cyclic voltammetry using 5 mM Fe(CN)63−/Fe(CN)64− redox probe. Electrochemical experiment results showed that acid treatment of CC resulted in a significant increase in peak current compared to bare CC, indicating formation of functional groups on the electrode surface and improved electrical conductivity.

Bi-metallic electrochemical deposition on 3D pyrolytic carbon architectures for potential application in hydrogen evolution reaction

ABSTRACT 3D printing has emerged as a highly efficient process for fabricating electrodes in hydrogen evolution through water splitting, whereas metals are the most popular choice of materials in hydrogen evolution reactions (HER) due to their catalytic activity. However, current 3D printing solutions face challenges, including high cost, low surface area, and sub-optimal performance. In this work, we introduce metal-deposited 3D printed pyrolytic carbon (PyC) as a facile and cost-effective HER electrode. We adopt an integrated approach of resin 3D printing, pyrolysis, and electrochemical metal deposition. 3D printing of a resin and its subsequent pyrolysis led to 3D complex architectures of the conductive substrate, facilitating the electrochemical metal deposition and leading to layered 3D metal architecture. Both monolayers of metals (such as copper and nickel) and bi-metallic 3D PyC structures are demonstrated. Each metal layer thickness ranges from 6 to10 µm. The metal coatings, particularly the bi-metallic configurations, result in achieving significantly higher mechanical properties under compressive loading and improved electrical properties due to the synergistic contributions from each metal counterpart. The metalized PyC structures are further demonstrated for HER catalysts, contributing to the development of highly efficient and durable catalyst systems for hydrogen production. Among the materials studied here, Ni@Cu bimetallic 3D PyC electrodes are particularly well-suited, demonstrating a low HER overpotential value of 264 mV (100 mA/cm2, KOH (1 M)) with corresponding Tafel slopes of 107 mV/dec, with exceptional stability during a 10 h operation at a high applied current of −50 mA/cm2.

Ambient Air-Synthesized CsPbBr3 Nanocrystals Coupled with TiO2 Film as an Efficient Hybrid Photoanode for Photoelectrochemical Methanol-to-Formaldehyde Conversion.

Due to its exceptional optoelectronic properties in the visible spectrum, cesium lead bromide (CsPbBr3) perovskite has attracted considerable attention in solar-driven organic transformations via photoelectrochemical (PEC) cells. However, the performance of the devices is adversely affected by electron-hole recombination occurring between a transparent conductive substrate, such as fluorine-doped tin dioxide (FTO), and a perovskite layer. Herein, to mitigate this issue, a compact layer of titanium dioxide (TiO2) was employed as both an electron transport layer and a hole blocking layer to diminish charge recombination while facilitating electron transfer in such perovskite material. At the oxidation peak potential of 0.70 V vs Ag/AgNO3, a hybrid photoanode of CsPbBr3/TiO2/FTO exhibited a significant increase in photocurrent density, from 15 to 41 μA/cm2, compared to a configuration without a TiO2 layer. Furthermore, the introduction of methanol as a hole scavenger in the PEC system using the hybrid photoanode facilitated the separation of electron-hole pairs, which led to an enhanced photocurrent density of 60 μA/cm2 and promoted the production of formaldehyde. High-performance liquid chromatography (HPLC) confirmed the generation of formaldehyde at a concentration of 26.69 μM with a Faradaic efficiency of 92% under an applied potential of 0.50 V vs Ag/AgNO3 for 60 min of PEC reaction. In addition to the enhanced PEC performance achieved from this hybrid photoanode, CsPbBr3 nanocrystals (NCs) in this work were synthesized by the modified one-pot method under ambient air, where highly uniform and high-purity NCs were obtained. This work signifies the groundbreaking exploration of CsPbBr3 NCs with TiO2 as a photoelectrode material in the organic-based PEC cells, which efficiently improved the interfacial charge transfer within the photoanode for the conversion of methanol to formaldehyde, marking a significant advancement in the field.

Nanoflower-like NiCoFe layered hydroxide by in-situ electrochemical corrosion as highly efficient electrocatalyst for water oxidation

Layered double hydroxides have been widely applied for oxygen evolution reaction (OER) in the alkaline water electrolysis. However, the issues of poor connection between the catalyst and nickel foam and the specific mechanisms for active sites has not been fully documented. In this study, the in-situ nickel foam etching in a mixed solution of ferric chloride and cobalt nitrate at low temperatures was adopted for NiCoFe layered ternary hydroxides (NiCoFe LTHs) synthesis with a better tight integration. Physicochemical characterization indicated that the NiCoFe LTHs could grow directly through corroding nickel foam with a nano-flower-like morphology and structures. That is favorable for electron transfer from the catalytic layer to the conductive substrate. With the transition metal ions interaction and the tight integration construction, NiCo1Fe4-LTH-T60/NF presented an enhanced electrolysis performance with the overpotential of 234 mV (1.464 V vs. RHE) at current density of 100 mA cm−2 in 1 M KOH electrolyte. The Tafel slope for NiCo1Fe4-LTH-T60/NF electrode was 36.19 mV dec−1 for an enhanced OER kinetics. Besides, it demonstrated faster interfacial charge transfer process, better intrinsic electrochemical activity and stability in large current stability testing. It was revealed that the synergistic effect of the transition metal ions interaction enhancement and the mechanism of oxygen evolution elementary reaction for NiCo1Fe4-LTH-T60/NF during the water electrolysis by the electrochemical and theoretical calculation. This work provides theoretical basis and experimental support for the design and synthesis of future OER catalyst and substrate, which is significant for hydrogen and oxygen generation from water electrolysis.

Hydrogen evolution reaction catalyzed by Co-based metal-organic frameworks and their derivatives

In this study, Co-bearing Metal-Organic Frameworks (MOFs) are grown via a facile solvothermal process on the surface of two kinds of conductive substrates – titanium dioxide nanotubes (TiO2NT) and fluorine-doped tin oxide (FTO) glass and tested as electrodes in the electrochemical hydrogen evolution reaction (HER). The materials derived from three organic linkers - terephthalic acid (Co-BDC), 2-aminoterephthalic acid (Co-BDCNH2), and trimesic acid (Co-BTC) are characterized by FTIR, Raman, XRD, SEM-EDS, BET, and XPS. Among the layers on FTO without post-synthesis treatment, Co-BTC shows the highest activity (overpotential of HER 1.72 V vs. Ag/AgCl/KCl). The effects of substrate change on TiO2NT and annealing of Co-BTC layers in air and argon on their electrocatalytic properties are also studied. Using TiO2 nanotubes as a substrate and annealing the material in air results in a reduction of the hydrogen evolution overpotential to 1.44 V vs. Ag/AgCl/KCl and a significant reduction in the exchange current density.

Highly Conductive Two-Dimensional FeTHBQ/Graphene Nanocomposite as the Cathode Material for Lithium-Ion Batteries.

Constructing high-performance coordination polymer (CP) cathodes for lithium-ion batteries based on the redox reactions of both high-potential transition metal ions and high-capacity organic ligands has attracted extensive attention. However, CP cathodes suffer from structural degradation, low electrical conductivity, and sluggish diffusion kinetics, resulting in poor cycling stability and inferior rate capability. Herein, the ultrafine FeTHBQ (THBQ = tetrahydroxy-1,4-benzoquinone) CP nanoparticles in situ grew on both sides of graphene nanosheets to form the uniform two-dimensional (2D) FeTHBQ/Graphene nanocomposite with a sandwich structure via a one-pot solvothermal method. The highly conductive graphene skeleton promotes the electronic conduction and structural stability for the 2D FeTHBQ/Graphene nanocomposite. Besides, compared with bulk FeTHBQ, the primary FeTHBQ nanoparticles in the FeTHBQ/Graphene nanocomposite have smaller particle sizes with larger specific surface areas. This not only shortens the Li+ diffusion distance in the FeTHBQ crystal but also benefits Li+ transfer between the electrolyte and the electrode. In the FeTHBQ/Graphene nanocomposite, the active material of FeTHBQ manifested multiple redox centers of transition metal ions (Fe3+/Fe2+) and carbonyls (C═O/C-O-) in THBQ ligands. Owing to the enhancements of structural stability, electronic conduction, and Li+ diffusion kinetics, the 2D FeTHBQ/Graphene nanocomposite presented a high lithium-ion storage capacity of 217.2 mA h g-1 at 50 mA g-1, a fast rate capability of 79.1 mA h g-1 at 5000 mA g-1, and a stable cycling performance of 87.2 mA h g-1 at 500 mA g-1 after 100 cycles. This work sheds light on the great opportunity for optimizing the electrochemical performances of CP-based functional electrode materials by combining with conductive substrates.

Material Selection and Design Methods for Flexible RFID Tag Antenna

In recent years, advancements in flexible printed electronics have significantly propelled the development of wearable devices, especially in areas of integration, comfort, and streamlined manufacturing. By incorporating electronic components and conductive coatings onto flexible substrates, circuits gain enhanced flexibility and some degree of stretchability. Among these circuits, radio frequency identification (RFID) tag antennas have emerged as a focal point in wearable device communication due to their adaptability in power selection and their compatibility with printed circuit technologies. When designing flexible and stretchable RFID tag antennas using printed electronics, two critical factors need to be addressed. The first is the antenna’s structural design, which must account for varying environments and usage contexts. The second is the development of the antenna prototype, involving the selection of conductive coatings and flexible substrates, as well as the printing processes and performance evaluation standards. This paper will explore common conductive coatings and substrate materials used in flexible printed electronics, along with the design methods of printed tag antennas for wearable applications. Lastly, a novel approach is proposed in which the flexible and stretchable RFID tag antenna itself functions as a strain sensor for posture or pressure detection. Unlike conventional strain sensors, this design eliminates the need for additional communication modules, offering a simplified structure that can be easily printed onto clothing, thereby streamlining the production process.

Toward Finding the Role of Surface Iron Ions in Enhancing Oxygen-Evolution Reaction.

The oxygen evolution reaction (OER) in alkaline media is crucial for energy conversion technologies, and Fe-based catalysts have garnered significant attention for their efficacy. In this study, we provide an investigation of Fe-based catalysts under OER conditions using some techniques. Our findings reveal minimal structural alterations in the bulk FeHxOy framework during OER, indicating that the bulk structure remains largely intact. Instead, the catalytic activity is primarily localized on the material's surface. This conclusion is corroborated by the measured low electrochemical surface area (ECSA) of FeHxOy, suggesting that its limited OER performance stems from a paucity of active sites rather than low intrinsic activity. The superior efficiency of Fe ions in conductive oxides or on conductive metal substrates (e.g., copper and gold) in OER is attributed to the increased availability of surface-active sites in these systems. To further elucidate this phenomenon, we investigated two additional systems: NiFe and VFe (hydr)oxides. For NiFe (hydr)oxides, we demonstrate that only surface Fe ions contribute actively to OER. In contrast, in VFe (hydr)oxides, the removal of vanadium resulted in a marked increase in ECSA and the generation of defect sites, significantly enhancing OER activity. These findings provide critical insights into the surface-specific role of Fe ions in catalytic activity and could inform future design strategies for more efficient OER catalysts by optimizing the availability and reactivity of surface-active Fe sites.

Innovative Air Cathode with Ni-Doped Cobalt Sulfide in Highly Ordered Macroporous Carbon Matrix for Rechargeable Zn-Air Battery.

To realize the practical application of rechargeable Zn-Air batteries (ZABs), it is imperative to develop a non-noble metal-based electrocatalyst with high electrochemical performance for the oxygen reduction reaction (ORR) and oxygen evolution reaction (OER). Herein, Ni-doped Co9S8 nanoparticles dispersed on an inverse opal-structured N, S co-doped carbon matrix (IO─NixCo9-xS8@NSC) as a bifunctional electrocatalyst is presented. The unique 3D porous structure, arranged in an inverse opal pattern, provides a large active surface area. Also, the conductive carbon substrate ensures the homogeneous dispersion of NixCo9-xS8 nanocrystals, preventing aggregation and increasing the exposure of active sites. The introduction of heteroatom dopants into the Co9S8 structure generates defect sites and enhances surface polarity, thereby improving electrocatalytic performance in alkaline solutions. Consequently, the IO─NixCo9-xS8@NSC shows excellent bifunctional activity with a high half-wave potential of 0.926V for ORR and a low overpotential of 289mV at 10mA cm-2 for OER. Moreover, the rechargeable ZAB assembled with prepared electrocatalyst exhibits a higher specific capacity (768 mAh gZn -1), peak power density (180.2mW cm-2), and outstanding stability (over 160h) compared to precious metal-based electrocatalyst.

Solution-Crystalized AgBiS2 Films for Solar Cells Generating a Photo-Current Density Over 31mA cm-2.

In response to the toxic heavy metal absorbers in perovskite solar cells (PSCs), this work focuses on the development of an environmentally friendly simple solution-processed infrared (IR) absorber. In this work, a simple solution-crystallized IR-absorbing AgBiS2 film is reported by spin-coating silver, bismuth nitrates, and thiourea dissolved in dimethylformamide (DMF) to produce thick AgBiS2 film. Extensive optimization of the precursor concentrations thicknesses and conductive substrates used allow for obtaining 250nm AgBiS2 film with different crystal sizes. When applied as an absorber in solar cells, solution-crystalized AgBiS2 thick film delivers an extraordinarily high current density of over 31mA cm-2. The devices show high stability under continuous 100mW cm-2 illumination and when stored in the dark for more than six months. When the AgBiS2 layer is fabricated in a gradient fashion combining one layer of 0.25m and three layers of 0.5m precursor concentrations, the efficiency of 5.15% is registered which is the highest reported for the simple solution-crystallized AgBiS2 films.

Engineering intervention to disrupt the evolution of ZIF-67: Ultra-fast synthesis of arrayed Co(OH)2@ZIF-L in dozens of seconds for high-energy charge storage

Designing rational heterostructures of high-performance electroactive materials on conductive substrates with hierarchical structures is critical for advancing electrochemical energy storage technologies. In this study, a unique spatial structure is fabricated by vertically aligning two-dimensional (2D) structures of Co-ZIF-L on conductive nickel foam (NF) substrate through interruption of ZIF-67 formation. This is followed by an innovative electrochemical synthesis method that disrupts unstable surface coordination bonds in Co-ZIF-L, enabling the in-situ generation of Co(OH)2. The resulting Co(OH)2@ZIF-L/NF binder-free electrodes feature a hierarchical spatial structure and are synthesized in approximately 30 s. These electrodes showcase exceptional area capacity of 3.1 C cm−2 at 1 mA cm−2, attributed to their high specific surface area and layered architecture that promotes electrolyte penetration. Density Functional Theory (DFT) calculations reveal that the Co(OH)2@ZIF-L nanostructures have superior electrical conductivity compared to the individual components. Furthermore, a hybrid supercapacitor (HSC) based on Co(OH)2@ZIF-L/NF//AC exhibits an impressive energy density of 42 Wh kg−1 at a power density of 184.7 W kg−1. This research provides new insights into the efficient synthesis of high-performance electroactive materials with unique spatial structures and expands the potential applications of ZIF materials.