On-demand Control Research Articles

Calcium carbonate-modified plant sporopollen capsule as an eco-friendly microvehicle for controlled release of pesticide.

In this work, natural club moss (Lycopodium clavatum, LC) spores with a porous surface morphology and highly uniform size distribution were engineered into controlled-release microvehicles for pesticide delivery. As a proof of concept, a widely used fungicide, fluazinam (FLU), was successfully loaded into LC spores and then modified with different amounts of CaCO3 (CaC) to extend the efficacy duration of FLU. Significantly, as the control target of FLU, clubroot disease is a worldwide destructive disease of cruciferous crops, and its development is favored by acidic soils and can be suppressed at high Ca concentrations. Fabricated FLU@LC-CaC microcapsules, FLU loading and CaCO3 deposition were systematically characterized by field emission scanning electron microscopy, Fourier transform infrared spectroscopy, and thermogravimetric analysis. The as-prepared FLU@LC-CaC microcapsules showed sustained-release behaviors and were potentially able to supplement the Ca concentration in acidic environments. This approach synergistically enhanced in vivo bioactivity for the on-demand control of clubroot disease. An in vivo bioassay revealed that the control efficacy of FLU@LC-CaC against clubroot disease in pak choi (Brassica chinensis) (66.4%) was 1.7-fold higher than that of a commercial FLU suspension concentrate (38.2%) over the course of the cultivation period (35 days). This work provides new ideas not only for developing eco-friendly and scalable microvehicles for pesticide delivery based on natural sporopollen, but also for unconventional research perspectives in on-demand pest management based on their occurrence characteristics. © 2022 Society of Chemical Industry.

Cost-Effective Smart Window: Transparency Modulation via Surface Contact Angle Controlled Mist Formation

Implementing simple and inexpensive energy-saving smart technologies in households is quite effective to accomplish on-demand privacy control and reduction in energy consumption. Conventional smart glasses face difficulty in making inroads into the consumer market due to utilizing expensive active layers, electrolytes, and transparent electrodes. Thus, the need of the hour is to develop an unconventional smart window, which should be cost-effective, power-efficient, and simple to fabricate. Against this backdrop, we report the fabrication of a new class of smart partition windows termed "mist-driven transparency switching glass". The fabrication protocol includes surface energy modification of two glass panes, followed by assembling them into a square or rectangular-shaped narrow cell with appropriate inlets and outlets for mist. In its pristine state, the device is transparent, as expected of two plain glasses forming a cell. Insertion of cool mist into the device produces tiny droplets onto the inner walls due to condensation enabling scattering of light, thereby producing the translucent state. The optimized device shows a transmittance modulation of as much as ∼65% at 550 nm, allowing it to reduce the indoor temperature by more than 30% compared to a regular glass windowpane. To realize commercial viability, a large area device (30 × 30 cm2) was fabricated, which could be operated wirelessly through a cellphone application paving the way for incorporating the Internet of Things into the technology.

Carbon network-hosted porphyrin as a highly biocompatible nanophotosensitizer for enhanced photodynamic therapy.

Photodynamic therapy (PDT) has the characteristics of being simple and non-invasive, and with on-demand light control. However, most photosensitizers exhibit strong hydrophobicity, low quantum yields in water and low tumor selectivity. In this study, carbon network-hosted porphyrins (CPs) with high biocompatibility and efficient singlet oxygen (1O2) generation were developed to reduce the biotoxicity of photosensitizers and avoid quenching caused by hydrophobic aggregation for enhanced PDT. The CPs were prepared by a simple solid-phase synthesis method using porphyrin, green non-toxic citric acid and urea as the raw materials. The CPs exhibited excellent water solubility and high biocompatibility. Even when the concentration reached 1.5 mg mL-1, cells still had good biological activity. By separately fixing the porphyrins in the carbon network, the CPs avoided aggregation-induced inactivation and had high generation efficiency of 1O2. Furthermore, in order to improve the PDT effect, the CPs were modified with the upper nuclear targeting peptide TAT (T-CPs), which was used to target the nucleus and generate 1O2in situ to directly destroy genetic material. The proposed strategy provides a simple and green path to prepare nanophotosensitizers with high biocompatibility and efficient 1O2 generation for PDT.

Advanced stimuli-responsive membranes for smart separation.

Membranes have been extensively studied and applied in various fields owing to their high energy efficiency and small environmental impact. Further conferring membranes with stimuli responsiveness can allow them to dynamically tune their pore structure and/or surface properties for efficient separation performance. This review summarizes and discusses important developments and achievements in stimuli-responsive membranes. The most commonly utilized stimuli, including light, pH, temperature, ions, and electric and magnetic fields, are discussed in detail. Special attention is given to stimuli-responsive control of membrane pore structure (pore size and porosity/connectivity) and surface properties (wettability, surface topology, and surface charge), from the perspective of determining the appropriate membrane properties and microstructures. This review also focuses on strategies to prepare stimuli-responsive membranes, including blending, casting, polymerization, self-assembly, and electrospinning. Smart applications for separations are also reviewed as well as a discussion of remaining challenges and future prospects in this exciting field. This review offers critical insights for the membrane and broader materials science communities regarding the on-demand and dynamic control of membrane structures and properties. We hope that this review will inspire the design of novel stimuli-responsive membranes to promote sustainable development and make progress toward commercialization.

Spin-switching effect and giant magnetoresistance in quantum structure of monolayer MoS<sub>2</sub> nanoribbons with ferromagnetic electrode

Spintronics is a new type of electronics based on electron spin rather than charge as the information carrier, which can be stored and calculated by regulating and manipulating the spin. The discovery and application of the giant magnetoresistance effect opens the door to the application of electron spin properties. Realizing on-demand control of spin degree of freedom for spin-based devices is essential. The two-dimensional novel material, monolayer transition metal dichalcogenide (TMD) (MoS<sub>2</sub> is a typical example from the family of TMD materials), has become an excellent platform for studying spintronics due to its novel physical properties, such as direct band gap and strong spin-orbit coupling. Obtaining high spin polarization and achieving controllability of degrees of freedom are fundamental problems in spintronics. In this paper, we construct the monolayer zigzag MoS<sub>2</sub> nanoribbon quantum structure of electrically controlled ferromagnetic electrode to solve this problem. Based on the non-equilibrium Green’s function method, the regulation of the magnetic exchange field and electrostatic barrier on the spin transport in parallel configuration and anti-parallel configuration are studied. It is found that in the parallel structure, spin transport is obviously related to the magnetic exchange field, and 100% spin filtering can occur near the Fermi energy level to obtain pure spin current. When an additional electric field is applied to the middle region, the spin filtering effect is more significant. Therefore, the spin switching effect can be achieved by regulating the incident energy. In addition, it is also found that within a specific energy range, electrons in the parallel configuration are excited to participate in transport, while electrons in the anti-parallel structure are significantly inhibited. Consequently, a noticeable giant magnetoresistance effect can be obtained in this quantum structure. Moreover, it can be seen that the magnetic exchange field strength can effectively modulate the giant magnetoresistance effect. These results provide valuable theoretical references for the development of giant magnetoresistance devices and spin filters based on monolayer zigzag MoS<sub>2</sub> nanoribbons.

Microfluidics in the eye: a review of glaucoma implants from an engineering perspective.

Glaucoma is a progressive optic neuropathy in the eye, which is a leading cause of irreversible blindness worldwide and currently affects over 70 million individuals. Clinically, intraocular pressure (IOP) reduction is the only proven treatment to halt the progression of glaucoma. Microfluidic devices such as glaucoma drainage devices (GDDs) and minimally invasive glaucoma surgery (MIGS) devices are routinely used by ophthalmologists to manage elevated IOP, by creating an artificial pathway for the over-accumulated aqueous humor (AH) in a glaucomatous eye, when the natural pathways are severely blocked. Herein, a detailed modelling and analysis of both the natural microfluidic pathways of the AH in the eye and artificial microfluidic pathways formed additionally by the various glaucoma implants are conducted to provide an insight into the causes of the IOP abnormality and the improvement schemes of current implant designs. The mechanisms of representative glaucoma implants have been critically reviewed from the perspective of microfluidics, and we have categorized the current implants into four groups according to the targeted drainage sites of the AH, namely Schlemm's canal, suprachoroidal space, subconjunctival space, and ocular surface. In addition, we propose to divide the development and evolution of glaucoma implant designs into three technological waves, which include microtube (1st), microvalve (2nd) and microsystem (3rd). With the emerging trends of minimal invasiveness and artificial intelligence in the development of medical implants, we envision that a comprehensive glaucoma treatment microsystem is on the horizon, which is featured with active and wireless control of IOP, real-time continuous monitoring of IOP and aqueous rate, etc. The current review could potentially cast light on the unmatched needs, challenges, and future directions of the microfluidic structural and functional designs of glaucoma implants, which would enable an enhanced safety profile, reduced complications, increased efficacy of lowering IOP and reduced IOP fluctuations, closed-loop and on-demand control of IOP, etc.

Collective Behaviors of Active Matter Learning from Natural Taxes Across Scales.

Taxis orientation is common in microorganisms, and it provides feasible strategies to operate active colloids as small-scale robots. Collective taxes involve numerous units that collectively perform taxis motion, whereby the collective cooperation between individuals enables the group to perform efficiently, adaptively, and robustly. Hence, analyzing and designing collectives is crucial for developing and advancing microswarm toward practical or clinical applications. In this review, natural taxis behaviors are categorized and synthetic microrobotic collectives are discussed as bio-inspired realizations, aiming at closing the gap between taxis strategies of living creatures and those of functional active microswarms. As collective behaviors emerge within a group, the global taxis to external stimuli guides the group to conduct overall tasks, whereas the local taxis between individuals induces synchronization and global patterns. By encoding the local orientations and programming the global stimuli, various paradigms can be introduced for coordinating and controlling such collective microrobots, from the viewpoints of fundamental science and practical applications. Therefore, by discussing the key points and difficulties associated with collective taxes of different paradigms, this review potentially offers insights into mimicking natural collective behaviors and constructing intelligent microrobotic systems for on-demand control and preassignedtasks.

Lipidoid Artificial Compartments for Bidirectional Regulation of Enzyme Activity through Nanomechanical Action.

Photoresponsive inhibitor and noninhibitor systems have been developed to achieve on-demand enzyme activity control. However, inhibitors are only effective for a specific and narrow range of enzymes. Noninhibitor systems usually require mutation and modification of the enzymes, leading to irreversible loss of enzymatic activities. Inspired by biological membranes, we herein report a lipidoid-based artificial compartment composed of azobenzene (Azo) lipidoids and helper lipids, which can bidirectionally regulate the activity of the encapsulated enzymes by light. In this system, the reversible photoisomerization of Azo lipidoids triggered by UV/vis light creates a continuous rotation-inversion movement, thereby enhancing the permeability of the compartment membrane and allowing substrates to pass through. Moreover, the membrane can revert to its impermeable state when light is removed. Thus, enzyme activity can be switched on and off when encapsulating enzymes in the compartments. Importantly, since neither mutation nor modification is required, negligible loss of activity is observed for the encapsulated enzymes after repeated activation and inhibition. Furthermore, this approach provides a generic strategy for controlling multiple enzymes by forgoing the use of inhibitors and may broaden the applications of enzymes in biological mechanism research and precision medicine.

Non-volatile chirality switching by all-optical magnetization reversal in ferromagnetic Weyl semimetal Co3Sn2S2

Weyl semimetals show unique physical properties exemplified by the colossal anomalous Hall effect, arising from exotic quasiparticles called Weyl fermions emerging around the Weyl nodes. Manipulating these topologically protected Weyl nodes is anticipated to play a leading role towards the on-demand control of quantum properties in Weyl semimetals. We demonstrate non-volatile chirality switching in a ferromagnetic Weyl semimetal Co3Sn2S2 via all-optical magnetization reversal. When excited by circularly polarized mid-infrared light pulses, the sign reversal of the anomalous Hall conductivity stemming from the Berry curvature is observed, manifesting the switching of the chirality of the Weyl nodes accompanying with the magnetization reversal. Magneto-optical imaging measurements reveal that the mechanism of the magnetization/chirality switching is attributed to the helicity-dependent deterministic magnetization associated with the magnetic circular dichroism.

Surface-limited reactions for spatial control of kinesin-microtubule motility assays using indirect irradiation of an electron beam.

Gliding of microtubules (MTs) on kinesins has been applied to lab-on-a-chip devices, which enable autonomous transportation and detection of biomolecules in the field of bioengineering. For rapid fabrication and evaluation of the kinesin-MT based devices, optical control techniques have been developed for control of kinesin activity and density; however, use of caged molecules lacks spatial controllability for long-term experiments, and direct irradiations of UV light onto kinesin-coated surfaces are inherently damaging to MTs due to their depth limit since the heights of the kinesin-MT systems are at the tens of a nanometer scale. Considering surface electric fields in electrolytic solutions are shielded at the nanometer scale due to Debye shielding, in this study, we show that fine spatial control of kinesin density and activity is enabled using surface-limited electrochemical reactions induced by indirect irradiations of an electron beam (EB). An EB is indirectly irradiated onto the kinesins through a 100-nm-thick silicon nitride membrane, and the electrons scattered in the membrane can cause localized electrochemical effects to the kinesins. We show that these localized electrochemical effects cause both ablation of kinesins and motility control of kinesin activity by changing the EB acceleration voltage. In particular, the latter is achieved without complete ablation of MTs, though the MTs are indirectly irradiated by the EB. As a demonstration of on-demand control of gliding MTs, we show the accumulation of the MTs on a target area by scanning the EB. The proposed accumulation technique will lead to rapid prototyping of microdevices based on MT-kinesin motility assay systems.

Probing Fast Transformation of Magnetic Colloidal Microswarms in Complex Fluids.

The rapidly transformed morphology of natural swarms enables fast response to environmental changes. Artificial microswarms can reconfigure their swarm patterns like natural swarms, which have drawn extensive attention due to their active adaptability in complex environments. However, as a prerequisite for biomedical applications of microswarms in confined environments, achieving on-demand control of pattern transformation rates remains a challenge. In this work, we report a strategy for optimizing pattern transformation rates of colloidal microswarms by coordinating the inner interactions. The influences of magnetic field parameters on pattern transformation rates are theoretically and experimentally studied, which elucidates the mechanism for optimal transformation rate control. The feasibility of the strategy is then validated in viscous Newtonian fluids and non-Newtonian biofluids. Moreover, the strategy is further validated in dynamic flow environments, exhibiting a promising future for practical applications in targeted delivery tasks with an optimal pattern transformation manner.

Robotic Arm-Protected Microsurgical Pericallosal and Middle Cerebral Artery Aneurysm Clipping: A Technical Note and Case Series.

Managing intraoperative aneurysm rupture (IAR) during intracranial aneurysm clipping can be challenging given the excessive hemorrhage and limited field of view under the microscope for visualizing the proximal artery and safe temporary clipping. To describe the first known use of robotic arm for safeguarding IAR in microsurgical aneurysm clipping. A robotic arm was used to safeguard 3 microsurgical clipping cases (1 pericallosal and 2 middle cerebral artery) performed by a single surgeon. The device was installed onto the side rail of the operating table along with the clip applier attachment. After dissecting the cerebral artery segment proximal to the aneurysm, a temporary aneurysm clip was loaded and established at the appropriate segment before dissecting distally toward the aneurysm. Setup for the robotic arm and temporary clip was simple, quick, precise, and without any unforeseen accommodations needed in all 3 instances. The temporary clip acted as an emergency gate and could be deployed either manually or remotely through a controller. IAR occurred in case 1, and the robotic-assisted temporary clip deployment achieved immediate hemostasis without complications. This method bypassed the need for significant suctioning, packing, and further exploration for safe temporary clipping. Case 2 and 3 demonstrated the feasibility for middle cerebral artery protection and ease of intraoperative readjustment. This technical note highlights the feasibility and relative ease of using a robotic arm as a safeguard device, and it enables on-demand control of proximal blood flow and may enhance the safety of microsurgical aneurysm procedures.

Enhanced photocontrollable dynamic adhesion of nematic elastomers on rough surfaces

Polymers with switchable adhesion properties are important for efficient catch-and-release processes in robotic hand applications and handgrips with on-demand adhesion control. However, counter objects often have a rough surface topography, which requires a dynamic adhesion system that balances adhesion and detachment performances. Here, we demonstrate that a photosensitive nematic main-chain liquid crystal elastomer (LCE) has suitable photoswitchable adhesion properties on surfaces with micrometer-scale roughness, resulting in a large adhesion change. The nematic LCE exhibits the so-called “soft elasticity,” wherein it can deform at a certain strain without increasing the elastic energy. Such deformation can be maintained owing to arrested relaxation, enabling the LCE to deform along with a rough surface upon light pressure. This increases the contact area and consequently enhances adhesion ability. On the other hand, the LCE exhibits rubber elasticity after proper light irradiation owing to a phase transition from the nematic to the isotropic phase. As rubber elasticity limits deformation, the contact area on the rough surface, and thus the adhesion, is greatly reduced. This LCE with photoswitchable elasticity has great merit as a dynamic adhesive pad for treating objects with rough surfaces, which may expand the versatility of stimuli-responsive adhesive systems.

Anti-Adhesive Organosilane Coating Comprising Visibility on Demand.

There is a wide application field for anti-adhesive and hydrophobic coatings, stretching from self-cleaning surfaces over anti-graffiti and release coatings to demolding aids in the production of polymers. The typical materials for the latter are hard coatings, including TiN, CrN, diamond-like carbon, etc. Alternatively, organosilane coatings based on perfluorinated compounds or molecules with long alkyl side chains can be employed. Although these functional layers are generally required to be invisible, there is a demand for a straightforward approach, which enables the temporary control of successful and homogeneous application as well as abrasion and wear of the coatings during use. For this purpose, a visibility-on-demand property was introduced to an already established anti-adhesive organosilane coating by incorporation of 1,8-naphthalimide-N-propyltriethoxysilane (NIPTES) as a fluorescent marker molecule. While the naphthalimide unit provides blue fluorescence under UV irradiation, the ethoxy groups of NIPTES enable the covalent coupling to the coating as a result of the hydrolysis and condensation reactions. As a consequence, the fluorescent marker molecule NIPTES can simply be added to the coating solution as an additional organosilane component, without the need for changes in the approved deposition procedure. The generated fluorescent anti-adhesive coatings were characterized by contact angle measurements, atomic force microscopy (AFM), as well as by different spectroscopic techniques, including FTIR, UV-Vis, fluorescence and X-ray photoelectron spectroscopy (XPS). In addition, the on-demand control function provided by the introduced fluorescence properties was evaluated along an injection molding process.

Modeling and demand-based control of responsive building envelope with integrated thermal mass and active thermal insulations

The static nature of current envelope design and operation is diametric to the mutable and transient forces and energies acting on our building stocks. Responsive building envelopes (or RBEs) have shown substantial energy saving potential for buildings by adaptively providing passive cooling/heating. In this research, an easy-to-implement yet flexible ‘demand-based’ control rule is proposed based on demand analysis to optimally control RBEs that integrate active insulation systems (AISs) and a sensible thermal energy storage (TES) layer. The controller developed herein calculates the desired thermal resistance for AIS layers and provides on-demand control of the heat flow into and out of the thermal mass to reduce AC load. It provides several benefits over the simple temperature-based controllers while does not require the complex formulation as needed for model predictive control. To quantify the thermal behavior and energy performance, a thermal network model is developed for RBEs to perform wholebuilding energy simulations of a residential thermal zone in six representative cities in the US. The results show apparent benefits of demand-based control strategy over traditional temperature-based control by offering higher energy savings and LPD reduction, especially in mild climate zones and during transitional seasons. Some design and implementation considerations for REBs with integrated AISs and TES are also discussed.

Regulation of the Inevitable Water-Responsivity of Silk Fibroin Biopolymer by Polar Amino Acid Activation.

In nature, water is vital for maintaining homeostasis. Particularly, organisms (e.g., plant leaf, bird feather) exploit water fluidics for motions. Hydration-adaptive crystallization is the representative water-responsive actuation of biopolymers. This crystallization has inspired the development of intelligent human-robot interfaces. At the same time, it hinders the consistent adhesion of tissue adhesive. As hydration-adaptive crystallization is inevitable, the on-demand control of crystallization is desirable in the innovative biopolymeric biomedical systems. To this end, this study developed an amino acid-based technology to artificially up- or down-regulate the inevitable crystallization of silk fibroin. A case II diffusion model was constructed, and it revealed that the activity of polar amino acid is related to crystallization kinetics. Furthermore, the water dynamics study suggested that active amino acid stabilizes crystallization-triggering water molecules. As a proof-of-concept, we verified that a 30% increase in the activity of serine resulted in a 50% decrease in the crystallization rate. Furthermore, the active amino acid-based suppression of hydration-adaptive crystallization enabled the silk fibroin to keep its robust adhesion (approximately 160 kJ m-3) by reducing the water-induced loss of adhesive force. The proposed silk fibroin was demonstrated as a stable tissue adhesive applied on ex vivo porcine mandible tissue. This amino acid-based regulation of hydration-adaptive crystallization will pioneer next-generation biopolymer-based healthcare.

Tuning Mechanical Properties of Polymeric Hydrogels Using Orthogonally Functionalized Crosslinkers

A unique orthogonal crosslinker-induced hydrogel, whose mechanical strength can be tunable by the crosslinker topology upon thermal treatment, is described herein. The crosslinker containing cationic moieties and crosslinkable styrenyl groups was employed for the preparation of orthogonally crosslinked hydrogels having ionic and covalent characteristics. The manipulation of the orthogonal crosslinkers topology and the ionic bond strength between cationic and anionic moieties facilitated the control of the mechanical properties. Short-term temporal modulation of hydrogel moduli, a key factor of the substrates for cell development, was demonstrated and could provide dynamic microenvironment for biological process. In addition, on-demand control of the elastic properties of the hydrogels by application of a thermal stimulus provides new avenues to regulate cell growth. Furthermore, the orthogonality of the crosslinkers allowed molecular functionalization of a wide range of molecules of interest to the hydrogels by thiol-ene Michael addition (nucleophilic addition of sulfhydryl and carbon-carbon double bonds) in a friendly manner as demonstrated in our work.

Advanced Strategies of Enzyme Activity Regulation for Biomedical Applications.

Enzymes are important macromolecular biocatalysts that accelerate chemical and biochemical reactions in living organisms. Most human diseases are related to alterations in enzyme activity. Moreover, enzymes are potential therapeutic tools for treating different diseases, such as cancer, infections, and cardiovascular and cerebrovascular diseases. Precise remote enzyme activity regulation provides new opportunities to combat diseases. This review summarizes recent advances in the field of enzyme activity regulation, including reversible and irreversible regulation. It also discusses the mechanisms and approaches for on-demand control of these activities. Furthermore, a range of stimulus-responsive inhibitors, polymers, and nanoparticles for regulating enzyme activity and their prospective biomedical applications are summarized. Finally, the current challenges and future perspectives on enzyme activity regulation are discussed.

Tuning super-lubricity via molecular adsorption

The state of vanishing friction known as super-lubricity is highly desirable to reduce parasitic energy loss. However, without efficient means to turn on and off the super-lubricity, it would be difficult to realize its full potential in engineering applications. Here we report that the nanoscale super-lubricity between amorphous silica tip and graphite basal plane can be tuned by physisorbing various molecules from the environment. In particular, the super-low fiction can be further reduced by about 54% in n-pentanol vapor, but increases by around 25 and 45 times in water and phenol vapor respectively. The vapor molecules influence the friction by adsorbing onto the silica surface and being entrained into the sliding interface. Based on the structures of adsorbed molecules, it could be deduced that adsorbates with high conformational entropy can suppress the interfacial commensuration and enhance the super-lubricity, while the ones that can facilitate commensurate interactions with the graphite surface increase friction. This finding provides the basic principle enabling on-demand control of friction into and out of the super-lubricious state of solid interface.

Raspberry-Shaped Microgels Assembled at the Oil–Water Interface by Heterocoagulation of Complementary Microgels

Raspberry-shaped particles have attracted increasing interest due to their tunable surface morphologies and physicochemical properties. A variety of covalent and noncovalent strategies have been developed for the fabrication of raspberry-shaped particles. However, most of these strategies are complex or require precise control of solution conditions. In this work, we develop a direct approach for the fabrication of noncovalent raspberry-shaped microgels. Our strategy works through the electrostatically driven heterocoagulation of binary microgels with complementary functional groups at the oil-water interface. By introducing hexanoic acid (HA) into the oil phase, stable inverse water-in-oil (w/o) Pickering emulsions could be stabilized solely by HA-swollen microgels or self-assembled raspberry-shaped microgels. Furthermore, the formation mechanism and the interfacial properties of interfaces laden with raspberry-shaped microgels were investigated. The results indicate that HA can effectively improve the hydrophobicity and interfacial activity of microgels. In addition, raspberry-shaped microgels achieve high coverage on the droplet surface, resulting in the elastic interface and excellent stability of emulsions. We envision that these results will not only fill a knowledge gap in the field of soft matter interfacial self-assembly, but also will shed light on the rational design of raspberry-shaped soft colloids and the on-demand control of interfacial rheology. In addition, we expect that our results will contribute to wider applications of microgel-stabilized emulsions, including cascade catalysis, microreactor, and in vivo drug delivery.