PPy Shell Research Articles

Synergistically magnetic and dielectric properties of two dimensional Fe3Al@PPy lamellae exhibiting broadband and strong electromagnetic wave absorption

Addressing the issue of low impedance characteristics is essential to improve the electromagnetic wave absorption performance of magnetic materials. Herein, two dimensional Fe3Al@polypyrrole (PPy) lamellae with synergistic magnetic and dielectric properties are fabricated by a mechanical alloying, ordering transformation and polymerization process, which exhibits excellent electromagnetic wave absorption performance. By carefully controlling the thickness of the PPy shell, the optimized Fe3Al@PPy lamellae show a minimum reflection loss of −45.6 dB and an effective absorption bandwidth of 9.1 GHz at a thickness of only 1.5 mm. The conformal growth of Fe3Al@PPy lamellae can induce strong interfacial polarization, dipole polarization, multiple scattering effect and magnetic loss behaviors for the attenuation of electromagnetic waves. This study demonstrates a facile strategy for the development of efficient Fe3Al@PPy composite absorbents showing great potential for practical applications.

MOF-derived metal oxides with hollow porous nanocube structure realize ultra-wideband, lightweight, and anticorrosion microwave absorber

High density, skin effect, and environmental instability are significant limitations that restrict the application of metal-based microwave absorbers in achieving lightweight, high performance, and long service life. This study broke from traditional methods for preparing a microwave absorber Mn2O3-Fe3O4@PPy (polypyrrole) by employing an innovative annealing process to convert metal into metal oxide by the introduction of metal organic framework (MOF), which effectively achieving a more lightweight absorber material with hollow porous nanocube structure. Subsequently, PPy was coated onto the metal oxide surface to form a core-shell structure by a situ chemical oxidation synthesis method. The combination of metal oxide of the hollow porous nanocube structure and the core-shell structure formed by highly conductive PPy shell significantly enhanced heterogeneous interfaces and electromagnetic (EM) wave reflection. Excellent dielectric loss and impedance matching contributed evidently to the ultra-wideband EM wave absorption performance. It was demonstrated that, with a filling amount of only 20 wt%, the prepared Mn2O3-Fe3O4@PPy achieved an effective bandwidth (EAB) of 10.0 GHz at a thickness of 3.08 mm, with EABmax reaching 13 GHz. At a filling amount of only 10 wt%, the reflection loss (RL) was −62.13 dB, achieving an EAB of 7.4 GHz at 2.98 mm thickness, with EABmax reaching 11.4 GHz. Furthermore, the proposed strategy incorporating metal oxide and PPy enhanced corrosion resistance with higher charge transfer resistance.

Size-progressively-reduced FeCoNi@C nanoparticles spatially confined within polypyrrole-derived hollow carbon nanoboxes against electromagnetic contamination

Pyrolytic prussian blue analogues (PBAs) are usually faced with serious agglomeration problem, which restrains their application in the field of microwave absorption to some extent. Given that polymer-based encapsulating layer is propitious for resolving the above issue, herein, with the assistance of polypyrrole (Ppy), a series of carbon-coated FeCoNi alloy nanoparticles (FeCoNi@C) spatially confined within hollow carbon nanoboxes (HCNB) are successfully fabricated using FeCoNi PBAs@Ppy with core–shell structure as the precursors. By quantitatively manipulating the thickness of Ppy encapsulating layer, it is found that there exists a competitive correlation between two kinds of forces with opposite directions under high-temperature inert atmosphere, eventually resulting in distinguishable differences in the configurations of derivatives. Specifically, if the thermal-induced inward contraction (FC) of the inner FeCoNi PBAs core is stronger than the heterointerface interaction (FI) provided by interfacial carbon layer derived from the outer Ppy shell, the derivative will exhibit yolk-shell microstructure, and otherwise, the architecture with hollow configuration can be created. When the thickness of Ppy encapsulating layer is optimized, the resultant yolk-shell sample with moderate Ppy-derived carbon content (ca. 32.6 wt%) delivers a broad maximum effective absorption bandwidth (EAB) value of 5.8 GHz and a desirable minimum reflection loss (RL) intensity of − 52.4 dB, which mainly benefit from its eligible impedance matching characteristic and the synergistic effect of dielectric and magnetic losses. It is believed that this work will enrich the pertinent researches about microwave absorbing materials (MAMs) with outstanding performance derived from polymer-encapsulated PBAs.

Fabrication of Polypyrrole Hollow Nanospheres by Hard-Template Method for Supercapacitor Electrode Material.

Conducting polymers like polypyrrole, polyaniline, and polythiophene with nanostructures offers several advantages, such as high conductivity, a conjugated structure, and a large surface area, making them highly desirable for energy storage applications. However, the direct synthesis of conducting polymers with nanostructures poses a challenge. In this study, we employed a hard template method to fabricate polystyrene@polypyrrole (PS@PPy) core-shell nanoparticles. It is important to note that PS itself is a nonconductive material that hinders electron and ion transport, compromising the desired electrochemical properties. To overcome this limitation, the PS cores were removed using organic solvents to create hollow PPy nanospheres. We investigated six different organic solvents (cyclohexane, toluene, tetrahydrofuran, chloroform, acetone, and N,N-dimethylformamide (DMF)) for etching the PS cores. The resulting hollow PPy nanospheres showed various nanostructures, including intact, hollow, buckling, and collapsed structures, depending on the thickness of the PPy shell and the organic solvent used. PPy nanospheres synthesized with DMF demonstrated superior electrochemical properties compared to those prepared with other solvents, attributed to their highly effective PS removal efficiency, increased specific surface area, and improved charge transport efficiency. The specific capacitances of PPy nanospheres treated with DMF were as high as 350 F/g at 1 A/g. And the corresponding symmetric supercapacitor demonstrated a maximum energy density of 40 Wh/kg at a power density of 490 W/kg. These findings provide new insights into the synthesis method and energy storage mechanisms of PPy nanoparticles.

Core-shell Fe3Al@polypyrrole composites with tunable shell thickness and enhanced microwave absorption performance

Nowadays, core-shell structures have attracted considerable attention as microwave absorbers (MAs) due to the synergistic effect between dielectric and magnetic loss. Herein, core-shell Fe3Al@polypyrrole (Fe3Al@PPy) composites were successfully fabricated by the thermit reaction and chemical oxidation polymerization method with the assistance of ammonium persulfate and p-toluene sulfonic acid. Due to the regulation of the impedance matching by the electromagnetic coupling and core-shell structure, the Fe3Al@PPy composites showed enhanced electromagnetic wave (EMW) absorption performance compared with the pure Fe3Al. Furthermore, the thickness of the PPy shell increased from 0.23 µm to 1.50 µm as the addition of pyrrole (Py) increased from 0.25 mL to 1.0 mL. Meanwhile, the core-shell Fe3Al@PPy composites exhibited the optimal wave absorption performance when the PPy shell thickness was 0.80 µm, and the reflection loss (RL) could reach − 40.53 dB with the thickness of 2.0 mm at 13.3 GHz. This work provides a new idea for the design of large-scale electromagnetic (EM) coupled MAs with core-shell structures.

Fabrication of versatile Ag-P/Ppy core-shell nanocomposite: Adsorption efficacy for chromium (VI) removal and assessment of antioxidant and antibacterial activities

This study reports the synthesis, via in-situ chemical oxidative polymerisation, of conducting polymer-based silver phosphate Polypyrrole (Ag-P/Ppy) core-shell nanocomposite, exhibiting antioxidant and antibacterial characteristics, for the adsorption of chromium (VI) ions from aqueous solutions. Filtering away Cr (VI) ions efficiently also improves the filtered water with antibacterial and antioxidant properties. P-XRD, ATR-FTIR, FESEM, EDAX, TEM, zeta potential, TGA, and BET studies characterized Ag-P/Ppy. The core-shell nanostructure of Ag-P/Ppy was determined by TEM micrographs, which indicated the presence of an Ag-P core and a Ppy shell. pH value, adsorbent dose, stirring rate, contact time, and Cr (VI) pollutant concentration, were investigated as potential influencing factors. At pH 2, 99.4 % of Cr(VI) was removed in 55 min. The adsorption kinetics was effectively depicted by a pseudo-second-order kinetics model, signifying that chemisorption played a momentous role in the total adsorption capacity. Freundlich, Temkin, Redlich-Peterson, and Sips isotherm models were fitted to adsorption data. Temkin and Redlich-Peterson models have a higher (0.99) correlation coefficient than Freundlich (0.95) and Sips (0.98). The maximum adsorption capacity (qm) evaluated using the Sips model was 138.5 mg g−1, which was quite close to the 130.55 mg g−1 value obtained from experiments. The manufactured nanocomposite showed 91.2 % radical scavenging activity in a 1,1-diphenyl-2-picrylhydrazyl (DPPH) radical scavenging assay. Antibacterial activity of the Ag-p/Ppy core-shell nanocomposite contrary to gram-positive (S. aureus) and gram-negative (P. aeruginosa, E. coli, and K. pneumoniae) bacteria was assessed by means of the agar well diffusion technique. Compared to the positive control, it inhibited S. aureus, E. coli, K. Pneumoniae, and P. Aeruginosa by 82.35 %, 79.5 %, 63.63 %, and 76.7 % respectively. Therefore, the Ag-P/Ppy core-shell nanocomposite has the potential as a potent and versatile adsorbent for the exclusion of Cr (VI) ions from water.

Selective CO2 Electroreduction to Formate on Polypyrrole-Modified Oxygen Vacancy-Rich Bi2 O3 Nanosheet Precatalysts by Local Microenvironment Modulation.

Challenges remain in the development of highly efficient catalysts for selective electrochemical transformation of carbon dioxide (CO2 ) to high-valued hydrocarbons. In this study, oxygen vacancy-rich Bi2 O3 nanosheets coated with polypyrrole (Bi2 O3 @PPy NSs) are designed and synthesized, as precatalysts for selective electrocatalytic CO2 reduction to formate. Systematic material characterization demonstrated that Bi2 O3 @PPy precatalyst can evolveintoBi2 O2 CO3 @PPy nanosheets with rich oxygen vacancies (Bi2 O2 CO3 @PPy NSs) via electrolyte-mediated conversion and function as the real active catalyst for CO2 reduction reaction electrocatalysis. Coating catalyst with a PPy shell can modulate the interfacial microenvironment of active sites, which work in coordination with rich oxygen vacancies in Bi2 O2 CO3 and efficiently mediate directional selective CO2 reduction toward formate formation. With the fine-tuning of interfacial microenvironment, the optimized Bi2 O3 @PPy-2 NSs derived Bi2 O2 CO3 @PPy-2 NSs exhibit a maximum Faradaic efficiency of 95.8% at -0.8V (versus.reversible hydrogen electrode) for formate production. This work might shed some light on designing advanced catalysts toward selective electrocatalytic CO2 reduction through local microenvironment engineering.

Biaxial Stretching Array Based on High-Energy-Efficient MXene-Based Al-Ion Micro-supercapacitor Island and Editable Stretchable Bridge.

Employment of multivalent charge carriers with higher charge density to replace frequently used univalent ones can effectively increase the areal capacitance of micro-supercapacitors utilizing few-layered MXene self-assembled electrodes. However, their larger charge density and ionic size usually lead to a sluggish extraction/insertion dynamic between MXene interlayers with limited free space, greatly offsetting the benefits. Herein, we show how to facilitate de-/intercalation of high-valence charge carriers (Al3+) by using polypyrrole-coated bacterial cellulose (BC@PPy) nanospacers to expand MXene interlayer space. Together with the longitudinal electron transport path between interlayers synchronously constructed by the conductive PPy shell, a significant 496% areal capacitance enhancement (232.79 mF cm-2) is realized in the fabricated symmetric Al3+-ion micro-supercapacitors (AMSCs) with the obtained MXene/BC@PPy hybrid film electrodes employing polyacrylamide/1 M AlCl3·6H2O hydrogel electrolyte relative to the cell with pure MXene film electrodes (39.02 mF cm-2). Further benefiting from a high output voltage of 1.2 V, the AMSCs acquire an areal energy density up to 45.3 μW h cm-2. As a device demonstration, we further fabricate a biaxially stretchable AMSC array, simulate its spatial strain distribution during biaxial stretching, and characterize its electrochemical and mechanical properties up to an extreme areal strain of 300%. The proposed rational fabrication paradigm achieves a new level of combined energy density, stretch performance, and architectural simplicity, which presents a route toward a commercially viable stretchable micro energy-storage system with high energy efficiencies.

Cyclodextrin-Functionalized Polypyrrole Particles for the Extraction of Aromatics from Water.

We describe the preparation of oil-in-water (o/w) colloidal particles with a polypyrrole (pPy) shell in which cyclodextrin has been incorporated at the oil-water interface via either physical adsorption or reaction with the pPy shell. The utility of these particles was assessed by the extraction of organic dyes from water. In all cases, we found that cyclodextrin incorporation significantly improved dye uptake, giving up to 78 ± 11% dye extraction in the case of a 100 ppm solution of 4-nitroaniline with a covalently incorporated cyclodextrin. We demonstrated the ability of our colloidal particles to extract nicotine-derived nitrosamine ketone (NNK), a potent carcinogen, from aqueous solution. By treating the solution containing 100 ppm NNK with our particles over 24 and 48 h, we found that NNK removal reached 65 ± 2 and 83 ± 1%, respectively. The uptake could be improved by re-treating a solution with additional freshly prepared particles, to achieve 95 ± 1% NNK extraction with a covalently incorporated cyclodextrin.

Biomimetic Core-Shell-Structured Nanofiber Membranes for Rapid and Portable Water Purification.

Rapid and portable water purification (RPWP) technologies, helping travelers survive in the wild, have attracted increasing interest due to increasing activities, such as exploration, field hiking, and excursion. Field water is usually pathogenic because of various soluble and insoluble contaminants. In this study, fish-gill-like biomimetic core-shell-structured nanofiber membranes are designed and synthesized by an in situ oxidation polymerization coating process. A polyimide nanofiber membrane and a polypyrrole (PPy) coating layer are employed as a core and shell, respectively. The biomimetic membranes exhibit dual-functional capacities: a rapid removal of insoluble contaminants owing to the highly porous network and broad-spectrum adsorption of soluble contaminants enabled by the PPy shell. Model studies confirm the excellent ability of the membranes to purify Cr(VI)-contaminated water to drinkable water with a safe capacity of ∼1415 L m-2. Actual application tests show that the membrane can efficiently remove coliform and suspended solids in a muddy water sample taken from a river in Suzhou, China. This study provides a promising route for the design of a single-layer membrane with dual functions for highly efficient RPWP.

Boosting visible photocatalytic degradation of 2,4-dichlorophenol and phenol efficiency by stable core@shell hybrid Ag3PO4@polypyrrole

In this paper, conjugated conductive polymer polypyrrole molecules were coated on Ag3PO4 nanoparticles by chemical adsorption method. The photocatalytic activity of Ag3PO4 @polypyrrole (Ag3PO4 @PPy) was enhanced significantly with introducing PPy. Under visible light, Ag3PO4 @PPy (1.5 wt%) degraded 100 % of phenol in 12 min and 98.39 % of 2,4-dichlorophenol in 24 min, which was 2.01 times and 1.89 times higher than pure Ag3PO4, respectively. In addition, the degradation activity of core-shell structure catalyst Ag3PO4 @PPy remains 91.26 % after five cycles. The increased stability and activity of as-prepared core-shell Ag3PO4 @PPy was mainly attributed to the synergistic effect of Ag3PO4 and PPy. The high-stability PPy shell inhibits the dissolution of Ag3PO4 nanoparticles. The core-shell structure increases the contact area and a chemical bond was formed on the interface. In addition, the matched energy level structure and the outstanding charge transfer ability of PPy conjugated large π bond accelerates the photo-generated charge separation thereby improves the photoactivity and stability of Ag3PO4.

Sb2O4 @PPy core-shell nanospheres as anode materials for lithium-ion storage

Globular Sb2O4 @PPy core-shell nanospheres are synthesized via a facile method combining controllable synthesis of nanospheres and conductive nanocomposite engineering. Sb2O4 nanospheres an ultrastable structure generates the relatively large void space and shorten the distance of diffusion, and the thin conductive PPy shell can alleviate the giant volume change. The obtained Sb2O4 @PPy core-shell nanospheres in anode material for lithium-ion batteries exhibit an enhanced electrochemical performance with 932.2 mA h g−1 at 100 mA g−1 after 100 cycles and high rate property (552.8 mA h g−1 at 2000 mA g−1). Notably, a specific reversible capacity about 542.8 mA h g−1 still can be delivered even after 250 long cycles at the high current density of 1000 mA g−1.

Polyrrole-encapsulated Cu2Se nanosheets in situ grown on Cu mesh for high stability sodium-ion battery anode

PPy-encapsulated Cu 2 Se nanosheets in-situ grown on the Cu mesh (Cu 2 Se@PPy) acts as a high-performance anode for sodium-ion batteries, capable of delivering a high specific capacity of 293.0 mAh g −1 at 1.0 A g −1 , impressive rate capacity of 263.5 mAh g −1 under 10.0 A g −1 over 2000 cycles. • Cu 2 Se nanosheets were in-situ grown on Cu mesh at room temperature. • PPy coating layer enables robust structure stability and fast charge transport. • Cu 2 Se@PPy as a SIBs anode gives high specific capacity. • Cu 2 Se@PPy as a SIBs anode offers outstanding cycling durability. Copper selenide (Cu 2 Se) features high theoretical capacity and quasi-2D characteristics built by repeating sextuple layers of Se-Cu-Cu-Cu-Cu-Se, making it a fascinating anode for sodium-ion batteries (SIBs). However, it experiences huge volume variation during repeated discharge–charge processes. Here, a productive approach to preserve the structure of Cu 2 Se anode via in-situ coating conductive polymer carbon is proposed. As a demonstration, Cu 2 Se nanosheets encapsulated by polypyrrole (PPy) were anchored on Cu mesh (Cu 2 Se@PPy) and regarded as an electrode material for SIBs. The PPy shell enjoys double functions that improves the electronic conductivity as well as alleviates the significant volume swelling of Cu 2 Se. As a result, Cu 2 Se@PPy gives a satisfactory electrochemical performance, including high specific capacity of 293.0 mAh g −1 at 1.0 A g −1 , impressive rate capacity (263.5 mAh g −1 under 10.0 A g −1 over 2000 cycles). This work describes the uncomplicated approaches available for designing high stability metal selenides anodes for sodium storage.

Nanostructured Co9S8/polypyrrole hybrids grown on carbon cloth for battery-type supercapacitor electrode

Nanostructured hybrids of Co9S8 and polypyrrole (PPy) were grown on carbon cloth (CC) for battery-type supercapacitor electrode. Zeolitic imidazolate framework (ZIF-67) was first self-assembled on CC, which was further hydrothermally converted to Co9S8. After electrodeposition of PPy on the surface of CC/Co9S8, the electrochemical performances of the CC/Co9S8/PPy were greatly enhanced. After 2500 cycles of charge/discharge, the capacity retention can remain 83.5%. The high cyclic stability of the CC/Co9S8/PPy might be due to the buffered volume change of Co9S8 during the redox process by the introduction of PPy shell.

Diameter-optimized PVA@PPy nanofibers: MXene interlayer space expansion without sacrificing electron transport

PVA@PPy nanofibers are proposed as a novel spacer for MXene electrode interlayer space expansion in Zn-ion micro-supercapacitors. The PPy shell mitigates the well-known challenge of electron transport degradation due to the expansion.

Minimal TiO2 Coupled with Conductive Polymer-Stimulated Synergistic Effect on Fast and Reversible Sodium-Ion Storage for Bismuth Sulfide.

Designing multiphase composition is believed to availably boost the structural integrity and electrochemical properties of sodium-ion battery anodes. Herein, a conceive of nanoflowers, assembled with Bi2S3 nanorods, is demonstrated to construct the multiphase composition involving TiO2 coating and polypyrrole (PPy) encapsulation. Bi2S3 acted as the dominating active material, in consideration of the low content of TiO2, which ensured the high capacity of the composite. The dual-structural restrain of the TiO2 and PPy coatings can effectively alleviate volume variation based on the pseudo-"zero-strain" effect of TiO2 and high flexibility of PPy shells. Meanwhile, the heterointerface greatly enhanced the coupling effect between Bi2S3 and TiO2 and thus improved the electrochemical performance, which was proved by the results of density functional theory calculation and electrochemical tests. Combining the regulation from the Bi2S3/TiO2 heterojunction and the dual-structural restrain effect, the Bi2S3/TiO2@PPy electrode exhibited excellent rate performance and superior cycle stability (275.8 mA h g-1 over 500 cycles at 10 A g-1). This study indicates that designing multiphase composition can be very promising and provides a structural insight to construct high stability in electrodes for sodium-ion batteries.

Design and Characterization of a Novel ZnO-Ag/Polypyrrole Core-Shell Nanocomposite for Water Bioremediation.

Incorporating nanostructured metal and metal oxide in a polymer matrix is a strategic way to develop a novel candidate for water bioremediation. In this study, under microwave irradiation, a ZnO–Ag/polypyrrole (PPy) nanocomposite with a core/shell structure was prepared by interfacial polymerization of pyrrole in the presence of ZnO nanoparticles and AgNO3 as an oxidant. The antimicrobial behavior of the ZnO–Ag core combined with the electrical properties of the conducting PPy shell created a special ZnO–Ag/PPy nanocomposite with inherent adsorption behavior and antimicrobial properties. More impressively, the as-prepared ZnO–Ag/PPy displayed enhanced adsorption of Cd2+ and PO43− ions in the mixed solution. At pH 8, it had overall removal efficiencies of 95% and 75% for Cd2+and PO43− ions, respectively. The Freundlich adsorption model, rather than the Langmuir adsorption model, better fits the adsorption isotherm results. The adsorption kinetics also followed the pseudo-second-order kinetic model. Additionally, the engineered nanocomposite demonstrated antifungal activity against different fungi, as well as remarkable antibacterial activity against Gram-negative and Gram-positive bacteria. The synergistic combination of crystallinity, coherence of the ZnO–Ag core in the PPy matrix, and the negative zeta potential all contribute to this nanocomposite’s high efficiency. Our results have significant consequences in the wastewater bioremediation field using a simple operation process.

Preparation of Polyimide@Polypyrrole/Palladium Hollow Composites with Applications in Catalysis

Polyimide based hollow composites were successfully prepared by combining the situ and template methods together. Firstly, the complete words (PPy) shell was covered on the surface of polystyrene nanoparticles, then the polyamide acid and PdCl2 were covered on the surface of the materials after the calcination. Finally, PI@ PPy/Pd hollow composites were obtained by a chemical process. The structure and composition of composites were characterized by scanning electron microscopy X-ray diffraction, thermo gravimetric analyzer and differential scanning calorimeter, respectively. Palladium (Pd) nanoparticles were densely and uniformly anchored on the surface of PPy shell due to the coordination interaction between amino groups on PPy backbone and Pd2+ ions. They are ideal candidates as nanoreactors for heterogeneous catalysis due to their special structure. The catalytic performance of PI@ PPy/Pd hollow composites were studied by the reduction of NaBH4 as a reducing agent. The catalytic performance of composites was characterized by ultraviolet and visible spectrophotometer. The PI@PPy/Pd composites showed excellent catalytic performance in the reduction of methylene blue with sodium borohydride as reducing agent. The dye completely turned colorless as seen within 2.0 minutes.

Microwave absorption enhancement of 2-dimensional CoZn/C@MoS2@PPy composites derived from metal-organic framework

Metal-organic framework (MOF) materials have caused widespread concerns in the field of microwave absorption, due to the unique microstructure and electronic state. Herein, the CoZn/C@MoS2@polypyrrole (PPy) composites were prepared through MOF self-template method. The MoS2 sheets and PPy shell incorporated for optimizing impedance matching of two-dimensional (2D) CoZn/C composites. The introduction of MoS2 sheets and PPy shell endowed the composites with enhanced microwave absorption. The as-prepared CoZn/C@MoS2@PPy composites showed a minimum reflection loss (RL) of −49.18 dB with the thickness of 1.5 mm. In addition, the effective absorption bandwidth (EAB, RL values exceeding −10 dB) covered 4.56 GHz, which showed greater performances than CoZn/C composites under a lower thickness (<2 mm). This work not only provides a facile route for fabricating MOF-derived carbon-based composites as microwave absorbers, but also broadens the application of MOF materials.

Monodispersed Nitrogen-Containing Carbon Capsules Fabricated from Conjugated Polymer-Coated Particles via Light Irradiation.

Near-infrared (NIR) light irradiation induced the transformation of polypyrrole (PPy) to nitrogen-containing carbon (NCC) material due to its light-to-heat photothermal property. The temperature of the PPy increased over 700 °C within a few seconds by the NIR laser irradiation, and elemental microanalysis confirmed the decreases of hydrogen and chloride contents and increases of carbon and nitrogen contents. Monodispersed polystyrene (PS)-core/PPy shell particles (PS/PPy particles) synthesized by aqueous chemical oxidative seeded polymerization were utilized as a precursor toward monodispersed NCC capsules. When the NIR laser was irradiated to the PS/PPy particles, the temperature rose to approximately 300 °C and smoke was generated, indicating that the PS component forming the core was thermally decomposed and vaporized. Scanning electron microscopy studies revealed the successful formation of spherical and highly monodispersed capsules, and Fourier transform infrared spectroscopy, Raman spectroscopy, and X-ray photoelectron spectroscopy studies confirmed the capsules consisted of NCC materials. Furthermore, sunlight was also demonstrated to work as a light source to fabricate NCC capsules. The size and thickness of the capsules can be controlled between 1 and 80 μm and 146 and 231 nm, respectively, by tuning the size of the original PS/PPy particles and PPy shell thickness.