Synthesis and Photocatalytic Application of Stable Lead-Free Cs2 AgBiBr6 Perovskite Nanocrystals.

Lead halide perovskite nanocrystals (NCs) have demonstrated great potential as appealing candidates for advanced optoelectronic applications. However, the toxicity of lead and the intrinsic instability toward moisture hinder their mass production and commercialization. Herein, to solve such thorny problems, novel lead-free Cs2 AgBiBr6 double perovskite NCs fabricated via a simple hot-injection method are reported, which exhibit impressive stability in moisture, light, and temperature. Such materials are then applied into photocatalytic CO2 reduction, achieving a total electron consumption of 105 µmol g-1 under AM 1.5G illumination for 6 h. This study offers a reliable avenue for Cs2 AgBiBr6 perovskite nanocrystals preparation, which holds a great potential in the further photochemical applications.

A CsPbBr3 Perovskite Quantum Dot/Graphene Oxide Composite for Photocatalytic CO2 Reduction.

Halide perovskite quantum dots (QDs), primarily regarded as optoelectronic materials for LED and photovoltaic devices, have not been applied for photochemical conversion (e.g., water splitting or CO2 reduction) applications because of their insufficient stability in the presence of moisture or polar solvents. Herein, we report the use of CsPbBr3 QDs as novel photocatalysts to convert CO2 into solar fuels in nonaqueous media. Under AM 1.5G simulated illumination, the CsPbBr3 QDs steadily generated and injected electrons into CO2, catalyzing CO2 reduction at a rate of 23.7 µmol/g h with a selectivity over 99.3%. Additionally, through the construction of a CsPbBr3 QD/graphene oxide (CsPbBr3 QD/GO) composite, the rate of electron consumption increased 25.5% because of improved electron extraction and transport. This study is anticipated to provide new opportunities to utilize halide perovskite QD materials in photocatalytic applications.

ATP selection in a random peptide library consisting of prebiotic amino acids.

Based upon many theoretical findings on protein evolution, we proposed a ligand-selection model for the origin of proteins, in which the most ancient proteins originated from ATP selection in a pool of random peptides. To test this ligand-selection model, we constructed a random peptide library consisting of 15 types of prebiotic amino acids and then used cDNA display to perform six rounds of in vitro selection with ATP. By means of next-generation sequencing, the most prevalent sequence was defined. Biochemical and biophysical characterization of the selected peptide showed that it was stable and foldable and had ATP-hydrolysis activity as well.

[A model for the evaluation of groundwater ecological compensation budget]. / åœ°ä¸‹æ°´ç”Ÿæ€è¡¥å¿æ ‡å‡†æ ¸ç®—æ¨¡åž‹.

Groundwater, one of the important water resources, plays an important role in maintaining sustainable social and economic development. The ecological compensation of groundwater is a beneficial tool for guaranteeing reasonable exploitation and utilization of groundwater resources. However, there is a lack of associated studies, especially compensation budget. We proposed an integrated groundwater compensation standard model, which consisted of four components: base, stimulus and punishment, research and development, and potential risk. The priority level of compensation was estimated by considering regional climate and economic conditions comprehensively. The model was applied to a total of 11 cities in Shanxi Province to calculate the groundwater ecolo-gical compensation standard. The results showed that the base compensation accounted for the largest proportion in the total compensation, with the non-market value contributing more than 60%. Our results indicated that groundwater had a high regulated service value. From 2008 to 2017, the development coefficient of each city had significantly increased, suggesting the improved regional economic level and enhanced compensation capacity. Compensation priority was affected by the non-market value of groundwater and economic level, and obvious difference in the compensation priority existed in all the cities, implying the requirement for the implement of groundwater ecological compensation. Meanwhile, we suggested that groundwater risk compensation system should be improved, special funds should be set up for supporting research projects on groundwater ecological compensation, and long-term effective compensation mechanisms should be established.

Why the c-Fos/c-Jun complex is extremely conserved: An in vitro evolution exploration by combining cDNA display and proximity ligation.

Transcriptional regulation involves a series of sophisticated protein-protein and protein-DNA interactions (PPI and PDI). Some transcriptional complexes, such as c-Fos/c-Jun and their binding DNA fragments, have been conserved over the past one billion years. Considering the thermodynamic principle for transcriptional complex formation, we hypothesized that the c-Fos/c-Jun complex may represent a thermodynamic summit in the evolutionary space. To test this, we invented a new method, termed One-Pot-seq, which combines cDNA display and proximity ligation to analyse PPI/PDI complexes simultaneously. We found that the wild-type c-Fos/c-Jun complex is indeed the most thermodynamically stable relative to various mutants of c-Fos/c-Jun and binding DNA fragments. Our method also provides a universal approach to detect transcriptional complexes and explore transcriptional regulation mechanisms.

In Situ Growth of 120 cm2 CH3 NH3 PbBr3 Perovskite Crystal Film on FTO Glass for Narrowband-Photodetectors.

Organometal trihalide perovskites have been attracting intense attention due to their enthralling optoelectric characteristics. Thus far, most applications focus on polycrystalline perovskite, which however, is overshadowed by single crystal perovskite with superior properties such as low trap density, high mobility, and long carrier diffusion length. In spite of the inherent advantages and significant optoelectronic applications in solar cells and photodetectors, the fabrication of large-area laminar perovskite single crystals is challenging. In this report, an ingenious space-limited inverse temperature crystallization method is first demonstrated to the in situ synthesis of 120 cm2 large-area CH3 NH3 PbBr3 crystal film on fluorine-doped tin oxide (FTO) glass. Such CH3 NH3 PbBr3 perovskite crystal film is successfully applied to narrowband photodetectors, which enables a broad linear response range of 10-4 -102 mW cm-2 , 3 dB cutoff frequency (f 3 dB ) of ≈110 kHz, and high narrow response under low bias -1 V.

A micron-scale laminar MAPbBr3 single crystal for an efficient and stable perovskite solar cell.

Nowadays, obtaining a thin and large-area perovskite single-crystal (SC) is still challenging. Herein, we report a novel strategy to prepare a laminar MAPbBr3 SC with a controllable thickness of 16 µm and a size of 6 × 8 mm. Additionally, the SC solar cell achieves an intriguing efficiency of 7.11% with an impressive stability, maintaining 93% initial PCE after aging for 1000 h.

3,4-Phenylenedioxythiophene (PheDOT) Based Hole-Transporting Materials for Perovskite Solar Cells.

Two new electron-rich molecules based on 3,4-phenylenedioxythiophene (PheDOT) were synthesized and successfully adopted as hole-transporting materials (HTMs) in perovskite solar cells (PSCs). X-ray diffraction, absorption spectra, photoluminescence spectra, electrochemical properties, thermal stabilities, hole mobilities, conductivities, and photovoltaic parameters of PSCs based on these two HTMs were compared with each other. By introducing methoxy substituents into the main skeleton, the energy levels of PheDOT-core HTM were tuned to match with the perovskite, and its hole mobility was also improved (1.33×10(-4)  cm(2) V(-1) s(-1) , being higher than that of spiro-OMeTAD, 2.34×10(-5)  cm(2) V(-1) s(-1)). The PSC based on MeO-PheDOT as HTM exhibits a short-circuit current density (Jsc) of 18.31 mA cm(-2) , an open-circuit potential (Voc ) of 0.914 V, and a fill factor (FF) of 0.636, yielding an encouraging power conversion efficiency (PCE) of 10.64 % under AM 1.5G illumination. These results give some insight into how the molecular structures of HTMs affect their performances and pave the way for developing high-efficiency and low-cost HTMs for PSCs.

3D Cathodes of Cupric Oxide Nanosheets Coated onto Macroporous Antimony-Doped Tin Oxide for Photoelectrochemical Water Splitting.

Cupric oxide (CuO), a narrow-bandgap semiconductor, has a band alignment that makes it an ideal photocathode for the renewable production of solar fuels. However, the photoelectrochemical performance of CuO is limited by its poor conductivity and short electron diffusion lengths. Herein, a three-dimensional (3D) architecture consisting of CuO nanosheets supported onto transparent conducting macroporous antimony-doped tin oxide (mpATO@CuONSs) is designed as an excellent photocathode for promoting the hydrogen evolution reaction (HER). Owing to the 3D structure affording superior light-harvesting characteristics, large contact areas with the electrolyte, and highly conductive pathways for separation and transport of charge carriers, the mpATO@CuONSs photocathode produces an impressively high photocurrent density of -4.6 mA cm-2 at 0 V versus the reversible hydrogen electrode (RHE), which is much higher than that of the CuONSs array onto planar FTO glass (-1.9 mA cm-2 ).

Achieving Highly Efficient Photoelectrochemical Water Oxidation with a TiCl4 Treated 3D Antimony-Doped SnO2 Macropore/Branched α-Fe2O3 Nanorod Heterojunction Photoanode.

Utilizing photoelectrochemical (PEC) cells to directly collecting solar energy into chemical fuels (e.g., H2 via water splitting) is a promising way to tackle the energy challenge. α-Fe2O3 has emerged as a desirable photoanode material in a PEC cell due to its wide spectrum absorption range, chemical stability, and earth abundant component. However, the short excited state lifetime, poor minority charge carrier mobility, and long light penetration depth hamper its application. Recently, the elegantly designed hierarchical macroporous composite nanomaterial has emerged as a strong candidate for photoelectrical applications. Here, a novel 3D antimony-doped SnO2 (ATO) macroporous structure is demonstrated as a transparent conducting scaffold to load 1D hematite nanorod to form a composite material for efficient PEC water splitting. An enormous enhancement in PEC performance is found in the 3D electrode compared to the controlled planar one, due to the outstanding light harvesting and charge transport. A facile and simple TiCl4 treatment further introduces the Ti doping into the hematite while simultaneously forming a passivation layer to eliminate adverse reactions. The results indicate that the structural design and nanoengineering are an effective strategy to boost the PEC performance in order to bring more potential devices into practical use.