Multifunctional System Research Articles

Ni‐MOF Engineered System Targeting Macrophage Aurora A Kinase for Bone Loss Prevention Through PD‐L1 Activation

AbstractPostmenopausal bone loss due to estrogen deficiency necessitates effective therapeutic strategies. Our study explores targeting macrophage Aurora A kinase to mitigate bone loss. Aurora A kinase phosphorylation is observed being increased in bone marrow‐derived macrophages (BMDMs) from ovariectomy (OVX) mice, along with a reduction in programmed death‐ligand 1 (PD‐L1) expression. Detailed analysis reveals that PD‐L1 plays an immunomodulatory role by lowering the ratio of T helper 17 cells and regulatory T cells. The metabolic shift toward glycolysis through transcriptome sequencing, induced by Aurora A kinase inhibition, is essential for PD‐L1 expression in BMDMs. The interaction between Aurora A kinase and cytochrome C oxidase subunit 5B is found to enhance PD‐L1 expression. To apply these findings therapeutically, a multifunctional system is developed using a Nickel‐metal organic framework combined with bisphosphonate and MLN8237 (BP@Ni‐MOF/MLN8237). This system targets bone tissues through bisphosphonate and effectively delivers MLN8237 to macrophages, promoting PD‐L1 expression for a favorable immune environment. Moreover, this system exhibits an obvious angiogenic effect. The present study highlights the crucial roles of macrophage Aurora A kinase and PD‐L1 in maintaining bone homeostasis as well as the angiogenesis effect by Ni‐MOF engineered system, presenting a promising therapeutic approach to prevent postmenopausal bone loss.

One-pot sequential aldol condensation and hydrodeoxygenation of furfural and acetone to 1-octanol over multifunctional acid-based catalytic system

One-pot sequential aldol condensation and hydrodeoxygenation of furfural and acetone to 1-octanol over multifunctional acid-based catalytic system

Soft-templating of biomass derivatives into edge-N doped 3D-interconnected hierarchical porous carbon for multi-scenario supercapacitive energy storage

Rational design of the pore structure for carbon materials is of great significance for solving the low specific capacitance and poor rate capability of supercapacitors. A novel soft-templating strategy is proposed by using biomass-derived sodium lignosulphonate as a carbon precursor and sublimable hexamethylenetetramine as a soft template. The hexamethylenetetramine nanoparticles are formed in the confined spaces of the precursor, and then these templates sublime to leave mesopores after the lignosulfonate transformed from linear structure to bulk structure by thermostabilization treatment. A high nitrogen content of 40 wt% in hexamethylenetetramine is also beneficial for the subsequent in-situ N-doping. The as-obtained nitrogen-doped hierarchical porous carbon microspheres possess a high specific surface area of 1416 m2 g−1 with an N-doping content of 4.32 % (86.26 % edge-N). In a two-electrode system, the soft-templating carbon exhibits a decent specific capacitance of 234 F g−1 at 0.1 A g−1, an excellent rate capability of 62.4 % at 50 A g−1, and a high energy density of 8.1 Wh kg−1 at 15.0 kW kg−1 in 6 M KOH aqueous electrolyte. Moreover, advanced additive manufacturing technology of direct ink writing was applied to construct a quasi-solid-state in-plane interdigital microsupercapacitor by using the soft-templating carbon, and it presents a superior areal/volumetric capacitance, rate performance, mechanical stability, and flexibility with PVA/H2SO4 gel electrolyte. This work broadens the pore structure engineering methodology by novel soft-templating biocarbon for multi-functional and multi-scenario energy storage systems.

Photoregulated Supramolecular Polymerization through Halogen Bonding

Supramolecular polymers are able to change their structure, morphology and function in response to external stimuli. However, controlling the independence of stimuli‐responses in these systems is challenging. Herein, we exploit halogen bonding (XB) as a reversible network element to regulate the photoresponsive and adaptive behavior of supramolecular polymers. To this end, we have designed a system comprising an amphiphilic XB acceptor with the ability to self‐assemble in aqueous media (OPE‐Py) and a molecule with a dual photoresponsive and XB donor function [(E)‐Azo‐I]. OPE‐Py self‐assembles in aqueous media into supramolecular polymers, which transform into nanoparticle assemblies upon co‐assembly with (E)‐Azo‐I. Interestingly, a third type of assembly (2D sheets) is obtained if OPE‐Py is treated with (E)‐Azo‐I and exposed to photoirradiation. At ambient conditions, both nanoparticles and 2D sheets remain invariant over time. However, heating dissociates the XB interactions present in both assemblies, resulting in their transformation to the original fiber‐like morphology of OPE‐Py. Thus, breaking the communication between self‐assembly and the stimuli‐responses upon heating restores the original state of the system, drawing parallels to feedback loops in programming language. This work broadens the still limited scope of XB in solution assemblies and paves the way for multifunctional adaptive supramolecular systems.

The Combined Effect of Hypoxia Activation and Radiosensitization by a Multifunctional Nanoplatform System Enhances the Therapeutic Efficacy of Chemoradiotherapy in Pancreatic Cancer

BackgroundPancreatic cancer is a highly malignant tumor, which is still a major global health problem. Chemotherapy and radiotherapy are regularly used in adjuvant therapy for pancreatic cancer but their therapeutic efficacy is limited. MethodsIn the present study, nanoparticle（MSN-AuNPs） was used as a drug carrier loaded with tirapazamine(TPZ) and hyaluronic acid (HA) to synthesize a multifunctional nanoplatform HA@TPZ-MSN-AuNPs (HTMA) for hypoxia activation and radiotherapy sensitization, which can be combined with radiotherapy therapy and synergistically enhance the therapeutic effect in pancreatic cancer. The anti-tumor performance of the nano platform was verified by in vivo and in vitro experiments. ResultFirst, the HA@TPZ-MSN-AuNPs (HTMA) was successfully synthesized. Drug release experiments showed that acidic environment and hyaluronidase promoted drug release in the nanoplatform. In vitro experiments, CCK-8, live-dead staining, clonal formation assay and flow cytometry confirmed the combined anti-tumor effect of hypoxia activation and radiotherapy sensitization with HTMA. In the drug uptake experiment, the nanoplatform showed the function of targeting and binding pancreatic cancer cells. In vivo, HTMA demonstrated good antitumor properties and good biocompatibility. ConclusionsThe nanoplatform had a good targeting effect and synergistic anti-tumor effect. The combination of hypoxia activation and radiotherapy sensitization is a promising strategy for the treatment of pancreatic cancer.

Photoregulated Supramolecular Polymerization through Halogen Bonding.

Supramolecular polymers are able to change their structure, morphology and function in response to external stimuli. However, controlling the independence of stimuli-responses in these systems is challenging. Herein, we exploit halogen bonding (XB) as a reversible network element to regulate the photoresponsive and adaptive behavior of supramolecular polymers. To this end, we have designed a system comprising an amphiphilic XB acceptor with the ability to self-assemble in aqueous media (OPE-Py) and a molecule with a dual photoresponsive and XB donor function [(E)-Azo-I]. OPE-Py self-assembles in aqueous media into supramolecular polymers, which transform into nanoparticle assemblies upon co-assembly with (E)-Azo-I. Interestingly, a third type of assembly (2D sheets) is obtained if OPE-Py is treated with (E)-Azo-I and exposed to photoirradiation. At ambient conditions, both nanoparticles and 2D sheets remain invariant over time. However, heating dissociates the XB interactions present in both assemblies, resulting in their transformation to the original fiber-like morphology of OPE-Py. Thus, breaking the communication between self-assembly and the stimuli-responses upon heating restores the original state of the system, drawing parallels to feedback loops in programming language. This work broadens the still limited scope of XB in solution assemblies and paves the way for multifunctional adaptive supramolecular systems.

In Situ Encapsulation of Atomically Precise Nanoclusters in Reticular Frameworks via Mechanochemical Synthesis.

The combination of atomically precise nanoclusters (APNCs) and reticular frameworks is promising for generating component-specific nanocomposites with emergent properties. However, traditional liquid-phase synthesis often hampers this potential by damaging APNCs and limiting combination diversity. Here, mechanochemical synthesis to explore the encapsulation of diverse oil- and water-soluble APNCs within various reticular frameworks is employed, establishing a database of 21 unique APNC-framework combinations, including metal-organic frameworks (MOFs), covalent-organic frameworks (COFs), hydrogen-bonded organic frameworks (HOFs), and multivariate MOFs. These framework coatings not only spatially immobilize APNCs but also secure their structures, preventing aggregation and degradation while enhancing stability and activity. Encapsulating Au25 in HOFs resulted in a remarkable 315-fold increase in catalytic activity compared to Au25 homogeneous catalyst, highlighting the framework's crucial role in catalytic enhancement. The mechanochemical synthesis strategy facilitates tailored support screening, catering to specific needs, and shows promise for developing multifunctional systems, including enzyme-APNC@frameworks material for cascade reactions.

Multifunctional nano co-delivery system for efficiently eliminating neuroblastoma by overcoming cancer heterogeneity

The high heterogeneity of neuroblastoma (NB) is currently the main challenge in clinical treatment, impeding the complete eradication of the tumor through monotherapy alone. In this study, we propose a combination strategy using a targeted nano co-delivery system (ADRF@Ag2Se) comprising phototheranostic agents, differentiation inducers and chemotherapy drugs for sequential therapy of NB. Upon intravenous injection, ADRF@Ag2Se demonstrates effective tumor targeting by the specific binding of AF7P to MMP14, which is overexpressed on the surface of NB cells. Subsequent implementation of local photothermal therapy (PTT) leverages the robust photothermal conversion capabilities of the amphiphilic photothermal reagent PF. This is followed by the temperature-triggered release of differentiation-inducing agent 13-cis-retinoic acid and chemo-drug doxorubicin to synergistically eliminate the residual lesions. This nanotherapeutic strategy facilitatesin vivotargeted delivery and PTT under the supervision of NIR-II fluorescence, and it also enhances the chemotherapeutic response through differentiation induction of poorly differentiated cancer cells. In the NB tumor model, this co-delivery strategy effectively inhibited tumor growth and significantly prolonged the survival of the mice.

Polarization-multiplexed zoom Moiré metalens for edge-enhanced imaging

Optical image processing with high operational efficiency has been applied as a pre-processing imaging system for image recognition. Edge-enhanced imaging as a high-efficiency optical image processing method is of great significance for feature extraction and target recognition. However, the edge-enhanced imaging system based on the 4F system and the spatial filter transforms mainly work under coherent light illumination conditions, without continuously zooming to track the spatial position of the target. Here, we demonstrate a polarization-multiplexed zoom Moiré metalens for edge-enhanced imaging under incoherent light illumination. Metalens is designed to generate polarization-dependent optical transfer functions that produce edge-enhanced images with a resolution of 1.2 µm by digital subtraction. Furthermore, continuous zoom at the range of 1-2× is realized by constructing a Moiré metalens composed of cascaded metasurfaces. The cascaded metasurfaces consist of two center-aligned dielectric metasurfaces, each with a Moiré phase sensitive to the rotation angle. By rotating the metasurface, the phase profile of the cascaded metasurfaces changes, and the effect of continuous zoom is realized. The focal length can be actively changed from 38 µm to 77 µm with the focusing efficiency of 50.3%. This metalens can be applied to machine vision, microscopic imaging, and promotes the development of multi-functional integrated optical systems.

Design and In Vitro Evaluation of Fluorescent MOF-Core CaCO₃-PEI-FA Shell Nanoparticles for Targeted Therapy of Laryngeal Cancer Cells.

Laryngeal cancer, a common malignant respiratory tumor, is primarily treated through surgery. However, challenges such as recurrence, metastasis, and drug resistance persist. In recent years, multifunctional drug delivery systems (DDS) based on nanoparticles have shown great potential in improving drug loading and release. We developed a biocompatible core-shell nanoparticle system with a zinc-based metal-organic framework (MOF) as the core, named CP1. The shell, composed of polyethyleneimine (PEI), folic acid, and calcium carbonate, forms a composite called CaCO3-PEI-FA. This system enhances biocompatibility and increases the efficacy of biomedical applications. Encapsulating CP1 within the CaCO3-PEI-FA shell allows for the targeted delivery of the anticancer drug doxorubicin (DOX) to laryngeal cancer cells (Hep-2), resulting in the CaCO3-PEI-FA@CP1@DOX system. The CaCO3-PEI-FA composite exhibits strong fluorescence with a peak around 350nm, confirming successful synthesis and demonstrating its potential as a bioimaging probe. Importantly, the nanoparticle system without DOX showed low toxicity to normal human skin fibroblasts (HSF). In vitro cytology experiments revealed a 38% inhibition rate of Hep-2 cells after 24h, highlighting the nanocomposite's significant potential in inhibiting laryngeal cancer cell proliferation and inducing apoptosis, underscoring its promise in targeted laryngeal cancer therapy.

Подходы в совершенствовании нормативной базы в отношении применения мультифокальных интраокулярных линз при хирургическом лечении катаракты

Ultrasound phacoemulsification with intraocular lens (IOL) implantation is the “gold standard” for cataract treatment. Considering the existing requirements for the quality of vision after surgery, there is an increasing demand from patients for IOL implantation, which provides comfortable vision not only at a long distance, but also at a short one without the use of reading glasses (IOL with multifocal properties). The analysis of the existing regulatory framework regarding the possibility and obligation of using this medical product in the provision of specialized medical care – surgical treatment of cataract within the framework of the state guarantee program shows the possibility of using this consumable material without the obligation of the medical organization to consider the wishes of the patient. The change in the structure of the payment tariff for medical care for patients with cataract in 2023, the reduction in the tariff for providing specialized medical care to patients with uncomplicated forms affected the availability of multifocal IOL for patients without specifying the way to obtain this type of service, which makes it relevant to analyze approaches to improving the regulatory framework regarding the use of multifocal intraocular lenses in cataract surgical treatment. There are unsettled clinical, organizational, and economic issues regarding the use of multifocal intraocular lenses (artificial lenses) in the surgical treatment of cataract. There are various approaches (clinical-organizational, economic, legal, information) to improving the regulatory framework, but the approach of decision makers should be complex based on a comprehensive assessment of the economic, clinical, and technological components. Approaches are only a means to achieve a goal: the development of a multifunctional system of state guarantees in the provision of medical services, rational use of available resources.

Microenvironmental pH modulating oxygen self-boosting microalgal prodrug carboxymethyl chitosan/hyaluronic acid/puerarin hydrogel for accelerating wound healing in diabetic rats

Chronic diabetic wounds are characterized by a range of detrimental features, including hypoxia, elevated levels of reactive oxygen species, impaired angiogenesis, chronic inflammation, and an increased susceptibility to bacterial infections. We have developed an innovative multifunctional hydrogel system based on carboxymethyl chitosan, which incorporates embedded microalgae PCC7942 along with hyaluronic acid and puerarin, termed PCC7942@carboxymethyl chitosan/hyaluronic acid/puerarin hydrogel. It demonstrated outstanding capabilities in exudate absorption, mechanical flexibility, hemostatic action, and antibacterial efficacy. Furthermore, it effectively modulated the pH of wound microenvironment through the hydrolysis of amide bonds, thereby establishing a favorable low-pH microenvironment. Microalgae in hydrogel covered in the wound exhibited stable and continuous oxygen production within 24 h, with more efficiency in dissolved oxygen penetration through skin. Furthermore, prodrugs such as hyaluronic acid and puerarin from hydrogel displayed the controlled release behavior and facilitated the fast and enhanced accumulation of drugs at wound site, thereby accelerating the process of wound healing via enhanced angiogenesis and anti-inflammation effects. In summary, the healing-promoting effect of PCC7942@carboxymethyl chitosan/hyaluronic acid/puerarin hydrogel in type 1 diabetic rats can be attributed to the synergistic effects of microalgae, hyaluronic acid, and puerarin, which collectively accelerated wound healing rate and improved the quality of wound recovery.

Silk Composite-Based Multifunctional Pellets for Controlled Release.

Chronic wounds present significant clinical challenges due to the high risk of infections and persistent inflammation. While personalized treatments in point-of-care settings are crucial, they are limited by the complex fabrication techniques of the existing products. The calcium sulfate hemihydrate (CSH)-based drug delivery platform enables rapid fabrication but lacks antioxidant and antibacterial properties, essential to promote healing. To develop a multifunctional platform, a tannic acid (TA)-silk fibroin (SF) complex is engineered and incorporated as an additive in CSH cement. This cement is then cast into pellets to create silk/bioceramic-based composite drug delivery systems, designed for point-of-care use. Compared to neat CSH pellets, the composite pellets exhibit a 7.5-fold increase in antioxidant activity and prolonged antibacterial efficacy (up to 13 d). Moreover, the subcutaneous implantation of the pellets shows no hallmarks of local or systemic toxicity in a rodent model. The pellets are optimized in composition and fabrication to ease market translation. Clinically, the pellets have the potential to be further developed into products to place on wound beds or fill into bone cavities that are designed to deliver the intended therapeutic effect. The developed multifunctional system proves to be a promising solution for personalized treatment in point-of-care settings.

Exploring Wettability: A Key to Optimizing Liquid-Solid Triboelectric Nanogenerators.

Nowadays, the liquid-solid triboelectric nanogenerator (L-S TENG) has gained much attention among researchers because of its ability to be a part of self-powering technology by harvesting ultra-low-frequency vibration in the environment. The L-S TENG works with the principle of contact electrification (CE) and electrostatic induction, in which CE takes place between the solid and liquid. The exact mechanism behind the CE at the L-S interface is still a debatable topic because many physical parameters of both solid and liquid triboelectric layers contribute to this process. In the L-S TENG device, water or solvents are commonly used as liquid triboelectric layers, for which their wettability over the solid triboelectric layer plays a significant role. Hence, this review is extensively focused on the influence of the wettability of solid surfaces on the CE and the corresponding impact on the output performance of L-S TENGs. The present review starts with introducing the L-S TENG, a mechanism that contributes to CE at the L-S interface, the significance of hydrophobic materials/surfaces in TENG devices, and their fabrication methods. Further, the impact of the contact angle over the electron/ion transfer over various surfaces has been extensively analyzed. Finally, the challenges and future prospects of the fabrication and utilization of superhydrophobic surfaces in the context of L-S TENGs have been included. This review serves as a foundation for future research aimed at optimizing the L-S TENG performance and inspiring new approaches in material design and multifunctional energy-harvesting systems.

Transferable, highly crystalline covellite membrane for multifunctional thermoelectric systems

AbstractEmerging freestanding membrane technologies, especially using inorganic thermoelectric materials, demonstrate the potential for advanced thermoelectric platforms. However, using rare and toxic elements during material processing must be circumvented. Herein, we present a scalable method for synthesizing highly crystalline CuS membranes for thermoelectric applications. By sulfurizing crystalline Cu, we produce a highly percolated and easily transferable network of submicron CuS rods. The CuS membrane effectively separates thermal and electrical properties to achieve a power factor of 0.50 mW m−1 K−2 and thermal conductivity of 0.37 W m−1 K−1 at 650 K (estimated value). This yields a record‐high dimensionless figure‐of‐merit of 0.91 at 650 K (estimated value) for covellite. Moreover, integrating 12 CuS devices into a module resulted in a power generation of ~4 μW at ΔT of 40 K despite using a straightforward configuration with only p‐type CuS. Furthermore, based on the temperature‐dependent electrical characteristics of CuS, we develop a wearable temperature sensor with antibacterial properties.image

An Ultrasensitive and Broad-Spectrum MoS2 Photodetector with Extrinsic Response Using Surrounding Homojunction.

As unique building blocks for advancing optoelectronics, 2D semiconducting transition metal dichalcogenides have garnered significant attention. However, most previously reported MoS2 photodetectors respond only to visible light with limited absorption, resulting in a narrow spectral response and low sensitivity. Here, a surrounding homojunction MoS2 photodetector featuring localized p-type nitrogen plasma doping on the surface of n-type MoS2 while preserving a high-mobility underlying channel for rapid carrier transport is engineered. The establishment of p-n homojunction facilitates the efficient separation of photogenerated carriers, thereby boosting the device's intrinsic detection performance. The resulting photoresponsivity is 6.94×104AW-1 and specific detectivity is 1.21×1014 Jones @ 638nm, with an optimal light on/off ratio of ≈107 at VGS = -27V. Notably, the introduction of additional bands within MoS2 bandgap through nitrogen doping leads to an extrinsic broadband response to short-wave infrared. The device exhibits a photoresponsivity of 34AW-1 and a specific detectivity of up to 5.92×1010 Jones @ 1550nm. Furthermore, the high-performance broadband response is further demonstrated through imaging and integration with waveguides, paving the way for next generation of multifunctional imaging systems and high-performance photonic chips.

Magnetic vortex γ-Fe2O3 nanospheres decorated with gold nanoparticles for dual hyperthermia treatment

In this work, multifunctional systems with potential applications for dual control of thermal heat delivery are developed. For this purpose, the nanosystems produced consist of vortex iron oxide nanospheres (VIONS) decorated with different amounts of gold nanoparticles (AuNPs). The VIONS were synthesized using the solvothermal reduction method, resulting in a 204 ± 24 nm diameter and meeting the requirements for biomedical applications. Magnetic measurements revealed that these systems are composed mainly of maghemite (γ-Fe2O3), exhibiting relatively low coercivity and moderate saturation magnetization, both of which serve as indicative attributes of an exceptional magnetic vortex state as validated by electron holography microscopy. The decoration with gold NPs was achieved through deposition-precipitation, involving the deposition of gold hydroxide on the surface of the previously amine-modified iron oxide NPs, followed by the concurrent reduction of Au3+. Furthermore, the gold NP size modulation was investigated by consecutively adding Au3+ to obtain gold NPs that interact with light differently depending on their size. The study provides crucial information that can aid the decoration of magnetic iron oxide nanospheres with AuNPs with tailored magnetic and optical properties; consequently, they may be promising candidates for magnetic and photothermal hyperthermia based on three-dimensional magnetic vortex structures.

Inspiration from Visual Ecology for Advancing Multifunctional Robotic Vision Systems: Bio-inspired Electronic Eyes and Neuromorphic Image Sensors.

In robotics, particularly for autonomous navigation and human-robot collaboration, the significance of unconventional imaging techniques and efficient data processing capabilities is paramount. The unstructured environments encountered by robots, coupled with complex missions assigned to them, present numerous challenges necessitating diverse visual functionalities, and consequently, the development of multifunctional robotic vision systems has become indispensable. Meanwhile, rich diversity inherent in animal vision systems, honed over evolutionary epochs to meet their survival demands across varied habitats, serves as a profound source of inspirations. Here, recent advancements in multifunctional robotic vision systems drawing inspiration from natural ocular structures and their visual perception mechanisms are delineated. First, unique imaging functionalities of natural eyes across terrestrial, aerial, and aquatic habitats and visual signal processing mechanism of humans are explored. Then, designs and functionalities of bio-inspired electronic eyes are explored, engineered to mimic key components and underlying optical principles of natural eyes. Furthermore, neuromorphic image sensors are discussed, emulating functional properties of synapses, neurons, and retinas and thereby enhancing accuracy and efficiency of robotic vision tasks. Next, integration examples of electronic eyes with mobile robotic/biological systems are introduced. Finally, a forward-looking outlook on the development of bio-inspired electronic eyes and neuromorphic image sensors is provided.

New Insights for High-Throughput CO2 Hydrogenation to High-Quality Fuel.

In the case of CO2 thermal-catalytic hydrogenation, highly selective olefin generation and subsequent olefin secondary reactions to fuel hydrocarbons in an ultra-short residence time is a huge challenge, especially under industrially feasible conditions. Here, we report a pioneering synthetic process that achieves selective production of high-volume commercial gasoline with the assistance of fast response mechanism. In situ experiments and DFT calculations demonstrate that the designed NaFeGaZr presents exceptional carbiding prowess, and swiftly forms carbides even at extremely brief gas residence times, facilitating olefin production. The created successive hollow zeolite HZSM-5 further reinforces aromatization of olefin diffused from NaFeGaZr via optimized mass transfer in the hollow channel of zeolite. Benefiting from its rapid response mechanism within the multifunctional catalytic system, this catalyst effectively prevents the excessive hydrogenation of intermediates and controls the swift conversion of intermediates into aromatics, even in high-throughput settings. This enables a rapid one-step synthesis of high-quality gasoline-range hydrocarbons without any post-treatment, with high commercial product compatibility and space-time yield up to 0.9 kggasoline ⋅ kgcat -1 ⋅ h-1. These findings from the current work can provide a shed for the preparation of efficient catalysts and in-depth understanding of C1 catalysis in industrial level.

Ultra‐Durable Solar‐Driven Seawater Electrolysis for Sustainable Hydrogen Production

AbstractIons in seawater hinder direct sewage electrolysis due to the extreme corrosion of Cl− to the anode and reaction of Mg2+ and Ca2+ on the cathode producing solid substances, which reduce the electrolytic efficiency. However, traditional desalination consuming fossil fuel with massive CO2 emissions threatens human survival. Therefore, zero‐carbon emission, ultra‐durable, large‐scale production of freshwater from seawater for water electrolysis is urgently needed. Herein, a multifunctional system for seawater is demonstrated electrolysis based on ultra‐durable solar desalination outdoors. The solar evaporators reach an evaporation flux of 1.88 kg m−2 h−1 with a photothermal conversion efficiency of solar energy as high as 91.3% with excellent ultra‐durable salt resistance even for saturated saltwater due to the Marangoni effects. Moreover, the condensation of pure water from solar desalination based on the evaporation system reaches 0.54 L m−2 h−1 outdoors, which is suitable for a 20 cm × 20 cm engineered electrode equipped with a Janus membrane powered by a solar panel to produce H2 outdoors. The ultrafast unidirectional transport of H2 bubbles enabled by Janus membranes can greatly improve the H2 production efficiency at a rate approaching 85 mL h−1 for continuous 24 h outdoors.