The Effect of the Alkyl Chains of the Alkylammonium Pesudohalide Additives on the Performance of Dion Jacobson Perovskite Solar Cells.

Dion-Jacobson perovskite (DJP) films suffer from the high structural disorder and non-compact morphology, leading to inefficient and unstable solar cells (SCs). Here, how the alkyl chains of alkylammonium pseudohalide additives including methylammonium thiocyanate (MASCN) and ethylammonium thiocyanate (EASCN), and propylammonium thiocyanate (PASCN), impact the microstructures, optoelectronic properties and the performance of the solar cells is investigated. These additives substantially improve the structural order and the morphology of the DJP films, yielding more efficient and stable solar cells than the control device. They behave quite differently in modifying the morphological features. Particularly, EASCN outstands the additives in terms of the superior morphology, which is compact and uniform and consists of the largest flaky grains. Consequently, the corresponding device delivers a power conversion efficiency (PCE) of 15.27% and maintains ≈86% of the initial PCE after aging in the air for 182 h. Conversely, MASCN as an additive produces uneven DJP film and the device maintains only 46% of the initial PCE. PASCN as an additive produces the finest grains in the DJP film, and the corresponding device yields a PCE of 11.95%. From the economical point of view, it costs 0.0025 yuan per device for the EASCN additive, allowing for cost-effective perovskite solar cells.

The impact of alternate wetting and drying and continuous flooding on antimony speciation and uptake in a soil-rice system.

The accumulation of trace elements in rice, such as antimony (Sb), has drawn special attention owing to the potential increased risk to human health. However, the effects of two common irrigation methods, alternate wetting and drying and continuous flooding, on Sb behaviors and subsequent accumulation in rice is unclear. In this study a pot experiment with various Sb additions (0, 50, 200, 1000 mg Sb kg-1) was carried out with these two irrigation methods in two contrasting paddy soils (an Anthrosol and a Ferralic Cambisol). The dynamics of Sb in soil porewater indicated that continuous flooding generally immobilized more Sb than alternate wetting and drying, concomitant with a pronounced reduction of Sb(V) in porewater. However, a higher phytoavailable fraction of Sb was observed under continuous flooding. The content of Sb in the rice plant decreased in the order of root > shoot > husk > grain, and continuous flooding facilitated Sb accumulation in rice root and shoot as compared with alternate wetting and drying. The differences of Sb content in root, shoot, and husk between the two irrigation methods was smaller in aboveground parts, and almost no difference in Sb was observed in grain between the two methods. The findings of this study facilitates the understanding of Sb speciation and behavior in soils with these common yet different water management regimes.

Speciation and location of arsenic and antimony in rice samples around antimony mining area.

Arsenic (As) and antimony (Sb) are considered as priority environmental pollutants and their accumulation in crop plants particularly in rice has posed a great health risk. This study endeavored to investigate As and Sb contents in paired soil-rice samples obtained from Xikuangshan, the world largest active Sb mining region, situated in China, and to investigate As speciation and location in rice grains. The soil and rice samples were analyzed by coupling the wet chemistry, laser ablation-inductively coupled plasma mass spectrometry (LA-ICP-MS), synchrotron-based micro X-ray fluorescence mapping (µ-XRF) and micro X-ray absorption near-edge structure (µ-XANES) spectroscopy. The results of field survey indicated that the paddy soil in the region was co-polluted by Sb (5.91-322.35 mg kg-1) and As (0.01-57.21 mg kg-1). Despite the higher Sb concentration in the soil, rice accumulated more As than Sb indicating the higher phytoavailability of As. Dimethylarsinic acid (DMA) was the predominant species (>60% on average) in the rice grains while the percentage of inorganic As species was 19%-63%. The µ-XRF mapping of the grain section revealed that the most of As was distributed and concentrated in rice husk, bran and embryo. Sb was distributed similarly to As but was not in the endosperm of rice grain based on LA-ICP-MS. The present results deepened our understanding of the As/Sb co-pollution and their association with the agricultural-product safety in the vicinity of Sb mining area.

Recent Progress in Metal-Organic Frameworks and Their Derived Nanostructures for Energy and Environmental Applications.

Metal-organic frameworks (MOFs), as a very promising category of porous materials, have attracted increasing interest from research communities due to their extremely high surface areas, diverse nanostructures, and unique properties. In recent years, there is a growing body of evidence to indicate that MOFs can function as ideal templates to prepare various nanostructured materials for energy and environmental cleaning applications. Recent progress in the design and synthesis of MOFs and MOF-derived nanomaterials for particular applications in lithium-ion batteries, sodium-ion batteries, supercapacitors, dye-sensitized solar cells, and heavy-metal-ion detection and removal is reviewed herein. In addition, the remaining major challenges in the above fields are discussed and some perspectives for future research efforts in the development of MOFs are also provided.

Effect of dopant concentration on visible light driven photocatalytic activity of Sn1-xAgxS2.

Tin(iv) sulfide (SnS2), as a mid-band-gap semiconductor shows good potential as an excellent photocatalyst due to its low cost, wide light spectrum response and environment-friendly nature. However, to meet the demands of large-scale water treatment, a SnS2 photocatalyst with a red-shifted band gap, increased surface area and accelerated molecule and ion diffusion is required. Doping is a facile method to manipulate the optical and chemical properties of semiconductor materials simultaneously. In this work, SnS2 photocatalysts with varied Ag doping content are synthesized through a facile one-step hydrothermal method. The product is characterized by XRD, SEM, TEM and UV-Vis spectrometry. The photocatalytic activity of the as-prepared Sn1-xAgxS2 is studied by the degradation of methylene blue (MB) dye under solar light irradiation. It is found that increasing the Ag dopant concentration can effectively increase the solar light adsorption efficiency of the photocatalyst and accelerate heterogeneous photocatalysis. The optimal concentration of Ag dopant is found to be 5% with the highest rate constant being 1.8251 hour-1. This study demonstrates that an optimal amount of Ag doping can effectively increase the photocatalytic performance of SnS2 and will promote the commercialization of such photocatalysts in the photocatalytic degradation of organic compounds.

Novel CoS2 embedded carbon nanocages by direct sulfurizing metal-organic frameworks for dye-sensitized solar cells.

Owing to its excellent electrocatalytic properties, cobalt disulfide (CoS2) is regarded as a promising counter electrode (CE) material for dye-sensitized solar cells (DSSCs). However, hindered by its relatively poor electrical conductivity and chemical instability, it remains a challenge to apply it into high-performance DSSCs. In this work, we have developed novel CoS2 embedded carbon nanocages as a CE in DSSCs, using ZIF-67 (zeolitic imidazolate framework 67, Co(mim)2, mim = 2-methylimidolate) as a template. The CoS2 samples sulfurized for different time lengths are prepared through a facile solution process. It is found that the sulfurization time can be optimized to maximize the DSSC efficiency and the DSSC based on the CoS2 embedded carbon nanocages sulfurized for 4 hours exhibits the highest photovoltaic conversion efficiency (PCE) of 8.20%, higher than those of DSSCs consisting of other CoS2 CEs and Pt-based DSSC (7.88%). The significantly improved DSSC PCE is contributed by the synergic effect of inner CoS2 nanoparticles and an amorphous carbon matrix, leading to a CE with high catalytic activity, good electrical conductivity and excellent durability. This study demonstrates that the CE based on inexpensive CoS2 embedded carbon nanocages is a prospective substitute to expensive platinum and provides a new approach for commercializing high-efficiency DSSCs.

Hierarchical Sandwich-Like Structure of Ultrafine N-Rich Porous Carbon Nanospheres Grown on Graphene Sheets as Superior Lithium-Ion Battery Anodes.

A sandwich-like, graphene-based porous nitrogen-doped carbon (PNCs@Gr) has been prepared through facile pyrolysis of zeolitic imidazolate framework nanoparticles in situ grown on graphene oxide (GO) (ZIF-8@GO). Such sandwich-like nanostructure can be used as anode material in lithium ion batteries, exhibiting remarkable capacities, outstanding rate capability, and cycling performances that are some of the best results among carbonaceous electrode materials and exceed most metal oxide-based anode materials derived from metal orgainc frameworks (MOFs). Apart from a high initial capacity of 1378 mAh g(-1) at 100 mA g(-1), this PNCs@Gr electrode can be cycled at high specific currents of 500 and 1000 mA g(-1) with very stable reversible capacities of 1070 and 948 mAh g(-1) to 100 and 200 cycles, respectively. At a higher specific current of 5000 mA g(-1), the electrode still delivers a reversible capacity of over 530 mAh g(-1) after 400 cycles, showing a capacity retention of as high as 84.4%. Such an impressive electrochemical performance is ascribed to the ideal combination of hierarchically porous structure, a highly conductive graphene platform, and high-level nitrogen doping in the sandwich-like PNCs@Gr electrode obtained via in situ synthesis.

Hierarchical Graphene-Encapsulated Hollow SnO2@SnS2 Nanostructures with Enhanced Lithium Storage Capability.

Complex hierarchical structures have received tremendous attention due to their superior properties over their constitute components. In this study, hierarchical graphene-encapsulated hollow SnO2@SnS2 nanostructures are successfully prepared by in situ sulfuration on the backbones of hollow SnO2 spheres via a simple hydrothermal method followed by a solvothermal surface modification. The as-prepared hierarchical SnO2@SnS2@rGO nanocomposite can be used as anode material in lithium ion batteries, exhibiting excellent cyclability with a capacity of 583 mAh/g after 100 electrochemical cycles at a specific current of 200 mA/g. This material shows a very low capacity fading of only 0.273% per cycle from the second to the 100th cycle, lower than the capacity degradation of bare SnO2 hollow spheres (0.830%) and single SnS2 nanosheets (0.393%). Even after being cycled at a range of specific currents varied from 100 mA/g to 2000 mA/g, hierarchical SnO2@SnS2@rGO nanocomposites maintain a reversible capacity of 664 mAh/g, which is much higher than single SnS2 nanosheets (374 mAh/g) and bare SnO2 hollow spheres (177 mAh/g). Such significantly improved electrochemical performance can be attributed to the unique hierarchical hollow structure, which not only effectively alleviates the stress resulting from the lithiation/delithiation process and maintaining structural stability during cycling but also reduces aggregation and facilitates ion transport. This work thus demonstrates the great potential of hierarchical SnO2@SnS2@rGO nanocomposites for applications as a high-performance anode material in next-generation lithium ion battery technology.

Effect of iron plaque on antimony uptake by rice (Oryza sativa L.).

Although iron (Fe) plaque has been shown to significantly affect the uptake of toxic antimony (Sb) by rice, knowledge about the influence of iron plaque on antimony (Sb) (amount, mechanisms, etc) is, however, limited. Here, the effect of Fe plaque on Sb(III) and Sb(V) (nominal oxidation states) uptake by rice (Oryza sativa L.) was investigated using hydroponic experiments and synchrotron-based techniques. The results showed that iron plaque immobilized Sb on the surface of rice roots. Although the binding capacity of iron plaque for Sb(III) was markedly greater than that for Sb(V), significantly more Sb(III) was taken up by roots and transported to shoots. In the presence of Fe plaque, Sb uptake into rice roots was significantly reduced, especially for Sb(III). However, this did not translate into decreasing Sb concentrations in rice shoots and even increased shoot Sb concentrations during high Fe-Sb(III) treatment.

Photo-induced oxidation of Sb(III) on goethite.

Goethite widely exists in soils and sediments, and plays a very important role in the environmental fate of toxic metal(loid)s. In the present study, photo-induced oxidation of antimonite [Sb(III)] on goethite was investigated with kinetic measurements and X-ray photoelectron spectroscopy (XPS) techniques. Effects of environmental factors including solution pH, the content of goethite as well as humic acid on the photo-induced oxidation of antimonite were tested. The results indicated that no oxidation of antimonite occurred in goethite suspension in the dark, but significant amounts of antimonite were transformed to antimonate when the suspension was exposed to light. Ferrous ions were found in the solution during the antimonite oxidation process, and its concentration decreased with increasing solution pH, which strongly affected the oxidation rate of antimonite. The initial solution pH has great impact on Sb oxidation. After 2h illumination, the highest oxidation rate was found at pH 3, while the initial oxidation rate was even higher at pH 9. In conclusion, the antimonite can be adsorbed and oxidized on goethite irradiated with light, which will greatly reduce its environmental risk.

Improving carbene-copper-catalyzed asymmetric synthesis of α-aminoboronic esters using benzimidazole-based precursors.

By using a benzimidazole core and N-substitutions to tune the electronic properties of the corresponding N-heterocyclic carbenes, a one-pot protocol for efficient synthesis of α-aminoboronic esters without the need of a glovebox was developed in this work. The starting materials for the transformation can also be extended from aldehydes to ketones. An alternative protocol with short reaction time using preformed carbene-copper chloride is also described.