Sustainable Recycling of Selenium-Based Optoelectronic Devices.

Selenium (Se), the world's oldest optoelectronic material, has been widely applied in various optoelectronic devices such as commercial X-ray flat-panel detectors and photovoltaics. However, despite the rare and widely-dispersed nature of Se element, a sustainable recycling of Se and other valuable materials from spent Se-based devices has not been developed so far. Here a sustainable strategy is reported that makes use of the significantly higher vapor pressure of volatile Se compared to other functional layers to recycle all of them from end-of-life Se-based devices through a closed-space evaporation process, utilizing Se photovoltaic devices as a case study. This strategy results in high recycling yields of ≈ 98% for Se and 100% for other functional materials including valuable gold electrodes and glass/FTO/TiO2 substrates. The refabricated photovoltaic devices based on these recycled materials achieve an efficiency of 12.33% under 1000-lux indoor illumination, comparable to devices fabricated using commercially sourced materials and surpassing the current indoor photovoltaic industry standard of amorphous silicon cells.

Static magnetic field increases aerobic nitrogen removal from hypersaline wastewater in activated sludge with coexistence of fungi and bacteria.

Fungi have been found to exist in activated sludge treating saline wastewater, but their role in removing pollution has been neglected. This study explored the aerobic removal of total inorganic nitrogen (TIN) from saline wastewater under static magnetic fields (SMFs) with several strengths. Compared to the control, the aerobic removal of TIN was significantly increased by 1.47 times in 50 mT SMF, due to the increased dissimilation nitrogen removal by fungi and bacteria. Under SMF, fungal nitrogen dissimilation removal was significantly increased by 3.65 times. The fungal population size decreased, and its community composition changed significantly under SMF. In contrast, bacterial community composition and population remained relatively stable. Under SMFs, heterotrophic nitrification - aerobic denitrification bacteria Paracoccus and the fungi denitrifying Candida formed a synergistic interaction. This study elucidates the fungal role in aerobic TIN removal and provides an efficient solution to improve TIN removal from saline wastewater by SMF.

Mitigating Electron Leakage of Solid Electrolyte Interface for Stable Sodium-Ion Batteries.

The interfacial stability is highly responsible for the longevity and safety of sodium ion batteries (SIBs). However, the continuous solid-electrolyte interphase(SEI) growth would deteriorate its stability. Essentially, the SEI growth is associated with the electron leakage behavior, yet few efforts have tried to suppress the SEI growth, from the perspective of mitigating electron leakage. Herein, we built two kinds of SEI layers with distinct growth behaviors, via the additive strategy. The SEI physicochemical features (morphology and componential information) and SEI electronic properties (LUMO level, band gap, electron work function) were investigated elaborately. Experimental and calculational analyses showed that, the SEI layer with suppressed growth delivers both the low electron driving force and the high electron insulation ability. Thus, the electron leakage is mitigated, which restrains the continuous SEI growth, and favors the interface stability with enhanced electrochemical performance.

Indoor photovoltaics awaken the world's first solar cells.

Selenium (Se) solar cells were the world's first solid-state photovoltaics reported in 1883, opening the modern photovoltaics. However, its wide bandgap (~1.9 eV) limits sunlight harvesting. Here, we revisit the world's oldest but long-ignored photovoltaic material with the emergence of indoor photovoltaics (IPVs); the absorption spectrum of Se perfectly matches the emission spectra of commonly used indoor light sources in the 400 to 700 nm range. We find that the widely used Te adhesion layer also passivates defects at the nonbonded Se/TiO2 interface. By optimizing the Te coverage from 6.9 to 70.4%, the resulting Se cells exhibit an efficiency of 15.1% under 1000 lux indoor illumination and show no efficiency loss after 1000 hours of continuous indoor illumination without encapsulation, outperforming the present IPV industry standard of amorphous silicon cells in both efficiency and stability. We further fabricate Se modules (6.75 cm2) that produce 232.6 µW output power under indoor illumination, powering a radio-frequency identification-based localization tag.

[Research progress of Angelicae Sinensis Radix and predictive analysis on its quality markers].

Angelicae Sinensis Radix, as a medicinal and edible Chinese medicinal herb, is widely used in clinical practice. It is mainly cultivated in Minxian, Tanchang, Zhangxian and Weiyuan counties of Gansu province. In recent years, with the comprehensive and in-depth study of Angelicae Sinensis Radix in China and abroad, its chemical composition, pharmacological effects and application and development have attracted much attention. In this study, the chemical composition, traditional efficacy, and modern pharmacological effects of Angelicae Sinensis Radix were summarized. On this basis, combined with the core concept of quality markers(Q-markers), the Q-markers of Angelicae Sinensis Radix were discussed from the aspects of mass transfer and traceability and chemical composition specificity, availability, and measurability, which provided scientific basis for the quality evaluation of Angelicae Sinensis Radix.

Promoting enrichment of sulfur-oxidizing autotrophic denitrifiers via static magnetic fields: Performance and mechanism of magnetic biological effects.

Sulfur-driven autotrophic denitrification (SADN) is a promising technology for nitrogen removal from wastewater. In this study, different-strength SMFs (0, 5, 20, 50, 70 mT) were evaluated to investigate the potential of external static magnetic field (SMF) for enriching sulfur-oxidizing autotrophic denitrifiers (SOAD). 50-mT and 70-mT SMFs were most suitable to accelerate the growth of SOAD and the elimination of non-SOAD. The relative abundance of Thiobacillus significantly increased (p < 0.01) from 6.26% in control reactor to 36.15% under 50 mT and 52.51% under 70 mT. Under 50 mT, Thiobacillus denitrificans accumulated most rapidly, with the largest population. Furthermore, functional gene forecast by high-throughput and metagenomic sequencing indicated that SMF changed the two-component system, the adenosine 5'-monophosphate-activated protein kinase (AMPK) signaling system, the phosphotransferase system (PTS), as well as N/S-related enzymes to regulate stress-response and promote the growth of SOAD. The findings indicated that SMF accelerated the start-up of SADN.

Surface-Defect States in Photovoltaic Absorber GeSe.

GeSe is an emerging promising light-harvesting material for photovoltaics due to its excellent optoelectronic properties, nontoxic and earth-abundant constituents, and high stability. In particular, perovskite-like antibonding states at the valence band maximum arising from Ge-4s and Se-4p coupling enable the bulk-defect-tolerant properties in GeSe. However, a fundamental understanding of surface-defect states in GeSe, another important factor for high-performance photovoltaics, is still lacking. Here, we investigate the surface-defect properties of GeSe through first-principle calculations. We find that different from common semiconductors possessing numerous surface dangling bonds, some GeSe surfaces are prone to reconstruction, thus eliminating the dangling bonds. The rearranged armchair edges exhibit unexpected benign defect properties, similar to those of bulk GeSe, arising from the formation of bulk-like [GeSe3] tetrahedrons. We further show that the stable exposed (111) surfaces are hard to reconstruct due to the stiff structure but are effectively passivated by the addition of H.

[Net ecosystem carbon exchange and its affecting factors in a deciduous broad-leaved forest in Songshan, Beijing, China]. / åŒ—äº¬æ¾å±±å¤©ç„¶è½å¶é˜”å¶æž—ç”Ÿæ€ç³»ç»Ÿå‡€ç¢³äº¤æ¢ç‰¹å¾åŠå ¶å½±å“å› å­.

Forests play an important role in terrestrial carbon cycles. The mechanism underlying carbon balance in temperate deciduous broad-leaved forests is not clear. In this study, net ecosystem exchange (NEE) and environmental factors, including air temperature (Ta), soil temperature (Ts), photosynthetically active radiation (PAR), vapor pressure deficit (VPD), soil water content (SWC) and precipitation (P) were continually measured using eddy covariance techniques in 2019 in a deciduous broad-leaved forest in Songshan, Beijing. We analyzed the characteristics of NEE and its response to environmental factors. The results showed that, at diurnal scale, the monthly averaged NEE exhibited a "U" shape curve (i.e., being a carbon sink over daytime while being a carbon source during nighttime) over the growing season. During the non-growing season, NEE was positive (i.e., carbon source) at diurnal scale. At the seasonal scale, NEE exhibited a unimodal curve. The annual cumulative NEE was -111 g C·m-2·a-1. Annual ecosystem respiration was 555 g C·m-2·a-1, while gross ecosystem productivity was 666 g C·m-2·a-1. Carbon sequestration peaked in June, while emission peaked in November. PAR was the dominant factor affecting daytime NEE (NEEd). VPD was the main factor that indirectly affected daytime NEEd, with an optimal VPD value that maximizes daytime NEE around 1-1.5 kPa. Soil temperature was the main factor affecting nighttime NEE (NEEn). SWC was a limiting factor for NEEn. Too high or too low SWC would inhibit NEEn, with an optimal SWC value of 0.28 m3·m-3.

In†Situ Scanning Tunneling Microscopy of Cobalt-Phthalocyanine-Catalyzed CO2 Reduction Reaction.

We report a molecular investigation of a cobalt phthalocyanine (CoPc)-catalyzed CO2 reduction reaction by electrochemical scanning tunneling microscopy (ECSTM). An ordered adlayer of CoPc was prepared on Au(111). Approximately 14 % of the adsorbed species appeared with high contrast in a CO2 -purged electrolyte environment. The ECSTM experiments indicate the proportion of high-contrast species correlated with the reduction of CoII Pc (-0.2 V vs. saturated calomel electrode (SCE)). The high-contrast species is ascribed to the CoPc-CO2 complex, which is further confirmed by theoretical simulation. The sharp contrast change from CoPc-CO2 to CoPc is revealed by in situ ECSTM characterization of the reaction. Potential step experiments provide dynamic information for the initial stage of the reaction, which include the reduction of CoPc and the binding of CO2 , and the latter is the rate-limiting step. The rate constant of the formation and dissociation of CoPc-CO2 is estimated on the basis of the in situ ECSTM experiment.

Microscopic investigations on the surface-state dependent moisture stability of a hybrid perovskite.

Hybrid organic-inorganic perovskite (HOIP) materials have caught significant attention in photovoltaics and photoelectronics for their outstanding photovoltaic properties. However, their instability to various environment, such as illumination, temperature, moisture and oxygen, hinders their way to commercialization. To figure out the interaction mechanism between H2O and CH3NH3PbI3 (MAPbI3), extensive theoretical studies have been carried out; however, the experimental results are insufficient and inconsistent. Here, we systematically investigate and compare the influence of H2O on MAPbI3 perovskite films with or without DMF) post-annealing in dark or light condition. The interaction between H2O and the surface of pristine MAPbI3 leads to the fusion of grain boundaries thus grain growth into micron level in short-time moisture exposure. While the penetration of H2O into MAPbI3 results in swelled crystalline whisker, cracking into smaller grains in long-time exposure upon the release of H2O. However, no degradation occurs in dark condition. As the DMF post-annealing treatment changes the surface states of MAPbI3, the interactions between the external H2O and internal MAPbI3 significantly varies from the pristine MAPbI3. Three different surface states with different topographies have influence on the interaction process and mechanism with H2O, leading to different decomposition rates, the striped surface that is the most rough among the three and experiencing the minimum change in surface potential with exposure to 80% humidity decomposes into PbI2 fastest. However, the addition of light will once again affect the aforementioned process. It is found that even ambient light could severely speed up the moisture-induced decomposition of MAPbI3, while the N,N-dimethylformamide (DMF) post-annealing treatment significantly improves the stability of MAPbI3 films upon exposure to humidity and illumination, benefiting from the MAI-deficient thus H2O resistant surface.

Ultra-thin solid electrolyte interphase evolution and wrinkling processes in molybdenum disulfide-based lithium-ion batteries.

Molybdenum disulfide is considered one of the most promising anodes for lithium-ion batteries due to its high specific capacity; however, it suffers from an unstable solid electrolyte interphase. Understanding its structural evolution and reaction mechanism upon charging/discharging is crucial for further improvements in battery performance. Herein, the interfacial processes of solid electrolyte interphase film formation and lithiation/delithiation on ultra-flat monolayer molybdenum disulfide are monitored by in situ atomic force microscopy. The live formation of ultra-thin and dense films can be induced by the use of fluoroethylene carbonate as an additive to effectively protect the anode electrodes. The evolution of the fluoroethylene carbonate-derived solid electrolyte interphase film upon cycling is quantitatively analysed. Furthermore, the formation of wrinkle-structure networks upon lithiation process is distinguished in detailed steps, and accordingly, structure-reactivity correlations are proposed. These quantitative results provide an in-depth understanding of the interfacial mechanism in molybdenum disulfide-based lithium-ion batteries.

Temperature-Dependent Local Electrical Properties of Organic-Inorganic Halide Perovskites: In Situ KPFM and c-AFM Investigation.

Organic-inorganic halide perovskite materials are emerging as a new class of photoelectric materials for its low cost, easy preparation, and, especially, outstanding optoelectronic properties. Although tremendous efforts have been made on the regulation and optimization of perovskite materials and their microscopic electrical properties for high-efficiency solar cells, few reports focus on the evolution of electrical properties with temperature changes, especially at the microscopic scale, which will directly affect the device performances at varying temperatures. Here, we map the contact potential difference and photocurrent distribution of MAPbI3 at different temperatures in situ by Kelvin probe force microscopy and conductive atomic force microscopy, emphasizing the different influences of variable temperature and phase transition on the photoelectric properties of grains and grain boundaries (GBs). It is discovered that both the Fermi level and photocurrent decrease as the sample is heated from 30 to 80 °C gradually because of the variation of effective carrier concentration and the degradation of carrier mobility implicated by lattice vibration scattering. The difference between the Fermi level at GBs and that on the grains ascends first and then descends, peaking at 50 °C, near which MAPbI3 transforms from a tetragonal phase to a cubic phase. This peak is speculated as a comprehensive consequence of the increasing difference of the Fermi level of semiconductors with different doping concentrations and the converging properties of grains and GBs with the temperature rising because the lower ion activation energy of the cubic phase at higher temperatures facilitates greatly the ions' movement between grains and GB. The variation trend of the difference of the photocurrent is the same. These findings advance the knowledge on the temperature-induced variations of microscopic photoelectrical properties of organic-inorganic hybrid perovskite materials, which may guide the development of strategies for improving their thermal stability.

Rational design of two-dimensional covalent tilings using a C6-symmetric building block via on-surface Schiff base reaction.

Three types of well-ordered covalent two-dimensional tilings including triangular, rhombille and semi-regular Archimedean tilings were successfully constructed via on-surface Schiff base reaction. Among them, the covalent organic framework (COF) constructed from a C6 symmetry monomer and C3 symmetry monomer is the first reported COF with kgd (rhombille tiling) topology.

The sequence and de novo assembly of hog deer genome.

Hog deer (Axis porcinus) is a small deer species in family Cervidae and has been undergoing a serious and global decline during the past decades. Chengdu Zoo currently holds a captive population of hog deer with sufficient genetic diversity in China. We sequenced and de novo assembled its genome sequence in the present study. A total of six different insert-size libraries were sequenced and generated 395 Gb of clean data in total. With aid of the linked reads of 10X Genomics, genome sequence was assembled to 2.72 Gb in length (contig N50, 66.04 Kb; scaffold N50, 20.55 Mb), in which 94.5% of expected genes were detected. We comprehensively annotated 22,473 protein-coding genes, 37,019 tRNAs, and 1,058 Mb repeated sequences. The newly generated reference genome is expected to significantly contribute to comparative analysis of genome biology and evolution within family Cervidae.

Formation of multicomponent 2D assemblies of C 2v-symmetric terphenyl tetracarboxylic acid at the solid/liquid interface: recognition, selection, and transformation.

We report on the two-dimensional self-assembly of C 2v-symmetric [1,1':3',1''-terphenyl]-3,3'',5,5''-tetracarboxylic acid (TPTA) at the solid/liquid interface by using scanning tunneling microscopy (STM). Two kinds of different self-assembly structure, i.e. a close-packed and porous rosette structure, are formed by TPTA molecules through intermolecular hydrogen bonds. When adding coronene (COR) as a guest into the TPTA assembly, structural transformation from a densely packed row structure to a rosette network structure is observed. It was found that two kinds of cavities with different sizes in the rosette network structure can be used to realize the selective co-adsorption of guest molecules with appropriate shape and size. Three-component 2D host-guest structures were successfully constructed by using 1,2,3,4,5,6-hexakis(4-bromophenyl)benzene (HBPBE) and copper phthalocyanine (CuPc) as guest molecules.

Highly Selective Production of Compound K from Ginsenoside Rd by Hydrolyzing Glucose at C-3 Glycoside Using ß-Glucosidase of Bifidobacterium breve ATCC 15700.

To investigate a novel ß-glucosidase from Bifidobacterium breve ATCC 15700 (BbBgl) to produce compound K (CK) via ginsenoside F2 by highly selective and efficient hydrolysis of the C-3 glycoside from ginsenoside Rd, the BbBgl gene was cloned and expressed in E. coli BL21. The recombinant BbBgl was purified by Ni-NTA magnetic beads to obtain an enzyme with specific activity of 37 U/mg protein using pNP-Glc as substrate. The enzyme activity was optimized at pH 5.0, 35°C, 2 or 6 U/ml, and its activity was enhanced by Mn2+ significantly. Under the optimal conditions, the half-life of the BbBgl is 180 h, much longer than the characterized ß-glycosidases, and the Km and Vmax values are 2.7 mM and 39.8 µmol/mg/min for ginsenoside Rd. Moreover, the enzyme exhibits strong tolerance against high substrate concentration (up to 40 g/l ginsenoside Rd) with a molar biotransformation rate of 96% within 12 h. The good enzymatic properties and gram-scale conversion capacity of BbBgl provide an attractive method for large-scale production of rare ginsenoside CK using a single enzyme or a combination of enzymes.

Directed assembly of fullerene on modified Au(111) electrodes.

Here we show a conceptual approach to realize the scanning tunneling microscopy based induced-assembly of fullerene (C60) molecules on top of a buffer organic adlayer at room temperature in a solution environment. The realization of spatially-defined C60 assembly is attributed to the modulation of substrate-molecular interactions with the assistance of a buffer layer.

Potential- and concentration-dependent self-assembly structures at solid/liquid interfaces.

We report the potential and concentration controlled assembly of an alkyl-substituted benzo[1,2-b:4,5-b']dithiophene (DDBDT) on an Au(111) electrode by in situ electrochemical scanning tunneling microscopy (ECSTM). It is found that a lamellar structure is formed at low concentrations, while herringbone-like and rhombus structures are obtained at high concentrations. In situ STM results reveal that herringbone-like and rhombus structures could transform into lamellar structures when the electrode potential is tuned negatively. A phase diagram is obtained to illustrate the relationship and effects of concentration and substrate potential on the interfacial structures of DDBDT. Both the substrate potential and the solute concentration can modulate the self-assembly structure through changing the molecular surface density. The results provide important insights into the understanding and precise control of molecular self-assembly on solid surfaces through a combination of different approaches.

Direct Visualization of Nucleation and Growth Processes of Solid Electrolyte Interphase Film Using in Situ Atomic Force Microscopy.

An understanding of the formation mechanism of solid electrolyte interphase (SEI) film at the nanoscale is paramount because it is one of the key issues at interfaces in lithium-ion batteries (LIBs). Herein, we explored the nucleation, growth, and formation of SEI film on highly oriented pyrolytic graphite (HOPG) substrate in ionic liquid-based electrolytes 1-butyl-1-methyl-pyrrolidinium bis(fluorosulfonyl)imide ([BMP]+[FSI]-) and 1-butyl-1-methylpyrrolidinium bis(trifluoromethanesulfonyl)imide ([BMP]+[TFSI]-) by in situ atomic force microscopy (AFM) and found that the types of anions have significant influence on the structure of the formed SEI. In [BMP]+[FSI]- containing LiFSI, a compact and thin SEI film prefers to grow in the plane of HOPG substrate, while a rough and loose film tends to form in [BMP]+[TFSI]- containing LiTFSI. On the basis of in situ AFM observations, the relationship between the SEI structure and the electrochemical performance was clarified.

General Space-Confined On-Substrate Fabrication of Thickness-Adjustable Hybrid Perovskite Single-Crystalline Thin Films.

Organic-inorganic hybrid perovskite single-crystalline thin films (SCTFs) are promising for enhancing photoelectric device performance due to high carrier mobility, long diffusion length, and carrier lifetime. However, bulk perovskite single crystals available today are not suitable for practical device application due to the unfavorable thickness. Herein, we report a facile space-confined solution-processed strategy to on-substrate grow various hybrid perovskite SCTFs in a size of submillimeter with adjustable thicknesses from nano- to micrometers. These SCTFs exhibit photoelectric properties comparable to bulk single crystals with low defect density and good air stability. The clear thickness-dependent colors allow fast visual selection of SCTFs with a suitable thickness for specific device application. The present substrate-independent growth of perovskite SCTFs opens up opportunities for on-chip fabrication of diverse high-performance devices.