Digital therapeutics as an emerging new therapy for diabetes mellitus: potentials and concerns.

The global burden of controlling and managing diabetes mellitus (DM) is a significant challenge. Despite the advancements in conventional DM therapy, there remain hurdles to overcome, such as enhancing medication adherence and improving patient prognosis. Digital therapeutics (DTx), an innovative digital application, has been proposed to augment the traditional disease management workflow, particularly in managing chronic diseases like DM. Several studies have explored DTx, yielding promising results. However, certain concerns about this innovation persist. In this review, we aim to encapsulate the potential of DTx and its applications in DM management, thereby providing a comprehensive overview of this technique for public health policymakers.

The potential of the Medical Digital Twin in diabetes management: a review.

Diabetes is a chronic prevalent disease that must be managed to improve the patient's quality of life. However, the limited healthcare management resources compared to the large diabetes mellitus (DM) population are an obstacle that needs modern information technology to improve. Digital twin (DT) is a relatively new approach that has emerged as a viable tool in several sectors of healthcare, and there have been some publications on DT in disease management. The systematic summary of the use of DTs and its potential applications in DM is less reported. In this review, we summarized the key techniques of DTs, proposed the potentials of DTs in DM management from different aspects, and discussed the concerns of this novel technique in DM management.

TiO2 -Based Heterostructures with Different Mechanism: A General Synergistic Effect toward High-Performance Sodium Storage.

The general synergistic effect of TiO2 -based heterostructures has been discovered to improve the sodium storage of anodes, involving conversion, alloying, and insertion mechanism materials. Herein, metal sulfides (MS2 , M = Sn2+ , Co2+ , Mo2+ ), metallic Sb and Sn, as well as, carbon nanotubes (CNTs) are chosen as the model examples from the three kinds. The electrochemical testing demonstrates a better performance of heterostructrues involving TiO2 than the pristine anode components. The introduction of TiO2 into the MS2 and Sb or Sn systems induces a built-in electric field as the charge transfer force at the heterojunctions, greatly reducing the ion transfer resistance and promoting interfacial electron transfer. In the CNT/TiO2 structure, the chemical growth of TiO2 nanoparticles on the outer surface of CNTs makes the interface more compact than the physical blending case, offering better improvement of electrochemistry. The synergy should work via the growth of heterostructures, relying on the interface effects, which always plays the promotion role through the formation of driving force or grain boundaries and/or condense phase interface to facilitate charge transfer at the interface during the storage process. Therefore, the construction of reasonable heterostructures can endow materials with intriguing electrochemical performance based on the synergistic effect.

Unusual formation of NiCo2O4@MnO2/nickel foam/MnO2 sandwich as advanced electrodes for hybrid supercapacitors.

A facile three-step method is designed for large-scale preparation of a NiCo2O4@MnO2/nickel foam/MnO2 sandwich architecture with robust adhesion as an advanced electrode for high-performance supercapacitors. The synthesis contains the hydrothermal reaction of a cobalt-nickel hydroxide precursor on a nickel foam (NF) support and subsequent thermal conversion into spinel mesoporous NiCo2O4 nanowire arrays, followed by a hydrothermal oxidation reaction to synthesize NiCo2O4@MnO2/nickel foam/MnO2 sandwiches. Moreover, the tactics reported in this study enable easy control of the growth of NiCo2O4 on one side of the NF and MnO2 nanosheets on both sides of the NF to obtain novel NiCo2O4@MnO2/nickel foam/MnO2 sandwiches. Because of the unusual structural and compositional features, the obtained NiCo2O4@MnO2/nickel foam/MnO2 sandwiches manifest excellent performance with high specific capacitance (1.70 C cm-2 at 2 mA cm-2), exceptional rate capability (78.5% retention at 20 mA cm-2) and ultralong cycling stability (91% retention over 30 000 cycles at 20 mA cm-2) as a battery-type electrode material for supercapacitors. When further assembled into an aqueous hybrid supercapacitor, it can deliver an energy density of 53.5 W h kg-1 at a power density of 80 W kg-1 and 20.7 W h kg-1 at 8 kW kg-1. This novel sandwich electrode provides a new idea for improving the electrochemical performance of hybrid supercapacitors.

Embedding MnO@Mn3 O4 Nanoparticles in an N-Doped-Carbon Framework Derived from Mn-Organic Clusters for Efficient Lithium Storage.

The first synthesis of MnO@Mn3 O4 nanoparticles embedded in an N-doped porous carbon framework (MnO@Mn3 O4 /NPCF) through pyrolysis of mixed-valent Mn8 clusters is reported. The unique features of MnO@Mn3 O4 /NPCF are derived from the distinct interfacial structure of the Mn8 clusters, implying a new methodological strategy for hybrids. The characteristics of MnO@Mn3 O4 are determined by conducting high angle annular dark-field scanning transmission electron microscopy (HAADF-STEM) and electron energy loss spectroscopy (EELS) valence-state analyses. Due to the combined advantages of MnO@Mn3 O4 , the uniform distribution, and the NPCF, MnO@Mn3 O4 /NPCF displays unprecedented lithium-storage performance (1500 mA h g-1 at 0.2 A g-1 over 270 cycles). Quantitative analysis reveals that capacitance and diffusion mechanisms account for Li+ storage, wherein the former dominates. First-principles calculations highlight the strong affiliation of MnO@Mn3 O4 and the NPCF, which favor structural stability. Meanwhile, defects of the NPCF decrease the diffusion energy barrier, thus enhancing the Li+ pseudocapacitive process, reversible capacity, and long cycling performance. This work presents a new methodology to construct composites for energy storage and conversion.