Insight into the interface engineering between methylammonium lead halide perovskites and gallium oxide: a first-principles approach.

Interface engineering of the organo-lead halide perovskite devices has shown the potential to improve their efficiency and stability. In this study, the atomic, electronic, optical and transport characteristics of MAPbI3/Ga2O3 and MAPbCl3/Ga2O3 interfaces were investigated by using first-principles calculations. Eight different interfacial models were established and the interfacial properties were discussed. The results show that the PbI/O configuration exhibits the largest bonding strength out of all eight interfacial configurations. Owing to the larger interfacial interaction, the charge transfer at the PbI/O interface is significantly more than that at the other interfaces. The analysis of absorption spectra indicates that the Ga-terminated perovskite/Ga2O3 heterostructures are expected to have great potential for efficient optoelectronic applications. The analysis of transmission spectra shows that the MA/O configurations with more transmission peaks near the Fermi level exhibit lower resistance compared to others. The results of our study could help understand the interfacial engineering mechanism between perovskite and Ga2O3.

DEAD-box RNA helicase Dbp2 binds to G-quadruplex nucleic acids and regulates different conformation of G-quadruplex DNA.

G-quadruplexes (G4s) are important in regulating DNA replication, repair and RNA transcription through interactions with specialized proteins. Dbp2 has been identified as a G4 DNA binding protein from Saccharomyces cerevisiae cell lysates. The majority of G4 motifs in Saccharomyces cerevisiae display 5-50 nt loops, only a few have 1-2 nt loops. Human DDX5 could unfold MycG4 DNA, whether Dbp2 also participates in remodeling G4 motifs with short loops in Saccharomyces cerevisiae remains elusive. Here we find that Dbp2 prefers G-rich substrates and binds MycG4 with a high affinity. Dbp2 possesses a dual function for different conformations of MycG4, destabilizing the folded MycG4 and inducing further folding of the unfolded MycG4. Similarly, DDX5 can unfold MycG4, but it exhibits a weaker MycG4 folding-promoting activity relative to Dbp2. Furthermore, Dbp2 facilitates DNA annealing activity in the absence of ATP, suggesting that Dbp2 can work on DNA substrates and possibly participate in DNA metabolism. Our results demonstrate that Dbp2 plays an important role in regulating the folding and unfolding activities of MycG4.

A Simple Route to Produce Highly Efficient Porous Carbons Recycled from Tea Waste for High-Performance Symmetric Supercapacitor Electrodes.

High-performance porous carbons derived from tea waste were prepared by hydrothermal treatment, combined together with KOH activation. The heat-treatment-processed materials possess an abundant hierarchical structure, with a large specific surface of 2235 m2 g-1 and wetting-complemental hydrophilicity for electrolytes. In a two-electrode system, the porous carbon electrodes' built-in supercapacitor exhibited a high specific capacitance of 256 F g-1 at 0.05 A g-1, an excellent capacitance retention of 95.4% after 10,000 cycles, and a low leakage current of 0.014 mA. In our work, the collective results present that the precursor crafted from the tea waste can be a promising strategy to prepare valuable electrodes for high-performance supercapacitors, which offers a practical strategy to recycle biowastes into manufactured materials in energy storage applications.

Replication protein A plays multifaceted roles complementary to specialized helicases in processing G-quadruplex DNA.

G-quadruplexes (G4s) are non-canonical DNA structures with critical roles in DNA metabolisms. To resolve those structures that can cause replication fork stalling and genomic instability, single-stranded DNA-binding proteins and helicases are required. Here, we characterized the interplay between RPA and helicases on G4s using single-molecule FRET. We first discovered that human RPA efficiently prevents G4 formation by preempting ssDNA before its folding. RPA also differentially interacts with the folded G4s. However, helicases such as human BLM and yeast Pif1 have different G4 preferences from RPA mainly based on loop lengths. More importantly, both RPA and these helicases are required for the stable G4 unfolding, as RPA promotes helicase-mediated repetitive unfolding into durative linear state. Furthermore, BLM can traverse G4 obstacles temporarily disrupted by RPA and continue to unwind downstream duplex. We finally proposed the mechanisms underlying above functions of RPA in preventing, resolving, and assisting helicases to eliminate G4s.

High-performance double ion-buffering reservoirs of asymmetric supercapacitors based on flower-like Co3O4-G>N-PEGm microspheres and 3D rGO-CNT>N-PEGm aerogels.

Novel 3D flower-like Co3O4-G>N-PEGm composites have been synthesized by employing a solvothermal method, in which the incorporating graphene nanosheets are modified with methoxypolyethylene glycol (mPEG) via nitrene chemistry to form 2D macromolecular brushes. In Co3O4-G>N-PEGm, the flower-like Co3O4 microspheres can anchor on the G>N-PEGm nanosheets, corresponding to the coordination bonds between the lone pair of electrons on the mPEG polymer chains of the G>N-PEGm macromolecular brushes and cobalt ions. Owing to the novel structure, a high specific capacitance value of 1625.6 F g-1 at a current density of 0.5 A g-1 can be achieved in KOH solution. Meanwhile, 3D rGO-CNT>N-PEGm aerogels (GCA), as the negative electrode of electrical double-layer capacitor materials, exhibit a high reversible specific capacitance of 313.8 F g-1 at a current density of 2 A g-1. Based on the high electrochemical performance of both electrode materials, the double ion-buffering reservoirs of asymmetric supercapacitors configured with the Co3O4-G>N-PEGm as the positive electrode and 3D GCA as the negative electrode can deliver a high energy density of 34.4 W h kg-1 at a power density of 400 kW kg-1.