Crystalline MnCO3@Amorphous MnOx Composite as Cathode Material for High-Performance Aqueous Zinc-Ion Batteries.

Rechargeable aqueous zinc-ion batteries (RAZIBs) have received extensive attention because of their advantages of low cost, high safety, and nontoxicity. However, problems such as dissolution of the active cathode material, dendrites/passivation of the zinc anode, and slow reaction kinetics hindered their further applications. In this work, a crystalline/amorphous composite-type material composed of crystalline MnCO3 and amorphous MnOx was prepared and used as the cathode material for RAZIBs. The MnCO3@amorphous MnOx (MnCO3@A-MnOx) composite possesses the merits of both the pure crystalline phase of MnCO3 and the amorphous phase of MnOx, which can deliver better electrochemical performance than the corresponding single component in repeated cycles. In addition, crystalline MnCO3 undergoes a complex phase transition to the active MnO2 during the first charge process, providing the composite with a stable structure and additional electrochemical capacity. The electrochemical measurement results indicate that the MnCO3@A-MnOx electrode can display high reversible discharge capacity at 0.1 A g-1, excellent rate performance at 5.0 A g-1, and long cycling stability over 2000 cycles, showing great potential as a cathode material for high-performance RAZIBs.

The elemental pegging effect in locally ordered nanocrystallites of high-entropy oxide enables superior lithium storage.

High-entropy oxides (HEOs) can be well suited for lithium-ion battery anodes because of their multi-principal synergistic effect and good stability. The appropriate selection and combination of elements play a crucial role in designing conversion-type anode materials with outstanding electrochemical performance. In this study, we have successfully built a single-phase spinel-structured HEO material of (Mn0.23Fe0.23Co0.22Cr0.19Zn0.13)3O4 (HEO-MFCCZ). When the HEO-MFCCZ materials transform into a coexisting state of amorphous and nanocrystalline structures during the cycling process, the inert Zn element can initiate a pegging effect, causing enhanced stability. The transition also introduces many defect sites, effectively reducing the potential barrier for ion transport and accelerating ion transport. The increased electronic and ionic conductivities and pseudocapacitive contribution significantly enhance the rate performance. As a result, a unique and practical approach is provided for developing anode materials for lithium-ion batteries.

Synergetic Coupling of Redox-Active Sites on Organic Electrode Material for Robust and High-Performance Sodium-Ion Storage.

Organic electrode materials (OEMs), valued for their sustainability and structural tunability, have been attracting increasing attention for wide application in sodium-ion batteries (SIBs) and other rechargeable batteries. However, most OEMs are plagued with insufficient specific capacity or poor cycling stability. Therefore, it's imperative to enhance their specific capacity and cycling stability through molecular design. Herein, we designed and synthesized a heteroaromatic molecule 2,3,8,9,14,15-hexanol hexaazatrinaphthalene (HATN-6OH) by the synergetic coupling of catechol (the precursor of ortho-quinone)/ortho-quinone functional groups and HATN conjugated core structures. The abundance of catechol/ortho-quinone and imine redox-active moieties delivers a high specific capacity of nine-electron transfer for SIBs. Most notably, the π-π interactions and intermolecular hydrogen bond forces among HATN-6OH molecules secure the stable long-term cycling performance of SIBs. Consequently, the as-prepared HATN-6OH electrode exhibited a high specific capacity (554 mAh g-1 at 0.1 A g-1 ), excellent rate capability (202 mAh g-1 at 10 A g-1 ), and stable long-term cycling performance (73 % after 3000 cycles at 10 A g-1 ) in SIBs. Additionally, the nine-electron transfer mechanism is confirmed by systematic density functional theory (DFT) calculation, attenuated total reflection Fourier transform infrared spectroscopy (ATR-FTIR), and Raman analysis. The achievement of the synergetic coupling of the redox-active sites on OEMs could be an important key to the enhancement of SIBs and other metal-ion batteries.

An analysis of nutritional risk factors in older adults with gastrointestinal tumours.

INTRODUCTION: The aim of this study was to investigate risk factors for nutritional risk in older adults with gastrointestinal tumours. MATERIALS AND METHODS: A total of 170 eligible hospitalised older adults with gastrointestinal tumours were included. Their clinical characteristics were collected, their nutritional risk was screened by NRS 2002, and then patients were divided into a nutritional risk group and a non-nutritional risk group. The observation indicators included body mass index (BMI), muscle mass, muscle strength, and calf circumference. The third lumbar skeletal muscle index (L3 SMI) was calculated using abdominal computed tomography (CT) scan results, and grip strength/muscle strength, 6-m walking speed and calf circumference were measured. Sarcopenia was diagnosed according to the criteria of the Asian Sarcopenia Working Group (AWGS). Finally, we analysed the relationship between nutritional risk and sarcopenia and other related factors (BMI, calf circumference, L3 SMI, grip strength/muscle strength, 6-m walking speed) in older adults with gastrointestinal tumours by multivariate logistic regression analysis. RESULTS: Older adults with gastrointestinal tumours who were at nutritional risk accounted for 51.8% of patients in this study. The differences between sex, tumour stage, age, BMI, calf circumference, L3 SMI, grip strength/muscle strength, 6-m walking speed, and prevalence of sarcopenia were statistically significant in two groups (all P < 0.05). Multivariate logistic regression analysis showed that age, BMI, grip strength/muscle strength, and sarcopenia were risk factors of nutritional risk in older adults with gastrointestinal tumours (all P < 0.05). DISCUSSION: Older adults with gastrointestinal cancer had a higher proportion of nutritional risk, and L3 SMI, grip strength/muscle strength were independent risk factors for nutritional risk. In clinical practice, attention to nutritional risk screening and sarcopenia development in older adults with gastrointestinal cancer is warranted.

In Situ Construction of Zn2Mo3O8/ZnO Hierarchical Nanosheets on Graphene as Advanced Anode Materials for Lithium-Ion Batteries.

Transition-metal oxides as anodes for lithium-ion batteries (LIBs) have attracted enormous interest because of their high theoretical capacity, low cost, and high reserve abundance. Unfortunately, they commonly suffer from poor electronic and ionic conductivity and relatively large volume expansion during discharge/charge processes, thereby triggering inferior cyclic performance and rate capability. Herein, a molybdenum-zinc bimetal oxide-based composite structure (Zn2Mo3O8/ZnO/rGO) with rectangular Zn2Mo3O8/ZnO nanosheets uniformly dispersed on reduced graphene oxide (rGO) has been prepared by using a simple and controllable cyanometallic framework template method. The Zn2Mo3O8/ZnO rectangular nanosheets with desirable porous features are composed of nanocrystalline subunits, facilitating the exposure of abundant active sites and providing sufficient contact with the electrolyte. Benefiting from the composition and structural merits as well as the induced synergistic effects, the Zn2Mo3O8/ZnO/rGO composite as LIB anodes delivers superior electrochemical properties, including high reversible capacity (960 mA h g-1 after 100 cycles at 200 mA g-1), outstanding rate performance (417 mA h g-1 at 10,000 mA g-1), and admirable long-term cyclic stability (862 mA h g-1 after 400 cycles at 1000 mA g-1). The mechanism of lithium storage and the formation of SEI film are systematically elucidated. This work provides an effective strategy for synthesizing promising Mo-cluster compound-based anodes for high-performance LIBs.

Noncrystalline Carbon Anodes for Advanced Sodium-Ion Storage.

Developing an anode with excellent rate performance, long-cycle stability, high coulombic efficiency, and high specific capacity is one of the key research directions of sodium-ion batteries. Among all the anode materials, noncrystalline carbon (NCC) has great possibilities according to its supreme performance and low cost, but with the complexity and variability of the structure. With the in-depth study of the sodium storage behaviors of NCC in recent years, three modes of interlayer intercalation, clustering into micropores, and adsorption are reported and summarized. Although the storage mechanism has gradually become more evident, the complex behavior of the ions at different voltage regions, especially in the low-voltage (plateau) region, still remains controversial. It is essential to understand further the relationship between ions and NCC structure during energy storage processes. Based on the summary of previous works, this article has reviewed the storage mechanism of sodium ions in NCC and evaluated the structure-behavior relationship between sodium-ion storage and the carbon structure.

Operando mechanistic and dynamic studies of N/P co-doped hard carbon nanofibers for efficient sodium storage.

In situ Raman and electrochemical results reveal that Na+ adsorbs on the surface/defective sites of N/P-HCNF and inserts randomly into its turbostratic nanodomains in the dilute state without a staged formation, which can facilitate fast Na+ diffusion kinetics for efficient sodium storage.

Oxygen vacancies boosted the electrochemical kinetics of Nb2O5-x for superior lithium storage.

The introduction of oxygen vacancies (OVs) into Nb2O5 can not only provide more active sites for lithium storage but also change the electronic structure of Nb2O5 to boost electron/ion transport kinetics. Consequently, the defective Nb2O5-x exhibits high lithium storage capacity, superior rate capability, and cycling stability.

Size-controllable synthesis of Zn2GeO4 hollow rods supported on reduced graphene oxide as high-capacity anode for lithium-ion batteries.

Germanium-based ternary oxides have aroused wide attention as an anode for high-performance lithium-ion batteries (LIBs). Nevertheless, they usually suffer a large volume expansion and rapid capacity fading during lithiation/delithiation cycles. To address this issue, herein, Zn2GeO4/RGO composites are synthesized with Zn2GeO4 hollow rods in-situ grown on reduced graphene oxide (RGO) sheets. The Zn2GeO4 hollow rods can be facilely adjusted from nano- to micro-size. The lithium storage performances of the composites strongly depend on the size of Zn2GeO4 hollow rods and the content of RGO. The optimized Zn2GeO4/RGO composite exhibits a pseudocapacitance-dominated Li+ storage performance, with a large reversible capacity of 1005 mAh g-1 after 100 cycles at 0.5 A g-1, an excellent rate capability (515 mAh g-1 at a high rate of 5 A g-1) and a good long cycling stability of 500 cycles with a low capacity loss of 0.05% per cycle at 1 A g-1. The outstanding electrochemical performance can be attributed to the unique composition and microstructure of the material as well as the synergistic effect of the conductive RGO sheets and the hollow Zn2GeO4 nanostructure. This work provides a promising anode for high-performance LIBs and a useful inspiration for further improving the Ge-based ternary oxide anodes.

Interface Engineering of CoS/CoO@N-Doped Graphene Nanocomposite for High-Performance Rechargeable Zn-Air Batteries.

Low cost and green fabrication of high-performance electrocatalysts with earth-abundant resources for oxygen reduction reaction (ORR) and oxygen evolution reaction (OER) are crucial for the large-scale application of rechargeable Zn-air batteries (ZABs). In this work, our density functional theory calculations on the electrocatalyst suggest that the rational construction of interfacial structure can induce local charge redistribution, improve the electronic conductivity and enhance the catalyst stability. In order to realize such a structure, we spatially immobilize heterogeneous CoS/CoO nanocrystals onto N-doped graphene to synthesize a bifunctional electrocatalyst (CoS/CoO@NGNs). The optimization of the composition, interfacial structure and conductivity of the electrocatalyst is conducted to achieve bifunctional catalytic activity and deliver outstanding efficiency and stability for both ORR and OER. The aqueous ZAB with the as-prepared CoS/CoO@NGNs cathode displays a high maximum power density of 137.8 mW cm-2, a specific capacity of 723.9 mAh g-1 and excellent cycling stability (continuous operating for 100 h) with a high round-trip efficiency. In addition, the assembled quasi-solid-state ZAB also exhibits outstanding mechanical flexibility besides high battery performances, showing great potential for applications in flexible and wearable electronic devices.

Multiple Active Sites of Carbon for High-Rate Surface-Capacitive Sodium-Ion Storage.

Although sodium ion batteries (SIBs) possess many beneficial features, their rate performance, cycling stability, and safety need improvement for commercial applications. Based on the mechanisms of the sodium ions storage in carbon materials, herein we present a multiple active sites decorated amorphous carbon (MAC) with rich structural defects and heteroatom doping as an anode material for SIBs. The full utilization of fast bonding-debonding processes between the active sites and sodium ions could bring a capacitive strategy to achieve superior sodium storage properties. Consequently, after materials characterization and electrochemical evaluation, the as-prepared electrode could deliver high rate and long-life performance. This active-site-related design could be extended to other types of electrode materials, thereby contributing to future practical SIB applications.

Porous Nb4N5/rGO Nanocomposite for Ultrahigh-Energy-Density Lithium-Ion Hybrid Capacitor.

To meet the increasing demands for high-performance energy storage devices, an advanced lithium-ion hybrid capacitor (LIHC) has been designed and fabricated, which delivers an ultrahigh energy density of 295.1 Wh kg-1 and a power density of 41 250 W kg-1 with superior cycling stability. The high-performance LIHC device is based on the uniform porous Nb4N5/rGO nanocomposite, which has an intimate interface between the firmly contacted Nb4N5 and rGO through the Nb(Nb4N5)-O(rGO)-C(rGO) bonds, significantly improving the electron transport kinetics. Moreover, the introduction of rGO nanosheets can prevent the Nb4N5 nanoparticles from agglomeration, not only resulting in a larger specific surface area to provide more active sites but also accommodating the strain during Li ion insertion/deinsertion. Therefore, the Nb4N5/rGO nanocomposite exhibits a higher reversible specific capacity and better rate and cycling performance than the Nb4N5 nanoparticle. In view of the scalable preparation and superior electrochemical characteristics, the Nb4N5/rGO nanocomposite would have great potential practical applications in the future energy storage devices.

Pseudocapacitive performance of binder-free nanostructured TT-Nb2O5/FTO electrode in aqueous electrolyte.

TT-Nb2O5 nanoparticles grown on electrically conducting fluorine-doped tin oxide (FTO) glass were successfully synthesized by a facile one-pot hydrothermal method at low temperature. The as-prepared nanostructured TT-Nb2O5/FTO was directly used as the working electrode to investigate its pseudocapacitive performance without any binder or conductive agent, which exhibited a high specific capacitance of 322 F g-1 at a current density of 3.68 A g-1, excellent rate capability (258.1 F g-1 at a high scan rate of 100 mV s-1 is about 91.6% of that at 5 mV s-1), and good cycling stability (the capacitance retention is 74.3% after 3000 cycles). More importantly, it is the first time electrochemical measurements for Nb2O5 electrode in aqueous electrolyte, which are low-cost and easy to operate, have been carried out.

Nickel-cobalt-layered double hydroxide nanosheet arrays on Ni foam as a bifunctional electrocatalyst for overall water splitting.

Bifunctional electrocatalysts, which are active both for the oxygen evolution reaction (OER) and hydrogen evolution reaction (HER), can increase the efficiency of overall water splitting, which is considered an attractive technology for hydrogen production. In this study, we report NiCo-LDH ultrathin nanosheets grown on nickel foam as a bifunctional electrocatalyst for overall water splitting. When used as OER and HER electrodes, NiCo-LDH/NF demonstrated excellent water splitting performance, achieving a current density of 10 mA cm-2 at 1.66 V. Thus, the synthesis of hierarchical 3D porous structure composed of 2D ultrathin nanosheets in NiCo-LDH/NF demonstrated the significance of structural features for achieving a high electrocatalytic activity in overall water splitting.

Graphitic carbon nitride/BiOCl composites for sensitive photoelectrochemical detection of ciprofloxacin.

Ciprofloxacin, as a second generation of fluoroquinolone antibiotics, has been proved to cause environmental harm and exhibits toxic effects on the wastewater and surface water even at low concentrations due to their continuous input and persistence. Despite tremendous efforts, developing ciprofloxacin detection method with accuracy and sensitivity at low-cost remains a great challenge. Herein, graphitic carbon nitride/BiOCl composite (g-CN/BiOCl) has been designed for a facile and sensitive photoelectrochemical (PEC) monitoring platform of ciprofloxacin at first time. BiOCl can be modified with the g-CN nanosheets which are obtained via solvothermal process at low-temperature conditions. The use of g-CN is shown to strongly enhance the PEC response of BiOCl due to the formation of heterojunctions. The photocurrent generated at the g-CN/BiOCl-modified ITO (with 13wt%g-CN content) is much higher and more stable than that of a BiOCl-modified ITO. Based on these findings, the g-CN/BiOCl-modified ITO was used to design a PEC assay for the antibiotic ciprofloxacin. Furthermore, the limit of detection of the ciprofloxacin PEC sensor has been significantly lowered to 0.2ngmL(-1). In addition, the PEC sensor can detect ciprofloxacin in the wide range of 0.5-1840ngmL(-1).

Photoelectrochemical sensing of 4-chlorophenol based on Au/BiOCl nanocomposites.

The Au/BiOCl composites have been prepared by a facile one-pot ethylene glycol (EG) assisted solvothermal reaction in the presence of ionic liquid 1-hexadecyl-3-methylimidazolium chloride ([C16mim]Cl). During the synthesis procedure, the [C16mim]Cl has been used as Cl source, solvent of this system, and dispersing agent to effectively disperse Au on the surface of BiOCl. The as-prepared samples have been systematically characterized by multiple instruments to investigate the structure, morphology, and photoelectrochemical properties. According to the photoelectrochemical data, the Au/BiOCl composites exhibit better photoelectrochemical performance toward the detection of 4-chlorophenol than that of the pure BiOCl. The photocurrent response of Au/BiOCl modified electrode is high and stable under light irradiation. The proposed Au/BiOCl modified electrode shows a wide linear response ranging from 0.16 to 20mgL(-1) with detection limit of 0.05mgL(-1). It indicates a dramatically promising application of bismuth oxyhalides in photoelectrochemical detection. It will be expected that the present study may be lightly extended to the monitor of other organic pollutants by photoelectrochemical detection of the Au/BiOCl composites.

Multifunctional SA-PProDOT Binder for Lithium Ion Batteries.

An environmentally benign, highly conductive, and mechanically strong binder system can overcome the dilemma of low conductivity and insufficient mechanical stability of the electrodes to achieve high performance lithium ion batteries (LIBs) at a low cost and in a sustainable way. In this work, the naturally occurring binder sodium alginate (SA) is functionalized with 3,4-propylenedioxythiophene-2,5-dicarboxylic acid (ProDOT) via a one-step esterification reaction in a cyclohexane/dodecyl benzenesulfonic acid (DBSA)/water microemulsion system, resulting in a multifunctional polymer binder, that is, SA-PProDOT. With the synergetic effects of the functional groups (e.g., carboxyl, hydroxyl, and ester groups), the resultant SA-PProDOT polymer not only maintains the outstanding binding capabilities of sodium alginate but also enhances the mechanical integrity and lithium ion diffusion coefficient in the LiFePO4 (LFP) electrode during the operation of the batteries. Because of the conjugated network of the PProDOT and the lithium doping under the battery environment, the SA-PProDOT becomes conductive and matches the conductivity needed for LiFePO4 LIBs. Without the need of conductive additives such as carbon black, the resultant batteries have achieved the theoretical specific capacity of LiFePO4 cathode (ca. 170 mAh/g) at C/10 and ca. 120 mAh/g at 1C for more than 400 cycles.

Photoelectrochemical characterization of hydrogenated TiO2 nanotubes as photoanodes for sensing applications.

In this work, hydrogenated TiO2 nanotubes (H-TNTs) electrodes were successfully fabricated via the anodization of a titanium sheet followed by a hydrogenation process. Oxygen vacancies were induced in the crystalline structure of TiO2 nanotubes (TNTs) as shallow donors that enhance the electronic conductivity of the TNTs. This improvement in the electronic conductivity and photoelectrocatalytic (PEC) performance was confirmed and evaluated by a photoelectrochemical characterization. Most importantly, the H-TNTs electrode was able to degrade potassium hydrogen phthalate (strong adsorbent) and glucose (weak adsorbent) indiscriminately. The corresponding photocurrents at the H-TNTs were 2-fold greater than that of the TNTs samples for the same concentrations of the organic compounds. This suggests that the H-TNTs electrode can be a promising sensor for the PEC determination of individual organic compounds or as an aggregative parameter of organic compounds (e.g., chemical oxygen demand).