Electrolyte engineering via fluorinated additives is promising to improve cycling stability and safety of high‐energy Li‐metal batteries. Here, an electrolyte is reported in a porous lithium fluoride ...(LiF) strategy to enable efficient carbonate electrolyte engineering for stable and safe Li‐metal batteries. Unlike traditionally engineered electrolytes, the prepared electrolyte in the porous LiF nanobox exhibits nonflammability and high electrochemical performance owing to strong interactions between the electrolyte solvent molecules and numerous exposed active LiF (111) crystal planes. Via cryogenic transmission electron microscopy and X‐ray photoelectron spectroscopy depth analysis, it is revealed that the electrolyte in active porous LiF nanobox involves the formation of a high‐fluorine‐content (>30%) solid electrolyte interphase layer, which enables very stable Li‐metal anode cycling over one thousand cycles under high current density (4 mA cm−2). More importantly, employing the porous LiF nanobox engineered electrolyte, a Li || LiNi0.8Co0.1Mn0.1O2 pouch cell is achieved with a specific energy of 380 Wh kg−1 for stable cycling over 80 cycles, representing the excellent performance of the Li‐metal pouch cell using practical carbonate electrolyte. This study provides a new electrolyte engineering strategy for stable and safe Li‐metal batteries.
Electrolyte engineering via fluorinated additives is promising to improve the cycling stability and safety of high‐energy Li‐metal batteries. The electrolyte in an active porous LiF nanobox involves the formation of a high‐fluorine‐content (>30%) solid electrolyte interphase layer to achieve a ≈3.5 Ah Li || LiNi0.8Co0.1Mn0.1O2 pouch cell with a specific energy of 380 Wh kg−1 under a practical carbonate electrolyte.
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BFBNIB, FZAB, GIS, IJS, KILJ, NLZOH, NUK, OILJ, SBCE, SBMB, UL, UM, UPUK
Thermochromic phosphors are intriguing materials for realizing thermochromic behaviors of light‐emitting diodes. Here a highly luminescent and stable thermochromic phosphor based on one‐dimensional ...Cu4I6(4‐dimethylamino‐1‐ethylpyridinium)2 is reported. This unique ionic copper‐iodine chain‐based hybrid exhibits near‐unity photoluminescence efficiency owing to the through‐space charge‐transfer character of relevant electronic transitions. More importantly, an alternative mechanism of thermochromic phosphorescence was unraveled, supported by a first principles simulation of concerted copper atom migration in the copper‐iodine chain. Furthermore, we successfully fabricate a bright thermochromic light‐emitting diode using this Cu4I6(4‐dimethylamino‐1‐ethylpyridinium)2 thermochromic phosphor. Our reported flexible ionic copper‐iodine chain‐based thermochromic luminescent material represents a new type of cost‐effective functional phosphor.
A novel thermochromic 1D‐Cu4I6(4‐dimethylamino‐1‐ethylpyridinium)2 hybrid phosphor with near‐unity photoluminescence efficiency is reported involving a mechanism of reversible single‐crystal‐to‐single‐crystal transformation induced by temperature‐responsive concerted Cu atom migration in ionic copper‐iodine chains.
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BFBNIB, FZAB, GIS, IJS, KILJ, NLZOH, NUK, OILJ, SBCE, SBMB, UL, UM, UPUK
Chiral chromophores and their ordered assemblies are intriguing for yielding circularly polarized luminescence (CPL) and exploring intrinsic structure–light emission relationships. With the ...extensively studied chiral organic molecules and inorganic nanoparticle assemblies for the amplified CPL, the assemblies of copper halide hybrid clusters have attracted intensive attention due to their potential efficient CPL. Here, we report robust chiral phosphine–copper iodide hybrid clusters and their layered assemblies in crystalline states for amplified CPL. We reveal that the intermolecular interactions endow the clusters with the capability of assembling into chiral crystalline CPL materials, including hexagonal platelet-shaped microcrystals (g lum ≈ 9.5 × 10–3) and highly oriented crystalline films (g lum ≈ 5 × 10–3). Owing to the high crystalline feature of the thin film, we demonstrate an electroluminescent device with bright electroluminescence (1200 cd m–2).
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IJS, KILJ, NUK, PNG, UL, UM
Enormous efforts have been devoted to the reduction of carbon dioxide (CO2) by utilizing various driving forces, such as heat, electricity, and radiation. However, the efficient reduction of CO2 is ...still challenging because of sluggish kinetics. Recent pioneering studies from several groups, including us, have demonstrated that the coupling of solar energy and thermal energy offers a novel and promising strategy to promote the activity and/or manipulate selectivity in CO2 reduction. Herein, we clarify the definition and principles of coupling solar energy and thermal energy, and comprehensively review the status and prospects of CO2 reduction by coupling solar energy and thermal energy. Catalyst design, reactor configuration, photo‐mediated activity/selectivity, and mechanism studies in photo‐thermo CO2 reduction will be emphasized. The aim of this Review is to promote understanding towards CO2 activation and provide guidelines for the design of new catalysts for the efficient reduction of CO2.
A bundle of energy: The coupling of solar energy and thermal energy is a promising strategy to mediate the activity and/or selectivity of CO2 reduction. The status and prospects of this topic are reviewed, with the aim of providing guidelines for the design of new catalysts.
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BFBNIB, FZAB, GIS, IJS, KILJ, NLZOH, NUK, OILJ, SBCE, SBMB, UL, UM, UPUK
Solar-to-fuel conversion through photocatalytic processes is regarded as promising technology with the potential to reduce reliance on dwindling reserves of fossil fuels and to support the ...sustainable development of our society. However, conventional semiconductor-based photocatalytic systems suffer from unsatisfactory reaction efficiencies due to limited light harvesting abilities. Recent pioneering work from several groups, including ours, has demonstrated that visible and infrared light can be utilized by plasmonic catalysts not only to induce local heating but also to generate energetic hot carriers for initiating surface catalytic reactions and/or modulating the reaction pathways, resulting in synergistically promoted solar-to-fuel conversion efficiencies. In this perspective, we focus primarily on plasmon-mediated catalysis for thermodynamically uphill reactions converting CO
2
and/or H
2
O into value-added products. We first introduce two types of mechanism and their applications by which reactions on plasmonic nanostructures can be initiated: either by photo-induced hot carriers (plasmonic photocatalysis) or by light-excited phonons (photothermal catalysis). Then, we emphasize examples where the hot carriers and phonon modes act in concert to contribute to the reaction (plasmonic photothermal catalysis), with special attention given to the design concepts and reaction mechanisms of the catalysts. We discuss challenges and future opportunities relating to plasmonic photothermal processes, aiming to promote an understanding of underlying mechanisms and provide guidelines for the rational design and construction of plasmonic catalysts for highly efficient solar-to-fuel conversion.
Hot carrier activation and photothermal heat can be constructively coupled using plasmonic photothermal catalysts for synergistically promoted solar-to-fuel conversion efficiency.
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IJS, KILJ, NUK, UL, UM, UPUK
Dissolved gas analysis (DGA) of insulating oil can provide an important basis for transformer fault diagnosis. To improve diagnosis accuracy, this paper presents a new transformer fault diagnosis ...method based on deep belief networks (DBN). By analyzing the relationship between the gases dissolved in transformer oil and fault types, the Non-code ratios of the gases are determined as the characterizing parameter of the DBN model. DBN adopts multi-layer and multi-dimension mapping to extract more detailed differences of fault types. In this process, the diagnosis parameters are pre-trained. A back-propagation algorithm adjusts them with the labels of the samples and optimizes the parameters. To verify the effect of the proposed method, the diagnostic DBN model is constructed and tested using various oil chromatographic datasets collected from the State Grid Corporation of China and previous publications. The performances of the DBN diagnosis model are analyzed by different characterizing parameters, different training datasets and sample datasets. In addition, the influence of discharge and overheating multiple faults on the diagnosis model is studied. The performance of the proposed approach is compared with that derived from support vector machine (SVM), back-propagation neural network (BPNN) and ratio methods respectively. The results show that the proposed method significantly improves the accuracy of power transformer fault diagnosis.
Fast charging of lithium ion batteries is essential for next‐generation energy‐storage systems. However, the poor ionic and electronic transport of anodes with its rather high mass loading limits the ...practical applications of this technology. Herein, a multiscale design from niobium titanium oxide anode material to electrode structure is proposed for fast charging lithium ion batteries with a practical level of areal capacity (3 mAh cm−2). At the atomic scale, the introduction of oxygen vacancy and surface carbon coating enables niobium titanium oxide (TiNb2O7−x@C) to possess excellent ionic and electronic conductivity. For the microscopic electrode structure, 1D TiNb2O7−x@C fibers are tightly assembled to form a high‐speed transport network of ions and electrons throughout the electrode. As a result, the obtained TiNb2O7−x@C electrode shows excellent rate capability (1.83 mAh cm−2 at 1 C) and cycling stability under an areal capacity of 3 mAh cm−2 (2.35 mAh cm−2 after 100 cycles at 0.5 C) in half‐cells. Significantly, a full‐cell coupled with practical level mass loading of lithium cobalt oxide cathode is demonstrated to deliver 1.55 mAh cm−2 at 3 C for the first time.
A multiscale electrode design strategy is reported to achieve fast ionic and electronic transport for improving the electrochemical performance of TiNb2O7 electrodes at high mass loading (>11 mg cm−2). Moreover, a TiNb2O7–x@C/LiCoO2 full‐cell with practical level mass loading is fabricated, which displays excellent fast‐charging performance.
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BFBNIB, FZAB, GIS, IJS, KILJ, NLZOH, NUK, OILJ, SBCE, SBMB, UL, UM, UPUK
Holey defective g‐C3N4 photocatalysts, which are easily prepared via a novel photoassisted heating process, are reported. The photoassisted treatment not only helps to create abundant holes, endowing ...g‐C3N4 with more exposed catalytic active sites and crossplane diffusion channels to shorten the diffusion distance of both reactants from the surface to bulk and charge carriers from the bulk to surface, but also introduces nitrogen vacancies in the tri‐s‐triazine repeating units of g‐C3N4, inducing the narrowing of intrinsic bandgap and the formation of defect states within bandgap to extend the visible‐light absorption range and suppress the radiative electron–hole recombination. As a result, the holey defective g‐C3N4 photocatalysts show much higher photocatalytic activity for H2O2 production with optimized enhancement up to ten times higher than pristine bulk g‐C3N4. The newly developed synthetic strategy adopted here enables the sufficient utilization of solar energy and shows rather promising for the modification of other materials for efficient energy‐related applications.
A holey defective g‐C3N4 photocatalyst can be prepared through a novel photo‐assisted heating process, and it shows much higher photocatalytic activity for H2O2 production with optimized enhancement up to 10 times higher than pristine bulk g‐C3N4, which is due to the introduction of abundant holes and nitrogen vacancies.
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BFBNIB, FZAB, GIS, IJS, KILJ, NLZOH, NUK, OILJ, SBCE, SBMB, UL, UM, UPUK
The histone demethylase lysine‐specific demethylase 4A (KDM4A) is reported to be overexpressed and plays a vital in multiple cancers through controlling gene expression by epigenetic regulation of ...H3K9 or H3K36 methylation marks. However, the biological role and mechanism of KDM4A in prostate cancer (PC) remain unclear. Herein, we reported KDM4A expression was upregulation in phosphatase and tensin homolog knockout mouse prostate tissue. Depletion of KDM4A in PC cells inhibited their proliferation and survival in vivo and vitro. Further studies reveal that USP1 is a deubiquitinase that regulates KDM4A K48‐linked deubiquitin and stability. Interestingly, we found c‐Myc was a key downstream effector of the USP1‐KDM4A/androgen receptor axis in driving PC cell proliferation. Notably, upregulation of KDM4A expression with high USP1 expression was observed in most prostate tumors and inhibition of USP1 promotes PC cells response to therapeutic agent enzalutamide. Our studies propose USP1 could be an anticancer therapeutic target in PC.
This study identifies USP1 as a critical deubiquitinase for stabilizing KDM4A, thereby promoting prostate cancer growth and tumorigenesis. Targeting KDM4A stabilization through pharmacological inhibition of USP1 by ML323 could thus open an avenue for therapeutic intervention in prostate cancer patients.
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BFBNIB, FZAB, GIS, IJS, KILJ, NLZOH, NUK, OILJ, SBCE, SBMB, UL, UM, UPUK
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