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In hybrid perovskite solar cells (PSCs), the reaction of hydrogens (H) located in the amino group of the organic A-site cations with their neighboring halides plays a central role in degradation. Inspired by the retarded biological activities of cells in heavy water, we replaced the light H atom with its abundant, twice-as-heavy, nonradioactive isotope, deuterium (D) to hamper the motion of H. This D substitution retarded the formation kinetics of the detrimental H halides in Pb-based PSCs, as well as the H bond-mediated oxidation of Sn2+ in Sn–Pb-based narrow-bandgap PSCs, evidenced by accelerated stability studies. A computational study indicated that the zero point energy of D-based formamidinium (FA) is lower than that of pristine FA. In addition, the smaller increase in entropy in D-based FA than in pristine FA accounts for the increased formation free energy of the Sn2+ vacancies, which leads to the retarded oxidation kinetics of Sn2+. In this study, we show that substituting active H with D in organic cations is an effective way to enhance the stability of PSCs without sacrificing photovoltaic (PV) performance. This approach is also adaptable to other stabilizing methods.

The utilization of metal-organic frameworks (MOFs) in photocatalysis applications requires light-responsive architectures with tunable optical bandgaps. Here, we demonstrate a facile approach to optical bandgap tuning via post-synthetic modifica-tions of pbz-MOF-1, a Zr-based MOF with polyphenylene ligands. A simple reaction of pbz-MOF-1 with FeCl3 was shown to induce three different chemical reactions of the ligands: oxidative dehydrogenation, chlorination and one/two electron oxi-dation of the ligands. The result of these reactions was a gradual decrease in the optical bandgap from 2.95 eV to as little as 0.69 eV. Time-resolved optical spectroscopy and electron paramagnetic resonance spectroscopy, coupled with density functional theory calculations provide insights into the mechanisms of bandgap tuning using chemical oxidation methods. The facile bandgap tuning report here has promising application in the utilization of photo-responsive MOFs in photocatalysis, sensing and other light-triggered applications.

The mechanism of photochemical CO2 reduction to formate by PCN-136, a Zr-based metal-organic framework (MOF) that incorporates light-harvesting nanographene ligands, has been investigated using steady-state and time-resolved spectroscopy and density functional theory (DFT) calculations. The catalysis was found to proceed via a “photoreactive capture” mecha-nism, where Zr-based nodes serve to capture CO2 in the form of Zr-bicarbonates, while the nanographene ligands have a dual role to absorb light and to store one-electron equivalents needed for catalysis. We also find that the process occurs via a “two-for-one” route, where a single photon initiates a cascade of electron/hydrogen atom transfers from the sacrificial donor to the CO2-bound MOF. The mechanistic findings obtained here illustrate several advantages of MOF-based architectures in the molecular photocatalyst engineering and provide insights on ways to achieve high formate selectivity.

Methionine (Met) was introduced to modify the Li-Al layered double hydroxides (LDHs) film prepared on 6063 aluminum alloy by in situ method for the first time. Fourier transform infrared spectroscopy, X-ray photoelectron spectroscopy, Scanning electron microscopy, and X-ray diffraction confirmed the successful insertion of Met into LDHs film and revealed that the introduction of Met could make the LDHs film much denser. Electrochemical tests illustrated that the corrosion rate of the Met modified LDHs film was reduced by more than an order of magnitude compared with the bare Al alloy. Moreover, the corrosion rate of the modified LDHs film after immersion in 3.5 wt.% NaCl solution for 21 days was almost the same as that without immersion, which indicates that the modified film has good corrosion durability. The corrosion resistance of the scratched modified film could recover to the level without a scratch on the 14th day based on the scratch test results, meaning the modified film has a good self-healing property. Finally, the anti-corrosion mechanism of the Met was proved by molecular dynamic simulations and found that the enhanced corrosion resistance may be attributed to the addition of Met that slowed the diffusion of the corrosive medium Cl− and water molecules.

Background. Side effects of the use of opioid analgesics during painless delivery are the main factors that affect rapid postpartum recovery. Opioid use can result in dangerous respiratory depression in the patient. Opioids can also disrupt the baby’s breathing and heart rate. The nonopioid analgesic dexmedetomidine, a new a2-adrenergic agonist, possesses higher selectivity, greater analgesic effects, and fewer side effects. Moreover, epidural administration of dexmedetomidine also reduces local anesthetic consumption. Objective. Our study aims to compare the analgesic effects as well as the side effects of ropivacaine with dexmedetomidine against sufentanyl as an epidural labor analgesia. Methods. This study is a randomized, double-blinded, controlled trial (registration no. ChiCTR2200055360) involving 120 primiparous (a woman who has given birth once), singleton pregnancy women who are greater than 38 weeks into gestation and have requested epidural labor analgesia. The participants were randomized to receive 0.1% ropivacaine with sufentanyl (0.4 μg/ml) or dexmedetomidine (0.4 μg/ml). The primary outcomes included Visual Analogue Score (VAS), duration of first epidural infusions, the requirement of additional PCEA bolus, and adverse reactions during labor analgesia. Results. Of the 120 subjects who consented, 91 parturient women (women in the condition of labor) had complete data for analysis. Demographics and VAS, as well as maternal and fetal outcomes, were similar between the groups. The duration of first epidural infusions in dexmedetomidine was significantly longer than sufentanyl (median value: 115 vs 68 min, P P P

Background: Sheep is an important meat-producing animal, and low tail fat deposition level has become one of the main targets of meat production. LncRNAs have recently received special attention due to their critical role in many important biological processes. There are few reports on its regulatory function in ovine fat deposition. In this study, two sheep populations with different tail types in Xinjiang, Bashby sheep (fat-tailed) and the hybrid population of Bashby sheep and wild argali (small-tailed), were selected for whole transcriptome resequencing from their tail tissues. Results: First, 728 differentially expressed lncRNA (DElncRNAs) of tail fat between Bashby and F2 sheep were identified by RNA-seq. Second, the tissue expression profile and relative expression difference between Bashby and F2 sheep of 7 of 728 DE lncRNAs were analyzed by RT-PCR. We conclude that MSTRG.37980, MSTRG.38164, MSTRG.36912 and MSTRG.36913 positively regulate fat deposition, while MSTRG.8169, MSTRG.24995 and MSTRG.31389 inhibit fat deposition. Third, GO and KEGG analysis revealed that lncRNA targets were mainly participated in energy metabolism, growth and development and immunity, such as viral carcinogenesis, Chemokine signaling pathway, B cell receptor signaling pathway. And the expression pattern of target genes in each tissue was similar to that of the corresponding lncRNAs, which required us to conduct further research on target genes. Conclusions: This study was the first to systematically identify fat deposition-associated lncRNAs in ovine tail fat and construct DElncRNAs profiles. Our findings will help understand the molecular mechanism of fat deposition from transcriptomic perspectives.

Stimuli-responsive materials with switchable wettability for bidirectional oil-water separation show great potential in practical applications. Inspired by mussels, we use dopamine as an anchor molecule to construct a polydopamine (PDA) coating on the surface of copper foam (CF). Silver particles are deposited on the PDA coated surface to construct a multiscale composite structure, and the long-chain alkylthiol with carboxyl and methyl groups at the end is subsequently self-assembled to the modified copper foam surface. The as-modified copper foam has unique pH responsiveness, that is, the water contact angle (WCA) is measured to be about 140° under acidic and neutral conditions, while alkaline conditions radically change the surface property from superhydrophobic to superhydrophilic due to the measured WCA turning to 0°. It can be used efficiently for the bidirectional separation of an oil-water mixture, e.g., the separation efficiency of a 1,2-dichloroethane/water mixture can reach as high as 98.2%. Besides, it maintains 98% separation efficiency and stable wettability for an octane/water mixture, together with excellent mechanical durability; the WCA of the surface maintains at about 130° after ten wear cycles.