Porous Hollow Research Articles

Rh Nanoparticles Encaged in Hollow Porous Silica Nanospheres as Catalysts for Toluene Hydrogenation under Mild Reaction Conditions

Rh Nanoparticles Encaged in Hollow Porous Silica Nanospheres as Catalysts for Toluene Hydrogenation under Mild Reaction Conditions

A novel TFNi pervaporation membrane with g-C3N4 quantum dots for high-efficiency IPA dehydration

Pervaporation (PV) shows significant potential for the highly selective isopropanol (IPA). The pursuit of developing PV membranes with outstanding separation effect and enduring high purity permeation is an indispensable goal. Based on polyamide (PA) separation layers, a polydopamine (PDA) mixed g-C3N4 quantum dots (gCNQDs) coating as the interlayer was deposited onto a porous ceramic hollow fiber substrate to fabricate thin-film nanocomposite membranes with an interlayer (TFNi). The nanocomposite interlayer enabled the formation of a smoother and highly separated selective polyamide layer. The separation factor exhibited a 31-fold enhancement with the augmentation of the blending fraction of gCNQDs during the PDA coating process. The resulting TFNi membrane attained an exceedingly high separation factor of 10270 ± 90 with a permeate water concentration of 99.9% and demonstrated a satisfactory flux of 1.40 ± 0.08 kg⋅m-2⋅h-1 during the PV process of 90 wt% IPA dehydration at 60 °C. This study presents a fresh perspective on the implementation of nanocomposite interlayers, which is expected to expand the application of high-performance TFNi membranes in PV dehydration processes.

Enhanced flame retardancy and thermal insulation of epoxy resins composites incorporated with ammonium polyphosphate and ionic liquids loaded CuO-ZnO hollow spheres

Epoxy resin, as a thermosetting polymer material with good performance, has been limited in application due to its high flammability. In this investigation, porous CuO-ZnO hollow spheres (CZHS) were prepared by a hydrothermal method. By incorporation with ionic liquids loaded CuO-ZnO hollow spheres (CZHS@Ils) and ammonium polyphosphate (APP) into epoxy resin (EP) matrix, a new composite flame retardant material, named as EP/7.5APP/1.5CZHS@ILs, was developed for improvement of their thermal insulation and flame retardancy. The thermal conductivity of EP/7.5APP/1.5CZHS@ILs was measured to be 0.0197 W m −1 K −1, which is lesser than that of APP incorporated epoxy resin (EP/APP), demonstrating good thermal insulation capability. The flame retardancy were assessed using the limiting oxygen index (LOI) test, the Vertical flame testing (UL-94) test, and the cone calorimeter (CC) test. The results obtained from LOI test show that the EP/7.5APP/1.5CZHS@ILs has good flame retardancy with a LOI value of up to 28, better than that of pure EP which has a LOI value of 19.2. Moreover, a V-0 level of the EP/7.5APP/1.5CZHS@ILs was observed from the UL-94 test. The peak heat release rate (PHRR) was reduced to 257.9 kW m−2, which is 74.8 % lower than that of the pure EP. Such results are attributed to the synergy effect of CZHS@ILs and APP which offers the epoxy resin excellent flame retardancy. Taking advantages of the excellent thermal insulation, flame retardancy and better mechanical properties, the as-resulted EP/7.5APP/1.5CZHS@ILs may hold great potential for future thermal insulation and flame-retardant applications of energy saving building.

An electrochemical sensor based on porous heterojunction hollow NiCo-LDH/Ti3C2Tx MXenes composites for the detection of quercetin in natural plants.

Cubic hollow-structured NiCo-LDH was synthesized using a solvothermal method. Subsequently, clay-like Ti3C2Tx MXenes were electrostatically self-assembled with NiCo layered double hydroxides (NiCo-LDH) to form composites featuring three-dimensional porous heterostructures. The composites were characterized using SEM, TEM, XRD, XPS, and FT-IR spectroscopy. Ti3C2Tx MXenes exhibit excellent electrical conductivity and hydrophilicity, providing abundant binding sites for NiCo-LDH, thereby promoting an increase in ion diffusion channels. The formation of three-dimensional porous heterostructural composites enhances charge transport, significantly improving sensor sensitivity and response speed. Consequently, the sensor demonstrates excellent electrochemical detection capabilityfor quercetin (Qu), with a detection range of 0.1-20 µM and a detection limit of 23 nM. Additionally, it has been applied to the detection of Qu in natural plants such as onion, golden cypress, and chrysanthemum. The recovery ranged from 97.6 to 102.28%.

Fluorinated Hollow Porous Carbon Spheres as High-Performance Cathode Material for Primary Battery

Fluorinated carbon cathode materials have extremely high theoretical specific energy among known cathode materials of lithium primary batteries. Nevertheless, current fluorinated carbon cannot meet the performance demands of future applications due to the rate performance. This work innovatively applies hollow carbon spheres with a porous structure as carbon sources to prepare fluorinated hollow porous carbon spheres (FHPCS) with high energy density and power density. The porous structure provides more reaction sites for the fluorination process and also shortens the diffusion path of lithium ions during the discharge. Additionally, the hollow porous structure offers more interfacial contact areas and reduces volumetric expansion during discharge reactions. The Li/CFx primary battery has a maximum specific energy of 2007 Wh kg−1 and a maximum power density of 30,400 W kg−1 and can have a capacity retention rate of 80.8% at a current density of 16 A g−1. In addition, FHPCS also has the highest specific energy of 1999 Wh kg−1 and 1711 Wh kg−1 in Na/CFx and K/CFx primary batteries, respectively. The diffusion efficiency of an alkali metal ion is analyzed by the different discharge depths with electrochemical impedance spectroscopy and galvanostatic intermittent titration technique. This effort introduces a new high-performance fluorinated carbon featuring a hollow porous structure and puts forward an innovative approach to designing fluorinated carbon materials.

Boosting the H2/CO2 and H2/N2 selectivities of a graphene oxide membrane by shrinking the membrane interlayer spacing via thermal treatment

Graphene oxide (GO) membranes have been widely studied and used for gas separation processes, but some structural changes are necessary to guarantee high membrane selectivities. The thermal reduction process stands out for reducing the interlayer channel size of the GO nanosheets to improve the molecular sieving mechanism. Herein, thermally annealed GO layers were deposited on the outer surface of porous alumina hollow fiber substrates and the produced composite membranes were tested for selective hydrogen (H2) separations. The influence of the thermal annealing process at different mild temperatures (80 and 160 °C) on the characteristics of the GO structure was investigated towards the improvement of the membrane efficiency for H2 separation. ATR-FTIR results confirmed the elimination of oxygenated groups, and XRD analyses showed the GO interlayer space decreased from 8.71 to 7.38 Å after the thermal annealing process at 160 °C. The GO thermally annealed membrane presented an H2 permeance of 2032.47 ± 101.69 GPU and an H2/N2 selectivity of 12.16 ± 0.30, which is 315% greater than the selectivity of the pristine GO membrane. Hence, the application of the thermal reduction method to produce GO membranes with greater selectivities is a viable alternative to deal with gas separation processes.

Nitrogen‐Doped Hollow Porous Carbon Bowls Optimizing Maleic Acid Dissolution for Fast Kinetic and Long‐Life Lithium‐Organic Batteries

Nitrogen‐Doped Hollow Porous Carbon Bowls Optimizing Maleic Acid Dissolution for Fast Kinetic and Long‐Life Lithium‐Organic Batteries

Pyrene Funtionlized Hollow Porous Carbon/S-Dib Composite As a Cathode for Lithium-Sulfur Batteries

Lithium-sulfur batteries (LiSBs) stand out as promising candidates for the next-generation energy storage system. However, challenges such as the “shuttling effects” of intermediate lithium polysulfides and sluggish conversion between sulfur and lithium sulfide have led to low specific capacity under high current and a shortened cycling life for LiSBs. Extensive research has explored porous carbon materials as hosts for sulfur in LiSBs cathodes. Nevertheless, overcoming the “shuttling effects” and ensuring the uniform deposition of lithium sulfide without using metals or metal-containing species remains a challenge.Taking advantage of its aromatic properties, which promotes robust π-π interactions with sp2-hybridized carbon, pyrene with various functionalized groups emerges as a viable solution for surface modification through non-covalent bonding to carbon. In this study, we present the synthesis of X-pyrene (X=OH, NH2, Cl) modified hollow porous carbon (HPC) serving as a micro-reactor for inverse vulcanization, resulting in the formation of S-DIB/X-HPC (X=OH, NH2, Cl) with a uniform structure. Abundant oxygen-, nitrogen- and chloride interfaces were designed to act as adsorption catalytic sites, accelerating conversion kinetics and mitigating shuttle effects.Hollow porous carbon (HPC) nanoparticles were prepared from ZIF-8 by carbonization at 950 °C under argon atmosphere. (Figure 1a). The cross-sectional view in Figure 1b reveals numerous individual hexagonal structures with abundant internal pores. This structure helps accommodate inverse vulcanization (IV) reactions and ensures the uniform distribution of the final product (S-DIB). To evaluate the adsorption quantity of pyrene on the carbon surface, standard solutions of varying pyrene concentrations in dimethyl sulfoxide (DMSO) were prepared and analyzed using Ultraviolet–visible spectroscopy (UV-VIS). A linear relationship is fitted between the intensity of these peaks with the standard pyrene solution. Therefore, the concentration in the filtrate is verified to be approximately 2 mM, in contrast to the initial concentration of 10 mM before adsorption. This observed concentration decrease implies an effective adsorption of pyrene molecules onto the HPC surface. To further investigate the catalytic effect of Cl-pyrene and NH2-pyrene for sulfur redox reactions, potentiostatic nucleation of Li2S on the HPC, Cl-HPC and NH2-HPC electrodes were conducted to clarify the involved multiphase transition process. As shown in Figure 3, the capacity of precipitated Li2S on Cl-HPC (160.62 mAh gS −1) and NH2-HPC (135.75 mAh gS −1) are both higher than that on HPC (99. 93 mAh gS −1). As a result, superior to S-DIB/HPC, the S-DIB/Cl-HPC cathode exhibits a higher initial specific capacity of 1208 mA h g−1 at 0.1 C and a capacity of 643 mA h g−1 at 3 C, and still retain 913 mAh g−1 while returning to 0.1 C. Furthermore, the S-DIB/NH2-HPC cathode possesses excellent cyclability with a high capacity retention of 652 mAh g−1 at 1 C over 300 cycles, yielding an average capacity decline of only 0.076% per cycle. Additionally, we investigate the impact of native surface groups on the deposition of lithium sulfide and the conversion of polysulfides. Figure 1

Nanoscopic catalyst-loaded porous metal oxide hollow frameworks using porous block copolymer templates for high performance formaldehyde sensors

Porous and hollow nanostructures functionalized with nanoscopic catalysts have attracted considerable interest in a wide range of applications depending on surface reactions. In this study, we present an efficient and versatile synthetic strategy of porous metal oxide hollow frameworks (HFs) decorated with noble metal nanoparticles (NPs). The key lies in the use of porous and bicontinuous polystyrene-block-poly(4-vinylpyridine) (PS-b-P4VP) microparticles as templates, which feature pores on the order of several hundred nanometers in size. Homogeneous Pt loading on the surface of the porous microparticles is achieved through the preferential adsorption of Pt precursors onto the P4VP block via electrostatic interactions. Subsequent SnO2 thin film deposition and calcination ultimately yield honeycomb-like SnO2 HFs with macropores and uniform distribution of Pt NPs. The Pt NP-loaded SnO2 HFs exhibit exceptional formaldehyde (HCHO) sensing capabilities, characterized by remarkable sensitivity (31.4 at 5 ppm), rapid response time (4.7 s at 5 ppm), ultra-low detection limit of 10 ppb, and remarkable cross-selectivity. These outstanding features result from their high surface area, gas permeability within porous hollow structures, and well-dispersed Pt NPs, which catalytically activate the sensor. Our study provides great promise for advancing surface catalytic reactions due to their exceptional surface area and gas permeability, paving the way for future applications.

Atomically dispersed Au single sites and nanoengineered structural defects enable a high electrocatalytic activity and durability for hydrogen evolution reaction and overall urea electrolysis

The development of exceptionally active and stable trifunctional electrocatalysts is essential to facilitate industrial applications of proton exchange membrane electrolyzers. Rare earth catalysts have a wide range of applications in alkaline solution oxidation, but limitations in their stability and activity prevent their further application. In this paper, Au doped CeO2 coated porous Aux/CeO2 (x = 1,2,3) was designed as a three-function electrocatalyst with excellent performance and stability. At 1 M KOH conditions, both the oxygen evolution reaction (OER) and the hydrogen evolution reaction (HER) reactions exhibit excess potentials of 159.6 and 320.8 mV at a current density of 10 mA cm-2. In addition, when incorporated into an Au2/CeO2 (0.05 mmol, HAuCl4·4H2O) microparticles, the catalyst exhibits the potential of 1.42 V(10 mA cm-2) containing 0.33 M urea in 1 M KOH. Remarkably, for hydrogen production driven by urea electrolysis, Au2/CeO2 demonstrated exceptional performance by requiring only a voltage input of 1.63 V. The reducing agent that forms the Au/CeO2 heterojunction modulates the electronic structure of the Au active site and optimizes the adsorption of the intermediate. In addition, the interaction of the Au monolayer with the CeO2 nanosphere effectively prevents excessive oxidation and dissolution of Au, and the porous hollow structure provides additional exposed active sites and facilitates mass transfer.

Probing Ion Diffusion and Ion Sieving through Hollow Porous Silica Shells by Imaging the Mobility of Colloids Inside the Shells

AbstractIonic transport through porous membranes and porous materials has received enormous attention due to its importance to many applications. An innovative methodology is proposed to study ion diffusion and ion sieving through mesoporous silica membranes (shells). The mobility of fluorescently labeled core particles within a hollow porous shell, filled with an index‐matched electrolyte solution, is observed using confocal laser scanning microscopy. The core motion range, i.e., the area explored by the core within the hollow compartment, sensitively changed depending on the local ionic concentration. Monitoring transitions in the core motion range is a practical way to detect which ions can migrate through the shells and on what timescale. For instance, lithium and chloride ions easily diffused through the porous silica shells, resulting in a core motion range that changed relatively quickly upon change of the ion concentrations outside of the shell. However, the motion range changed significantly slower upon changing to a bigger cation (tetraoctylammonium ion). This proof of principle experiment can be explained by the Gibbs‐Donnan effect, revealing that the detection of core motion ranges is a good probe to measure both ion diffusion and ion sieving through porous membranes.

Construction of CuCo2O4 hollow microspheres/Ti3C2Tx MXene composite for electrode material of hybrid supercapacitors

CuCo2O4 is a promising active electrode material for its considerable theoretical capacities and natural abundance, however, also is plagued by the disadvantages of the intrinsic low electrical conductivity, slow reaction kinetics and relatively low specific capacity in the practical applications, hence, the precise hybridization with high conductivity and active surface matrix is a promising strategy to overcome these limitations. Herein, porous CuCo2O4 hollow microspheres (CuCo2O4-HS) with the diameter of about 500 nm are hybridized with Ti3C2Tx MXene nanosheets (CuCo2O4-HS/MXene) by electrostatic self-assembly. The crystal structure, morphology and elemental composition of prepared CuCo2O4-HS/MXene are confirmed by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM) and X-ray photoelectron spectroscopy (XPS). Electrochemical test results show that the CuCo2O4-HS/MXene-3 electrode delivers an outstanding specific capacity of 1341.4 C g−1 at 1 A g−1 and retained excellent cyclic stability of 90.9% retention during 10000 cycles of charge/discharge at 5 A g−1. Additionally, the hybrid supercapacitors (HSC) device from CuCo2O4-HS/MXene-3 demonstrated excellent specific energy of 66.3 Wh kg−1 and 49.8 W h kg−1 at specific power of 724.3 W kg−1 and 7229.8 W kg−1 respectively. Significantly, two HSCs connected in series can light a commercial blue LED (3 V) for about 10 mins, demonstrating promising prospect for practical applications.

Nanosponges: A Targeted Drug Delivery System

The latest advances in nanotechnology have resulted in the development of a targeted drug delivery system. However, in order to efficiently target a molecule to a specific place with a drug delivery system, a specialized drug delivery system is required. The discovery of nanosponge has been a big step toward overcoming challenges such as drug toxicity, low bioavailability, and predictable drug release because they can accept both hydrophilic and hydrophobic drugs. Nanosponges, a newly developed colloidal system, have the potential to address concerns such as medicine toxicity, lower bioavailability, and drug release over a large region because they can be adjusted to operate with both hydrophilic and hydrophobic pharmaceuticals. Nanosponges are small structures with a three-dimensional network and porous hollow. Nanosponges are small structures with a three-dimensional network and porous hollow. They can be easily created by crosslinking cyclodextrins with various chemicals. Because of Cyclodextrin's excellent biocompatibility, stability, and safety, a number of Cyclodextrin-based drug delivery systems have been rapidly developed. The nanosponge drug delivery system has a wide range of applications, including cancer, autoimmune illnesses, theranostic uses, increased bioavailability, and stability. This review delves into the benefits and downsides, preparation procedures, factors influencing their preparation, characterisation techniques, applications, and the most recent advancements in nanosponges. Nanosponges can also act as an efficient carrier of enzymes, proteins, vaccines, and antibodies. The current review focuses on the method of preparation, characterisation, and possible application in drug delivery systems.

Synthesis of Stable and Efficient Electrocatalysts for Hydrogen Evolution: Hierarchical NiMo-Based Hollow Nanotubes

Large-scale development of low-cost, efficient, and stable powder electrocatalysts for the hydrogen evolution reaction (HER) in alkaline solutions is a key step toward commercial hydrogen production. Herein, a hierarchical NiMo-MoO3-x hollow nanotube (NiMo-MoO3-x-HNT) with bifunctional groups as an efficient HER electrocatalyst was strategically invented using an MoO3 nanorod (MoO3−NR) as the precursor. The synthesis mechanism of the NiMo-MoO3-x-HNT is established based on in-depth investigations using diffraction, spectral, and microscopy results. Experimental results suggest that the NiMo-MoO3-x-HNT exhibits excellent electrocatalytic HER performance in 1 M KOH, with a low overpotential of 26.5 mV@10.0 mA cm-2 and a small Tafel slope of 32.6 mV dec–1. These values are comparable to those of cutting-edge electrocatalysts based on platinum-group metals. Moreover, it exhibits an almost unaffected cyclic stability over 50,000 cycles and robust durability over 98 h. This remarkable performance is attributed to its bifunctional groups and the porous hierarchical hollow nanotubular morphology. In summary, this study proposes a novel, efficient, and cost-effective strategy for the development of noble metal-free, high-performance HER electrocatalysts.

High performance Ce0.8Nd0.2O2-δ-carbonate hollow fiber membrane for high-temperature CO2 separation

Ceramic-carbonate dual phase (CCDP) membrane consisting of oxygen ionic conductor and molten carbonate has potential applications in clean energy delivery as it enabling the direct CO2 separation or capture at the elevated temperatures. The performance of previous CCDP membranes is not ideal either with a low CO2 flux or with a poor operational stability. In the present work, we looked at the CeO2-based oxygen ionic conductor (neodymium doped cerium (NDC)) as the porous ceramic hollow fiber support to form NDC-carbonate hollow fiber membranes. The NDC hollow fiber was fabricated by the combined phase inversion and sintering techniques and the preparation conditions were optimized to better accommodate the carbonate phase and maintain the mechanical stability. The NDC hollow fibers possessed good bending strength, reaching 91.5 MPa upon sintering at 1500 °C. The effects of feed gas composition and sweep flow rates on the CO2 separation performance were carefully investigated. The resultant dual phase hollow fiber membranes exhibited appreciably high CO2 permeation fluxes at temperatures exceeding 800 °C, which was required to activate both conductions of oxygen and carbonate ions. The achieved maximum CO2 flux of the optimized NDC-carbonate hollow fiber membranes was up to 5.08 mL min−1 cm−2 with 50%CO2–50%N2 as the feed gas at 900 °C. At 700 °C, the membrane exhibited a relatively stable CO2 permeation behavior over 120 h and the spent membrane maintained a stable structure. The high flux and good operational stability of the developed membrane make a huge step towards practical applications.

Enhanced photoelectrochemical water splitting by a 3D hierarchical sea urchin-like structure: ZnO nanorod arrays on TiO2 hollow hemisphere

A hierarchical sea urchin-like hybrid metal oxide nanostructure of ZnO nanorods deposited on TiO2 porous hollow hemispheres with a thin zinc titanate interface layer is specifically designed and synthesized to form a combined type I straddling and type II staggered junctions. The HHSs, synthesized by electrospinning, facilitate light trapping and scattering. The ZnO nanorods offer a large surface area for improved surface oxidation kinetics. The interface layer of zinc titanate (ZnTiO3) between the TiO2 HHSs and ZnO nanorods regulates the charge separation in a closely coupled hierarchy structure of ZnO/ZnTiO3/TiO2. The synergistic effects of the improved light trapping, charge separation, and fast surface reaction kinetics result in a superior photoconversion efficiency of 1.07% for the photoelectrochemical water splitting with an outstanding photocurrent density of 2.8 mA cm−2 at 1.23 V versus RHE.

In situ TEM study of structure evolution of porous hollow carbon sphere/sulfur cathodes

Great progresses on improving capability and stability of lithium-sulfur batteries (LSBs) by developing novel electrodes and electrolytes have been achieved. However, the study on the electrochemical conversion of sulfur with their volume expansion is limited, but provides another promising approach to further promote the practical application of LSBs. Herein, we successfully synthesize porous hollow carbon spheres as the host for sulfur in LSBs. In situ transmission electron microscopy (TEM) is applied to track the real-time morphological and structural evolutions of the porous hollow carbon sphere/sulfur composite when lithiation occurs. A small volume expansion of 39.4% from its original state is observed, benefiting from the highly porous structure of carbon. As a result, the composite electrode achieves a high residual capacity of 712 mAh g−1 after 200 cycles.

Hollow Porous Cu2S Nano-Spheres as High-Rate Magnesium Battery Cathode

The magnesium ion batteries are gaining huge attention in the field of battery energy due to high energy density, low cost potential and high safety performance. So far, the research of magnesium ion batteries has been slow. The surface and structural properties of cathode electrode materials greatly limiting the discharge performance of magnesium ion battery. Herein, a facile synthesis of Cu2S nano-hollow spheres for high performance magnesium ion battery cathode electrode materials was reported. This nano-hollow spheres have a large specific surface area (12.84 m2 g−1) which can reduce the volume expansion caused by magnesium ions during embedding and detachment, and facilitate ion diffusion during the discharge-charging process. Consequently, the nano-hollow porous Cu2S deliver a 152 mAh g−1 after 850 cycles at 560 mA g−1 hold a long-term cycling stability as cathode materials for magnesium ion battery. This work not only demonstrates the great potential of NHP-Cu2S materials, for application in magnesium ion batteries, but also sheds a new light on the application of metal sulfides in magnesium ion batteries.

A new coaxial flow-through probe for electromembrane extraction of methadone from clinical samples on-line coupled to capillary electrophoresis

BackgroundA new design of a flow-through coaxial electromembrane extraction (EME) probe that can be on-line coupled with CE instrument is described and tested. The supporting base of the probe is a PDMS microchip with T-shaped channels into which two coaxially arranged capillaries for inlet and outlet solutions are inserted. The extraction part of the probe is a porous polypropylene hollow fiber, sealed at one end and modified with nitrophenyloctyl ether (NPOE) extraction fluid. The internal volume of the extraction probe is 1.1 μL. ResultsThe EME probe was tested on laboratory samples and methadone was extracted into 3.0 M AcOH as acceptor. The concentration dependence was linear in the range of 0.1–1.0 μg mL−1 at EME 300 s/150 V and in the range of 0.5–10.0 μg mL−1 at EME 100 s/150 V. The enrichment factor was greater than 30 and the LOD was 0.21 μg mL−1. The EME of methadone in clinical samples showed a linear concentration dependence in human urine and a nonlinear concentration dependence in serum. The distribution of methadone in each phase of the extraction system and the effect of extraction membrane thickness on the enrichment factor were studied. The EME probe can be applied repeatedly. SignificanceThe supporting base of EME probe and flow gating interface (FGI) are realized by a microfluidic PDMS microchips cast in the laboratory without the use of lithography. A supporting PDMS chip with coaxially arranged capillaries and extraction membrane forms a compact analytical instrument. The entire EME/CE analysis process is performed on a laboratory-made instrument and automated by LabView.

Enhancing thermal mechanical properties of polymer composites with hollow porous fillers

Incorporating inorganic fillers is a common strategy for reducing the coefficient of thermal expansion (CTE) in polymers, but it is often associated with limited efficiency and a sacrifice in mechanical compliance. Current approaches mainly involve surface modification of fillers to overcome these challenges, but a significant proportion of fillers remain underutilized. In this study, we introduced hollow porous SiO2 particles as fillers, utilizing both their external and internal surfaces to interact with the matrix. Moreover, the hollow porous structure allows the matrix to penetrate into the filler cavities, creating a unique mechanical interlock with the matrix. These combined effects result in a higher efficiency for CTE reduction and a significant improvement in the glass transition temperature. Furthermore, the hollow structure reduces the modulus of the fillers, resulting in a lower composite modulus compared to solid SiO2 counterparts. This approach offers a new avenue for enhancing the thermal mechanical properties of polymer composites.