Ampere-hour-scale soft-package potassium-ion hybrid capacitors enabling 6-minute fast-charging

Extreme fast charging of Ampere-hour (Ah)-scale electrochemical energy storage devices targeting charging times of less than 10 minutes are desired to increase widespread adoption. However, this metric is difficult to achieve in conventional Li-ion batteries due to their inherent reaction mechanism and safety hazards at high current densities. In this work, we report 1 Ah soft-package potassium-ion hybrid supercapacitors (PIHCs), which combine the merits of high-energy density of battery-type negative electrodes and high-power density of capacitor-type positive electrodes. The PIHC consists of a defect-rich, high specific surface area N-doped carbon nanotube-based positive electrode, MnO quantum dots inlaid spacing-expanded carbon nanotube-based negative electrode, carbonate-based non-aqueous electrolyte, and a binder- and current collector-free cell design. Through the optimization of the cell configuration, electrodes, and electrolyte, the full cells (1 Ah) exhibit a cell voltage up to 4.8 V, high full-cell level specific energy of 140 Wh kg-1 (based on the whole mass of device) with a full charge of 6 minutes. An 88% capacity retention after 200 cycles at 10 C (10 A) and a voltage retention of 99% at 25 ± 1 °C are also demonstrated

Reversing relaxation-induced embrittlement by high-temperature thermal cyclic annealing in Zr-based metallic glass

Annealing usually induces structural relaxation and reduction of liquid-like regions, leading to embrittlement in bulk metallic glasses (BMGs). Here, we find that the short-term high-temperature thermal cycling (HTC) annealed Zr41.2Ti13.8Cu12.5Ni10Be22.5 (Vit1) BMG shows an improved plasticity without sacrificing their yield strength. And only relaxation behavior with increased hardness is observed after HTC, which is different from the rejuvenation effect usually observed in cryogenic thermal cycling (CTC). We revealed that this embrittlement reversal is attributed to enhanced fluctuations of full width at half maximum (FWHM) of the hardness’ distribution at micrometer and larger scales induced by short-term HTC. The enhanced fluctuations of mechanical heterogeneities across the diameter on a cross-section of the short-term HTC sample may increase the number and decrease the size of shear transformation zones (STZs) activated at high stress and promote the deflection of shear bands (SBs) during their propagation to form multiple SBs. The enhanced plasticity after HTC induced relaxation contradicts the common sense that relaxation accompanying with annihilation of free volume or liquid-like region usually causes embrittlement. Present results indicate that short-term HTC could be a powerful mean to tune the mechanical performance, shedding new lights on the interplay among relaxation, mechanical/structural heterogeneity, and plasticity of MGs

Effect of Cr and La co-doping on the photocatalytic hydrogen production performance of Sr1-xLaxTi1-xCrxO3 nanofibers

The Sr1-xLaxTi1-xCrxO3 (x = 0–0.05) nanofibers were synthesized by electrospinning based on Pechini sol-gel method. The prepared Sr1-xLaxTi1-xCrxO3 nanofibers were analyzed by XRD, Raman, UV–vis spectra, XPS, SEM, TEM, transient photocurrent, electrochemical impedance and photocatalytic hydrogen evolution tests. The results showed that CrLa co-doped can expand the light absorption region of SrTiO3 from the ultraviolet region to the visible light, and significantly narrowed its band gap. Under visible light irradiation, Sr1-xLaxTi1-xCrxO3 nanofibers exhibited the best hydrogen evolution activity at x = 0.03, and the hydrogen evolution rate reached 106.2 μmol∙g−1∙h−1. This may be the result of the combined effect of the intermediate band gap and the band gap variation due to Cr doping

Ampere-hour-scale soft-package potassium-ion hybrid capacitors enabling 6-minute fast-charging

Acknowledgements: This work was financially supported by the National Natural Science Foundation of China (Grant nos. 52274298 (H. Zhou), 51974114 (H. Zhou), 51672075 (Y. Kuang) and 21908049 (Y. Kuang)), and Faraday Institute - Battery Study and Seed Research Project (Rational design and manufacture of stacked Li-CO2 pouch cells) (FIRG052, Y. Zhao). National Supercomputing Center in CHANGSHA is acknowledged for allowing the use of computational resources including TIANHE-1.Extreme fast charging of Ampere-hour (Ah)-scale electrochemical energy storage devices targeting charging times of less than 10 minutes are desired to increase widespread adoption. However, this metric is difficult to achieve in conventional Li-ion batteries due to their inherent reaction mechanism and safety hazards at high current densities. In this work, we report 1 Ah soft-package potassium-ion hybrid supercapacitors (PIHCs), which combine the merits of high-energy density of battery-type negative electrodes and high-power density of capacitor-type positive electrodes. The PIHC consists of a defect-rich, high specific surface area N-doped carbon nanotube-based positive electrode, MnO quantum dots inlaid spacing-expanded carbon nanotube-based negative electrode, carbonate-based non-aqueous electrolyte, and a binder- and current collector-free cell design. Through the optimization of the cell configuration, electrodes, and electrolyte, the full cells (1 Ah) exhibit a cell voltage up to 4.8 V, high full-cell level specific energy of 140 Wh kg−1 (based on the whole mass of device) with a full charge of 6 minutes. An 88% capacity retention after 200 cycles at 10 C (10 A) and a voltage retention of 99% at 25 ± 1 °C are also demonstrated

Ampere-hour-scale soft-package potassium-ion hybrid capacitors enabling 6-minute fast-charging

Acknowledgements: This work was financially supported by the National Natural Science Foundation of China (Grant nos. 52274298 (H. Zhou), 51974114 (H. Zhou), 51672075 (Y. Kuang) and 21908049 (Y. Kuang)), and Faraday Institute - Battery Study and Seed Research Project (Rational design and manufacture of stacked Li-CO2 pouch cells) (FIRG052, Y. Zhao). National Supercomputing Center in CHANGSHA is acknowledged for allowing the use of computational resources including TIANHE-1.Extreme fast charging of Ampere-hour (Ah)-scale electrochemical energy storage devices targeting charging times of less than 10 minutes are desired to increase widespread adoption. However, this metric is difficult to achieve in conventional Li-ion batteries due to their inherent reaction mechanism and safety hazards at high current densities. In this work, we report 1 Ah soft-package potassium-ion hybrid supercapacitors (PIHCs), which combine the merits of high-energy density of battery-type negative electrodes and high-power density of capacitor-type positive electrodes. The PIHC consists of a defect-rich, high specific surface area N-doped carbon nanotube-based positive electrode, MnO quantum dots inlaid spacing-expanded carbon nanotube-based negative electrode, carbonate-based non-aqueous electrolyte, and a binder- and current collector-free cell design. Through the optimization of the cell configuration, electrodes, and electrolyte, the full cells (1 Ah) exhibit a cell voltage up to 4.8 V, high full-cell level specific energy of 140 Wh kg−1 (based on the whole mass of device) with a full charge of 6 minutes. An 88% capacity retention after 200 cycles at 10 C (10 A) and a voltage retention of 99% at 25 ± 1 °C are also demonstrated

Ampere-hour-scale soft-package potassium-ion hybrid capacitors enabling 6-minute fast-charging.

Acknowledgements: This work was financially supported by the National Natural Science Foundation of China (Grant nos. 52274298 (H. Zhou), 51974114 (H. Zhou), 51672075 (Y. Kuang) and 21908049 (Y. Kuang)), and Faraday Institute - Battery Study and Seed Research Project (Rational design and manufacture of stacked Li-CO2 pouch cells) (FIRG052, Y. Zhao). National Supercomputing Center in CHANGSHA is acknowledged for allowing the use of computational resources including TIANHE-1.Extreme fast charging of Ampere-hour (Ah)-scale electrochemical energy storage devices targeting charging times of less than 10 minutes are desired to increase widespread adoption. However, this metric is difficult to achieve in conventional Li-ion batteries due to their inherent reaction mechanism and safety hazards at high current densities. In this work, we report 1 Ah soft-package potassium-ion hybrid supercapacitors (PIHCs), which combine the merits of high-energy density of battery-type negative electrodes and high-power density of capacitor-type positive electrodes. The PIHC consists of a defect-rich, high specific surface area N-doped carbon nanotube-based positive electrode, MnO quantum dots inlaid spacing-expanded carbon nanotube-based negative electrode, carbonate-based non-aqueous electrolyte, and a binder- and current collector-free cell design. Through the optimization of the cell configuration, electrodes, and electrolyte, the full cells (1 Ah) exhibit a cell voltage up to 4.8 V, high full-cell level specific energy of 140 Wh kg-1 (based on the whole mass of device) with a full charge of 6 minutes. An 88% capacity retention after 200 cycles at 10 C (10 A) and a voltage retention of 99% at 25 ± 1 °C are also demonstrated

Large-area synthesis of superclean graphene via selective etching of amorphous carbon with carbon dioxide

Contamination commonly observed on the graphene surface is detrimental to its excellent properties and strongly hinders its application. It is still a great challenge to produce large-area clean graphene film in a low-cost manner. Herein, we demonstrate a facile and scalable chemical vapor deposition approach to synthesize meter-sized samples of superclean graphene with an average cleanness of 99 %, relying on the weak oxidizing ability of CO to etch away the intrinsic contamination, i.e., amorphous carbon. Remarkably, the elimination of amorphous carbon enables a significant reduction of polymer residues in the transfer of graphene films and the fabrication of graphene-based devices and promises strongly enhanced electrical and optical properties of graphene. The facile synthesis of large-area superclean graphene would open the pathway for both fundamental research and industrial applications of graphene, where a clean surface is highly needed

Regulating the Electron Distribution of Metal‐Oxygen for Enhanced Oxygen Stability in Li‐rich Layered Cathodes

Abstract Li‐rich Mn‐based layered oxides (LLO) hold great promise as cathode materials for lithium‐ion batteries (LIBs) due to their unique oxygen redox (OR) chemistry, which enables additional capacity. However, the LLOs face challenges related to the instability of their OR process due to the weak transition metal (TM)‐oxygen bond, leading to oxygen loss and irreversible phase transition that results in severe capacity and voltage decay. Herein, a synergistic electronic regulation strategy of surface and interior structures to enhance oxygen stability is proposed. In the interior of the materials, the local electrons around TM and O atoms may be delocalized by surrounding Mo atoms, facilitating the formation of stronger TM─O bonds at high voltages. Besides, on the surface, the highly reactive O atoms with lone pairs of electrons are passivated by additional TM atoms, which provides a more stable TM─O framework. Hence, this strategy stabilizes the oxygen and hinders TM migration, which enhances the reversibility in structural evolution, leading to increased capacity and voltage retention. This work presents an efficient approach to enhance the performance of LLOs through surface‐to‐interior electronic structure modulation, while also contributing to a deeper understanding of their redox reaction

Enhanced Photodynamic Efficacy of Zinc Phthalocyanine by Conjugating to Heptalysine

Zinc phthalocyanine (ZnPc) is a promising photosensitizer for photodynamic therapy, but faces some challenges: ZnPc is insoluble in water and thus requires either special formulation of ZnPc by, e.g., liposome or Cremophor EL, or chemical modification of <i>Pc</i> ring to enhance its bioavailability and photodynamic efficacy. Here, we conjugated monosubstituted ZnPc-COOH with a series of oligolysine moieties with different numbers of lysine residues (ZnPc-(Lys)_<i>n</i> (<i>n</i> = 1, 3, 5, 7, 9) to improve the water solubility of the ZnPc conjugates. We measured the photosensitizing efficacies and the cellular uptakes of this series of conjugates on a normal and a cancerous cell line. In addition, we developed a sensitive <i>in situ</i> method to distinguish the difference in photodynamic efficacy among conjugates. Our results showed that ZnPc-(Lys)₇ has the highest photodynamic efficacy compared to the other conjugates investigated