Latest ArticlesAs one of the most common gynecological malignancies, peritoneal metastasis is a common feature and cause of high mortality in ovarian cancer (OC). Currently, the standard treatment for OC and its peritoneal metastasis is maximal cytoreductive surgery (CRS) combined with platinum-based chemotherapy. Compared with intravenous chemotherapy, traditional intraperitoneal (IP) chemotherapy exhibits obvious pharmacokinetic (PK) advantages and systemic safety and has shown significant survival benefits in several clinical studies of OC patients. However, there remain several challenges in traditional IP chemotherapy, such as insufficient drug retention, a lack of tumor targeting, inadequate drug penetration, gastrointestinal toxicity, and limited inhibition of tumor metastasis and chemoresistance. Nanomedicine-based IP targeting delivery systems, through specific drug carrier design with tumor cells and tumor environment (TME) targeting, make it possible to overcome these challenges and maximize local therapy efficacy while reducing side effects. In this review article, the rationale and challenges of nanomedicine-based IP chemotherapies, as well as their in vivo fate after IP administration, which are crucial for their rational design and clinical translation, are firstly discussed. Then, current strategies for nanomedicine-based targeting delivery systems and the relevant clinical trials in IP chemotherapy are summarized. Finally, the future directions of the nanomedicine-based IP targeting delivery system for OC and its peritoneal metastasis are proposed, expecting to improve the clinical development of IP chemotherapy.
Urea-assisted water electrolysis offers a promising route to reduce energy consumption for hydrogen production and meanwhile treat urea-rich wastewater. Herein, we devised a shear force-involved polyoxometalate-organic supramolecular self-assembly strategy to fabricate 3D hierarchical porous nanoribbon assembly Mn-VN cardoons. A bimetallic polyoxovanadate (POV) with the inherent structural feature of Mn surrounded by [VO6] octahedrons was introduced to trigger precise Mn incorporation in VN lattice, thereby achieving simultaneous morphology engineering and electronic structure modulation. The lattice contraction of VN caused by Mn incorporation drives electron redistribution. The unique hierarchical architecture with modulated electronic structure that provides more exposed active sites, facilitates mass and charge transfer, and optimizes the associated adsorption behavior. Mn-VN exhibits excellent activity with low overpotentials of 86 mV and 1.346 V at 10 mA/cm2 for hydrogen evolution reaction (HER) and urea oxidation reaction (UOR), respectively. Accordingly, in the two-electrode urea-assisted water electrolyzer utilizing Mn-VN as a bifunctional catalyst, hydrogen production can occur at low voltage (1.456 V@10 mA/cm2), which has the advantages of energy saving and competitive durability over traditional water electrolysis. This work provides a simple and mild route to construct nanostructures and modulate electronic structure for designing high-efficiency electrocatalysts.
Rationally design the morphology and structure of electroactive nanomaterials is an effective approach to enhance the performance of aqueous batteries. Herein, we co-engineered the hollow architecture and interlayer spacing of layered double hydroxides (LDH) to achieve high electrochemical activity. The hierarchical hollow LDH was prepared from bimetallic zeolitic imidazolate frameworks (ZIF) by a facile cation exchange strategy. Zn and Cu elements were selected as the second metals incorporated in Co-ZIF. The characteristics of the corresponding derivatives were studied. Besides, the transformation mechanism of CoZn-ZIF into nanosheet-assembled hollow CoZnNi LDH (denoted as CoZnNi-OH) was systematically investigated. Importantly, the interlayer spacing of CoZnNi-OH expands due to Zn2+ incorporation. The prepared CoZnNi-OH offers large surface area, exposed active sites, and rapid mass transfer/diffusion rate, which lead to a significant enhancement in the specific capacitance, rate performance, and cycle stability of CoZnNi-OH electrode. In addition, the aqueous alkaline CoZnNi-OH//Zn showed a maximum energy density/power density of 0.924 mWh/cm2, 8.479 mW/cm2. This work not only raises an insightful strategy for regulating the morphology and interlayer spacing of LDH, but also provides a reference of designing hollow nickel-based nanomaterials for aqueous batteries.
Sodium metal batteries (SMBs) have drawn much attention as complement to lithium metal batteries for next generation high-energy batteries. However, it is still a big challenge to enhance their cycling stability without sufficient sodium reserve in anode, due to the non-uniform Na plating/stripping and uncontrolled Na dendrite growth. Herein, a dual layer host consists of sodiophilic graphene@antimony nanoparticles bottom layer and 3D polyacrylonitrile nanofiber top layer (PAN-G@Sb) is employed to enable highly reversible Na plating/stripping. Thanks to the uniform Na deposition, PAN-G@Sb delivers an outstanding average Coulombic efficiency of 99.8%, highly reversible Na plating/stripping for 1000 cycles at 2.0 mA/cm2, as well as over 1000 h of stable operation in symmetric cells. When paired with a high mass loading Na3V2(PO4)3 (NVP) cathode (16.2 mg/cm2), the full cell (N/P ratio = 1.4) also displays prominent capacity retention of 98.7% after 250 cycles with a high energy density of 284.6 Wh/kg. Moreover, PAN-G@SbNVP anode-free full cell also shows an excellent capacity retention of 91.0% after 50 cycles at 0.5 C, exhibiting the stable operation of high energy SMBs.
Silicon-air batteries (SABs), a new type of semiconductor air battery, have a high energy density. However, some side reactions in SABs cause Si anodes to be covered by a passivation layer to prevent continuous discharge, and the anode utilization rate is low. In this work, reduced graphene oxide (RGO) fabricated via high-temperature annealing or L-ascorbic acid (L.AA) reduction was first used to obtain Si nanowires/RGO-1000 (Si NWs/RGO-1000) and Si nanowires/RGO-L.AA (Si NWs/RGO-L.AA) composite anodes for SABs. It was found that RGO suppressed the passivation and self-corrosion reactions and that SABs using Si NWs/RGO-L.AA as the anode can discharge for more than 700 h, breaking the previous performance of SABs, and that the specific capacity was increased by 90.8% compared to bare Si. This work provides a new solution for the design of high specific capacity SABs with nanostructures and anode protective layers.
For realizing the goals of “carbon peak” and “carbon neutrality”, lithium-ion batteries (LIB) with LiFePO4 as the cathode material have been widely applied. However, this has also led to a large number of spent lithium-ion batteries, and the safe disposal of spent lithium-ion batteries is an urgent issue. Currently, the main reason for the capacity decay of LiFePO4 materials is the Li deficiency and the formation of the Fe3+ phase. In order to address this issue, we performed high-temperature calcination of the discarded lithium iron phosphate cathode material in a carbon dioxide environment to reduce or partially remove the carbon coating on its surface. Subsequently, mechanical grinding was conducted to ensure thorough mixing of the lithium source with the discarded lithium iron phosphate. The reaction between CO2 and the carbon coating produced a reducing atmosphere, reducing Fe3+ to Fe2+ and thereby reducing the content of Fe3+. The Fe3+ content in the repaired LiFePO4 material is reduced. The crystal structure of spent LiFePO4 cathode materials was repaired more completely compare with the traditional pretreatment method, and the repaired LiFePO4 material shows good electrochemical performance and cycling stability. Under 0.1 C conditions, the initial capacity can reach 149.1 mAh/g. It can be reintroduced for commercial use.
Sodium metal has been widely studied in the field of batteries due to its high theoretical specific capacity (~1,166 mAh/g), low redox potential (-2.71 V compared to standard hydrogen electrode), and low-cost advantages. However, problems such as unstable solid electrolyte interface (SEI), uncontrolled dendrite growth, and side reactions between solid-liquid interfaces have hindered the practical application of sodium metal anodes (SMAs). Currently, lots of strategies have been developed to achieve stabilized sodium metal anodes. Among these strategies, modified metal current collectors (MCCs) stand out due to their unique role in accommodating volumetric fluctuations with superior structure, lowering the energy barrier for sodium nucleation, and providing guided uniform sodium deposition. In this review, we first introduced three common metal-based current collectors applied to SMAs. Then, we summarized strategies to improve sodium deposition behavior by optimally engineering the surface of MCCs, including surface loading, surface structural design, and surface engineering for functional modification. We have followed the latest research progress and summarized surface optimization cases on different MCCs and their applications in battery systems.
The ultra-high nickel cathode material has important application prospect in power lithium-ion batteries. However, the poor structural stability and serious surface/interfacial side reactions during long cycles severely hinder the material's practical application. In this paper, Cs+ doping and polymethyl methacrylate (PMMA) coating are used to synergistically modify the NCM955 material. The results show that the corresponding discharge specific capacity of NCMCs-2@P-2 material reaches 152.02 mAh/g at 1 C (1 C = 200 mA/g) and 125.66 mAh/g at 5 C after 300 cycles, and the capacity retention is 78.11% and 72.21%, respectively. In addition, it still maintains 156.36 mAh/g discharge specific capacity at 10 C, and these rate and cycle properties exceed those reported on ultra-high nickel cathode material. Moreover, NCMCs-2@P-2 material has higher migration energy barrier of Ni2+ and lower migration energy barrier of Li+ than that of NCM955 material. Therefore, NCMCs-2@P-2 material has excellent electrochemical properties, which has been proved by a series of structural characterization, theoretical calculation and performance test. The synergistic enhancement of Cs+ doping and PMMA coating accelerates lithium ion diffusion kinetics, stabilizes crystal structure, and inhabits surface/interface side reaction.
The transition metal-catalyzed C-H activation have been considered as increasingly useful approach for installing new functional groups onto organic small molecules due to their high step- and atom-economy, the abundance of hydrocarbon compounds, and the potential for late-stage functionalization of complex organic molecules. The ortho- and meta-C-H activation and functionalization of aromatic compounds have been widely explored in recent years, however the distal para-C-H activation and functionalization has remained a significant challenge because of the difficulty in forming energetically favorable metallacyclic transition states. The utilization of appropriate directing groups or templates as well as the meticulous design of catalysts and ligands has proven to be effective in transition-metal-catalyzed remote para-C-H bonds activation and functionalization of aromatic compounds. This review aims to summarize the strategies for controlling para-selective C-H functionalization using the directing group, template engineering, and catalyst/ligand design under transition metals catalysis in recent years.
Electrocatalytic nitrate reduction reaction (NO3−RR) is a green and competitive method for removing nitrate from water, requiring highly active and long-term stable electrocatalysts. In this work, we report a Cu0 nanorod catalyst with disordered structure (re-Cu NRs), prepared by electrochemical in situ reconfiguration of copper-based nitrides (Cu3N NRs). The amorphous structure allows the exposure of abundant active sites to enhance the electrocatalytic activity because of the disordered atomic arrangement. At a potential of −1.2 V vs. Ag/AgCl, the re-Cu NRs catalyst achieved nearly 100% nitrate conversion within 120 min at a low nitrate concentration (50 mg/L), without the accumulation of nitrite. In-situ DEMS detection reveals that the NO3−RR on re-Cu NRs followed the pathway of *NO3−→ *NO2−→ *NO → *N → *NH → *NH2 → *NH3. Furthermore, combining this proposed pathway with electrochlorination could efficiently transform ammonia into harmless N2 (~99.41%). Theoretical calculations confirm that the amorphous structure on the surface of re-Cu NRs catalysts can facilitate strongly adsorbed nitrate, weaken the rate-determining step of *NH3 → NH3, and suppress hydrogen evolution reaction (HER). This study provides a new approach for designing efficient and stable amorphous catalysts for electrocatalytic nitrate reduction.
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