A critical challenge in the commercialization of layer‐structured Ni‐rich materials is the fast capacity drop and voltage fading due to the interfacial instability and bulk structural degradation of ...the cathodes during battery operation. Herein, with the guidance of theoretical calculations of migration energy difference between La and Ti from the surface to the inside of LiNi0.8Co0.1Mn0.1O2, for the first time, Ti‐doped and La4NiLiO8‐coated LiNi0.8Co0.1Mn0.1O2 cathodes are rationally designed and prepared, via a simple and convenient dual‐modification strategy of synchronous synthesis and in situ modification. Impressively, the dual modified materials show remarkably improved electrochemical performance and largely suppressed voltage fading, even under exertive operational conditions at elevated temperature and under extended cutoff voltage. Further studies reveal that the nanoscale structural degradation on material surfaces and the appearance of intergranular cracks associated with the inconsistent evolution of structural degradation at the particle level can be effectively suppressed by the synergetic effect of the conductive La4NiLiO8 coating layer and the strong TiO bond. The present work demonstrates that our strategy can simultaneously address the two issues with respect to interfacial instability and bulk structural degradation, and it represents a significant progress in the development of advanced cathode materials for high‐performance lithium‐ion batteries.
Ti‐doped and La4NiLiO8‐coated Ni‐rich layered oxide cathodes are synchronously and in situ synthesized with the guidance of theoretical calculations, which exhibit good surficial stability, fast interfacial kinetic behaviors, suppressed inconsistent structural degradation in combination with markedly improved electrochemical performance. This work opens a new avenue of designing simple modification approaches and advanced cathodes for high‐energy lithium‐ion batteries.
As an emerging solid‐state refrigeration technology with zero‐emission and high energy conversion efficiency, there is a compelling need for ferroelectric materials with giant electrocaloric effects ...(ECEs) at room temperature suitable for refrigeration applications. The complex perovskite antiferroelectric (AFE), PbMg0.5W0.5O3, containing non‐equivalent B‐site ions with a symmetric giant positive and negative ECE near room temperature is presented. At the Curie temperature of 36 °C, the first‐order AFE–paraelectric phase transition gives rise to a large enthalpy change of 3.92 J g−1, more than four times that of BaTiO3. This leads to a significant ECE under the influence of an electric field. The direct electrocaloric characterization shows that the adiabatic temperature change, ΔT, exhibits symmetric peaks with a giant positive maximum of 1.79 K (ΔS = 1.68 J kg−1 K−1) at 36 °C and a negative maximum of −2.02 K (ΔS = −1.93 J kg−1 K−1) at 34 °C. The ultrahigh magnitude of ΔT near room temperature makes PbMg0.5W0.5O3 a superior electrocaloric material far beyond traditional PbZrO3‐based AFEs. The coexistence of symmetric giant positive and negative ΔT to further improve cooling efficiency is expected. In addition, the good reversibility and negligible leakage current should pave the way for practical applications.
In ordered PbB′0.5B″0.5O3 perovskite oxide ceramic‐PbMg0.5W0.5O3, a first‐order antiferroelectric–paraelectric phase transition occurs near room temperature (36 °C), with a large enthalpy change of 3.92 J g−1. The resultant symmetric giant positive (ΔT = 1.79 K, ΔS = 1.68 J kg−1 K−1) and negative electrocaloric effect (ΔT = −2.02 K, ΔS = −1.93 J kg−1 K−1) favors solid‐state ferroelectric refrigeration application.
Bioactive peptides (BAPs) play a crucial physiological role in human health. To exert their biological effects after oral administration, BAPs have to be transported across the human intestinal ...barrier into the blood circulation system, and must reach their targets in an intact or active form. However, few reviews have summarized current understanding of BAP transport to exhibit activities (bioavailability) and its knowledge gaps.
To obtain a better insight into BAP absorption and aid the design of improved functional foods for humans, this review summarizes and discusses the mechanistic transport pathways, modulatory factors, human studies, solutions to improve the bioavailability, and future perspectives of BAPs.
Both passive (paracellular and passive transcellular diffusion) and active (transporter and transcytosis) routes are possible involved in the BAP transport process, which can be influenced by various properties of peptides, including hydrophobicity, charge, size, molecular weight, amino acid sequence, stability, and enzymatic degradation. Peptidase-resistant BAPs can be transported into the bloodstream at concentrations in the micromolar range and remain intact for several minutes to hours to excise bioactivities. Studies of the effects of BAPs in humans are required, and the bioavailability of BAPs will be at the forefront of future functional food research.
•Transport mechanisms of bioactive peptide are reviewed.•Both passive and active routes may be involved in transporting bioactive peptides.•Transport can be affected by various properties of bioactive peptides.•Bioactive peptides are transported intact into human blood to exert bioactivities.•More studies on the bioavailability of BAPs are required.
Owing to the diversity and ease of preparation of nanomaterials, the rational nanocarriers with a rational design have become increasingly popular in medical researches. Although nanoparticle-based ...drug delivery exhibits great potential, there are some challenges facing like rapid plasma clearance, triggering or aggravation of immune response, etc. Herein, cell-based targeted drug delivery systems have drawn more and more attention owing to low immunogenicity and intrinsic mutation rate, and innate ability to allow targeted delivery. Mesenchymal stem cells (MSCs) have been used in gene and drug delivery. The use of MSCs is a promising approach for the development of gene transfer systems and drug loading strategies because of their intrinsic properties, including homing ability and tumor tropism. By combining the inherent cell properties and merits of synthetic nanoparticles (NPs), cell membrane coated NPs emerge as the time requires. Overall, we provide a comprehensive overview of the utility of MSCs in drug and gene delivery as well as MSC membrane coated nanoparticles for therapy and drug delivery, aiming to figure out the significant room for development and highlight the potential future directions.
Display omitted
Anion and cation substitution is an effective way in modulating electrochemical properties of electrode materials to achieve enhanced performance. Herein, we report our finding in the fabrication of ...advanced binder-free supercapacitor electrodes of hierarchical anion- (phosphorus-) and cation- (zinc- and nickel-) substituted cobalt oxides (denoted as ZnNiCo-P) architectures assembled from nanosheets grown directly on Ni foam. In contrast to the reference Co-P systems, the as-prepared electrode manifests a markedly improved electrochemical performance with a high specific capacity of ~ 958 C g−1 at 1 A g−1 and an outstanding rate capability (787 C g−1 at 20 A g−1) due to its compositional and structural advantages. Density functional theory calculations confirm that the Co species partially replaced by Zn/Ni and O species by P can simultaneously improve the charge transfer behavior and facilitate the OH- adsorption and deprotonation/protonation reaction process. Moreover, an aqueous hybrid supercapacitor based on self-supported ZnNiCo-P nanosheet electrode demonstrates a high energy density of 60.1 Wh kg−1 at a power density of 960 W kg−1, along with a superior cycling performance (89% of initial specific capacitance after 8000 cycles at 10 A g−1 is retained). These findings offer insights into the rational design of transition metal compounds with multi-components and favorable architectures by manipulating the cations and anions of metal compounds for high-performance supercapacitors.
A high-performance mix-metal phosphide nanosheet electrode enables excellent capacity, rate capability, and cycle stability of hybrid supercapacitors. The electrode is composed of hierarchical Zn and Ni co-substituted Co phosphide nanosheet arrays grown on porous Ni foam. Display omitted
•Hierarchical ZnNiCo-P nanosheet arrays grown directly on Ni foam are constructed for the first time.•The resultant binder-free electrodes manifest outstanding electrochemical performances.•The synergetic contribution and structural features together contribute to outstanding electrochemical performance.•The assembled ZnNiCo-P//PPD-rGOs hybrid supercapacitor achieved a high energy density of 60.1 W h kg−1 at a power density of 960 W kg−1.
Neural stem cells (NSCs), capable of ischemia‐homing, regeneration, and differentiation, exert strong therapeutic potentials in treating ischemic stroke, but the curative effect is limited in the ...harsh microenvironment of ischemic regions rich in reactive oxygen species (ROS). Gene transfection to make NSCs overexpress brain‐derived neurotrophic factor (BDNF) can enhance their therapeutic efficacy; however, viral vectors must be used because current nonviral vectors are unable to efficiently transfect NSCs. The first polymeric vector, ROS‐responsive charge‐reversal poly(2‐acryloyl)ethyl(p‐boronic acid benzyl)diethylammonium bromide (B‐PDEA), is shown here, that mediates efficient gene transfection of NSCs and greatly enhances their therapeutics in ischemic stroke treatment. The cationic B‐PDEA/DNA polyplexes can effectively transfect NSCs; in the cytosol, the B‐PDEA is oxidized by intracellular ROS into negatively charged polyacrylic acid, quickly releasing the BDNF plasmids for efficient transcription and secreting a high level of BDNF. After i.v. injection in ischemic stroke mice, the transfected NSCs (BDNF‐NSCs) can home to ischemic regions as efficiently as the pristine NSCs but more efficiently produce BDNF, leading to significantly augmented BDNF levels, which in turn enhances the mouse survival rate to 60%, from 0% (nontreated mice) or ≈20% (NSC‐treated mice), and enables more rapid and superior functional reconstruction.
The first nonviral gene carrier, reactive‐oxygen‐species‐responsive charge‐reversal poly(2‐acryloyl)‐ethyl(p‐boronic acid benzyl)diethylammonium bromide (B‐PDEA), is shown to mediate efficient gene transfection to neural stem cells (NSCs). When BDNF gene plasmids are used, the transfected NSCs homing to the ischemic regions increase animal survival and reconstruct functions.
An improved understanding of the origin of the electrocatalytic activity is of importance to the rational design of highly efficient electrocatalysts for the hydrogen evolution reaction. Here, an ...ambipolar single‐crystal tungsten diselenide (WSe2) semiconductor is employed as a model system where the conductance and carrier of WSe2 can be individually tuned by external electric fields. The field‐tuned electrochemical microcell is fabricated based on the single‐crystal WSe2 and the catalytic activity of the WSe2 microcell is measured versus the external electric field. Results show that WSe2 with electrons serving as the dominant carrier yields much higher activity than WSe2 with holes serving as the dominant carrier even both systems exhibit similar conductance. The catalytic activity enhancement can be characterized by the Tafel slope decrease from 138 to 104 mV per decade, while the electron area concentration increases from 0.64 × 1012 to 1.72 × 1012 cm−2. To further understand the underlying mechanism, the Gibbs free energy and charge distribution for adsorbed hydrogen on WSe2 versus the area charge concentration is systematically computed, which is in line with experiments. This comprehensive study not only sheds light on the mechanism underlying the electrocatalysis processes, but also offers a strategy to achieve higher electrocatalytic activity.
An ambipolar single‐crystal tungsten diselenide (WSe2) semiconductor electrocatalyst is employed as a benchmark system for interfacial model catalysis. By tuning the external electric field, the conductance and carrier of ambipolar WSe2 can be individually modulated. Combining the experimental and theoretical study, it is demonstrated that the electron carrier plays a key role in the hydrogen evolution reaction.
Lithium (Li) metal with high theoretical capacity and low electrochemical potential is the most ideal anode for next-generation high-energy batteries. However, the practical implementation of Li ...anode has been hindered by dendritic growth and volume expansion during cycling, which results in low Coulombic efficiency (CE), short lifespan, and safety hazards. Here, we report a highly stable and dendrite-free Li metal anode by utilizing N-doped hollow porous bowl-like hard carbon/reduced graphene nanosheets (CB@rGO) hybrids as three-dimensional (3D) conductive and lithiophilic scaffold host. The lithiophilic carbon bowl (CB) mainly works as excellent guides during the Li plating process, whereas the rGO layer with high conductivity and mechanical stability maintains the integrity of the composite by confining the volume change in long-range order during cycling. Moreover, the local current density can be reduced due to the 3D conductive framework. Therefore, CB@rGO presents a low lithium metal nucleation overpotential of 18 mV, high CE of 98%, and stable cycling without obvious voltage fluctuation for over 600 cycles at a current density of 1 mA·cm
−2
. Our study not only provides a good CB@rGO host and pre-Lithiated CB@rGO composite anode electrode, but also brings a new strategy of designing 3D electrodes for those active materials suffering from severe volume expansion.
•Low-molecular-weight collagen peptides are associated with various health benefits.•Enzymatic hydrolysis remains the major way to prepare LMW collagen hydrolysates.•Cross-link and hydroxyproline in ...collagen contributes to its resistance to hydrolysis.
Collagen hydrolysates (peptides) derived from food processing byproducts have been used to produce commercially valuable food ingredients due to their potential to trigger certain desirable physiological responses in the body. Low-molecular-weight (LMW) collagen hydrolysates are generally thought to exert better bioactivities than their larger counterparts. However, the preparation of LMW collagen hydrolysates is often impeded by their special structure, cross-linking, and hydroxyproline. This review briefly introduces the motivation of the food industry to prepare LMW collagen hydrolysate from food processing byproducts. We further summarize recent progress on the preparation of LMW collagen hydrolysates and methods to determine the molecular weight. We then discuss the challenges and then provide perspectives on future directions in preparing LMW collagen hydrolysates.
PDF
