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Recently, the lead-free double perovskite Cs2AgBiBr6has been considered as a promising candidate for next-generation nonvolatile memory and artificial synapse devices due to its high stability and low toxicity compared to its lead-based counterparts. In this work, we developed a simple and effective method to produce high-quality lead-free double perovskite Cs2AgBiBr6thin films without pinholes and particles by applying a low-pressure assisted method under ambient condition with a relative humidity (RH) of about 45%. The formation of pinholes and Ag precipitation in the perovskite Cs2AgBiBr6 films is effectively suppressed by the proper ratio of N,N-dimenthylformamide (DMF) mixed in dimethyl sulfoxide (DMSO) solvents. Furthermore, the grain size of the Cs2AgBiBr6films can be significantly increased by increasing the post-annealing temperature. Finally, a sandwiched structure memristor with an ITO/Cs2AgBiBr6/Ta configuration was successfully demonstrated, featuring ultralow operation voltage (VSetâ¼ 57 ± 23 mV,VResetâ¼ -692 ± 68 mV) and satisfactory memory window (the ratio ofRHRS/RLRSâ¼ 10 times), which makes it suitable for low-power consumption information storage devices.
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The elimination of uranium from radioactive wastewater is crucial for the safe management and operation of environmental remediation. Here, we present a layered vanadate with high acid/base stability, [Me2NH2]V3O7, as an excellent ion exchanger capturing uranyl from highly complex aqueous solutions. The material possesses an indirect band gap, ferromagnetic characteristic and a flower-like morphology comprising parallel nanosheets. The layered structure of [Me2NH2]V3O7 is predominantly upheld by the H-bond interaction between anionic framework [V3O7]nn- and intercalated [Me2NH2]+. The [Me2NH2]+ within [Me2NH2]V3O7 can be readily exchanged with UO22+. [Me2NH2]V3O7 exhibits high exchange capacity (qm = 176.19 mg/g), fast kinetics (within 15 min), high removal efficiencies (>99%), and good selectivity against an excess of interfering ions. It also displays activity for UO22+ ion exchange over a wide pH range (2.00-7.12). More importantly, [Me2NH2]V3O7 has the capability to effectively remove low-concentration uranium, yielding a residual U concentration of 13 ppb, which falls below the EPA-defined acceptable limit of 30 ppb in typical drinking water. [Me2NH2]V3O7 can also efficiently separate UO22+ from Cs+ or Sr2+ achieving the highest separation factors (SFU/Cs of 589 and SFU/Sr of 227) to date. The BOMD and DFT calculations reveal that the driving force of ion exchange is dominated by the interaction between UO22+ and [V3O7]nn-, whereas the ion exchange rate is influenced by the mobility of UO22+ and [Me2NH2]+. Our experimental findings indicate that [Me2NH2]V3O7 can be considered as a promising uranium scavenger for environmental remediation. Additionally, the simulation results provide valuable mechanistic interpretations for ion exchange and serve as a reference for designing novel ion exchangers.
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Urânio , Vanadatos , Urânio/química , Vanadatos/química , Troca Iônica , Poluentes Radioativos da Água/química , CinéticaRESUMO
New insights are proposed into enhancing detection of uranyl ions (UO22+) by electropolymerization brilliant cresyl blue-modified glassy carbon electrode (PBCB/GCE). The mercury-free PBCB/GCE sensor was applied to determine UO22+ in water samples by differential pulse adsorptive stripping voltammetry (DPAdSV). The unique combination of the PBCB/GCE and DPAdSV significantly improves sensitivity due to the polymer of high electroactive area and fast electron transfer rate. The DPAdSV current using a 3 mm diameter PBCB/GCE was proportional to the UO22+ concentration in the range 2.0-90.0 µg·L-1 (- 0.113 V vs. SCE) with a detection limit of 0.650 µg·L-1, RSD = 3.1% (n = 10), and 4.5% reproducibility. In addition, the sensitivity for UO22+ determination was further improved at using an 1 mm diameter PBCB/GCE, which enhances the efficiency of UO22+ deposition due to its higher current density. The 1 mm diameter PBCB/GCE based on DPAdSV technique could be used to determine uranyl ions in the concentration range 0.20-2.0 µg·L-1 (- 0.113 V vs. SCE) with a detection limit of 0.067 µg·L-1, RSD = 5.7 % (n = 10) and 5.4% reproducibility. Hence, the PBCB/GCE is a suitable candidate to substitute the mercury electrode. Graphical abstract.
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Carbono , Mercúrio , Íons , Oxazinas , Polímeros , Reprodutibilidade dos Testes , ÁguaRESUMO
Achieving high photocatalytic activity of titania-graphene composites calls for well-controlled titania size and efficient charge transfer interfaces. However, it is rather difficult because of easy restacking of graphene sheets and random nucleation and growth of titania nanoparticles in solution. Here, we reported a facile way to control the TiO2 sizes and interfaces by localizing the nucleation and growth of titania on graphene sheets, which prohibits both restacking of graphene and random growth of TiO2. As a result, a composite with controllably less than 10-nm-sized TiO2 nanoparticles evenly distributed on thin graphene sheets was achieved. Thanks to the small size of titania and efficient charge transfer interfaces, the TiO2/graphene composite exhibits a significant enhancement of photocatalytic H2 evolution activity, reaching 1.35 mmol g-1 h-1. Furthermore, the composite also shows high photocatalytic activity on dye degradation under visible light illumination.
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Due to the limited electronic conductivity, the application of many metal oxides that may have attractive (photo)-electrochemical properties has been limited. Regarding these issues, incorporating low-dimensional conducting scaffolds into the electrodes or supporting the metal oxides onto the conducting networks are common approaches. However, some key electronic processes like interfacial charge transfer are far from being consciously concerned. Here we use a carbon-TiO2 contact as a model system to demonstrate the electronic processes occurring at the metal-semiconductor interface. To minimize the energy dissipation for fast transfer of electrons from semiconductor to carbon scaffolds, facilitating electron tunneling while avoiding high energy-consuming thermionic emission is desired, according to our theoretical simulation of the voltammetric behaviors. To validate this, we manage to sandwich ultrathin TiO2 interlayers with heavy electronic doping between the carbon conductors and dopant-free TiO2. The radially graded distribution of the electronic doping along the cross-sectional direction of carbon conductor realized by immobilizing the dopant species on the carbon surface can minimize the energy consumption for contacts to both the carbon and the dopant-free TiO2. Our strategy provides an important requirement for metal oxide electrode design.
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The development of effective, economical, and sustainable seawater extraction strontium techniques is of great significance to the environment and industrial needs. In this paper, an asymmetric pulsed current-assisted electrochemical (AP-CE) method was used to extract Sr(â ¡) from seawater using a carbon electrode modified by dibenzo-18-crown-6-ether and cellulose acetate. An asymmetric pulsed current was used to prevent unwanted cations from blocking adsorption sites to prevent water splitting. It also prevented the cellulose acetate membrane from sealing the crown ether. Compared with traditional physicochemical adsorption of Sr(â ¡), the AP-CE method achieved a higher removal efficiency and adsorption capacity. When the concentrations of Sr(â ¡) were 10, 20, 50, and 100 mg L-1, the removal efficiencies of Sr(â ¡) were 99.3%, 97.6%, 97.3%, and 96.1%, and the adsorption capacities of Sr(â ¡) were 14.9, 29.3, 73.0, and 144.2 mg g-1, respectively. This method exhibited excellent selectivity for Sr(â ¡) adsorption from simulated seawater, suggesting that the asymmetric pulse electrochemical method is promising for extracting strontium ions from seawater.
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Estrôncio , Poluentes Químicos da Água , Adsorção , Água do Mar , Água , Poluentes Químicos da Água/análiseRESUMO
Industrial robots are a strategic future technology and an important part of the development of artificial intelligence, and they are a necessary means for the intelligent transformation of manufacturing industry. Based on global industrial robot trade data from 1998 to 2017, this paper applies the dynamic complex network analysis method to reveal the spatial and temporal variation characteristics and trade status evolution of the global industrial robot trade network. The results show that the global industrial robot network density has steadily increased, and the industrial robot trade has been characterized by 'diversification'. The number of major industrial robot exporters in the world is increasing, and the import market is increasingly diversified. The export market structure is relatively tight, the centrality of the global industrial robot trade network shows a downward trend, and the dissimilarity of the 'core-edge' clusters decreases year by year. The trade status of 'catch-up' countries represented by China has rapidly increased. However, Japan, Germany, and Italy are still in the central position of the industrial robot trade. Moreover, trade of the 'catch-up' countries' is dominated by imports, and exports of industrial robot products are insufficient. Finally, policy suggestions are provided according to the results.
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Comércio/tendências , Robótica/tendências , Análise Espaço-Temporal , Inteligência Artificial , China , Comércio/estatística & dados numéricos , Alemanha , Itália , Japão , Robótica/estatística & dados numéricosRESUMO
A novel hierarchical nanostructure with graphite-like carbon and small Si nanocrystals, respectively, encapsulated in the mesopores and embedded in the silica framework of mesoporous silica nanoparticles has been facilely constructed and used as an anode for Li-ion batteries, which exhibits high specific storage capacity and extraordinarily high cycling stability.
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We demonstrate here the synthesis of a hierarchical TiO(2) architecture without any surfactants or templates. Two kinds of structure existed simultaneously, the ordered nanoarrays at bottom provided direct conduction pathway for photo generated electrons, while the upper micro-flowers consisted of nanobelt as building units increased the light harvesting ability as the scattering part. The formation mechanism of the hierarchical architecture has been proposed by studying the morphology evolution processes upon reaction time. The performance of dye-sensitized solar cells based on the obtained hierarchical anatase TiO(2) has been also studied, giving a J(SC) = 12.44 mA cm(-2), V(OC) = 0.64 V, FF = 69.05%, and η = 5.53%, which is superior than commercial TiO(2) (P25). The UV-vis results prove that the obtained morphology is beneficial to light-scattering and thus increases the light harvesting ability. This hierarchical TiO(2) structure offers great potential for the development of high-efficiency DSSCs.
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OBJECTIVE: To investigate the indication and effect of the application of Ligasure vessel sealing instrument in laparoscopic hepatectomy for liver cancer. METHODS: Eleven patients with liver cancer undergoing laparoscopic hepatectomy were analyzed for the tumor size and location, operation time, volume of intraoperative bleeding, postoperative hospital stay and short-term clinical outcomes. RESULTS: All the operations were performed successfully in the 11 cases. All the tumors were less than 7 cm in diameter, locating at the segments II, III, V, VI and VII. The mean operation time was 91 min (80-126 min), and the intraoperative blood loss averaged 82 ml (20-200 ml). The average postoperative hospital stay of the patients was 8 days (7-9 days). No complications were observed in these cases. CONCLUSION: Ligasure vessel sealing instrument in laparoscopic hepatectomy is applicable in cases of perimeter liver cancer. This instrument can decrease the operation time, reduce the intraoperative blood loss and postoperative hospital stay with good safety and minimal invasiveness.