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Recently, integrated photonics has attracted considerable interest owing to its wide application in optical communication and quantum technologies. Among the numerous photonic materials, lithium niobate film on insulator (LNOI) has become a promising photonic platform owing to its electro-optic and nonlinear optical properties along with ultralow-loss and high-confinement nanophotonic lithium niobate waveguides fabricated by the complementary metal–oxide–semiconductor (CMOS)-compatible microstructure engineering of LNOI. Furthermore, ferroelectric domain engineering in combination with nanophotonic waveguides on LNOI is gradually accelerating the development of integrated nonlinear photonics, which will play an important role in quantum technologies because of its ability to be integrated with the generation, processing, and auxiliary detection of the quantum states of light. Herein, we review the recent progress in CMOS-compatible microstructure engineering and domain engineering of LNOI for integrated lithium niobate photonics involving photonic modulation and nonlinear photonics. We believe that the great progress in integrated photonics on LNOI will lead to a new generation of techniques. Thus, there remains an urgent need for efficient methods for the preparation of LNOI that are suitable for large-scale and low-cost manufacturing of integrated photonic devices and systems.Photonics: Enabling new applications in optical communication and quantum technologiesA review of recent progress in the microstructure and domain engineering of lithium niobate film on insulator (LNOI) has concluded that it is a promising photonic material for developing integrated nonlinear photonic devices. The review, conducted by a team of researchers from China and led by Hong Liu from Shandong University, found that the high-performance electro-optic and nonlinear optical properties of LNOI makes it an ideal platform for integrated photonics. Furthermore, they also discovered that the microstructures could be constructed on LNOI platforms for photonic circuits using current manufacturing techniques such as complementary metal–oxide–semiconductor technology. The researchers concluded that the large-scale and low-cost manufacturing of integrated photonic devices and systems by mature manufacturing processes could lead to the development of new applications in optical communication and quantum technologies.

Proinflammatory (M1) macrophages play a vital role in antitumor immunity, and regulation of proinflammatory macrophage polarization is critical for immunotherapy. The polarization of macrophages can be regulated by biological or chemical stimulation, but investigations of the regulatory effect of physical stimulation are limited. Herein, regulating macrophage polarization with localized electrical signals derived from a piezoelectric β‐phase poly(vinylidene fluoride) (β‐PVDF) film in a wireless mode is proposed. Charges released on the surface of the β‐PVDF film driven by ultrasonic irradiation can significantly enhance the M1 polarization of macrophages. Mechanistic investigation confirms that electrical potentials rather than reactive oxygen species and mechanical forces enable Ca2+ influx through voltage‐gated channels and establishment of the Ca2+‐CAMK2A‐NF‐κB axis to promote the proinflammatory macrophage response during ultrasound treatment. Piezoelectric material‐mediated electrical signal‐activated proinflammatory macrophages significantly inhibit tumor cell proliferation. A method for electrogenetic regulation of immune cells as well as a powerful tool for engineering macrophages for immunotherapy is provided here. Regulating macrophage polarization with localized electrical signals derived from a piezoelectric β‐phase poly(vinylidene fluoride) (β‐PVDF) film in a wireless mode is proposed, providing a method for electrogenetic regulation of immune cells as well as a powerful tool for engineering macrophages for immunotherapy.

Pre‐intercalation of metal ions into vanadium oxide is an effective strategy for optimizing the performance of rechargeable zinc‐ion battery (ZIB) cathodes. However, the battery long‐lifespan achievement and high‐capacity retention remain a challenge. Increasing the electronic conductivity while simultaneously prompting the cathode diffusion kinetics can improve ZIB electrochemical performance. Herein, N‐doped vanadium oxide (N‐(Zn,en)VO) via defect engineering is reported as cathode for aqueous ZIBs. Positron annihilation and electron paramagnetic resonance clearly indicate oxygen vacancies in the material. Density functional theory (DFT) calculations show that N‐doping and oxygen vacancies concurrently increase the electronic conductivity and accelerate the diffusion kinetics of zinc ions. Moreover, the presence of oxygen vacancies substantially increases the storage sites of zinc ions. Therefore, N‐(Zn,en)VO exhibits excellent electrochemical performance, including a peak capacity of 420.5 mA h g−1 at 0.05 A g−1, a high power density of more than 10 000 W kg−1 at 65.3 Wh kg−1, and a long cycle life at 5 A g−1 (4500 cycles without capacity decay). The methodology adopted in our study can be applied to other cathodic materials to improve their performance and extend their practical applications. N‐doping and oxygen vacancies were introduced on the VO framework by nitridation treatment, which reduced the interaction between the intercalated Zn2+ and the framework, accelerated the migration of Zn ions, and improved the electrochemical performance of the electrode. In addition, the formation mechanism of nitrogen doping and oxygen vacancies were systematically analyzed. The proposed N‐doping mechanism provides a reference for the construction of high‐performance cathode materials.

Suppressing the recombination of photogenerated charges is one of the most important routes for enhancing the catalytic performance of semiconductor photocatalysts. In addition to the built‐in field produced by semiconductor heterostructures and the photo‐electrocatalysis realized by applying an external electrical potential to photocatalysts assembled on electrodes, other strategies are waiting to be scientifically explored and understood. In this work, a Lorentz force–assisted charge carrier separation enhancement strategy is reported to improve the photocatalytic efficiency by applying a magnetic field to a photocatalytic system. The photocatalytic efficiency can be improved by 26% just by placing a permanent magnet beneath the normal photocatalytic system without any additional power supply. The mechanism by which the Lorentz force acts oppositely on the photogenerated electrons and holes is introduced, resulting in the suppression of the photoinduced charge recombination. This work provides insights into the specific role of the Lorentz force in suppressing the recombination of electron–hole pairs in their initial photogenerated states. This suppression would increase the population of charge carriers that would subsequently be transported in the semiconductor. It is believed that this strategy based on magnetic effects will initiate a new way of thinking about photoinduced charge separation. Suppressing the recombination of photogenerated charges is one of the most important routes to enhance the catalytic performance of semiconductor photocatalysts. By applying a magnetic field in a photocatalytic system, a 26% improvement of photocatalytic efficiency is achieved without additional energy supply. The Lorentz force promotes the separation of charge carriers at the initial state.

One‐dimensional (1D) ferroelectric nanostructures, such as nanowires, nanorods, nanotubes, nanobelts, and nanofibers, have been studied with increasing intensity in recent years. Because of their excellent ferroelectric, ferroelastic, pyroelectric, piezoelectric, inverse piezoelectric, ferroelectric‐photovoltaic (FE‐PV), and other unique physical properties, 1D ferroelectric nanostructures have been widely used in energy‐harvesting devices, nonvolatile random access memory applications, nanoelectromechanical systems, advanced sensors, FE‐PV devices, and photocatalysis mechanisms. This review summarizes the current state of 1D ferroelectric nanostructures and provides an overview of the synthesis methods, properties, and practical applications of 1D nanostructures. Finally, the prospects for future investigations are outlined. The current state of 1D ferroelectric nanostructures, including the synthesis methods, properties, and practical applications of 1D nanostructures, is reviewed. The prospects for future investigations are also outlined.

Electrical stimulation holds promise for enhancing neuronal differentiation of neural stem cells to treat traumatic brain injury. However, once the stem cells leave the stimulating material and migrate post transplantation, electrical stimulation on them is diminished. Here, we wrap the stem cells with wireless electrical nanopatches, the conductive graphene nanosheets. Under electromagnetic induction, electrical stimulation can thus be applied in-situ to individual nanopatch-wrapped stem cells on demand, stimulating their neuronal differentiation through a MAPK/ERK signaling pathway. Consequently, 41% of the nanopatch-wrapped stem cells differentiate into functional neurons in 5 days, as opposed to only 16.3% of the unwrapped ones. The brain injury male mice implanted with the nanopatch-wrapped stem cells and exposed to a rotating magnetic field 30 min/day exhibit significant recovery of brain tissues, behaviors, and cognitions, within 28 days. This study opens up an avenue to individualized electrical stimulation of transplanted stem cells for treating neurodegenerative diseases. Electrical stimulation holds promise for enhancing neuronal differentiation of neural stem cells to treat traumatic brain injury. Here, the authors wrap stem cells with wireless electrical nanopatches and apply electrical stimulation in-situ to individual nanopatch-wrapped stem cells on demand

Glioblastoma (GBM) is one of the most fatal central nervous system tumors and lacks effective or sufficient therapies. Ferroptosis is a newly discovered method of programmed cell death and opens a new direction for GBM treatment. However, poor blood–brain barrier (BBB) penetration, reduced tumor targeting ability, and potential compensatory mechanisms hinder the effectiveness of ferroptosis agents during GBM treatment. Here, a novel composite therapeutic platform combining the magnetic targeting features and drug delivery properties of magnetic nanoparticles with the BBB penetration abilities and siRNA encapsulation properties of engineered exosomes for GBM therapy is presented. This platform can be enriched in the brain under local magnetic localization and angiopep‐2 peptide‐modified engineered exosomes can trigger transcytosis, allowing the particles to cross the BBB and target GBM cells by recognizing the LRP‐1 receptor. Synergistic ferroptosis therapy of GBM is achieved by the combined triple actions of the disintegration of dihydroorotate dehydrogenase and the glutathione peroxidase 4 ferroptosis defense axis with Fe3O4 nanoparticle‐mediated Fe2+ release. Thus, the present findings show that this system can serve as a promising platform for the treatment of glioblastoma. A novel composite therapeutic platform combining the magnetic targeting features and drug delivery properties of magnetic nanoparticles with the blood–brain barrier penetration abilities and siRNA encapsulation properties of engineered exosomes for Glioblastoma therapy is presented. Synergistic ferroptosis therapy is achieved by the combined actions of the disintegration of ferroptosis defense axis with Fe3O4 nanoparticle‐mediated Fe2+ release.

Individual theranostic agents with dual-mode MRI responses and therapeutic efficacy have attracted extensive interest due to the real-time monitor and high effective treatment, which endow the providential treatment and avoid the repeated medication with side effects. However, it is difficult to achieve the integrated strategy of MRI and therapeutic drug due to complicated synthesis route, low efficiency and potential biosafety issues. In this study, novel self-assembled ultrasmall Fe 3 O 4 nanoclusters were developed for tumor-targeted dual-mode T 1 /T 2 -weighted magnetic resonance imaging (MRI) guided synergetic chemodynamic therapy (CDT) and chemotherapy. The self-assembled ultrasmall Fe 3 O 4 nanoclusters synthesized by facilely modifying ultrasmall Fe 3 O 4 nanoparticles with 2,3-dimercaptosuccinic acid (DMSA) molecule possess long-term stability and mass production ability. The proposed ultrasmall Fe 3 O 4 nanoclusters shows excellent dual-mode T 1 and T 2 MRI capacities as well as favorable CDT ability due to the appropriate size effect and the abundant Fe ion on the surface of ultrasmall Fe 3 O 4 nanoclusters. After conjugation with the tumor targeting ligand Arg-Gly-Asp (RGD) and chemotherapy drug doxorubicin (Dox), the functionalized Fe 3 O 4 nanoclusters achieve enhanced tumor accumulation and retention effects and synergetic CDT and chemotherapy function, which serve as a powerful integrated theranostic platform for cancer treatment.

Water splitting for production of hydrogen as a clean energy alternative to fossil fuel has received much attention, but it is still a tough challenge to synthesize electrocatalysts with controllable bonding and charge distribution. In this work, ultrafine S‐doped RuP nanoparticles homogeneously embedded in a N, P, and S‐codoped carbon sheet (S‐RuP@NPSC) is synthesized by pyrolysis of poly(cyclotriphosphazene‐co‐4,4′‐sulfonyldiphenol) (PZS) as the source of C/N/S/P. The bondings between Ru and N, P, S in PZS are regulated to synthesize RuS2 (800 °C) and S‐RuP (900 °C) by different calcination temperatures. The S‐RuP@NPSC with low Ru loading of 0.8 wt% with abundant active catalytic sites possesses high utilization of Ru, the mass catalytic activity is 22.88 times than 20 wt% Pt/C with the overpotential of 250 mV. Density functional theory calculation confirms that the surface Ru (−0.18 eV) and P (0.05 eV) are catalytic active sites for the hydrogen evolution reaction (HER), and the according charge redistribution of Ru is regulated by S and P with reverse electronegativity and electron–donor property to induce a synergistically enhanced reactivity toward the HER. This work provides a rational method to regulate the bonding and charge distribution of Ru‐based electrocatalysts by reacting macromolecules with multielement of C/N/S/P with Ru. Synthesis of electrocatalysts with controllable bonding and charge distribution can optimize charge distribution and phase composition to induce a synergistically enhanced reactivity toward the hydrogen evolution reaction. This work provides a rational method to produce platinum‐like electrocatalysts, and according catalytic active sites are regulated by bonding C/N/S/P in the same molecular structure with Ru.

Rechargeable aqueous zinc‐ion batteries (ZIBs) show promise for use in energy storage. However, the development of ZIBs has been plagued by the limited cathode candidates, which usually show low capacity or poor cycling performance. Here, a reversible Zn//(Na,Mn)V8O20·nH2O system is reported, the introduction of manganese (Mn) ions in NaV8O20 to form (Na,Mn)V8O20 exhibits an outstanding electrochemical performance with a capacity of 377 mA h g−1 at a current density of 0.1 A g−1. Through experimental and theoretical results, it is discovered that the outstanding performance of (Na,Mn)V8O20·nH2O is ascribed to the Mn2+/Mn3+‐induced high electrical conductivity and Na+‐induced fast migration of Zn2+. Other cathode materials derived from (Na,Mn)V8O20·nH2O by substituting Mn with Fe, Co, Ni, Ca, and K are explored to confirm the unique advantages of transition metal ions. With an increase in Mn content in NaV8O20, (Na0.33,Mn0.65)V8O20 ·nH2O can deliver a reversible capacity of 150 mA h g−1 and a capacity retention of 99% after 1000 cycles, which may open new opportunities for the development of high‐performance aqueous ZIBs. Mn‐doped NaV8O20 is synthesized via a one‐step hydrothermal reaction. The Mott–Schottky plots, Tafel curves and calculation results are given to explain the improved cycling performance of Mn‐doped NaV8O20. Other cathode materials derived from (Na,Mn)V8O20·nH2O by substituting Mn with Fe, Co, Ni, Ca, and K are explored to confirm the unique advantages of transition metal ions in NaV8O20.