Copper Intercalation Induces Amorphization of 2D Cu/WO3 for Room-Temperature Ferromagnetism.

Ferromagnetism in the two-dimensional limit has become an intriguing topic for exploring new physical phenomena and potential applications. To induce ferromagnetism in 2D materials, intercalation has been proposed to be an effective strategy, which could introduce lattice distortion and unpaired spin into the material to modulate the magnetocrystalline anisotropy and magnetic exchange interactions. To strengthen the understanding of the magnetic origin of 2D material, Cu was introduced into a 2D WO3 through chemical intercalation in this work (2D Cu/WO3). In contrast to the diamagnetic nature of the Cu and the WO3, room-temperature ferromagnetism was characterized for 2D Cu/WO3. Experimental and theoretical results attribute the ferromagnetism to the bound magnetic polaron in 2D Cu/WO3, which is consist of unpaired spins from W5+/W4+ with localized carriers from oxygen vacancies. Overall, this work provides a novel approach to introduce ferromagnetism into diamagnetic WO3, which could be applied for a wider scope of 2D materials.

Polyfluorinated Organic Diammonium Induced Lead Iodide Arrangement for Efficient Two-Step-Processed Perovskite Solar Cells.

The inefficient conversion of lead iodide to perovskite has become one of the major challenges in further improving the performance of perovskite solar cells fabricated by the two-step method. Herein, the discontinuous lead iodide layer realized by introduction of a polyfluorinated organic diammonium salt, octafluoro-([1,1'-biphenyl]-4,4'-diyl)-dimethanaminium (OFPP) iodide which does not form low-dimensional perovskites, can enable the satisfactory conversion of lead iodide into perovskite, leading to meliorated crystallinity and enlarged grains in the OFPP modulated perovskite (OFPP-PVK) film. Combined with the effective defect passivation, the OFPP-PVK films show enhanced charge mobility and suppressed charge recombination. Accordingly, the OFPP-based perovskite solar cells exhibit a champion efficiency of 24.76 % with better device stability. Moreover, a superior efficiency of 21.04 % was achieved in a large-area perovskite module (100 cm2). Our work provides a unique insight into the function of organic diammonium additive in boosting photovoltaic performance.

Suppressing interfacial nucleation competition through supersaturation regulation for enhanced perovskite film quality and scalability.

The growing interest in cost-effective and high-performing perovskite solar cells (PSCs) has driven extensive research. However, the challenge lies in upscaling PSCs while maintaining high performance. This study focuses on achieving uniform and compact perovskite films without pinholes and interfacial voids during upscaling from small PSCs to large-area modules. Competition in nucleation at concavities with various angles on rough-textured substrates during the gas-pumping drying process, coupled with different drying rates across the expansive film, aggravates these issues. Consequently, substrate roughness notably influences the deposition window of compact large-area perovskite films. We propose a supersaturation regulation approach aimed at achieving compact deposition of high-quality perovskite films over large areas. This involves introducing a rapid drying strategy to induce a high-supersaturation state, thereby equalizing nucleation across diverse concavities. This breakthrough enables the production of perovskite photovoltaics with high efficiencies of 25.58, 21.86, and 20.62% with aperture areas of 0.06, 29, and 1160 square centimeters, respectively.

CO2-Assisted synthesis of a crystalline/amorphous NiFe-MOF heterostructure for high-efficiency electrocatalytic water oxidation.

Modulating the crystalline phase and structure of metal organic frameworks (MOFs) for superior electrocatalytic oxygen evolution reaction (OER) performance is a significant but challenging topic. Herein, a facile CO2-assisted strategy is reported to fabricate a crystalline/amorphous NiFe-based MOF heterostructure (c/a-NiFe-MOF) that exhibited excellent OER performance with a low overpotential of only 236 mV at a current density of 10 mA cm-2 and a small Tafel slope of 30 mV dec-1. This work provides new insights for CO2-assisted preparation of novel MOF heterostructures with diverse crystalline phases and sheds light on the rational design of highly efficient OER electrocatalysts.

A Two-dimensional Amorphous Plasmonic Heterostructure of Pd/MoO3-x for Enhanced Photoelectrochemical Water Splitting Performance.

Two-dimensional (2D) heterostructures based on localized surface plasmon resonance (LSPR) have a great potential for solar energy harvesting applications. Exploring 2D amorphous plasmonic heterostructures with high light absorption and catalytic activity is desirable yet challenging. Herein, 2D Pd/MoO3-x amorphous heterostructures can be obtained by immobilizing Pd single atoms in unsaturated coordination sites of amorphous MoO3-x , because of strong metal-support interactions, and it reaches a current density of 50 µA cm-2 for photoelectrochemical response with good durability, and exhibits a high incident-photon-to-current-conversion efficiency (IPCE) of 14.8% at 460 nm. Such an enhanced catalytic effects are contributed to the enhanced light absorption in visible region and change of electronic structure owing to enhanced electron transfer through dominant Pd-O bonds, which facilitate water splitting. This work moves a step closer to the expansion of photovoltaic device with the high conversion efficiency for visible light for amorphous heterostructures.

Amorphous-MoO3-x/MoS2 heterostructure: in situ oxidizing amorphization of S-vacancy MoS2 for enhanced alkaline hydrogen evolution.

Cost-effective and durable electrocatalysts for the alkaline hydrogen evolution reaction (HER) are urgently required. The slow HER kinetics suppressed by water dissociation hinder the application of catalysts in alkaline media. Herein, we constructed an amorphous heterostructure that combined amorphous-MoO3-x (A-MoO3-x) and MoS2 by in situ oxidizing amorphization of S-vacancy MoS2. The optimal A-MoO3-x/MoS2 catalyst exhibited a competitive HER overpotential of -146 mV at η = -10 mA cm-2. DFT calculations indicate that A-MoO3-x can reduce the energy barriers of water dissociation and H2 formation, and the heterointerfaces can facilitate charge transfer.

High-Quality Concentrated Precursor Solution in N,N-Dimethylformamide for Thick Methylammonium Triiodoplumbate Layer in Solar Cells.

A high-quality precursor solution is essential for the fabrication of hybrid perovskite solar cells. This article reports a simple and efficient method for preparing a high-quality concentrated solution of methylammonium triiodoplumbate (MAPbI3) in N,N-dimethylformamide (DMF) by using MAPbI3 crystals instead of conventional lead iodine and methylammonium iodine blend. The MAPbI3 concentration of the precursor solution is easily and accurately adjusted from 0 up to 1.64 M. An investigation of the dissolution process of the MAPbI3 crystals reveals that the concentrated solution of MAPbI3 in DMF is metastable, and the transition from the concentrated solution to solvated intermediate MAPbI3·DMF determines the solubility of MAPbI3 in DMF. The high purity and precise stoichiometric ratio of the crystals eliminate the possible impurities that initialize the transition to MAPbI3·DMF and consequently suppress the transition and increase the stability of the concentrated solution. MAPbI3 films with different thicknesses up to 800 nm are prepared with the conventional film fabrication technique, and the highest power conversion efficiency of 20.7% is achieved on corresponding solar cells. This newly developed method for preparing a concentrated precursor solution can be easily combined with other fabrication techniques for further development of industrial-scale manufacture of solar cells.

Supercritical CO2 synthesis of Co-doped MoO3-x nanocrystals for multifunctional light utilization.

Here, we demonstrate, for the first time, that Co-MoO3-x nanocrystals (NCs) have been synthesized with the assistance of supercritical CO2. Their unique structural features of transition-metal doping and high oxygen vacancy concentrations, lead to synchronous outstanding surface enhanced Raman scattering (SERS) detection and photothermal conversion performances.

An advanced FeCoNi nitro-sulfide hierarchical structure from deep eutectic solvents for enhanced oxygen evolution reaction.

A tri-metal material system of FeCoNi-based nitro-sulfide (FeCoNi-NS) hierarchical structure has been successfully synthesized via a deep eutectic solvent annealing process. The as-prepared FeCoNi-NS possesses interesting N,S-binary heteroatoms evenly doped with Fe, Co, and Ni. By taking advantage of the unique structure including multi-metal sites, high BET area and porous structures, the as-prepared FeCoNi-NS exhibited excellent oxygen evolution reaction (OER) performance, achieving a current density of 10 mA cm-2 at an overpotential of 251 mV and a low Tafel slope of 58 mV dec-1 in 1 M KOH. Furthermore, FeCoNi-NS also demonstrated highly efficient mass/charge transportation, long-term stability with 2% deactivation after ten hours continuous operation and high faradaic efficiency of 98%. Such a facile synthetic strategy is applicable to the fabrication of more mutil-metal hierarchical structures for energy conversion and storage.

NIR light-activated upconversion semiconductor photocatalysts.

Harvesting of near infrared (NIR) light in the abundant and environmentally friendly solar spectrum is particularly significant to enhance the utilization rate of the cleanest energy on earth. Appreciating the unique nonlinear optical properties of upconversion materials for converting low-energy incident light into high-energy radiation, they become the most promising candidates for fabricating NIR light-active photocatalytic systems by integrating with semiconductors. The present review summarizes recent NIR light-active photocatalytic systems based on a sequence of NaYF4-based, fluoride-based, oxide-based and Ln3+ ion-doped semiconductor-based photocatalysts for degradation of organic molecules. In addition, we provide an in-depth analysis of various photocatalytic mechanisms and enhancement effects for efficient photo-redox performance of different upconversion semiconductor photocatalysts. We envision that this review can inspire multidisciplinary research interest in rational design and fabrication of efficient full-spectrum active (UV-visible-NIR) photocatalytic systems and their wider applications in solar energy conversion.

Catalytic Application and Mechanism Studies of Argentic Chloride Coupled Ag/Au Hollow Heterostructures: Considering the Interface Between Ag/Au Bimetals.

For an economical use of solar energy, photocatalysts that are sufficiently efficient, stable, and capable of harvesting light are required. Composite heterostructures composed of noble metals and semiconductors exhibited the excellent in catalytic application. Here, 1D Ag/Au/AgCl hollow heterostructures are synthesized by galvanic replacement reaction (GRR) from Ag nanowires (NWs). The catalytic properties of these as-obtained Ag/Au/AgCl hollow heterostructures with different ratios are investigated by reducing 4-nitrophenol (Nip) into 4-aminophenol (Amp) in the presence of NaBH4, and the influence of AgCl semiconductor to the catalytic performances of Ag/Au bimetals is also investigated. These hollow heterostructures show the higher catalytic properties than pure Ag NWs, and the AgCl not only act as supporting materials, but the excess AgCl is also the obstacle for contact of Ag/Au bimetals with reactive species. Moreover, the photocatalytic performances of these hollow heterostructures are carried out by degradation of acid orange 7 (AO7) under UV and visible light. These Ag/Au/AgCl hollow heterostructures present the higher photocatalytic activities than pure Ag NWs and commercial TiO2 (P25), and the Ag/Au bimetals enhance the photocatalytic activity of AgCl semiconductor via the localized surface plasmon resonance (LSPR) and plasmon resonance energy transfer (PRET) mechanisms. The as-synthesized 1D Ag/Au/AgCl hollow heterostructures with multifunction could apply in practical environmental remedy by catalytic manners.

CuO and Ag2O/CuO catalyzed oxidation of aldehydes to the corresponding carboxylic acids by molecular oxygen.

Furfural was oxidized to furoic acid by molecular oxygen under catalysis by 150 nm-sized Ag(2)O/CuO (92%) or simply CuO (86.6%). When 30 nm-size catalyst was used,the main product was a furfural Diels-Alder adduct. Detailed reaction conditions and regeneration of catalysts were investigated. Under optimal conditions, a series of aromatic and aliphatic aldehydes were oxidized to the corresponding acids in good yields.

Tunable and ultra-stable UV light-switchable fluorescent composites for information hiding and storage.

Advanced fluorescent materials have demonstrated great value in the anti-counterfeiting field for information storage and hiding. In this work, a novel strategy for producing UV light-switchable fluorescent patterns to hide and store information is proposed based on carbon dots (CDs) and Y2O3:Eu composites with exceptional optical properties. CDs can present blue emission under both 254 nm and 365 nm UV light excitation, but Y2O3:Eu can only arouse a red color under 254 nm light excitation. Under conventional 365 nm excitation, a single blue color and partial information are shown, however, the whole information in patterns can be displayed under specific 254 nm excitation. The functional anti-counterfeiting patterns are made by screen printing using as-prepared polyvinyl alcohol (PVA)-medium fluorescent inks. Moreover, the hidden information retained its integrity after printed patterns were exposed to an ambient environment for 90 days. Such invisible, tunable and ultra-stable fluorescent patterns utilizing 254 nm UV light well achieve information hiding and storage and increase information security for anti-counterfeiting applications.

Facile Synthesis of Silver Nanowires with Different Aspect Ratios and Used as High-Performance Flexible Transparent Electrodes.

Silver nanowires (Ag NWs) are the promising materials to fabricate flexible transparent electrodes, aiming to replace indium tin oxide (ITO) in the next generation of flexible electronics. Herein, a feasible polyvinylpyrrolidone (PVP)-mediated polyol synthesis of Ag NWs with different aspect ratios is demonstrated and high-quality Ag NWs transparent electrodes (NTEs) are fabricated without high-temperature thermal sintering. When employing the mixture of PVP with different average molecular weight as the capping agent, the diameters of Ag NWs can be tailored and Ag NWs with different aspect ratios varying from ca. 30 to ca. 1000 are obtained. Using these as-synthesized Ag NWs, the uniform Ag NWs films are fabricated by repeated spin coating. When the aspect ratios exceed 500, the optoelectronic performance of Ag NWs films improve remarkably and match up to those of ITO films. Moreover, an optimal Ag NTEs with low sheet resistance of 11.4 Ω/sq and a high parallel transmittance of 91.6% at 550 nm are achieved when the aspect ratios reach almost 1000. In addition, the sheet resistance of Ag NWs films does not show great variation after 400 cycles of bending test, suggesting an excellent flexibility. The proposed approach to fabricate highly flexible and high-performance Ag NTEs would be useful to the development of flexible devices.

Dimensional heterostructures of 1D CdS/2D ZnIn2S4 composited with 2D graphene: designed synthesis and superior photocatalytic performance.

The development of photocatalysts with superior photoactivity and stability for the degradation of organic dyes is very important for environmental remediation. In this study, we have presented a multidimensional (1D and 2D) structured CdS/ZnIn2S4/RGO photocatalyst with superior photocatalytic performance. The CdS/ZnIn2S4 helical dimensional heterostructures (DHS) were prepared via a facile solvothermal synthesis method to facilitate the epitaxial growth of 2D ZnIn2S4 nanosheets on 1D CdS nanowires. Ultrathin 2D ZnIn2S4 nanosheets have grown uniformly and perpendicular to the surface of 1D CdS nanowires. The as-obtained 1D/2D CdS/ZnIn2S4 helical DHS show good photocatalytic properties for malachite green (MG). Subsequently, 2D reduced graphene oxide (RGO) was introduced into the 1D/2D CdS/ZnIn2S4 helical DHS as a co-catalyst. The photoactivity and stability of the CdS/ZnIn2S4/RGO composites are significantly improved after 6 cycles. The enhanced photoactivity can be attributed to the high surface area of RGO, the improved adsorption of organic dyes and the efficient spatial separation of photo-induced charge carriers. The transfer of photo-generated electrons from the interface of CdS and ZnIn2S4 to RGO also restricted the photocorrosion of metal sulfide, suggesting an improved stability of the reused CdS/ZnIn2S4/RGO composited photocatalyst.

Zinc Oxide Coating Effect for the Dye Removal and Photocatalytic Mechanisms of Flower-Like MoS2 Nanoparticles.

Flower-like MoS2 nanoparticles (NPs) consist of ultra-thin MoS2 nanosheets are synthesized via a facile one-pot hydrothermal method. The MoS2/ZnO p-n heterostructure is formed by coating n-type ZnO on the surface of flower-like MoS2 NPs through the seed-mediate route and post-annealing treatment. The effects for the dye removal and photocatalytic performances after ZnO coating are systematically investigated. The results demonstrated that the coating of ZnO nanoparticles has a positive promotion to the photodegrading properties while negative effect on the adsorption capacity of the MoS2/ZnO heterostructures. The related mechanisms on the relationship of adsorption capacity and photocatalysis are discussed in detail.

Preparation and RGB upconversion optic properties of transparent anti-counterfeiting films.

Advanced anti-counterfeiting labels have aroused an intensive interest in packaging industry to avoid the serious issue of counterfeit. However, the preparation and cost of the existing labels associated with the drawbacks, including the complex and high-cost equipment, limit the protection of the authenticity of goods. Herein, we developed a series of anti-counterfeiting labels based on multicolor upconversion micro-particles (UCMPs) inks via straightforward and low-cost solutions, including spin-coating, stamping and screen printing. The UCMPs were synthesized through a facile hydrothermal process and displayed tunable red (R), green (G) and blue (B) color by doping different lanthanide ions, which are Er3+/Tm3+, Yb3+/Er3+ and Yb3+/Tm3+ in NaYF4 hosts, respectively. The optimal UCMPs inks were deposited on a flexible polyethylene terephthalate (PET) substrate to obtain transparent anti-counterfeiting labels possessing higher transmittance, stronger upconversion fluorescence intensity and good photostability. Under ambient conditions, the patterns and films were transparent, but could exhibit multicolor light under 980 nm laser excitation. They can be used as anti-counterfeiting labels for die-cutting packages to further elevate the security of goods. The tunable and designable transparent anti-counterfeiting labels based on RGB UCMPs inks exhibit the merits of low-cost, easy-manufacture and versatility, underlying the practical application in the field of anti-counterfeiting.

Benzoyl Peroxide as an Efficient Dopant for Spiro-OMeTAD in Perovskite Solar Cells.

Although organic small molecule spiro-OMeTAD is widely used as a hole-transport material in perovskite solar cells, its limited electric conductivity poses a bottleneck in the efficiency improvement of perovskite solar cells. Here, a low-cost and easy-fabrication technique is developed to enhance the conductivity and hole-extraction ability of spiro-OMeTAD by doping it with commercially available benzoyl peroxide (BPO). The experimental results show that the conductivity increases several orders of magnitude, from 6.2×10-6  S cm-1 for the pristine spiro-OMeTAD to 1.1×10-3  S cm-1 at 5 % BPO doping and to 2.4×10-2  S cm-1 at 15 % BPO doping, which considerably outperform the conductivity of 4.62×10-4  S cm-1 for the currently used oxygen-doped spiro-OMeTAD. The fluorescence spectra suggest that the BPO-doped spiro-OMeTAD-OMeTAD layer is able to efficiently extract holes from CH3 NH3 PbI3 and thus greatly enhances the charge transfer. The BPO-doped spiro-OMeTAD is used in the fabrication of perovskite solar cells, which exhibit enhancement in the power conversion efficiency.

Preparing of Highly Conductive Patterns on Flexible Substrates by Screen Printing of Silver Nanoparticles with Different Size Distribution.

A facile one-step polyol method is employed to synthesize the Ag nanoparticles (NPs) in large scale. The Ag NPs with different average diameter (from 52 to 120 nm) and particle size distribution are prepared by changing the mass ratio of AgNO3 and PVP. Furthermore, the as-obtained Ag NPs are prepared as conductive inks, which could be screen printed on various flexible substrates and formed as conductive patterns after sintering treatment. During the reaction process, PVP is used as the capping reagent for preventing the agglomeration of Ag NPs, and the influence of the mass ratio of AgNO3 and PVP to the size distribution of Ag NPs is investigated. The results of electronic properties reveal that the conductivity of printed patterns is highly dependent on the size distribution of as-obtained Ag NPs. Among all the samples, the optimal conductivity is obtained when the mass ratio of AgNO3 and PVP is 1:0.4. Subsequently, the sintering time and temperature are further investigated for obtaining the best conductivity; the optimal electrical resistivity value of 3.83 µΩ · cm is achieved at 160 °C for 75 min, which is close to the resistivity value of the bulk silver (1.58 µΩ · cm). Significantly, there are many potential advantages in printed electronics applications because of the as-synthesized Ag NPs with a low sintering temperature and low electrical resistivity.

Anchoring of Ag6Si2O7 nanoparticles on α-Fe2O3 short nanotubes as a Z-scheme photocatalyst for improving their photocatalytic performances.

Coupling two different semiconductors to form composite photocatalysts is the most significant method for environmental remediation. In this regard, tube-like α-Fe2O3/Ag6Si2O7 heterostructures are synthesized via anchoring p-type Ag6Si2O7 nanoparticles (NPs) on the surface of n-type α-Fe2O3 short nanotubes (SNTs) by conventional wet-chemical routes. α-Fe2O3 SNTs are firstly fabricated by a hydrothermal method with the assistance of dihydrogen phosphate and sulphate. Then, Ag6Si2O7 NPs are anchored on α-Fe2O3 SNTs by an in situ deposition method, and the α-Fe2O3/Ag6Si2O7 p-n heterostructures are finally obtained. The morphologies, crystal structure, photocatalytic performance and photocurrent properties of as-synthesized α-Fe2O3/Ag6Si2O7 heterostructures are investigated. Six organic dyes are used for determining the high-efficiency Z-scheme photocatalytic activities of the as-obtained photocatalysts under ultraviolet and visible light (mercury lamp, 300 W). Compared with pure α-Fe2O3 SNTs, the photocurrent intensity of the α-Fe2O3/Ag6Si2O7 heterostructures is improved 62 times. The enhanced significant photocatalytic performance of α-Fe2O3/Ag6Si2O7 heterostructures could be attributed to charge transfer between Ag6Si2O7 NPs and the charge separation between Ag6Si2O7 NPs and α-Fe2O3 SNTs. These composite heterostructures are proposed to be an example for the preparation of other composite silicate photocatalysts for practical application in environmental remediation issues.