High-rate lithium (Li) ion batteries that can be charged in minutes and store enough energy for a 350-mile driving range are highly desired for all-electric vehicles. A high charging rate usually leads to sacrifices in capacity and cycling stability. We report use of black phosphorus (BP) as the active anode for high-rate, high-capacity Li storage. The formation of covalent bonds with graphitic carbon restrains edge reconstruction in layered BP particles to ensure open edges for fast Li+ entry; the coating of the covalently bonded BP-graphite particles with electrolyte-swollen polyaniline yields a stable solid–electrolyte interphase and inhibits the continuous growth of poorly conducting Li fluorides and carbonates to ensure efficient Li+ transport. The resultant composite anode demonstrates an excellent combination of capacity, rate, and cycling endurance.

Lithium-sulfur (Li-S) batteries have been regarded as the most promising candidates as the next-generation energy storage systems because of high theoretical capacities (Li: 3860 mAh g −1 and S: 1675 mAh g −1 ), low mass densities (Li: 0.534 g cm −3Lithium-sulfur (Li-S) batteries are strongly considered as next-generation energy storage systems because of their high energy density. However, the shuttling of lithium polysulfides (LiPS), sluggish reaction kinetics, and uncontrollable Li-dendrite growth severely degrade the electrochemical performance of Li-S batteries. Herein, a dual-functional flexible free-standing carbon nanofiber conductive framework in situ embedded with TiN-VN heterostructures (TiN-VN@CNFs) as an advanced host simultaneously for both the sulfur cathode (S/TiN-VN@CNFs) and the lithium anode (Li/TiN-VN@CNFs) is designed. As cathode host, the TiN-VN@CNFs can offer synergistic function of physical confinement, chemical anchoring, and superb electrocatalysis of LiPS redox reactions. Meanwhile, the well-designed host with excellent lithiophilic feature can realize homogeneous lithium deposition for suppressing dendrite growth. Combined with these merits, the full battery (denoted as S/TiN-VN@ CNFs || Li/TiN-VN@CNFs) exhibits remarkable electrochemical properties including high reversible capacity of 1110 mAh g −1 after 100 cycles at 0.2 C and ultralong cycle life over 600 cycles at 2 C. Even with a high sulfur loading of 5.6 mg cm −2 , the full cell can achieve a high areal capacity of 5.5 mAh cm −2 at 0.1 C. This work paves a new design from theoretical and experimental aspects for fabricating high-energy-density flexible Li-S full batteries.

The ability to predict the response of a cancer patient to a therapeutic agent is a major goal in modern oncology that should ultimately lead to personalized treatment. Existing approaches to predicting drug sensitivity rely primarily on profiling of cancer cell line panels that have been treated with different drugs and selecting genomic or functional genomic features to regress or classify the drug response. Here, we propose a dual-layer integrated cell line-drug network model, which uses both cell line similarity network (CSN) data and drug similarity network (DSN) data to predict the drug response of a given cell line using a weighted model. Using the Cancer Cell Line Encyclopedia (CCLE) and Cancer Genome Project (CGP) studies as benchmark datasets, our single-layer model with CSN or DSN and only a single parameter achieved a prediction performance comparable to the previously generated elastic net model. When using the dual-layer model integrating both CSN and DSN, our predicted response reached a 0.6 Pearson correlation coefficient with observed responses for most drugs, which is significantly better than the previous results using the elastic net model. We have also applied the dual-layer cell line-drug integrated network model to fill in the missing drug response values in the CGP dataset. Even though the dual-layer integrated cell line-drug network model does not specifically model mutation information, it correctly predicted that BRAF mutant cell lines would be more sensitive than BRAF wild-type cell lines to three MEK1/2 inhibitors tested.

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Constructing artificial solid‐electrolyte interphase (SEI) on the surface of Li metal is an effective approach to improve ionic conductivity of surface SEI and buffer Li dendrite growth of Li metal anode. However, constructing of homogenous ideal artificial SEI is still a great challenge. Here, a mixed lithium‐ion conductive Li2S/Li2Se (denoted as LSSe) protection layer, fabricated by a facile and inexpensive gas–solid reaction, is employed to construct stable surface SEI with high ionic conductivity. The Li2S/Li2Se‐protected Li metal (denoted as LSSe@Li) exhibits a stable dendrite‐free cycling behavior over 900 h with a high lithium stripping/plating capacity of 3 mAh cm−2 at 1.5 mA cm−2 in the symmetrical cell. Compared to bare Li anode, full batteries paired with LiFePO4, sulfur/carbon, and LiNi0.6Co0.2Mn0.2O2 cathodes all present better battery cycling and rate performance when LSSe@Li anode is used. Moreover, Li2Se exhibits a lower lithium‐ion migration energy barrier in comparison with Li2S which is proved by density functional theory calculation.

To meet the requirements of the rapid development of large-scale energy storage systems, "Beyond Li-ion battery (LIB)" systems are attracting more and more attention. [1][2][3][4][5] Among various alkali metals ion batteries, potassium-ion batteries (KIBs) exhibit many advantages for large-scale energy storage system applications including: [6,7] 1) the low manufacturing costs because of the natural abundance of their raw materials; 2) much lower redox potential of K/K + (−2.93 V vs standard hydrogen electrode) leading to higher open-circuit voltage and higher energy density compared with sodiumion batteries (SIBs). [8][9][10] According to the advantages and properties of low production costs and high energy density, the KIB is considered as a promising energy storage system for large-scale energy storage application. However, KIBs suffer from inferior cyclic stability and insufficient power density resulting from the structure collapse of electrode materials due to the bigger K + Constructing 2D heterostructure materials by stacking different 2D materials can combine the merits of the individual building blocks while eliminating their shortcomings. Dichalcogenides are attractive anodes for potassium-ion batteries (KIBs) due to their high theoretical capacity. However, the practical application of dichalcogenide is greatly hampered by the poor electrochemical performance due to sluggish kinetics of K + insertion and the electrode structure collapse resulting from the large K + insertion. Herein, heterostructures of 2D molybdenum dichalcogenide on 2D nitrogen-doped carbon (MoS 2 , MoSe 2 -on-NC) are prepared to boost their potassium storage performance. The unique 2D heterostructures possess built-in heterointerfaces, facilitating K + diffusion. The robust chemical bonds (CS, CSe, CMo bonds) enhance the mechanical strength of electrodes, thus suppressing the volume expansion. The 2D N-doped carbon nanosheets interconnected as a 3D structure offer a fast diffusion path for electrons. Benefitting from these merits, both the MoS 2 -on-NC and the MoSe 2 -on-NC exhibit unprecedented cycle life. Moreover, the electrochemical reaction mechanism of MoSe 2 is revealed during the process of potassiation and depotassiation.The ORCID identification number(s) for the author(s) of this article can be found under https://doi.

To determine whether hormone-dependent changes in the levels of LH/CG receptor in the rat ovary are associated with changes in expression of LH/CG receptor mRNAs, total RNA from rat follicles and corpora lutea at various stages of development was prepared and analyzed by Northern blots and/or solution hybridization. Whereas small antral follicles contained lo amounts of LH/CG receptor mRNAs, the growth of preovulatory (PO) follicles was associated with an increase in all LH/CG receptor mRNA transcripts. Induction of LH/CG receptor mRNAs in granulosa cells of hypophysectomized rats was dependent on the synergistic effects of estradiol and FSH. An LH/CG surge in vivo or LH treatment of PO follicles in vitro caused a rapid decline of all LH/CG receptor mRNAs in PO follicles, which was prevented by cycloheximide. Newly formed corpora lutea (days 1-4 postovulation) contained low amounts of LH/CG receptor mRNAs unless the rats were pregnant or treated exogenously with PRL. During pregnancy, corpora lutea isolated on days 4-19 of gestation contained high levels of LH/CG receptor mRNAs, which decreased markedly on days 21 and 24, the time of functional luteolysis and decreasing LH/CG receptor levels. These studies demonstrate that hormonal regulation of LH/CG receptor mRNA in rat ovarian cells parallels changes in LH/CG receptor levels and involves diverse molecular mechanisms, including 1) low concentrations of cAMP (elicited by FSH) in developing follicles, 2) inhibition by high concentrations of cAMP (elicited by LH/CG) in PO follicles, and 3) induction and maintenance by PRL in corpora lutea of gestation.

To avoid the energy‐consuming step of direct N≡N bond cleavage, photocatalytic N2 fixation undergoing the associative pathways has been developed for mild‐condition operation. However, it is a fundamental yet challenging task to gain comprehensive understanding on how the associative pathways (i.e., alternating vs. distal) are influenced and altered by the fine structure of catalysts, which eventually holds the key to significantly promote the practical implementation. Herein, we introduce Fe dopants into TiO2 nanofibers to stabilize oxygen vacancies and simultaneously tune their local electronic structure. The combination of in situ characterizations with first‐principles simulations reveals that the modulation of local electronic structure by Fe dopants turns the hydrogenation of N2 from associative alternating pathway to associative distal pathway. This work provides fresh hints for rationally controlling the reaction pathways toward efficient photocatalytic nitrogen fixation.