Water-Enabled H2 Generation from Hydrogenated Silicon Nanosheets for Efficient Anti-Inflammation.

As an emerging therapeutic gas, hydrogen (H2) is gifted with excellent biosafety, high tissue permeability, and radical-trapping capacity and is extensively considered as a highly promising antioxidant in clinics. However, a facile and effective strategy of H2 production for major inflammatory disease treatments is still lacking. In this study, by a facile wet-chemical exfoliation synthesis, a hydrogen-terminated silicon nanosheet (H-silicene) has been synthesized, which can favorably react with environmental water to generate H2 rapidly and continuously without any external energy input. Furthermore, theoretical calculations were employed to reveal the mechanism of enhanced H2 generation efficacy of H-silicene nanosheets. The as-synthesized H-silicene has been explored as a flexible hydrogen gas generator for efficient antioxidative stress application for the first time, which highlights a promising prospect of this two-dimensional H-silicene nanomaterial for acute inflammatory treatments by on-demand H2 production-enabled reactive oxygen species scavenging. This study provides a novel and efficient modality for nanomaterial-mediated H2 therapy.

Enhanced Thermoelectric Performance in Ge0.955- x Sbx Te/FeGe2 Composites Enabled by Hierarchical Defects.

Manipulations of carrier and phonon scatterings through hierarchical structures have been proved to be effective in improving thermoelectric performance. Previous efforts in GeTe-based materials mainly focus on simultaneously optimizing the carrier concentration and band structure. In this work, a synergistic strategy to tailor thermal and electrical transport properties of GeTe by combination with the scattering effects from both Ge vacancies and other defects is reported. The addition of Fe in GeTe-based compounds introduces the secondary phase of FeGe2 , synchronously increasing the concentration of Ge vacancies and arousing more Ge planar defects. These hierarchical defects contribute to a large scattering factor, leading to a significant enhancement of Seebeck coefficient and further a splendid power factor. Meanwhile, benefiting from the reinforced phonon scatterings by multiscale hierarchical structures, an extremely low lattice thermal conductivity is successfully achieved. With simultaneously optimized electrical and thermal transport properties, a maximum figure of merit, zT, value of 2.1 at 750 K and an average zT value of 1.5 in 400-800 K are realized in Ge0.875 Sb0.08 Te/1.5%FeGe2 . This work demonstrates that manipulation of hierarchical defects is an effective strategy to optimize the thermoelectric properties.

Small nucleolar RNA Sf-15 regulates proliferation and apoptosis of Spodoptera frugiperda Sf9 cells.

BACKGROUND: Small nucleolar RNAs (snoRNAs) function in guiding 2'-O-methylation and pseudouridylation of ribosomal RNAs (rRNAs) and small nuclear RNAs (snRNAs). In recent years, more and more snoRNAs have been found to play novel roles in mRNA regulation, such as pre-mRNA splicing or RNA editing. In our previous study, we found a silkworm C/D box snoRNA Bm-15 can interact with Notch receptor gene in vitro. To further study the function of Bm-15, we cloned its homolog Sf-15 from Spodoptera frugiperda and investigate the function of Sf-15 in Sf9 cells. RESULTS: We showed that knocking down of Sf-15 can inhibit the proliferation, then induce apoptosis of insect S. frugiperda Sf9 cells, but the results were reversed when Sf-15 was overexpressed. De novo sequencing of transcriptome of Sf9 cells showed that the expression of 21 apoptosis-related genes were increased upon Sf-15 repression. Further analysis showed that a Ca2+-induced cell death pathway gene Cn (PPP3C, the serine/threonine-protein phosphatase 2B catalytic subunit), was significantly increased upon Sf-15 depression but decreased when Sf-15 was overexpressed, which indicated that Cn might be a potential target of Sf-15. CONCLUSIONS: We conclude that C/D box snoRNA Sf-15 can participate in apoptosis through regulating the expression of Ca2+-induced cell death pathway gene Cn in Sf9 cells. This is the first time that we found snoRNAs exhibiting dual functions in insect, which reveals a novel layer of ncRNA modulation in cell growth and death.

Identification and functional characterization of intermediate-size non-coding RNAs in maize.

BACKGROUND: The majority of eukaryote genomes can be actively transcribed into non-coding RNAs (ncRNAs), which are functionally important in development and evolution. In the study of maize, an important crop for both humans and animals, aside from microRNAs and long non-coding RNAs, few studies have been conducted on intermediate-size ncRNAs. RESULTS: We constructed a homogenized cDNA library of 50-500 nt RNAs in the maize inbred line Chang 7-2. Sequencing revealed 169 ncRNAs, which contained 58 known and 111 novel ncRNAs (including 70 snoRNAs, 27 snRNAs, 13 unclassified ncRNAs and one tRNA). Forty of the novel ncRNAs were specific to the Panicoideae, and 24% of them are located on sense-strand of the 5' or 3' terminus of protein coding genes on chromosome. Target site analysis found that 22 snoRNAs can guide to 38 2'-O-methylation and pseudouridylation modification sites of ribosomal RNAs and small nuclear RNAs. Expression analysis showed that 43 ncRNAs exhibited significantly altered expression in different tissues or developmental stages of maize seedlings, eight ncRNAs had tissue-specific expression and five ncRNAs were strictly accumulated in the early stage of leaf development. Further analysis showed that 3 of the 5 stage-specific ncRNAs (Zm-3, Zm-18, and Zm-73) can be highly induced under drought and salt stress, while one snoRNA Zm-8 can be repressed under PEG-simulated drought condition. CONCLUSIONS: We provided a genome-wide identification and functional analysis of ncRNAs with a size range of 50-500 nt in maize. 111 novel ncRNAs were cloned and 40 ncRNAs were determined to be specific to Panicoideae. 43 ncRNAs changed significantly during maize development, three ncRNAs can be strongly induced under drought and salt stress, suggesting their roles in maize stress response. This work set a foundation for further study of intermediate-size ncRNAs in maize.

Part-crystalline part-liquid state and rattling-like thermal damping in materials with chemical-bond hierarchy.

Understanding thermal and phonon transport in solids has been of great importance in many disciplines such as thermoelectric materials, which usually requires an extremely low lattice thermal conductivity (LTC). By analyzing the finite-temperature structural and vibrational characteristics of typical thermoelectric compounds such as filled skutterudites and Cu3SbSe3, we demonstrate a concept of part-crystalline part-liquid state in the compounds with chemical-bond hierarchy, in which certain constituent species weakly bond to other part of the crystal. Such a material could intrinsically manifest the coexistence of rigid crystalline sublattices and other fluctuating noncrystalline sublattices with thermally induced large-amplitude vibrations and even flow of the group of species atoms, leading to atomic-level heterogeneity, mixed part-crystalline part-liquid structure, and thus rattling-like thermal damping due to the collective soft-mode vibrations similar to the Boson peak in amorphous materials. The observed abnormal LTC close to the amorphous limit in these materials can only be described by an effective approach that approximately treats the rattling-like damping as a "resonant" phonon scattering.

Structure family and polymorphous phase transition in the compounds with soft sublattice: Cu2Se as an example.

Quite a few interesting but controversial phenomena, such as simple chemical composition but complex structures, well-defined high-temperature cubic structure but intriguing phase transition, coexist in Cu2Se, originating from the relatively rigid Se framework and "soft" Cu sublattice. However, the electrical transport properties are almost uninfluenced by such complex substructures, which make Cu2Se a promising high-performance thermoelectric compound with extremely low thermal conductivity and good power factor. Our work reveals that the crystal structure of Cu2Se at the temperature below the phase-transition point (∼400 K) should have a group of candidate structures that all contain a Se-dominated face-centered-cubic-like layered framework but nearly random site occupancy of atoms from the "soft" Cu sublattice. The energy differences among those structures are very low, implying the coexistence of various structures and thus an intrinsic structure complexity with a Se-based framework. Detailed analyses indicate that observed structures should be a random stacking of those representative structure units. The transition energy barriers between each two of those structures are estimated to be zero, leading to a polymorphous phase transition of Cu2Se at increasing temperature. Those are all consistent with experimental observations.

Structural Design Principle of Rocksalt Oxides for Li-Excess Cathode Materials.

Li-excess oxide cathodes have received increasing attention due to their high capacity derived from accumulated cation and anion redox activity. However, Li-excess layered oxides suffer from capacity and voltage decay due to the irreversible phase transition, while cation-disordered cathodes also have the problems of poor cycling stability and rate capability. The rocksalt oxides with a layered-disordered coexistence nanostructure can combine the advantages of both phases such as the inherent high capacity of Li-excess oxides, good rate capability of the layered phase, and structural stability resulting from the intergrown disordered phase. Herein, for rational design, we developed a descriptor by correlating the ionic radius and electronic configuration to predict layered, cation-disordered, and coexistent structures of Li-excess cathode materials. Accordingly, we experimentally synthesized Li1.2Ni0.4Mn0.2Nb0.2O2 oxide with a coexistent structure in which the layered and disordered phases are well combined in the nanoscale region, achieving a high capacity (312 mAh g-1) with good cycling stability and rate capability. The design principle with composition predicting structure provides a valuable strategy in controllably designing and preparing Li-excess cathode materials.

Enhancing anionic redox stability via oxygen coordination configurations.

Anionic redox in Li-rich cathode materials with disordered crystal structures has potential to increase battery energy density. However, capacity fading due to anionic redox-induced structural transformation hinders practical implementation. To address this challenge, it is crucial to understand the influence of the anion coordination structure on redox reversibility. By comprehensively studying the spinel-like Li1.7Mn1.6O3.7F0.3 and layered Li2MnO3 model systems, we found that tetrahedral oxygen exhibits higher kinetic and thermodynamic stability than octahedral oxygen in Li1.7Mn1.6O3.7F0.3 and Li2MnO3, effectively suppressing aggregation of oxidized anions. Electronic structure analysis showed that the 2p lone-pair states in tetrahedral oxygen lie deeper than those in octahedral oxygen. The Li-O-TM bond angle in a polyhedron is identified as a characteristic parameter to correlate anionic redox stability. TM substitutions using Co3+, Ti4+ and Mo5+ could effectively regulate the Li-O-Mn bond angle and anionic active electronic state. Our finding that anionic redox stability is influenced by the polyhedral structure offers new opportunities for designing high-energy-density Li-rich cathode materials.

Trinitroaromatic Salts as High-Energy-Density Organic Cathode Materials for Li-Ion Batteries.

Even though organic molecules with designed structures can be assembled into high-capacity electrode materials, only limited functional groups such as -C═O and -C═N- could be designed as high-voltage cathode materials with enough high capacity. Here, we propose a common chemical raw material, trinitroaromatic salt, to have promising potential to develop organic cathode materials with high discharge voltage and capacity through a strong delocalization effect between -NO2 and aromatic ring. Our first-principles calculations show that electrochemical reactions of trinitroaromatic potassium salt C6H2(NO2)3OK are a 6-electron charge-transfer process, providing a high discharge capacity of 606 mAh g-1 and two voltage plateaus of 2.40 and 1.97 V. Electronic structure analysis indicates that the discharge process from C6H2(NO2)3OK to C6H2(NO2Li2)3OK stabilizes oxidized [C6]n+ to achieve a stable conjugated structure through electron delocalization from -NO2 to [C6]n+. The ordered layer structure C6H2(NO2)3OK can provide large spatial pore channels for Li-ion transport, achieving a high ion diffusion coefficient of 3.41 × 10-6 cm2 s-1.

Unlock Restricted Capacity via OCe Hybridization for LiOxygen Batteries.

The aprotic Li-O2 battery (LOB) has the highest theoretical energy density of any rechargeable batteries. However, such system is largely restricted by the electrochemically formed lithium peroxide (Li2 O2 ) on the cathode surface, leading ultimately to low actual capacities and early cell death. In contrast to the surface-mediated growth of thin film with a thickness <50 nm, a non-crystalline Li2 O2 film with a thickness of >400 nm can be formed via an optimal OCe hybridized electronic structure. Specially, oxygen can react with dissolved cerium cations in the electrolyte via a cerium-oxygen reaction to form a high-energy faceted cerium oxide catalyst, which not only generates a great number of non-saturable active sites, but also erects electron transport bridges between the lattice O and adjacent Ce atoms. Such CeO orbital hybridization also forms a direct charge transfer channel from Ce-4f of CeO2 to O 2 2 - ${\rm{O}}_2^{2 - }$ -π* of Li2 O2 , eventually leading to submicron-thick Li2 O2 shells via a subsequent lithium-oxygen reaction. Relying on the above merits, this work unlocks the rechargeable capacities of LOB from restricted 1000 to unprecedented 10 000 mAh g-1 with good cyclabilities and reduced charge-discharge overpotentials.

lncR26319/miR-2834/EndophilinA axis regulates oogenesis of the silkworm, Bombyx mori.

Oocyte maturation is critical for insect reproduction. Vitellogenesis, the timely production and uptake of vitellogenin (Vg), is crucial for female fecundity. Vg is synthesized in fat body and absorbed by the oocytes through endocytosis during insect oogenesis. In the silkworm, Bombyx mori, we discovered that a nucleus-enriched long-noncoding RNA (lncRNA) lncR26319 regulates Endophilin A (EndoA) - a member of the endophilin family of endocytic proteins - through competitive binding to miR-2834. The lncR26319-miR-2834-EndoA axis was required for Vg endocytosis in the silkworm; loss of EndoA or overexpression of miR-2834 significantly reduced egg numbers in virgin moths. In addition, accumulation of miR-2834 resulted in pupal and adult deformation and reduced fecundity in females. The expression of Vg, 30-kDa (30K) protein, and egg-specific protein (Esp) decreased after knockdown of EndoA or overexpression of miR-2834, while knockdown of miR-2834 had an opposite effect on the expression of Vg, 30K protein gene, and Esp. These results suggest that the lncR26319-miR-2834-EndoA axis contributes to the endocytic activity in the Vg uptake and leads to the normal progression of oogenesis in the silkworm. Thus, miR-2834 and EndoA are crucial for female reproduction and could be potential targets for new pest management strategies in lepidopterans.

Origin of multiple voltage plateaus in P2-type sodium layered oxides.

Although layered transition metal (TM) oxides have attracted considerable attention for cathode materials of sodium-ion batteries, they suffer from uncontrolled multiple voltage plateaus due to local structure transformations such as TM-layer gliding and Na+/vacancy ordering upon Na+ extraction and insertion. However, the intrinsic origins of these local structure transformations are not fully understood, preventing the rational design of better cathode materials. Here, we concentrate on Na+/vacancy ordering in single phase domains to reveal the underlying mechanism of multiple voltage plateaus by tracking desodiation-induced electronic structure evolutions of two typical compounds, P2-Na0.6[Cr0.6Ti0.4]O2 and P2-NaCrO2. During desodiation, P2-NaCrO2 generates obvious multiple voltage plateaus, which are not observed in P2-Na0.6[Cr0.6Ti0.4]O2 due to TM disordering. A combination of first-principles desodiation calculations and electronic structure analysis reveals that charge localization accompanied by Na+ migration is an intrinsic feature of multiple voltage plateaus in P2-NaCrO2. A correlation between charge localization and multiple voltage plateaus is established by a comparative study in which P2-Na0.6[Cr0.6Ti0.4]O2 always follows the charge transfer order from high-activity to low-activity sites. This finding reveals that disordering design of active sites to avoid charge localization in redox is of much importance for developing high-performance Na-ion cathode materials.

Triple Conductive Wiring by Electron Doping, Chelation Coating and Electrochemical Conversion in Fluffy Nb2 O5 Anodes for Fast-Charging Li-Ion Batteries.

High-rate anode material is the kernel of developing fast-charging lithium ion batteries (LIBs). T-Nb2 O5 , well-known for its "room and pillar" structure and bulk pseudocapacitive effect, is expected to enable the fast lithium (de)intercalation. But this property is still limited by the low electronic conductivity or insufficient wiring manner. Herein, a strategy of triple conductive wiring through electron doping, chelation coating, and electrochemical conversion inside the microsized porous spheres consisting of dendrite-like T-Nb2 O5 primary particles is proposed to achieve the fast-charging and durable anodes for LIBs. The penetrative implanting of conformal carbon coating (derivative from polydopamine chelate) and NbO domains (induced by excess discharging) reinforces the global supply of electronically conductive wires, apart from those from Co/Mn heteroatom or O vacancy doping. The polydopamine etching on T-Nb2 O5 spheres promotes their evolution into fluffy morphology with better electrolyte infiltration. The synergic electron and ion wiring at different scales endow the modified T-Nb2 O5 anode with ultralong cycling life (143 mAh g-1 at 1 A g-1 after 8500 cycles) and high-rate performance (144.1 mAh g-1 at 10.0 A g-1 ). The permeation of multiple electron wires also enables a high mass loading of T-Nb2 O5 (4.5 mg cm-2 ) with a high areal capacity of 0.668 mAh cm-2 even after 150 cycles.

Hydrogenated Germanene Nanosheets as an Antioxidative Defense Agent for Acute Kidney Injury Treatment.

Acute kidney injury (AKI) is a sudden kidney dysfunction caused by aberrant reactive oxygen species (ROS) metabolism that results in high clinical mortality. The rapid development of ROS scavengers provides new opportunities for AKI treatment. Herein, the use of hydrogen-terminated germanene (H-germanene) nanosheets is reported as an antioxidative defense nanoplatform against AKI in mice. The simulation results show that 2D H-germanene can effectively scavenge ROS through free radical adsorption and subsequent redox reactions. In particular, the H-germanene exhibits high accumulation in injured kidneys, thereby offering a favorable opportunity for treating renal diseases. In the glycerol-induced murine AKI model, H-germanene delivers robust antioxidative protection against ROS attack to maintain normal kidney function indicators without negative influence in vivo. This positive in vivo antioxidative defense in living animals demonstrates that the present H-germanene nanoplatform is a powerful antioxidant against AKI and various anti-inflammatory diseases.

Identifying Metallic Transition-Metal Dichalcogenides for Hydrogen Evolution through Multilevel High-Throughput Calculations and Machine Learning.

High-performance electrocatalysts not only exhibit high catalytic activity but also have sufficient thermodynamic stability and electronic conductivity. Although metallic 1T-phase MoS2 and WS2 have been successfully identified to have high activity for hydrogen evolution reaction, designing more extensive metallic transition-metal dichalcogenides (TMDs) faces a large challenge because of the lack of a full understanding of electronic and composition attributes related to catalytic activity. In this work, we carried out systematic high-throughput calculation screening for all possible existing two-dimensional TMD (2D-TMD) materials to obtain high-performance hydrogen evolution reaction (HER) electrocatalysts by using a few important criteria, such as zero band gap, highest thermodynamic stability among available phases, low vacancy formation energy, and approximately zero hydrogen adsorption energy. A series of materials-perfect monolayer VS2 and NiS2, transition-metal ion vacancy (TM-vacancy) ZrTe2 and PdTe2, chalcogenide ion vacancy (X-vacancy) MnS2, CrSe2, TiTe2, and VSe2-have been identified to have catalytic activity comparable with that of Pt(111). More importantly, electronic structural analysis indicates active electrons induced by defects are mostly delocalized in the nearest-neighbor and next-nearest neighbor range, rather than a single-atom active site. Combined with the machine learning method, the HER-catalytic activity of metallic phase 2D-TMD materials can be described quantitatively with local electronegativity (0.195·LEf + 0.205·LEs) and valence electron number (Vtmx), where the descriptor is ΔGH* = 0.093 - (0.195·LEf + 0.205·LEs) - 0.15·Vtmx.

Hydrogen-bonded silicene nanosheets of engineered bandgap and selective degradability for photodynamic therapy.

Silicon, a highly biocompatible and ubiquitous chemical element in living systems, exhibits great potentials in biomedical applications. However, the silicon-based nanomaterials such as silica and porous silicon have been largely limited to only serving as carriers for delivery systems, due to the lack of intrinsic functionalities of silicon. This work presents the facile construction of a two-dimensional (2D) hydrogen-bonded silicene (H-silicene) nanosystem which is highlighted with tunable bandgap and selective degradability for tumor-specific photodynamic therapy facilely by surface covalent modification of hydrogen atoms. Briefly, the H-silicene nanosheet material is selectively degradable in normal neutral tissues but rather stable in the mildly acidic tumor microenvironment (TME) for achieving efficient photodynamic therapy (PDT). Such a 2D hydrogen-bonded silicene nanosystem featuring the tunable bandgap and tumor-selective degradability provides a new paradigm for the application of multi-functional two-dimensional silicon-based biomaterials towards the diagnosis and treatments of cancer and other diseases.

The order-disorder transition in Cu2Se and medium-range ordering in the high-temperature phase.

The high thermoelectric performance of cuprous selenide (Cu2Se) arises from its specific structures consisting of two independent sublattices, i.e. the rigid face-centered cubic (f.c.c.) Se sublattice and the flexible Cu sublattice showing a variety of ordered configurations at numerous interstitial sites. Upon increasing the temperature, the Cu sublattice undergoes an order-to-disorder transition but the details of the structural evolution have not been fully elucidated. Here, in situ transmission electron microscopy (TEM) is used to investigate the thermally induced structural changes of Cu2Se in both real and reciprocal spaces. Order-disorder transition was found to proceed in nanoblocks accompanied by the structural fluctuations between low-temperature and high-temperature phases. Electron diffraction revealed the emergence of medium-range ordering of Cu atoms in the high-temperature f.c.c. phase. By referring to the Coulomb interaction evaluations, the superstructures for the medium-range ordering were constructed. Such medium-range atomic ordering was sustained over a wide temperature range (from the phase transition temperature to over 800 K in the TEM) but gradually changed to short-range ordering as indicated by the appearance of diffuse scattering rings.

Stabilizing Low-Coordinated O Ions To Operate Cationic and Anionic Redox Chemistry of Li-Ion Battery Materials.

Conventional electrochemical processes are mainly operated by cationic redox chemistry. Developing cumulative cationic and anionic redox chemistry offers a transformative approach to increase the energy storage capacity of Li-ion batteries and active sites of catalysts. However, realizing the reversible anionic redox reaction to increase the specific capacity in Li-ion battery materials is a large challenge because uncontrollable anion-anion combination and gas evolutions cause poor cyclic performance. Here, we use open-framework metal-fluorides (FeF3·0.33H2O) to demonstrate cumulative cationic and anionic redox reactions to be realized through O substitution. Experimental studies verified that O substitution could form reductive O ions, and stabilizing this reductive low-coordinated O by p-d orbital hybridization and hydrogen-transfer-mediated O-H bond formation plays an important role in operating anionic electrochemistry. O substitution also exhibits an improved cyclic performance beyond the insertion-reaction capacity (150 mA h/g) of FeF3·0.33H2O (225 and 300 mA h/g). Theoretical calculations show that FeF2.67O0.33·0.33H2O exhibits a 50% higher insertion-reaction capacity (225 mA h/g) than FeF3·0.33H2O (150 mA h/g) before structural collapse, which is attributed to cumulative cationic (Fe3+ ↔ Fe2+) and anionic (O- ↔ O2-) redox reactions based on our electronic structure analysis. The present study opens a new avenue to develop cationic and anionic electrochemistry to improve the storage capacity and cyclic performance through stabilizing low-coordinated O ions.

Silicene: Wet-Chemical Exfoliation Synthesis and Biodegradable Tumor Nanomedicine.

Silicon-based biomaterials play an indispensable role in biomedical engineering; however, due to the lack of intrinsic functionalities of silicon, the applications of silicon-based nanomaterials are largely limited to only serving as carriers for drug delivery systems. Meanwhile, the intrinsically poor biodegradation nature for silicon-based biomaterials as typical inorganic materials also impedes their further in vivo biomedical use and clinical translation. Herein, by the rational design and wet chemical exfoliation synthesis of the 2D silicene nanosheets, traditional 0D nanoparticulate nanosystems are transformed into 2D material systems, silicene nanosheets (SNSs), which feature an intriguing physiochemical nature for photo-triggered therapeutics and diagnostic imaging and greatly favorable biological effects of biocompatibility and biodegradation. In combination with DFT-based molecular dynamics (MD) calculations, the underlying mechanism of silicene interactions with bio-milieu and its degradation behavior are probed under specific simulated physiological conditions. This work introduces a new form of silicon-based biomaterials with 2D structure featuring biodegradability, biocompatibility, and multifunctionality for theranostic nanomedicine, which is expected to promise high clinical potentials.

Superposed Redox Chemistry of Fused Carbon Rings in Cyclooctatetraene-Based Organic Molecules for High-Voltage and High-Capacity Cathodes.

Even though many organic cathodes have been developed and have made a significant improvement in energy density and reversibility, some organic materials always generate relatively low voltage and limited discharge capacity because their energy storage mechanism is solely based on redox reactions of limited functional groups [N-O, C═X (X = O, N, S)] linking to aromatic rings. Here, a series of cyclooctatetraene-based (C8H8) organic molecules were demonstrated to have electrochemical activity of high-capacity and high-voltage from carbon rings by means of first-principles calculations and electronic structure analysis. Fused molecules of C8-C4-C8 (C16H12) and C8-C4-C8-C4-C8 (C24H16) contain, respectively, four and eight electron-deficient carbons, generating high-capacity by their multiple redox reactions. Our sodiation calculations predict that C16H12 and C24H16 exhibit discharge capacities of 525.3 and 357.2 mA h g-1 at the voltage change from 3.5 to 1.0 V and 3.7 to 1.3 V versus Na+/Na, respectively. Electronic structure analysis reveals that the high voltages are attributed to superposed electron stabilization mechanisms, including double-bond reformation and aromatization from carbon rings. High thermodynamic stability of these C24H16-based systems strongly suggests feasibility of experimental realization. The present work provides evidence that cyclooctatetraene-based organic molecules fused with the C4 ring are promising in designing high-capacity and high-voltage organic rechargeable cathodes.