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Nanopores are ubiquitous across disciplines, ranging from bioscience to energy science. Enhancing their transport properties and energy storage capability is crucial to improving functionality. Dissolutive flow, which involves the removal of geometrical obstructions, can transform solid structures into shapes that are less obstructive. In this study, we utilized molecular dynamics simulations to optimize the shape of nanopores through a dissolution-based approach, resulting in optimized inlet and outlet configurations. Furthermore, we examined the distribution of pressure and stress to elucidate the mechanisms underlying shape evolution and edge effects. Conventional inlets impede liquid flow due to high pressure at the apex, a phenomenon we refer to as the reservoir pattern. As dissolution progresses, the apex pressure is significantly reduced over time, allowing a transition to the sliding pattern. By manipulating the dissolubility, wall velocity, and nanopore length, the optimized shape can be fine-tuned. Experiments conducted at the microscale confirmed the emergence of analogous optimized shapes. Additionally, we investigated the transport properties and energy storage capability of various nanopores using molecular dynamics simulations, demonstrating that the optimized nanopore can significantly reduce the hydrodynamic resistance and accelerate the charging rate. This research offers theoretical insights into nanopore dissolution and presents a viable strategy for the practical fabrication of optimized nanopores.

Recent advancements in radiative cooling technologies have highlighted their potential as sustainable and environmentally friendly cooling solutions. However, while this method offers significant energy savings during hot seasons, it may incur energy losses (overcooling leads to a waste of cooling energy) in colder conditions. The current solution has the problems of a complex process or easy leakage of materials. To address this challenge, we synthesized a SiO 2 nanohybrid (a SiO 2 nanoparticle with elongated polymer chains grafted onto its surface), which modifies the thermoresponsive behavior of radiative cooling composites. Upon incorporation of these nanohybrids into the radiative cooling matrix, it will display significant morphological changes in response to temperature variations, leading to changes in the emissivity of the resulting composite film. What's more, the reflectivity of the composite film was enhanced from 57.26 to 89.37%, increasing the cooling performance by 4 °C in hot weather. Results confirmed that the composite film maintained structural integrity without leakage, demonstrating a robust durability. Overall, the synthesized SiO 2 nanohybrids in this work will offer valuable insights for advancing radiative cooling applications.

Wearable temperature-sensitive electronic skin enables robots to rapidly detect environmental changes and respond intelligently, thereby reducing temperature-related mechanical failures. Additionally, this temperature-sensitive skin can measure and record the temperature of external objects, broadening its potential applications in the medical field. In this study, we designed a thermally sensitive artificial ionic skin using ionic liquids (ILs) as solvents and carbon nanotubes (CNTs) as thermally conductive fillers. The incorporation of ILs into the polymer network enhances thermal stability, while the CNTs establish dual thermal conduction pathways (CNTs-CNTs and CNTs-polymer chain segments), leading to rapid thermal response times of only 16 s. The initiation of IL dissociation at elevated temperatures boosts carrier density, resulting in a substantial improvement in thermal sensitivity (5%/°C). Furthermore, the skin displays remarkable self-healing properties (90%), thereby extending the lifespan of the skin in practical applications. This kind of skin can stably sense the wearer's body temperature and environmental temperature and provide an ideal temperature-sensitive and long-term stable new functional material for the development of human skin such as robots.

The threat posed by biological and chemical warfare agents (BCWA) to national security, the environment, and personal health underscores the need for innovative chemical protective clothing. To address the limitations of conventional activated carbon materials, which are prone to falling off and adsorption saturation, an efficient self-association approach was introduced. In this study, we proposed the immobilization of metal-organic framework (MOF) 808 and Ag nanoparticles onto a polypropylene (PP) fiber membrane using a rapid self-association method facilitated by chitosan (CS). The MOF 808/Ag-based (PP-CS/808-Ag) fiber membrane demonstrated exceptional degradation efficiency, achieving a remarkable rate of t within 2 h for the mustard simulant 2-chloroethyl ethyl sulfide (2-CEES) and a rate of 1/2 within 2 h for the mustard simulant 2-chloroethyl ethyl sulfide (2-CEES) and a rate of t 1/2 = 4.12 min for the G-series simulant dimethyl 4-nitrophenylphosphate (DMNP). A theoretical computational model was developed to determine the overall reaction mechanism, and it was verified that MOF 808 and Ag nanoparticles were mainly involved in the hydrolysis process against 2-CEES and DMNP. The PP-CS/808-Ag composite fiber film was prepared as the core layer, and the fracture strength, bending resistance, and moisture permeability were better than those specified by many countries for biochemical protective clothing, showing that it has a broad application prospect in developing a generation of broad-spectrum bioprotective clothing.

Electrohydrodynamic (EHD) printing is an additive manufacturing technique capable of producing micro/nanoscale features by precisely jetting ink under an electric field. However, as a new technique compared to more conventional methods, commercially available inks designed and optimized for EHD are currently very limited. To address this challenge, a new silver nanoink platform was developed by synthesizing silver nanoparticles in situ with biobased polymer 2-hydroxyethyl cellulose (HEC). Typically used as a thickening agent, HEC is cost-effect, biocompatible, and versatile in developing inks that meet the rheology criteria for high-resolution EHD jetting. This approach significantly outperforms the traditional use of polyvinylpyrrolidone (PVP), enabling the stabilization of high solids content (>50 wt %) nanoinks for over 10 months with an HEC dosage 20 times lower than that required by PVP. The HEC-synthesized silver ink displays excellent electrical properties, yielding resistivities as low as 2.81 μΩ cm upon sintering, less than twice that of pure silver. Additionally, the capability to sinter at low temperatures (<200 °C) enables the use of this ink on polymer substrates for flexible devices. The synthesized nanoinks were also found to be capable of producing precise, high-resolution features by EHD printing with smooth lines narrower than 5 μm printed using a 100 μm nozzle. Additionally, a semiempirical model was developed to reveal the relationship between printing resolution, ink properties, and printing parameters, enabling precise printing control. Moreover, for the first time, the unique ability of EHD to achieve precise fabrication under microgravity was conclusively demonstrated through a parabolic flight test utilizing the HEC-based nanoinks. The study greatly expands the potential of printing thin films for the on-demand manufacturing of electronic devices in space.

Nanoparticles have aroused widespread interest because of their unique surface structure and nano effect, which presents novel characteristics like as sound, light, electricity, magnetism, and thermal properties. However, two critical defects have hindered their applications: (1) poor processability resulting from the high melting temperature (e.g., >1000 °C) for some inorganic nanoparticles; (2) the restriction of the nano effect caused by the easy aggregation of the nanoparticles. To solve those issues, solvent-free nanofluids (SNFs) with hard cores and flexible organic chains were successfully designed and fabricated at the beginning of the twenty-first century. The promising technology of SNFs not only solved the dispersion problem of nanomaterials but also imparted novel functionalization to nanoparticles. Up to now, many researchers have been devoted to developing diverse cores and flexible organic polymer chains to endow SNFs with particular functions, such as conductivity, fluorescence, lubricity, and so on. However, there are few review reports on the research progress in the fabrication and applications of functional SNFs. To gain a better understanding of SNFs, this paper presents an overall investigation into the development, fabrication, as well as the applications of functional SNFs.

Light-propelled nanomotors, which can convert external light into mechanical motion, have shown considerable potential in the construction of a new generation of drug delivery systems. However, the therapeutic efficacy of light-driven nanomotors is always unsatisfactory due to the limited penetration depth of near-infrared-I (NIR-I) light and the inherent biocompatibility of the motor itself. Herein, an asymmetric nanomotor (Pd@ZIF-8/R848@M JNMs) with efficient motion capability is successfully constructed for enhanced photoimmunotherapy toward hepatocellular carcinoma. Under near-infrared-II (NIR-II) irradiation, Pd@ZIF-8/R848@M JNMs convert light energy into heat energy, exhibiting self-thermophoretic locomotion to penetrate deeper into tumor tissues to achieve photothermal therapy. At the same time, functionalized with an immune-activated agent Resiquimod (R848), our nanomotors could convert a "cold tumor" into a "hot tumor", transforming the immunosuppressive microenvironment into an immune-activated state, thus achieving immunotherapy. Dual photoimmunotherapy of the as-developed NIR-II light-driven Pd@ZIF-8/R848@M JNMs demonstrates considerable tumor inhibition effects, offering a promising therapeutic approach in the field of anticancer therapy.

Donor (D)-acceptor (A) copolymer-based organic mixed ionic-electronic conductors (OMIECs) exhibit intrinsic environmental stability for they have tailored energy levels. However, their figure-of-merit ( μC *) is still falling behind the D-D polymers because of morphology deterioration during the electrochemical doping process. Herein, we developed two D-A copolymers with precisely regulated backbone curvature, namely PTBT-P and PTTBT-P. Compared to the curved PTBT-P and previously reported copolymers, PTTBT-P better keeps its backbone linear, leading to a long-range ordered doping morphology, which is revealed by the in operando X-ray technique. This optimized doping morphology enables a significantly improved operando charge mobility ( μ ) of 2.44 cm 2 V -1 s -1 and a μ C * value of 342 F cm -1 V -1 s -1 , one of the highest values in D-A copolymer based on OECTs. Besides, we fabricated PTTBT-P-based electrochemical random-access memories and achieved ideal and robust conductance modulation. This study highlights the critical role of backbone curvature control in the optimization of doping morphology for efficient and robust organic electrochemical devices.

Manipulating magnetization via power-efficient spin-orbit torque (SOT) has garnered significant attention in the field of spin-based memory and logic devices. However, the damping-like SOT efficiency (ξ DL ) in heavy metal (HM)/ferromagnetic metal (FM) bilayers is relatively small due to the strong spin dephasing accompanied by additional spin polarization decay. Furthermore, the perpendicular magnetic anisotropy (PMA) originating from the HM/FM interface is constrained by the thickness of FM, which is unfavorable for thermal stability in practical applications. Consequently, it is valuable to develop systems that not only exhibit large ξ DL but also balance thermal stability. In this work, we designed antiferromagnetic-coupled [Co/Gd] N multilayers, where staggered Co and Gd magnetic moments effectively suppress the spin dephasing and additional spin polarization decay. The ordered Co-Gd arrangements along the out-of-plane direction provide bulk PMA, endowing Pt/[Co/Gd] N high thermal stability. The SOT of Pt/[Co/Gd] N was systematically studied with N, demonstrating a significantly large ξ DL of up to 0.66. The ξ DL of Pt/[Co/Gd] N is greater than those of Pt/Co and Pt/ferrimagnetic alloys. This significant enhancement relies on the effective suppression of spin dephasing in [Co/Gd] N . Our work highlights that the antiferromagnetic-coupled [Co/Gd] N multilayer is a promising candidate for low-consumption and high-density spintronic devices.

The synthesis of anode materials plays an important role in determining the production efficiency, cost, and performance of lithium-ion batteries (LIBs). However, a low-cost, high-speed, scalable manufacturing process of the anode with the desired structural feature for practical technology adoption remains elusive. In this study, we propose a novel method called in situ flash shunt-electrothermal shock (SETS) which is controllable, fast, and energy-saving for synthesizing metal oxide-based materials. By using the example of direct electrothermal decomposition of ZIF-67 precursor loaded onto copper foil support, we achieve rapid (0.1-0.3 s) pyrolysis and generate porous hollow cubic structure material consisting of carbon-coated ultrasmall (10-15 nm) subcrystalline CoO/Co nanoparticles with controllable morphology. It was shown that CoO/Co@N-C exhibits prominent electrochemical performance with a high reversible capacity up to 1503.7 mA h g -1 after 150 cycles at 0.2 A g -1 and stable capacities up to 434.1 mA h g -1 after 400 cycles at a high current density of 6 A g -1 . This fabrication technique integrates the synthesis of active materials and the formation of electrode sheets into one process, thus simplifying the preparation of electrodes. Due to the simplicity and scalability of this process, it can be envisaged to apply it to the synthesis of metal oxide-based materials and to achieve large-scale production in a nanomanufacturing process.

Piezoelectric ceramics, as essential components of actuators and transducers, have captured significant attention in both industrial and scientific research. The "entropy engineering" approach has been demonstrated to achieve excellent performance in lead-based materials. In this study, the "entropy engineering" approach was employed to introduce the morphotropic phase boundary (MPB) into the bismuth ferrite (BF)-based lead-free system. By employing this strategy, a serial of novel "medium to high entropy" lead-free piezoelectric ceramics were successfully synthesized, namely (1- x )BiFeO 3 - x (Ba 0.2 Sr 0.2 Ca 0.2 Bi 0.2 Na 0.2 )TiO 3 (BF- x BSCBNT, x = 0.15-0.5). Our investigation systematically examined the phase structure, domain configuration, and ferroelectric/piezoelectric properties as a function of conformational entropy. Remarkable performances with a largest strain of 0.50% at 100 kV/cm, remanent polarization ∼40.07 μC/cm 2 , coercive field ∼74.72 kV/cm, piezoelectric coefficient ∼80 pC/N, and d 33 * ∼500 pm/V were achieved in BF-0.4BSCBNT ceramics. This exceptional performance can be attributed to the presence of MPB, coexisting rhombohedral and cubic phases, along with localized nanodomains. The concept of high-entropy lead-free piezoelectric ceramics in this study provides a promising strategy for the exploration and development of the next generation of lead-free piezoelectric materials.

The advent of liquid-solid triboelectric nanogenerators (LS-TENGs) has ushered in a new era for harnessing and using energy derived from water. To date, extensive research has been conducted to enhance the output of LS-TENGs, thereby improving water utilization efficiency and facilitating their practical application. However, in contrast to intricate chemical treatment methods and specialized structures, a straightforward operational process and cost-effective materials are more conducive to the widespread adoption of LS-TENGs in practical applications. This work presents a novel method to enhance the output of LS-TENGs by increasing the liquid-solid contact area. The approach involves creating roughness on the solid surface through sandpaper grinding, which is simple in design and easy to operate and significantly reduces the cost of the experiment. The theory is applied to the solid triboelectric layer commonly used in the LS-TENG, demonstrating its universality and wide applicability to improve the output of the LS-TENG. The practical performance of the device is demonstrated by charging the capacitor and external load and driving the hygrometer and commercial 5 W LED light bulb, which can directly light up 300 commercial light-emitting diodes (LEDs) driven by a drop of water. This work provides a new method for the optimization of LS-TENGs and contributes to the wide application of LS-TENGs. This is a significant step forward in the field of energy harvesting and utilization.

Zirconium-based metal-organic frameworks have emerged as promising materials for detoxifying chemical warfare agents (CWAs) due to their remarkable stability and porosity. However, their practical application is hindered by issues with their powder form and poor catalytic performance in solid-phase degradation. To address these challenges, herein, a granular MOF-808 metal-organic gel (G808) is prepared under optimized conditions for catalytic degradation of the simulant 2-chloroethyl ethyl sulfide (2-CEES), a sulfide blister agent, in a neat state under different humidity conditions. The detoxification performance of G808 toward 2-CEES is significantly enhanced as the content of water present increases. The half-life of 2-CEES decontaminated by G808 can be shortened to 816 s, surpassing those of many other benchmark materials. To confirm the mechanism of catalytic degradation, we used gas chromatography, gas chromatography-mass spectrometry, and theoretical calculations. The findings revealed that hydrolysis was the predominant route. Additionally, granular G808 was reusable and adaptable to high-moisture environments, making it an excellent protective material with practical potential.

Tumor recurrence remains the leading cause of treatment failure following surgical resection of glioblastoma (GBM). M2-like tumor-associated macrophages (TAMs) infiltrating the tumor tissue promote tumor progression and seriously impair the efficacy of chemotherapy and immunotherapy. In addition, designing drugs capable of crossing the blood-brain barrier and eliciting the applicable organic response is an ambitious challenge. Here, we propose an injectable nanoparticle-hydrogel system that uses doxorubicin (DOX)-loaded mesoporous polydopamine (MPDA) nanoparticles encapsulated in M1 macrophage-derived nanovesicles (M1NVs) as effectors and fibrin hydrogels as in situ delivery vehicles. In vivo fluorescence imaging shows that the hydrogel system triggers photo-chemo-immunotherapy to destroy remaining tumor cells when delivered to the tumor cavity of a model of subtotal GBM resection. Concomitantly, the result of flow cytometry indicated that M1NVs comprehensively improved the immune microenvironment by reprogramming M2-like TAMs to M1-like TAMs. This hydrogel system combined with a near-infrared laser effectively promoted the continuous infiltration of T cells, restored T cell effector function, inhibited the infiltration of myeloid-derived suppressor cells and regulatory T cells, and thereby exhibited a strong antitumor immune response and significantly inhibited tumor growth. Hence, MPDA-DOX-NVs@Gel (MD-NVs@Gel) presents a unique clinical strategy for the treatment of GBM recurrence.

Composition optimization, structural design, and introduction of external magnetic fields into the catalytic process can remarkably improve the oxygen evolution reaction (OER) performance of a catalyst. NiFe 2 O 4 @(Ni, Fe)S/P materials with a heterogeneous core-shell structure were prepared by the sulfide/phosphorus method based on spinel-structured NiFe 2 O 4 nanomicrospheres. After the sulfide/phosphorus treatment, not only the intrinsic activity of the material and the active surface area were increased but also the charge transfer resistance was reduced due to the internal electric field. The overpotential of NiFe 2 O 4 @(Ni, Fe)P at 10 mA cm -2 (iR correction), Tafel slope, and charge transfer resistance were 261 mV, 42 mV dec -1 , and 3.163 Ω, respectively. With an alternating magnetic field, the overpotential of NiFe 2 O 4 @(Ni, Fe)P at 10 mA cm -2 (without iR correction) declined by 45.5% from 323 mV (0 mT) to 176 mV (4.320 mT). Such enhancement of performance is primarily accounted for the enrichment of the reactive ion OH - on the electrode surface induced by the inductive electric potential derived from the Faraday induction effect of the AMF. This condition increased the electrode potential and thus the charge transfer rate on the one hand and weakened the diffusion of the active substance from the electrolyte to the electrode surface on the other hand. The OER process was dominantly controlled by the charge transfer process under low current conditions. A fast charge transfer rate boosted the OER performance of the catalyst. At high currents, diffusion exerted a significant effect on the OER process and low OH - diffusion rates would lead to a decrease in the OER performance of the catalyst.

Aggregation-induced emission (AIE) is a unique photophysical process, and its emergence brings a revolutionary change in luminescence. However, AIE-based research has been limited to a few classical molecular skeletons, which is unfavorable for in-depth studies of the photophysical characteristics of AIE and the full exploitation of their potential values. There is an urgent need to develop new skeletons to rise to the challenges of an insufficient number of AIE core structures and difficult modification. Here, we report a novel dumbbell AIE skeleton, in which two phenyls are connected through ( E )-3-iminoprop-1-en-1-amine. This skeleton shows extremely strong solid-state emission with an absolute quantum yield up to 69.5%, a large Stokes shift, and typical AIE characteristics, which well resolves the challenge of difficult modification and low luminous efficiency of the traditional AIE skeletons. One-step reaction, high yield, and diversified modification endow the skeleton with great scalability from simple to complicated, or from symmetrical to asymmetrical structures, which establishes the applicability of the skeleton in various scenarios. These molecules self-assemble into highly ordered layer-, rod-, petal-, hollow pipe-, or helix-like nanostructures, which contribute to strong AIE emission. Crystallographic data reveal the highly ordered layer structures of the aggregates with different substituents, and a novel halogen bond-driven self-assembly mechanism that restricts intramolecular motion is clearly discovered. Taking advantage of these merits, a full-band emission system from green to red is successfully established, which displays great potential in the construction of light-emitting films and advanced light-emitting diodes. The discovery of this AIE skeleton may motivate a huge potential application value in luminescent materials and lead to hitherto impossible technological innovations.

Adsorbents, especially those with high removal efficiency, long life, and multi-purpose capabilities, are the most crucial components in an adsorption system. By taking advantage of the liquid-like mobility and crystal-like ordering of liquid crystal materials, a liquid crystal induction method is developed and applied to construct three-dimensional graphene-based adsorbents featuring excellent shape adaptability, a distinctive pore structure, and abundant surface functional groups. When the monoliths are used for water restoration, the large amount of residual oxygen-containing groups is more susceptible to electrophilic attack, thus contributing to cation adsorption (up to 705.4 mg g -1 for methylene blue), while the connected microvoids between the aligned graphene oxide sheets facilitate mass transfer, e.g., the high adsorption capacity for organic pollutants (196.2 g g -1 for ethylene glycol) and the high evaporation rate for water (4.01 kg m -2 h -1 ). This work gives a practical method for producing high-performance graphene-based functional materials for those applications that are sensitive to surface and mass transfer properties.

Renewable electricity from splitting water to produce hydrogen is a favorable technology to achieve carbon neutrality, but slow anodic oxygen evolution reaction (OER) kinetics limits its large-scale commercialization. Electron spin polarization and increasing the reaction temperature are considered as potential ways to promote alkaline OER. Here, it is reported that in the alkaline OER process under an AC magnetic field, a ferromagnetic ordered electrocatalyst can simultaneously act as a heater and a spin polarizer to achieve significant OER enhancement at a low current density. Moreover, its effect obviously precedes antiferromagnetic, ferrimagnetic, and diamagnetic electrocatalysts. In particular, the noncorrected overpotential of the ferromagnetic electrocatalyst Co at 10 mA cm -2 is reduced by a maximum of 36.6% to 243 mV at 4.320 mT. It is found that the magnetic heating effect is immediate, and more importantly, it is localized and hardly affects the temperature of the entire electrolytic cell. In addition, the spin pinning effect established on the ferromagnetic/paramagnetic interface generated during the reconstruction of the ferromagnetic electrocatalyst expands the ferromagnetic order of the paramagnetic layer. Also, the introduction of an external magnetic field further increases the orderly arrangement of spins, thereby promoting OER. This work provides a reference for the design of high-performance OER electrocatalysts under a magnetic field.

Although tremendous efforts have been dedicated to promote the electrochemical stability of sodium metal batteries (SMBs), the uncontrollable dendrites growth and inevitable side reactions at the sodium (Na) anode/electrolyte interface have not been effectively resolved. In this work, a flexible and functionalized 3D framework with mesoporous SnO 2 nanosheet arrays (SnO 2 @CC-12) is fabricated to serve as a sodiophilic matrix toward dendrite-free Na metal anode. The mesoporous SnO 2 nanosheet arrays provide abundant sodiophilic sites and sufficient internal voids, which can not only accelerate electron transport to reduce the local current density of Na anode surface but also manipulate the Na + flux deposition to suppress the growth of Na dendrites. Therefore, the SnO 2 @CC-12-Na symmetric cell exhibits an ultralow overpotential of 9 mV and superior Na plating/stripping stability over 2200 h at 1.0 mA cm -2 . Moreover, the full cells using Na 3 V 2 (PO 4 ) 3 cathode show favorable high-rate performance and impressive long cycling stability with 95.1% capacity retention over 1000 cycles at 500 mA g -1 . This work may provide a new insight into the design of functionalized interface layer with high sodiophilicity toward dendrite-free SMBs.

A promising magnetocaloric effect has been obtained in Ni-(Co)-Mn-X (X = Sn, In, Sb)-based Heusler alloys, but the low isothermal magnetic entropy change Δ S M restricts the further promotion of such materials. Defect engineering is a useful method to modulate magnetic performance and shows great potential in improving the magnetocaloric effect. In this work, dense Ni vacancies are introduced in Ni 41 Mn 43 Co 6 Sn 10 alloys by employing high-energy electron irradiation to adjust the magnetic properties. These vacancies bring about intense lattice distortion to change the distance between adjacent magnetic atoms, leading to a significant enhancement of the average magnetic moment. As a result, the saturation magnetization of ferromagnetic austenite is accordingly improved to generate a high isothermal magnetic entropy change Δ S M of 20.0 J/(kg K) at a very low magnetic field of ∼2 T.

Rechargeable lithium-ion batteries using high-capacity anodes and high-voltage cathodes can deliver the highest possible energy densities among all electrochemical devices. However, there is no single electrolyte with a wide and stable electrochemical window that can accommodate both a high-voltage cathode and a low-voltage anode so far. Here, we propose that a strategy of using a hybrid electrolyte should be applied to realize the full potential of a Ni-rich LiNi 0.8 Co 0.1 Mn 0.1 O 2 (NCM811)-silicon/carbon (Si/C) full cell by simultaneously achieving optimal redox chemistry at both the NCM811 cathode and the Si/C anode. The hybrid-electrolyte design spatially separates the cathodic electrolytes from anodic electrolytes by a Nafion-based separator. The ionic liquid electrolyte (LiTFSI-Pyr 13 TFSI) on the cathode side can stand high work potentials and form a stable cathodic electrolyte intermediate (CEI) on NCM811. Meanwhile, a stable solid electrolyte intermediate (SEI) and high cycling stability can also be achieved on the anode side, enabled by a localized high concentration of ether-based electrolytes (LiTFSI-DME/HFE). The decoupled NCM811-Si/C full cell exhibits excellent long-term cycling performance with ultrahigh capacity retention for over 1000 cycles, thanks to the synergy of the cathode-side and anode-side electrolytes. This hybrid-electrolyte strategy has been proven to be applicable for other high-performance battery systems such as dual-ion batteries (DIB).

Zinc ion batteries have become a new type of energy storage device because of the low cost and high safety. Among the various cathode materials, vanadium-oxygen compounds stand out due to their high theoretical capacity and variable chemistry valence state. Here, we construct a 3D spongy hydrated vanadium dioxide composite (O d -HVO/rG) with abundant oxygen vacancy defects and graphene modifications. Thanks to the stable structure and abundant active sites, O d -HVO/rG exhibits superior electrochemical properties. In aqueous electrolyte, the O d -HVO/rG cathode provides high initial charging capacity (428.6 mAh/g at 0.1 A/g), impressive rate performance (186 mAh/g even at 20 A/g), and cycling stability, which can still maintain 197.5 mAh/g after 2000 cycles at 10 A/g. Also, the superior specific energy of 245.3 Wh/kg and specific power of 14142.7 W/kg are achieved. In addition, MXene/O d -HVO/rG cathode materials are prepared and PAM/ZnSO 4 hydrogel electrolytes are applied to assemble flexible soft pack quasi-solid-state zinc ion batteries, which also exhibit excellent flexibility and cycling stability (206.6 mAh/g after 2000 cycles). This work lays the foundation for advances in rechargeable aqueous zinc ion batteries, while revealing the potential for practical applications of flexible energy storage devices.

The sluggish sulfur reduction reaction, severe shuttle effect, and poor conductivity of sulfur species are three main problems in lithium-sulfur (Li-S) batteries. Functional materials with a strong affinity and catalytic effect toward polysulfides play a key role in addressing these issues. Herein, we report a defect-rich amorphous a-Fe 3 O 4- x /GO material with a nanocube-interlocked structure as an adsorber as well as an electrocatalyst for the Li-S battery. The composition and defect structure of the material are determined by X-ray diffraction, high-resolution transmission electron microscopy, Raman spectroscopy, and X-ray photoelectron spectroscopy measurements. The distinctive open framework architecture of the as-engineered composite inherited from the metal-organic framework precursor ensures the stability and activity of the catalyst during extended cycles. The oxygen defects in the amorphous structure are capable of absorbing polysulfides and similarly work as catalytic centers to boost polysulfide conversion. Taking advantage of a-Fe 3 O 4- x /GO on the separator surface, the Li-S battery shows a capacity over 610 mA h g -1 at 1 C and a low decay rate of 0.12% per cycle over 500 cycles and superior rate capability. The functional material made via the low-cost synthesis process provides a potential solution for advanced Li-S batteries.

Previous results indicated that acceptor doping was considered an effective clue to substantially suppress electronic thermal conductivity and in the meanwhile hold a rather low lattice thermal conductivity in high Yb-filled skutterudites. However, the strength of ionized impurity scattering needs to be regulated elaborately to balance the enhanced Seebeck coefficient and the deteriorated carrier mobility. In this work, Ge doping not only synergistically modulates the Fermi energy level and strength of ionized impurity scattering to an optimal range and attains a benign power factor but also offers a valuable opportunity to further suppress κ e and κ in the classic Yb 0.3 Co 4 Sb 12 alloy. Since the Yb 0.3 Co 4 Sb 11.75 Ge 0.25 sample is endowed with the most highlighted ZT value in the device application temperature range, a promising average ZT value of 1.00 across the 300-823 K is achieved, reaching up to the level of a typical triple-filled skutterudite, which is highly desirable for achieving a satisfactory theoretical conversion efficiency of ∼14.5%. Our work corroborates that the ionized impurity strength is an extremely critical benchmark to obtain desirable thermoelectric performance in the high Yb-filled skutterudites.

3D monolithic reactor has shown great promise for varied heterogeneous catalysis reactions including water treatment, energy generation and storage, and clean fuel production. As a natural porous material, macroporous wood is regarded as an excellent support for inorganic catalyst due to its abundant polar functional groups and channels. On the other hand, a metal organic framework (MOF) has been widely used as heterogeneous catalyst due to its high specific surface area and large amount of microporosities. Combining macroporous wood and a microporous MOF is expected to produce a high-performance 3D reactor and is demonstrated here for Fischer-Tropsch synthesis. The carbonized MOF/wood reactor retains the original cellular structure with over 180 000 channels/cm 2 . When being decorated with hexagonal-shaped core-shell Co@C nanoparticles aggregates derived from Co-MOF, the MOF/wood reactor resembles a multi-cylinders reactor for Fischer-Tropsch synthesis. Because of the unique combination of macro- and microporous hierarchical structure, the 3D MOF/wood reactor demonstrates exceptional performance under high gas hourly space velocity (81.2% CO conversion and 48.5% C 5+ selectivity at 50 L·h -1 ·g cat -1 GHSV). This validates that MOF/wood can serve as a multi-cylinders and high-power reactor for catalytic reactions, which is expected to be applicable for environmental and energy applications.

A multi-functional polymer with aggregation-induced emission (AIE)-active salicylaldehyde azine (SA) functionality and reactive oxygen species (ROS)-responsive thioether groups is readily prepared via thiol-ene click polymerization of SA derivative diacrylate monomer, poly(ethylene glycol) diacrylate, and 3,6-dioxa-1,8-octanedithiol. The obtained AIE-active polymer exhibited an unexpected strong emission in amide solvents compared to that in other common organic solvents that was dramatically decreased by adding a trace amount of water, suggesting that the polymer could be utilized as a water trace indicator in amide solvents. In the backbone, the PEG segments make the polymer well dispersed in water and the ROS-responsive thioether groups enable this polymer as a promising ROS scavenger, with embedded SA moieties as a fluorescent indicator for the hemolysis determination. Due to the ability of SA moieties to complex with Cu 2+ , this AIE polymer can also be utilized as a fluorescent sensor for selective Cu 2+ detection in real-world water samples. Thus, this multi-functional polymer is anticipated to be well applied in biological and environmental applications.

Because of the prevailing environment and energy challenges, there has been a growing interest in biobased materials for thermal insulation application. Although cellulose aerogel has been considered as an excellent thermal insulating material, its thermal conductivity is generally negatively affected by the interconnected internal pores. Herein, it is demonstrated that a cellulose nanofibril (CNF)/emulsion composite aerogel with quasi-closed internal pores can be facilely fabricated by Pickering emulsion templating and solvent exchange methods. The CNF-stabilized oil-in-water Pickering emulsion (with an average diameter of 1.3 μm) can be converted into quasi-closed pores by sequential solvent exchange to acetone and tert -butanol (TBA), followed by freeze-drying from TBA to suppress the formation of large ice crystals. The presence of quasi-closed pores from emulsion templating is verified by both confocal microscopy and scanning electron microscopy images and is confirmed to reduce thermal conductivity to as low as 15.5 mW/(m K). Compared to the CNF aerogel, increasing emulsion content can lead to better volume retention with significantly reduced density (11.4 mg/cm 3 ), increased mesoporosity, and enhanced specific modulus (18.2 kPa/(mg/cm 3 )) and specific yield strength (1.6 kPa/(mg/cm 3 )). In addition, the CNF/emulsion composite aerogel also demonstrates superb flexibility and infrared shielding performance.

Although halogenation has been widely regarded as an effective approach to adjust the properties of organic semiconductors, systematic investigation on the comparison of nonhalogenated and halogenated polymer acceptors only received minor attention in all-polymer solar cell (all-PSC) community. Herein, we report three IDIC-based narrow band gap polymer acceptors, PIDIC2T, PIDIC2T2F, and PIDIC2T2Cl, which are composed of IDIC-C16 building blocks as acceptor units, linking pristine bithiophene, fluorinated bithiophene, or chlorinated bithiophene as donor units. Although these three polymer acceptors exhibit nearly identical lowest unoccupied molecular orbital (LUMO) levels of ca. -3.87 eV with a similar optical band gap of ca. 1.54 eV, we found that different halogen species significantly affect the electron mobility and thin-film morphology of the polymer acceptors. All-PSCs were fabricated by pairing three polymer acceptors with a PBDB-T polymer donor, while PIDIC2T2Cl delivered a highest power conversion efficiency (PCE) of 5.34% due to its favorable bulk morphology with smaller root-mean-square (rms) roughness values, which induce the relatively more balanced charge carrier mobilities. By blending the fluorinated analogue of PBDB-T, PM6, further improved V OC , J SC , and fill factor (FF) of devices were achieved (5.46% for PM6:PIDIC2T, 4.96% for PM6:PIDIC2T2F, 7.11% for PM6:PIDIC2T2Cl), which can be due to the synergistic effect of the deeper highest occupied molecular orbital (HOMO) energy level of PM6, enhanced crystallinity, and more matched charge transport. This systematic study provides an insight into the influence of halogenation (fluorination and chlorination) on the optoelectrical properties of n-type organic semiconductors and demonstrates an efficient strategy that the design guideline for polymer acceptors can be enriched by backbone halogenation to further develop high-performance all-PSCs.

Carbon dots (CDs) have been widely studied for their excellent properties. However, most of the prepared CDs only show strong emission in the blue to green region, which greatly limits the application of CDs in the biomedical field. In this report, a new design strategy of long-wavelength CDs was reported. The orange phenyl-CDs with good optical properties and biocompatibility were successfully prepared by changing the substituted group of the o -phenylenediamine and the main emission band of phenyl-CDs was in the far-red region. With the increase of polarity, the wavelength of phenyl-CDs red-shifts and the fluorescence intensity decreases, demonstrating their sensitive polarity response function. In addition, phenyl-CDs can achieve ultrafast target imaging of lysosome within 40 s through clathrin-mediated endocytosis. Finally, phenyl-CDs were successfully applied for monitoring lysosomal polarity induced by drugs, which is helpful in getting a better understanding of the physiological and pathological processes of lysosomes. This report provides an important theoretical basis for the rational design and precise synthesis of long-wavelength fluorescent CDs.

The development of membranes with low fuel crossover and high fuel efficiency is a key issue in direct borohydride fuel cells (DBFCs). In previous work, we produced a poly(vinyl alcohol) (PVA)-anion-exchange resin (AER) membrane with a low fuel crossover and a low fuel efficiency by introducing Co ions. In this work, a bilayer membrane was designed to improve the fuel efficiency and cell performance. The bilayer membrane was prepared by casting a PVA-AER wet gel onto the partially desiccated Co-PVA-AER gel. The bilayer membrane showed a borohydride permeability of 1.34 × 10 -6 cm 2 ·s -1 , which was even lower than that of the Co-PVA-AER membrane (1.98 ×10 -6 cm 2 ·s -1 ) and the PVA-AER membrane (2.80 × 10 -6 cm 2 ·s -1 ). The DBFC using the bilayer membrane exhibited a higher fuel efficiency (37.4%) and output power (1.73 Wh) than the DBFCs using the Co-PVA-AER membrane (33.3%, 1.27 Wh) and the PVA-AER membrane (34.3%, 1.2 Wh). Furthermore, the DBFC using the bilayer membrane achieved a peak power density of 327 mW·cm -2 , which was 2.14 times of that of the DBFC using the PVA-AER membrane (153 mW·cm -2 ). The drastic improvement benefited from the bilayer design, which introduced an interphase to suppress fuel crossover and avoided unnecessary borohydride hydrolysis.

Inspired by the gas-trapped mechanism underwater of Argyroneta aquatica , we prepared a superhydrophobic yarn with a fiber network structure via a facile and environmentally friendly method. Attributed to the low surface energy, the superhydrophobic fiber network structure on the yarn is able to trap and transport bubbles directionally underwater. The functional yarn has good superhydrophobic and superaerophilic properties underwater to realize the directional transport of bubbles underwater without being pumped. We designed demonstration experiments on the antibuoyancy directional bubble transportation, which indicated the feasibility in the applications of gas-related fields. Significantly, on further testing, where the superhydrophobic yarn is put into a U-shaped pipe, we obtain a gas-siphon underwater with a high flux. The superhydrophobic fiber structure yarn can trap the gas underwater to enable the self-starting behavior while no manual intervention is used. The gas-siphon can convey gas over the edge of a vessel and deliver it at a higher level without energy input, which is driven by the differential pressure. The relationship between the differential pressure and the volume flux of transport bubbles is investigated. The experimental results show that the prepared superhydrophobic yarn has the advantages of good stability, easy preparation, and low cost in bubble continuous transportation underwater, which provides a novel strategy for the development and application of new technologies such as directional transportation, separation, exhaustion, and collection of gases in water.

Herein, we demonstrate a synergistic combination of novel mechanisms in aluminum (Al)-alloyed Yb 0.3 Co 4 Sb 12 -based thermoelectric materials to address both reduction in thermal conductivity and concomitant enhancement in power factor (PF). Upon Al alloying, CoAl nanoprecipitates are embedded in the matrix, leading to (1) significant local strain and thus intensified phonon scattering and (2) carrier injection because of interphase electron transfer. Moreover, by decreasing the Yb filling fraction, not only is the electronic thermal conductivity significantly suppressed but also the carrier concentration is modulated to the optimum range, thus resulting in the dramatically boosted PF, especially below 773 K. As a result, a peak ZT value of 1.36 at 873 K and ZT ave of 0.96 from 300 to 873 K were obtained in Yb 0.21 Co 4 Sb 12 /0.32CoAl. Last but not the least, the mechanical properties of the Al-alloyed samples were considerably improved through CoAl precipitate hardening, offering great potential for commercial applications.

Bi-based Zintl phase CaMg 2 Bi 2 is a promising thermoelectric material. Here, we report that the high-concentration point defects induced by equivalent Zn doping on the Mg site significantly enhance phonon scattering and then suppress lattice thermal conductivity by 50% at room temperature. Subsequently, partial substitution of divalent calcium ions with alkali-ion doping (Li, Na, K) not only optimizes the electrical transport properties by increasing the carrier concentration but also further reduces the lattice thermal conductivity through crystal disorder. Finally, the synergistic effect of Zn and Li co-doping leads to a high ZT of ∼1.0 at 873 K and an average ZT of 0.6 between 300 and 873 K for Ca 0.995 Li 0.005 Mg 1.9 Zn 0.1 Bi 1.98 . This work demonstrates an instructive method to reduce the lattice thermal conductivity via doping at the Mg site, which has never been reported in the CaMg 2 Bi 2 system. Moreover, high-performance Ca 0.995 Li 0.005 Mg 1.9 Zn 0.1 Bi 1.98 alloy does not contain any toxic elements and expensive rare earth elements, which is of great significance for the development of environment-friendly thermoelectric materials.

A tiny amount of Mn is doped in In 0.15 Sb 1.85 Te 3 sample to tailor its carrier concentration, thus boosting the power factor and suppressing the bipolar effect. Furthermore, large amounts of nanotwins are constructed to effectively scatter the phonons and reduce the lattice thermal conductivity. As a result, the zT value of Mn 0.02 In 0.15 Sb 1.83 Te 3 is enhanced up to 1.0 at 673 K, making this material a robust candidate for medium-temperature (500-673 K) thermoelectric applications. Then combining with the low-temperature thermoelectric material Mn 0.0075 Bi 0.5 Sb 1.4925 Te 3 previously reported by our group and using nickel as a barrier layer, a high average zT value of 1.08 during a broad temperature range from 303 to 673 K together with an Ohmic contact interface bonding is achieved in the p-type segmented leg fabricated via simple one-step sintering. Finally, the maximum theoretical conversion efficiency with a temperature difference of 370 K reaches ∼12.7%.

Metal-free layered black phosphorus (BP) nanosheets with an excellent photothermal effect and large surface areas have been widely applied in biomedicine but are easily oxidized in ambient conditions yielding insulating phosphorus oxides adsorbed on its surface. Several chemical-functionalized strategies have been explored to protect thin layers of BP; however, the performance of passivated BP often decreases significantly, falling behind the single BP due to the strong structure perturbation. Herein, we designed and constructed 0D/2D hybrid photothermal agents by assembling NIR-II-responsive carbon dots (NIR-II-CDs) on BP nanosheets. NIR-II-CDs improve the ambient stability of BP by isolating them from water and oxygen and enhance the photothermal properties of BP nanosheets. Such NIR-II-CD/BP hybrids strengthen the light-harvesting ability, achieving high photothermal conversion efficiencies in the NIR-I (77.3%) and NIR-II (61.4%) windows, which is significantly higher than that of pristine BP (49.5 and 28.4% at 808 and 1064 nm). Owing to the intrinsic advantage of 1064 nm laser and the excellent PTT effect of our NIR-II-CD/BP hybrids, complete tumor eradication was realized in a deep-tissue tumor model.

Biological photonic nanostructures comprising a hierarchically self-assembled cellulose nanocrystal (CNC) have been exploited for the development of sensing, optoelectronics, and energy materials. Although multiple techniques are used for controlling the optical response and chiral nematic structure of CNC-derived materials, the presence of external studies that pristine CNC has chemoselectivity is not yet reported to implement this destination. Here, we report that the CNC film without modification shows a high optical sensitivity for glucose through color variation from blue to red. Moreover, various glucose homologs or analogs that only differ in terms of the orientation of a hydroxyl group are selectively distinguished through the naked eye. The excellent chemoselectivity of CNC is attributed to carbohydrate-carbohydrate selective hydrogen-bonding interactions. Close binding with glucose induces the rearrangement of a CNC chain and strengthens the repulsive interaction, thus increasing the helical pitch of the chiral nematic structure of the CNC film and changing its macroscopic color. This CNC chemoselectivity presents an unprecedented control of chiral nematic mesoporous carbon through monosaccharide species. The results provide a simple but highly efficient method to tune the optical and structural properties of CNC nanomaterials and to apply them for practical biosensors, chiral separation, and energy applications.

Nanocrystalline powders of 3 wt % Pd-doped SmFe 1- x Mg x O 3 ( x = 0, 0.1, 0.2, and 0.3) were prepared by a sol-gel method and annealed at 750 °C. Pd:SmFe 0.9 Mg 0.1 O 3 has a maximum response at 220 °C. When exposed to 0.5 ppm acetone vapor, the response of undoped SmFeO 3 is 2.26 and the response of Pd:SmFe 0.9 Mg 0.1 O 3 is 7.16. Under light illumination, Pd:SmFe 0.9 Mg 0.1 O 3 has a better sensing performance and lower optimal operating temperature. The sensor shows good selectivity and stability for acetone vapor. The high response and good selectivity of Pd:SmFe 0.9 Mg 0.1 O 3 to ultralow concentrations of acetone vapor indicate its potential for applications in many areas.

The highly specific affinity between probes and phosphopeptides is the fundamental interaction for selective identification of phosphoproteomes that uncover the mechanisms of signal transduction, cell cycle, enzymatic regulation, and gene expression in biological systems. In this study, a metal-affinity probe possessing both interactions of metal oxide affinity chromatography (MOAC) and immobilized metal ion affinity chromatography (IMAC) was facilely prepared by immobilizing zirconium(IV) on a zirconium-organic framework of UiO-66-NH 2 , which holds dual-metal centers of not only the inherent Zr-O cluster but also the immobilized Zr(IV) center. This dual-metal centered zirconium-organic framework (DZMOF) demonstrates as a highly specific metal-affinity probe toward the extraction of phosphopeptides due to the metal-affinity interactions of MOAC and IMAC toward either mono-phosphorylated or multi-phosphorylated peptides. The binding energies of zirconium 3d 5/2 and 3d 3/2 in this DZMOF are 183.07 and 185.47 eV, respectively, which are higher than those of the intact UiO-66-NH 2 (182.84 and 185.17 eV, respectively), confirming the higher metal-affinity interaction between the DZMOF and phosphopeptides. This high metal-affinity probe presents an unprecedented strong performance in anti-nonspecific interference during the capturing of phosphopeptides of β-casein with the molar ratio of β-casein vs bovine serum albumin up to ca. 1:5000. The enrichment of phosphopeptides from a human saliva sample by DZMOF further confirms the great potential of DZMOF in the extraction of low-abundance phosphopeptides for real complex biological samples.

A highly conductive sulfur cathode is crucial for improving the kinetic performance of a Li-S battery. The encapsulation of sulfur in porous nanocarbons is expected to benefit the Li(+) migration, yet the e(-) conduction is still to be improved due to a low graphitization degree of a conventional carbon substrate, especially that pyrolyzed from carbohydrates or polymers. Aiming at facilitating the e(-) conduction in the cathode, here we propose to use ketjen black, a highly graphitized nanocarbon building block to form a conductive network for electrons in a biomass-derived, hierarchically porous carbon sponge by a easily scaled-up approach at a low cost. The specifically designed carbon host ensures a high loading and good retention of active sulfur, while also provides a faster electron transmission to benefit the lithiation/delithiation kinetics of sulfur. The sulfur cathode prepared from the carbon network shows excellent cycling and rate performance in a Li-S battery, rendering its practicality for emerging energy storage opportunities such as grids or automobiles.

Utilizing and reducing carbon dioxide is a key target in the fight against global warming. The photocatalytic performance of bulk graphitic carbon nitride (g-C3N4) is usually limited by its low surface area and rapid charge carrier recombination. To develop g-C3N4 more suitable for photocatalysis, researchers have to enlarge its surface area and accelerate the charge carrier separation. In this work, novel hybrid graphitic carbon nitride and carbon (H-g-C3N4/C) composites with various carbon contents have been developed for the first time by a facile one-step pyrolysis method using melamine and natural soybean oil as precursors. The effect of carbon content on the structure of H-g-C3N4/C composites and the catalytic activity for the photoreduction of CO2 with H2O were investigated. The results indicated that the introduction of carbon component can effectively improve the textural properties and electronic conductivity of the composites, which exhibited imporved photocatalytic activity for the reduction of CO2 with H2O in comparison with bulk g-C3N4. The highest CO and CH4 yield of 22.60 μmol/g-cat. and 12.5 μmol/g-cat., respectively, were acquired on the H-g-C3N4/C-6 catalyst with the carbon content of 3.77 wt % under 9 h simulated solar irradiation, which were more than twice as high as that of bulk g-C3N4. The remarkably increased photocatalytic performance arises from the synergistic effect of hybrid carbon and g-C3N4.

We report on the application of pristine graphene as a drug carrier for phototherapy (PT). The loading of a photosensitizer, chlorin e6 (Ce6), was achieved simply by sonication of Ce6 and graphite in an aqueous solution. During the loading process, graphite was gradually exfoliated to graphene to give its composite with Ce6 (G-Ce6). This one-step approach is considered to be superior to the graphene oxide (GO)-based composites, which required pretreatment of graphite by strong oxidation. Additionally, the directly exfoliated graphene ensured a high drug loading capacity, 160 wt %, which is about 10 times larger than that of the functionalized GO. Furthermore, the Ce6 concentration for killing cells by G-Ce6 is 6-75 times less than that of the other Ce6 composites including GO-Ce6.

Solvent additive processing is important in optimizing an active layer's morphology and thus improving the performance of organic solar cells (OSCs). In this study, we find that how 1,8-diiodooctane (DIO) additive is removed plays a critical role in determining the film morphology of the bulk heterojunction OSCs in inverted structure based on a porphyrin small molecule. Different from the cases reported for polymer-based OSCs in conventional structures, the inverted OSCs upon the quick removal of the additive either by quick vacuuming or methanol washing exhibit poorer performance. In contrast, the devices after keeping the active layers in ambient pressure with additive dwelling for about 1 h (namely, additive annealing) show an enhanced power conversion efficiency up to 7.78% with a large short circuit current of 19.25 mA/cm(2), which are among the best in small molecule-based solar cells. The detailed morphology analyses using UV-vis absorption spectroscopy, grazing incidence X-ray diffraction, resonant soft X-ray scattering, and atomic force microscopy demonstrate that the active layer shows smaller-sized phase separation but improved structure order upon additive annealing. On the contrary, the quick removal of the additive either by quick vacuuming or methanol washing keeps the active layers in an earlier stage of large scaled phase separation.

To simultaneously enhance the osteogenic and antibacterial properties of titanium, we introduced magnesium (Mg), silver (Ag), or both by using the plasma immersion ion implantation (PIII) technique, producing three PIII sample groups, namely, Mg-doped titanium (Mg-PIII), Ag-doped titanium (Ag-PIII), and Mg and Ag codoped titanium (Mg/Ag-PIII). The in vitro antibacterial efficacy of Mg/Ag-PIII group was about 7-10% higher than that of Ag-PIII. In vitro and in vivo results demonstrated that osteogenic property of Mg/Ag PIII group was better than that of Ag-PIII or Mg-PIII. It was believed that the galvanic effects between Mg and Ag NPs played a key role in facilitating the release of Mg but reducing the release of silver, answering for the selective performances of the Mg/Ag-PIII group over bacterial and mammalian cells. This study demonstrated that the integration of multiple functional elements could be realized by the dual-source PIII technique, and in this case, the antibacterial properties and osteogenic property of titanium could be balanced.

Introducing hierarchical microstructure and bioactive trace elements simultaneously onto the surface of titanium implant is a very effective way to improve the osseointegration between bone and implant. In this work, hierarchical topography was prepared on Ti surface via acid etching and sandblasting (SLA) to form micropits and microcavities then underwent Ca plasma immersion ion implantation (Ca-PIII) process. The surface wettability and roughness did not change obviously before and after Ca-PIII process. The in vitro evaluations including cell adhesion, activity, alkaline phosphatase (ALP), osteogenic genes (Runx2, OSX, ALP, BSP, Col1a1, OPN, and OC), and protein (BSP, Col1a1, OPN, and OC) expressions revealed that the introduction of Ca ions onto the surface of SLA-treated Ti can promote greater osteoblasts adhesion, spread and proliferation, which in return further accelerated the maturation and mineralization of osteoblasts. More importantly, in vivo evaluations including Micro-CT evaluation, histological observations, push-out test, sequential fluorescent labeling and histological observations verified that Ca-SLA-treated Ti implants could efficiently promote new bone formation in early times. These promising results suggest that Ca-SLA-treated Ti has the potential for future application in orthopedic field.

Prevention of implant loosening and infection is crucial to orthopedic and dental surgeries. In this work, the surface of stainless steel (SS) was modified by silver-sourced plasma immersion ion implantation (Ag-PIII). Metallic silver nanoparticles with various diameters and distributions were fabricated on the SS surfaces after treatment with Ag-PIII for 0.5 and 1.5 h, respectively. The osteogenic activity and antimicrobial properties of SS before and after Ag-PIII treatment were evaluated using in vitro and in vivo tests. The results demonstrated that Ag-PIII treatment not only promoted the antibacterial activity of SS but also enhanced the osteogenic differentiation of human bone marrow stromal cells.

Different composite films prepared by coupling ZnO and nitrogen-doped ZnO (N-ZnO) were used to photodegrade humic acids (HA). The catalysts exhibit an activity in the order of glass/ZnO/N-ZnO > glass/N-ZnO >glass/ZnO > glass/N-ZnO/ZnO when light is irradiated from the film to glass substrate. However, glass/ZnO/N-ZnO exhibits a lower activity than glass/N-ZnO/ZnO when light is illuminated from glass to film. Moreover, glass/ZnO/N-ZnO shows a lower activity when light is irradiated from glass to film than that irradiated in the opposite direction. These results suggest that it is not always the case that the presence of a heterojunction at interface of two semiconductors can definitely result in improving the photoactivity of the heterostructure although it can suppress the recombination of photogenerated charge carriers. They also indicate that photodegradation of HA is mainly via the oxidization by HO• (rather than directly by O(2)(-) and h(+)), which is produced mainly by the reactions with h(+). This implies the importance of fabrication a right heterojunction at the interface between the composite materials when they are used for photocatalysis. We envision that this work will help to develop new photocatalysts, as well as to understand better the photocatalytic mechanism.