Low-Intensity Light Detection with a High Detectivity Using 2D-Sb2Se3 Nanoflakes on 1D-ZnO Nanorods as Heterojunction Photodetectors.

Multifunctional photodetectors (PDs) with broadband responsivity (R) and specific detectivity (D*) at low light intensities are gaining significant attention. Thus, we report a bilayer PD creatively fabricated by layering two-dimensional (2D) Sb2Se3 nanoflakes (NFs) on one-dimensional (1D) ZnO nanorods (NRs) using simple thermal transfer and hydrothermal processes. The unique coupling of these two layers of materials in a nanostructured form, such as 2D-Sb2Se3 NFs/1D-ZnO NRs, provides an effective large surface area, robust charge transport paths, and light-trapping effects that enhance light harvesting. Furthermore, the combination of both layers can effectively facilitate photoactivity owing to proper band alignment. The as-fabricated device demonstrated superior overall performance in terms of a suitable bandwidth, good R, and high D* under low-intensity light, unlike the single-layered 1D-ZnO NRs and 2D-Sb2Se3 NF structures alone, which had poor detectivity or response in the measured spectral range. The PD demonstrated a spectral photoresponse ranging from ultraviolet (UV) to visible (220-628 nm) light at intensities as low as 0.15 mW·cm-2. The PD yielded a D* value of 3.15 × 1013 Jones (220 nm), which reached up to 5.95 × 1013 Jones in the visible light region (628 nm) at a 3 V bias. This study demonstrated that the 2D-Sb2Se3 NFs/1D-ZnO NRs PD has excellent potential for low-intensity light detection with a broad bandwidth, which is useful for signal communications and optoelectronic systems.

Retraction: Progressive p-channel vertical transistors fabricated using electrodeposited copper oxide designed with grain boundary tunability.

Retraction of 'Progressive p-channel vertical transistors fabricated using electrodeposited copper oxide designed with grain boundary tunability' by Sung Hyeon Jung et al., Mater. Horiz., 2022, 9, 1010-1022, https://doi.org/10.1039/D1MH01568K.

Porous nanorods by stacked NiO nanoparticulate exhibiting corn-like structure for sustainable environmental and energy applications.

A porous 1D nanostructure provides much shorter electron transport pathways, thereby helping to improve the life cycle of the device and overcome poor ionic and electronic conductivity, interfacial impedance between electrode-electrolyte interface, and low volumetric energy density. In view of this, we report on the feasibility of 1D porous NiO nanorods comprising interlocked NiO nanoparticles as an active electrode for capturing greenhouse CO2, effective supercapacitors, and efficient electrocatalytic water-splitting applications. The nanorods with a size less than 100 nm were formed by stacking cubic crystalline NiO nanoparticles with dimensions less than 10 nm, providing the necessary porosity. The existence of Ni2+ and its octahedral coordination with O2- is corroborated by XPS and EXAFS. The SAXS profile and BET analysis showed 84.731 m2 g-1 surface area for the porous NiO nanorods. The NiO nanorods provided significant surface-area and the active-surface-sites thus yielded a CO2 uptake of 63 mmol g-1 at 273 K via physisorption, a specific-capacitance (CS) of 368 F g-1, along with a retention of 76.84% after 2500 cycles, and worthy electrocatalytic water splitting with an overpotential of 345 and 441 mV for HER and OER activities, respectively. Therefore, the porous 1D NiO as an active electrode shows multifunctionality toward sustainable environmental and energy applications.

Alkali Cation Engineered Chemical Self-Oxidation of Copper Oxide Nanowire-Based Photocathodes.

Hydrogen energy production through photoelectrochemical (PEC) water splitting has great potential in the field of renewable energy. This study focuses on the hydration enthalpy difference of cations (Li+ , Na+ , and K+ ) in an aqueous solution for the chemical self-oxidation process without an external applied bias. The thickness of the cation/H2 O double layer is controlled. The starting materials are low-cost copper foil and the synthesis uses alkali cation-engineered chemical self-oxidation. Li+ ions are strongly attracted to water molecules. This forms a sufficient OH- layer on the Cu foil surface. By accelerating the oxidation reaction, a large surface area of Cu(OH)x nanowires (NWs) with high purity and a uniform shape are obtained. This optimal p-type Cu2 O NWs photocathode is CuO-free, has the highest conductivity, and is fabricated through phase transition using precise vacuum annealing. The other alkali cations produce the Cu2 O/CuO mixed or CuO phases that degrade the PEC performances with severe corrosive reactions. The Cu/Li : Cu2 O/AZO/TiO2 /Pt photocathode has a 50 h stability with a photocurrent density of 8.4 mA cm-2 at 0 VRHE . The fabricated photoelectrode did not structurally collapse after stability measurements during this period. The captured hydrogen production was in agreement with the calculated faradaic efficiency.

Progressive p-channel vertical transistors fabricated using electrodeposited copper oxide designed with grain boundary tunability.

A strategically designed electrodeposition method is proposed for the coating of p-type copper(i) oxide (Cu2O) channels for oxide thin film transistors. To date, conventional p-type oxide semiconductors have revealed a poor mobility and stability and this has obstructed the development of all oxide based logic devices. Furthermore, previous studies on p-type oxide transistors have been limited by the use of a typical planar type configuration. Our Cu2O electrodeposition method designed by incorporating Sb element promotes vertical alignment of the grain boundaries (GBs) and it perfectly coincides with the charge transport direction from the source to the drain in the vertical field effect transistors. These vertically aligned GBs are bundle type GBs and are likely to be ideal for vertical transistors with supreme electrical performances owing to the structurally suppressed grain boundary charge scattering. This alignment of the GBs in the electrodeposited Sb doped Cu2O (Sb:Cu2O) also demonstrates a superior vertical taper profile with conventional wet chemical etching owing to the extremely preferential etching rate along the GBs. Surprisingly, the sidewall formation, with a smooth and steep morphology causes the formation of abrupt and non-defective gate insulator/channel interfaces for superior spacer-free vertical transistors. Consequently, the Cu2O vertical field effect transistors exhibit extraordinary transistor performances of Vth = 0.4 V, µFE = 8 cm2 V-1 s-1, subthreshold swing = 0.24 V dec-1, on/off current ratio = 2 × 108 and qualified electrical and long-term stability characteristics under various environments. To the best of our knowledge, this is the first reported study on an electrodeposited method to design troublesome p-type oxide Cu2O as novel vertical transistors. Finally, power efficient logic inverter circuits with unprecedented performances, such as good noise margins, remarkable gain values of 15.6 (2 VDD) and 62.7 (5 VDD), and high frequency operation up to 10 kHz, are demonstrated using these p-type Cu2O transistors by interconnecting n-type IGZO transistors.

A synergistic strategy to remove hazardous water pollutants by mimicking burdock flower morphology structures of iron oxide phases.

Artificially mimicking structures/morphologies available in the nature to develop multifunctional materials for catalysis is receiving greater attention. Particularly, the burdock flower morphology, which has a hollow-globe surrounded by spiky sheets, represents a multifunctional structure helpful in adsorption as well as intercalation of molecules. Given this, we have strategically developed a robust microwave (MW) bubble-template process to achieve highly uniform α-Fe2O3 and carbon-enriched Fe3O4 (Fe3O4@C) phases resembling the characteristics of spiky hollow burdock morphologies. The utilization of the MW bubble-templates as a pretreatment to the iron-based precursor solution helps in producing hollowed open-space ferrous glycolate burdock flower morphology with rapid production rate and without any addition of extra agents. Such burdock flower structures remain intact even after annealing in air/N2 ambiance providing highly photoactive α-Fe2O3 or magnetic Fe3O4@C, respectively. Utilizing the hollow burdock flower structures together with the individual photo/magnetic properties of iron oxide phases, a dual-layer filter was designed to remove hazardous dye molecules from water, which efficiently photodegraded (99.2 %) in natural sunlight as well as showed excellent adsorption (99.7 %) within minutes. Comparatively, a lower catalytic activity using simple iron oxide nanoparticles, closed, and faded burdock morphologies were seen. Hence, the high catalytic activity in removing the dye molecules, retention of structural phases after repeated use, and strong durability were a result of the synergetic effect of photo/magnetic properties, activated surface/spiky open burdock structure.

Energy Transfer-Induced Photoelectrochemical Improvement from Porous Zeolitic Imidazolate Framework-Decorated BiVO4 Photoelectrodes.

BiVO4 , which is a representative photoanode material for photoelectrochemical water splitting, intrinsically restricts high conversion efficiency, owing to faster recombination, low electron mobility, and short electron diffusion length. While the photocurrent density of typical BiVO4 corresponds to only 21.3% of the maximum photocurrent density (4.68 mA cm-2 ), decoration of the BiVO4 photoanode with zeolitic imidazolate framework-67 (ZIF-67) exhibits a synergetic effect to raise the overall photocatalytic ability at the BiVO4 surface region to a higher level via the energy-transfer process from BiVO4 to ZIF-67. The hybrid ZIF-67/BiVO4 photoanode follows two convenient photoelectrochemical pathways: 1) energy-transfer-induced water oxidation reaction in ZIF-67 and 2) water oxidation reaction by direct contact between the BiVO4 surface and electrolytes. Compared to the moderate photocurrent density (≈1 mA cm-2 ) of single-layer BiVO4 , the proposed ZIF-67/BiVO4 photoanodes show a remarkably high photocurrent (2.25 mA cm-2 ) with high stability, despite the lack of hole scavengers in the electrolyte. Furthermore, the absorbed photon-to-current efficiency of the ZIF-67/BiVO4 photoanode is ≈2.5 times greater than that of BiVO4 . This work proposes a promising solution for efficient water oxidation that overcomes the intrinsic material limitations of BiVO4 photoelectrodes by using energy transfer-induced photon recycling and the decoration of porous ZIFs.

ß-like FeOOH Nanoswords Activated by Ni Foam and Encapsulated by rGO toward High Current Densities, Durability, and Efficient Oxygen Evolution.

As an alternative to the oxygen evolution reaction (OER) electrocatalyst developed by a complex bi- or multimetal ion with layered double hydroxide (LDH) structures, we design a simple, self-supported, and single-metal-ion OER electrocatalyst having lower overpotentials and high current densities in alkaline water electrolyzers. Here, ß-like FeOOH nanosword structures encapsulated by reduced graphene oxide (rGO) were cost-effectively synthesized on formable Ni foam substrates as an efficient and highly durable OER catalyst. It is revealed that the rGO uniformly covered the ß-like FeOOH nanoswords to form a porous network achieving a lower overpotential of only 210 mV at 10 mA cm-2 with a stable operation for more than 40 h in alkali media. Moreover, a high current density of ∼300 mA cm-2 was achieved at less than 1.8 V. In-depth physical and electrochemical analysis indicated that the intrinsic charge transfer through activated Ni-foam, ß-like phase, and nanosword morphology was evidently beneficial for enhancing the OER activity of the bare FeOOH, and its encapsulation by rGO further improved the conductivity and long-life durability. Our integrated OER electrocatalyst developed by a simple method (repeated soaking and quenching process) will aid in scaling up ß-like FeOOH nanoswords for preparing uniform and large-area electrodes for industrial purposes.

Optimal n-Type Al-Doped ZnO Overlayers for Charge Transport Enhancement in p-Type Cu2O Photocathodes.

An effective strategy for improving the charge transport efficiency of p-type Cu2O photocathodes is the use of counter n-type semiconductors with a proper band alignment, preferably using Al-doped ZnO (AZO). Atomic layer deposition (ALD)-prepared AZO films show an increase in the built-in potential at the Cu2O/AZO interface as well as an excellent conformal coating with a thin thickness on irregular Cu2O. Considering the thin thickness of the AZO overlayers, it is expected that the composition of the Al and the layer stacking sequence in the ALD process will significantly influence the charge transport behavior and the photoelectrochemical (PEC) performance. We designed various stacking orders of AZO overlayers where the stacking layers consisted of Al2O3 (or Al) and ZnO using the atomically controlled ALD process. Al doping in ZnO results in a wide bandgap and does not degrade the absorption efficiency of Cu2O. The best PEC performance was obtained for the sample with an AZO overlayer containing conductive Al layers in the bottom and top regions. The Cu2O/AZO/TiO2/Pt photoelectrode with this overlayer exhibits an open circuit potential of 0.63 V and maintains a high cathodic photocurrent value of approximately -3.2 mA cm-2 at 0 VRHE for over 100 min.

Smart Bifunctional Sb2 Se3 Nanorods for Integrated Water Purification: Insoluble Liquid Separation and Photoelectrochemical Degradation.

Antimony selenide (Sb2 Se3 ) nanostructures enable bifunctional water purification by a single membrane through i) physical separation of water-insoluble oil and ii) photoelectrocatalytic degradation of water-soluble organic compounds. Sb2 Se3 nanorods with exposed surfaces of {h 0 0} and {h 0 l} planes exhibit superhydrophobicity (water contact angle of ≈159°) owing to extremely low surface energy of those dangling-bond-free van der Waals planes. Based on crystallographic understanding, superhydrophobic Sb2 Se3 nanorods were produced on a mesh-type substrate for utilization as a membrane for physical water/oil separation. Sb2 Se3 exhibited an optimal photocathodic response with p-type electrical conductivity under visible light along the longitudinal crystal direction. This indicated that the nanorods could be used as photoelectrocatalytic material for chemical water purification. A smart membrane with Sb2 Se3 nanostructures was proposed as a candidate for integrated water purification that can simultaneously accomplish water/oil separation and photoelectrocatalytic degradation of organic compounds in wastewater. Linear sweep voltammetry measurements of the Sb2 Se3 -membrane showed cathodic photocurrent generation (up to approximately 10 mA cm-2 at 0 V vs. reversible hydrogen electrode), which was enough to reduce O2 to an oxygen radical (O2 .- ) for degradation of methyl orange. Consequently, solar-driven integrated water purification was demonstrated for the first time by using a single material with a dual function of superhydrophobicity and photoactivity.

Highly Improved Quasi-Two-Dimensional Oxide Transistors via Non-centrosymmetric Nitrogen Dioxide Treatment, toward Extremely Low Process Temperature and Operant Self-Aligned Coplanar Structure.

Rapid degradations are typically encountered in low-temperature processed oxide thin-film transistors (TFTs) with a high indium composition and quasi-two-dimensional (Q2D) thin channel, owing to the breaking of numerous surface bonds of the Q2D oxide and the ineffectiveness of oxidation treatment. Strategically, a novel approach is proposed for the effective use of non-centrosymmetric nitrous oxide (NO2) as a reactive oxidizer gas for realizing the highly robust and rapid field-effect mobility properties of low-temperature-processed Q2D amorphous indium zinc oxide (a-IZO) TFTs. From the surface chemical analysis, it is found that NO2 stably reconstructs surface chemical bonding with NO3- ions by capturing the charged electrons and oxygen and the regions with and without NO2 treatment display extreme differences in their electrical conductivity. Thus, a new process design can be suggested for the fabrication of self-aligned coplanar Q2D transistors, with the aim of scaling down and replacing conventional hydrogen treatment or ultraviolet irradiation. This concept is tactically designed considering the problematic aging effect and impact of the NO2 treatment. The self-aligned coplanar top-gate Q2D a-IZO TFTs exhibit outstanding device performance with a field-effect mobility of 30.1 cm2 V-1 s-1 and a relatively low positive bias stress shift of 1.3 V at an extremely low process temperature of 80 °C.

Electrochemically Assembled Cu2O Nanoparticles Using Crystallographically Anisotropic Functional Metal Ions and Highly Expeditious Resistive Switching via Nanoparticle Coarsening.

We have developed an artificially controllable strategy of an electrodeposition process adequate for resistive random-access memory (ReRAM) applications of binary Cu2O. Typically, the precise control of OH- ion concentration (the intermediate supplier of oxygen ions) at the electrode's surface decides the overall reaction rate of the Cu2O. Here, the suggested Pb and Sb metal additives preferentially contribute to the consumption of OH- ions and the supply of OH- ions, respectively, during the Cu2O electrochemical reaction so that the final products are the (200) preferential quadrangular pyramids and the (111) preferential triangular pyramids. Interestingly, the coexistence of Sb/Pb precursors in the Cu electrolytes results in extraordinarily decreased reaction rate from the opposite action of OH- ion utilization as well as intense progressive growth behavior, and the resultant Cu2O films consist of crystallized small-size nanoparticles (NPs) in an amorphous-like matrix. In the case of ReRAM applications, while the polycrystalline film induces irregular device performance and the amorphous layer shows an easily irreparable electrical breakdown, our NP-assembled Cu2O films from Pb/Sb metal ions reveal the formation of a conduction bridge via phase change to a crystalline filament with no need for forming voltage and with superior electrical stability. It is attributed to the coalescence of crystal NPs into large grains during the set/reset cycle process for the heat dissipation of Joule heating. The Cu2O sample prepared with a 3 mM Sb + 3 mM Pb mixture solution exhibits forming-free ReRAM devices with high on/off resistance ratios of 1.2 × 104 and long-term electrical/thermal stability.

Toward Robust Photoelectrochemical Operation of Cuprous Oxide Nanowire Photocathodes Using a Strategically Designed Solution-Processed Titanium Oxide Passivation Coating.

To date, TiO2 films prepared by atomic layer deposition are widely used to prepare Cu2O nanowire (NW)-based photocathodes with photoelectrochemical (PEC) durability as this approach enables conformal coating and furnishes chemical robustness. However, this common approach requires complicated interlayers and makes the fabrication of photocathodes with reproducible performance and long-term stability difficult. Although sol-gel-based approaches have been well established for coating surfaces with oxide thin films, these techniques have rarely been studied for oxide passivation in PEC applications, because the sol-gel coating methods are strongly influenced by surface chemical bonding and have been mainly demonstrated on flat substrates. As a unique strategy based on solution processing, herein, we suggest a creative solution for two problems encountered in the conformal coating of surfaces with oxide layers: (i) how to effectively prevent corrosion of materials with hydrophilic surfaces by simply using a single TiO2 surface protection layer instead of a complex multilayer structure and (ii) guaranteeing perfect chemical durability. A Cu(OH)2 NW can be easily prepared as an intermediate phase by anodization of a Cu metal, where the former inherently possesses a hydrophilic hydroxylated surface and thus, enables thorough coating with TiO2 precursor solutions. Chemically robust nanowires are then generated as the final product via the phase transformation of Cu(OH)2 to Cu2O via sintering at 600 °C. The coated NWs exhibit excellent PEC properties and a stable performance. Consequently, the perfect chemical isolation of the Cu2O NWs from the electrolyte allows a remarkable PEC operation with the maintenance of the initial photocurrent for more than one day.

Contact angle measurements: a preliminary diagnostic tool for evaluating the performance of ZnFe2O4 nano-flake based supercapacitors.

Contact angle measurements (surface wettability) of the electrolytes (1 M KOH, NaOH and LiOH) and their combination (1 M 1 : 1 v/v LiOH + KOH, NaOH + KOH and LiOH + NaOH) in contact with ZnFe2O4 nano-flake based electrodes is used as an empirical diagnostic tool to pre-evaluate the performance of a supercapacitor prior to actual fabrication of the device.