Porous Silica Microspheres Research Articles

Ultrawhite and ultrablack asymmetric coatings for radiative cooling and solar heating

Passive daytime radiative cooling, a zero-energy and zero‑carbon cooling technology, has significant potential to substantially reduce reliance on compression-based cooling systems, combat the urban heat island effect, and mitigate global warming. However, current radiative cooling materials either exhibit low efficiency or are susceptible to overcooling, resulting in cooling penalties on winter days. In this work, we designed and fabricated the ultrawhite and ultrablack asymmetric coatings. The top-layer, designed for efficient radiative cooling, consists of a porous polymethyl methacrylate and hollow silica microspheres composite. The underlayer, tailored for solar heating, is composed of a carbon nanotubes and carbon black composite. The cooling side with an exceptional solar reflectivity of 0.98 and a mid-infrared emissivity of 0.97 achieves a comparable daytime subambient cooling of 7.6 °C, with a theoretical net cooling power of 98.8 W/m2. Conversely, the heating side with a solar absorptivity of 0.96, a ultra-high visible light absorptivity of 0.985, and a mid-infrared emissivity of 0.97, results in a daytime above-ambient heating of 12.8 °C, corresponding to a theoretical net heating power of 745 W/m2. Promisingly, our ultrawhite and ultrablack asymmetric coatings hold the promise of addressing the long-standing challenge of all-season temperature regulation, offering significant potential for electricity savings and CO2 emission reduction.

Fabrication of immobilized lipases from Candida rugosa on hierarchical mesoporous silica for enzymatic enrichment of ω-3 polyunsaturated fatty acids by selective hydrolysis

In this study, lipase from Candida rugosa was immobilized on hydrophobic hierarchical porous hollow silica microsphere (HPHSM-C3) via adsorption. The prepared biocatalyst HPHSM-C3@CRL exhibited higher activity, thermal and pH stability. HPHSM-C3@CRL remained 70.2% of initial activity after 30 days of storage at 24 °C and 50.4% of initial activity after 10 cycles. Moreover, HPHSM-C3@CRL was utilized in enzymatic enrichment of omega-3 polyunsaturated fatty acids (ω-3 PUFAs) in glycerides, achieving ω-3 PUFAs content of 53.42% with the hydrolysis rate of 48.78% under optimal condition. The Km and Vmax value of HPHSM-C3@CRL was 42.2% lower and 63.5% higher than those of CRL, respectively. The 3D structure analysis of CRL, substrates and pore structure of HPHSM-C3 suggested that the hierarchical pore improved activity and selectivity of immobilized lipase. This result demonstrated that HPHSM-C3@CRL may be an effective biocatalyst for the enzymatic enrichment of ω-3 PUFAs in food industries.

Green conversion of CO2 by N-heterocyclic carbene-CO2 adducts grafted hierarchical porous silica microspheres

The multiphase catalysts DMSNs-Cb-X containing NHC-CO2 adducts were synthesized by soft template method that is, first preparing dendritic multi-model pore silica nanoparticles (DMSNs) with central-radial structure, and then grafting imidazoline functional groups, and finally allowing to react with dimethyl carbonate to graft NHC-CO2 adducts. The investigations had the scope to improve the performance and to elucidate the effect of NHC-CO2 adducts on the CO2 cycloaddition reaction. The optimum catalyst DMSNs-Cb-1 and the optimum reaction conditions (200 mg, 100 °C, 10 h) were obtained via thermogravimetric analysis. CO2 cycloaddition reaction with epoxide DMSNs-Cb-1 can convert CO2 and epoxide to cyclic carbonate at ambient pressure without solvent and co-catalysts (1 bar, 100 °C). The reaction proceeds with high yield and high conversion frequency (TOF = 27.4 h−1). The prepared catalyst is easily recovered and still has high activity after five cycles of experiments. The excellent catalytic performance of the obtained catalyst can be attributed to the synergy of hierarchical porous structure and NHC-CO2 adducts acting as CO2 adsorption sites as well as zwitterionic catalytic sites. This work demonstrates an efficient strategy for green conversion of CO2 into cyclic carbonates.

Hyperactivation of lipase by oil-water interface in interfacial immobilization on hierarchical porous hollow silica microsphere: dynamics, mechanism and application

Lipases exhibit high activity at oil−water interfaces due to interfacial activation effect. In this work, the interfacial immobilization of lipase was developed based on Pickering emulsion through using lipase solution as the aqueous phase, n-hexane as oil phase, and stabilized by modified hierarchical porous hollow silica microsphere (HPHSM-C1). The prepared immobilized lipase HPHSM-C1@AY400-II achieved highest specific activity (6.4 IU/mg) with the amount of immobilized protein of 34.5 mg/g, surpassing traditional adsorptive immobilized lipase (HPHSM-C1@AY400) by 1.89-fold, and retained 70 % of residual activity after ten operational cycles. The conformational change of HPHSM-C1@AY400-II was confirmed by Fourier transform infrared. The interfacial adsorption at oil-water interface was influenced by intraparticle and surface diffusion, as evidenced by adsorption kinetic. Finally, the HPHSM-C1@AY400-II was applied in enzymatic enrichment of ω-3 polyunsaturated fatty acids (ω-3 PUFAs) in glycerides, and the content of ω-3 PUFAs in the glyceride significantly increased from 32.35 % to 54.78 % after 3 h of selective hydrolysis. This study opens a promising avenue to improve lipase activity in immobilization process, contributing to enzymatic synthesis of functional lipids.

Ionic liquid/covalent organic framework/silica composite material: Green synthesis and chromatographic evaluation

BackgroundDue to their large surface area and distinctive adsorption affinity, covalent organic frameworks (COFs) appear to be good candidates as liquid chromatographic separation materials with good application prospect. The development of COF materials in chromatographic science is currently in an exploratory stage. Especially, the practicability of COF@silica composite materials as liquid chromatographic stationary phases needs further exploration. Reasonably integrating a functional component such as ionic liquid (IL) into the COF@silica composite materials may provide customized functionality to achieve the purpose of synthesizing multi-functional COF based stationary phases. ResultsIn this study, an IL modified COF bonded silica composite material (IL-COF@SiO2) was successfully synthesized by using an environmentally friendly deep eutectic solvent as the reaction medium instead of the frequently-used organic solvent. The synthesized IL-COF@SiO2 composite material combines the excellent separation ability of COF and the excellent mass transfer function of spherical porous silica microsphere, and meanwhile, the introduction of IL endows COF@SiO2 with preferable separation performance. The slurry-packed IL-COF@SiO2 liquid chromatographic column could be applied to effectively separate hydrophobic and hydrophilic compounds with preferable separation selectivity and high column efficiency. By investigating the retention behavior and influencing factors, a mixed-mode retention mechanism was found. Multiple interaction forces endow the IL-COF@SiO2 with a hydrophilic-hydrophobic balance performance, demonstrating a good application prospect as a versatile liquid chromatographic separation material. SignificanceIn this study, a new strategy is proposed for greenly synthesizing a novel IL-COF@SiO2 composite material under mild conditions, which expands the potential application of COF materials in chromatographic science. One particular point to note is that the reaction medium in each step of the preparation process is low toxic and degradable deep eutectic solvent, which conforms to the concept of green chemistry.

Preparation of porous silica microspheres using silica nanoparticles with different morphologies and their properties as catalyst carriers

Preparation of porous silica microspheres using silica nanoparticles with different morphologies and their properties as catalyst carriers

A novel target-triggered signal chemiluminescence kit for thrombin detection based on fusiform Au/MIL-53(Fe)

In this work, a fusiform Au/MIL-53(Fe) catalyst was used to construct a chemiluminescence (CL) kit for the sensitive and rapid detection of thrombin (THR). The porous silica microspheres encapsulated with luminol in holes by thrombin aptamer (THR-APT/Luminol/SPSiO2) and the fusiform Au/MIL-53(Fe) modified with thrombin aptamer complementary chains (Au/MIL-53(Fe)-SSDNA) were prepared. Then, a CL kit for THR detection was constructed by using the prepared composites. When thrombin is added to the reaction system, it binds to its aptamer (THR-APT) to open the holes of SPSiO2, which cause luminol and Au/MIL-53(Fe) release. Released luminol enters the detection system and triggers the reaction of luminol–H2O2–NaOH with the catalyst of Au/MIL-53(Fe), and produces a CL signal. The detection limit and the linear range of the kit were 4.7 × 10−15 M and 1.5 × 10−14 – 3.5 × 10−10 M, respectively. The CL kit also showed high stability, selectivity and reproducibility, and was successfully applied to the determination of THR in serum samples. Therefore, the proposed method for detecting THR has great application potential in the diagnosis of blood-related disease markers.

Hybridization of helical poly(phenylacetylene)s bearing L-proline tripeptide pendants into porous silica microspheres as a solvent-tolerable chiral stationary phase for liquid chromatography.

A novel one-handed helical copoly(phenylacetylene) (CPA) bearing L-proline tripeptide pendants and a few triethoxysilyl residues was synthesized and hybridized into SiO2 porous microspheres (PMSs) during microsphere growth through the hydrolytic polycondensation of ethoxysilyl groups. Nuclear magnetic resonance and Fourier transform infrared spectroscopy results verified the successful preparation of CPA and its hybrid product using SiO2 PMSs. The chiral recognition ability of the resulting CPA with a hybridized-type chiral stationary phase (HCSP) for high-performance liquid chromatography (HPLC) was investigated, revealing its high recognition ability for selected racemates. Moreover, the HCSP showed good solvent tolerability, thus broadening the selection of suitable eluents. The separation effect of the HCSP for the racemate N,N-diphenylcyclohexane-1,2-dicarboxamide (7) improved significantly after introducing CHCl3 in the eluent, resulting in separation factors equivalent or superior to common commercially available polysaccharide-based chiral stationary phases. The proposed preparation strategy provides a new and valuable method for obtaining poly(phenylacetylene)-based HCSPs suitable for a wide range of applications and eluent conditions.

Metal salts assisted thermoplastic polymer NIPAM in-situ carbonization on porous silica microspheres surface

The preparation of different carbon-shell morphology microspheres and controllable surface area via using thermoplastic polymers as carbon source was still a challenge. In addition, the unique structure of porous Silica@Carbon (Sil@C) microspheres not only can provide larger surface area and active site, but also have the characteristics of high mechanical strength and easy modification. Herein, we report a simple method to in-situ fixation a series of different morphology graphitized carbon shell (rosa roxburghii, bulk, and carbon sphere shapes) on porous silica microspheres surface. Metal salt assisted polymer carbonization will not only prepare graphitized carbon with different morphology on silica surface, but also facilitate the in-situ carbonization of thermoplastic polymer on the silica microspheres surface instead of internal pores; the more heat of metal salt released during carbonization, the larger the specific surface area of Sil@C.

Bimetallic Pd‐Au Nanoparticles Supported Monodisperse Porous Silica Microspheres as an Efficient Heterogenous Catalyst for Fast Oxidation of Benzyl Alcohol

AbstractA bimetallic heterogeneous catalyst in the form of PdAu nanoparticle supported monodisperse‐porous SiO2 microspheres (PdAu@APTES@SiO2) was prepared for fast oxidation of benzyl alcohol (BzOH). The mesoporous support obtained by an originally developed staged‐shape templated hydrolysis‐condensation protocol provided large surface area and high pore volume for parking of noble metal nanoparticles. PdAu@APTES@SiO2 provided higher BzOH conversion, benzaldehyde (BzH) selectivity and BzH formation yield with respect to monometallic catalysts containing Pd or Au nanoparticles supported with SiO2 microspheres. BzOH conversions and BzH formation yields higher than 95 % were obtained in 30 min at 80 °C. The maximum TON and TOF values were determined as 300 and 600 h−1, respectively. BzOH conversions and TOF were also higher with respect to similar catalysts prepared using different supports also carrying PdAu nanoparticles. PdAu@APTES@SiO2 exhibited good stability with a decrease of BzOH conversion less than 2.5 % over five consecutive runs.

Synthesis and application of 5 μm monodisperse porous silica microspheres with controllable pore size using polymeric microspheres as templates for the separation of small solutes and proteins by high-performance liquid chromatography

High-performance liquid chromatography (HPLC) is a powerful tool to separate and analyze complex samples. Monodiseperse porous silica microspheres (MPSMs) have been widely used as column packings in HPLC. However, synthesis of MPSMs with controllable sizes of both particles and pores for the separation of small solutes and proteins in HPLC still remains a challenge. In this paper, an effective and facile approach to prepare MPSMs with controllable particle size and pore size by using porous polymer microspheres as templates is presented. By employing porous PGMA/EDMA microspheres as templates and tetraethyl orthosilicate (TEOS) as the silica source, 5 μm MPSMs with tunable pore sizes were synthesized successfully. The as-prepared MPSMs were characterized by scanning electron microscopy (SEM), Fourier transform infrared (FT-IR) spectroscopy, thermogravimetric analysis (TGA), dynamic laser scattering, and mercury intrusion porosimetry. The results indicated that the MPSMs obtained retained the original size of the polymer templating particles and calcination caused almost no shrinkage. Furthermore, the effects of the pore size of polymer template microspheres, different amino-functionalizations of PGMA/EDMA microspheres and the mass ratio of PGMA/EDMA microspheres/TEOS on the pore size of MPSMs were carefully studied. The results indicated that the pore size of MPSMs was adjusted from 20 to 69 nm by controlling the pore size of the polymer microspheres and the mass ratio of PGMA/EDMA microspheres/TEOS in the sol-gel process. In addition, the amino-functionalization of PGMA/EDMA microspheres with different structure-directing agents, such as (3-aminopropyl)triethoxysilane (APTES), trimethylamine hydrochloride (TMA) and tetraethylenepentamine (TEPA), also resulted in MPSMs with the different pore sizes. MPSMs with large pore sizes of more than 30 nm were fabricated by using TEPA-functionalized PGMA/EDMA microspheres as templates, while with TMA-functionalized PGMA/EDMA microspheres as templates, MPSMs with pore sizes of approximately 10 nm were obtained. The as-prepared MPSMs were further modified with different silanes, such as C4, C8 and C18, to explore as stationary phases for the separation of proteins and small solutes in reversed phase liquidi chromatography (RPLC). The results illustrated that the baseline separation of 7 kinds of proteins could be achieved based on MPSMs with pore sizes of 30 nm, and 6 kinds of alkyl benzenes and 5 kinds of aromatic alcohol homologs could be separated completely based on MPSMs with pore sizes of 11 nm. This work demonstrated that MPSMs prepared by applying the polymer templating method showed a promising potential applicability in HPLC.

Carbon Dots with an Emission in the Near Infrared Produced from Organic Dyes in Porous Silica Microsphere Templates.

Carbon dots (CDs) with an emission in the near infrared spectral region are attractive due to their promising applications in bio-related areas, while their fabrication still remains a challenging task. Herein, we developed a template-assisted method using porous silica microspheres for the formation of CDs with optical transitions in the near infrared. Two organic dyes, Rhodamine 6G and IR1061 with emission in the yellow and near infrared spectral regions, respectively, were used as precursors for CDs. Correlation of morphology and chemical composition with optical properties of obtained CDs revealed the origin of their emission, which is related to the CDs’ core optical transitions and dye-derivatives within CDs. By varying annealing temperature, different kinds of optical centers as derivatives of organic dyes are formed in the microsphere’s pores. The template-assisted method allows us to synthesize CDs with an emission peaked at 1085 nm and photoluminescence quantum yield of 0.2%, which is the highest value reported so far for CDs emitting at wavelengths longer than 1050 nm.

Bio-templated synthesis of porous silica nano adsorbents to wastewater treatment inspired by a circular economy

Water is an indispensable substance in human life activities. However, due to industrial discharge problems, water resources are polluted, so there is an urgent need for material and technology for wastewater treatment. This paper presents an innovative synthesis of porous silica microspheres (PSM) from a biomass template material (fish skin collagen) to treat protein from wastewater. The collagen from the biomass template was rich in amino, carboxyl, and hydroxyl groups that effectively controlled the hydrolysis rate of tetraethyl orthosilicate (TEOS) and promoted the synthesis of structured PSM. X-ray photoelectron spectroscopy (XPS), X-ray powder diffraction (XRD), nitrogen sorption isotherms measurements, scanning electron microscopy (SEM) and transmission electron microscopy (TEM) were utilized to characterize the chemical composition, crystalline structure, and pore architecture of the synthesized PSM. The characterization results confirmed that the PSM were spherical with the microporous and mesoporous structure in shape and approximately 400 nm in size. Moreover, the pore size could be tuned by addition of mesitylene (TMB). The large number of silicon hydroxyl groups on the PSM surface effectively bound proteins in wastewater and greatly improved the overall absorption rate. The PSM adsorption capacity for lysozyme (LZ) was 49.5 mg/g, and the adsorption behavior was well described by a pseudo-second-order kinetic model and the Langmuir model. Most importantly, the PSM effectively removed protein from actual industrial wastewater, thereby realizing a high value-added utilization of wastewater pollutants.

Fabrication of naphthol-based phenolic polymer coated-silica for mixed-mode chromatography

This paper introduces a novel phenolic resin-coated silica stationary phase grafted from the surface of amino-functionalized porous silica microspheres through copolymerization of 1,5-dihydroxynaphthalene and 1,3,5-trioxane in the dispersed state, followed by low-temperature calcination at 200 °C. The new material was identified by scanning electron microscopy, elemental analysis, thermogravimetric analysis and Fourier-transform infrared spectroscopy. The new column has the capability to separate different types of compounds. When utilizing hydrophilic interaction liquid chromatography, sulfonamide drugs and nucleosides/nucleobases could be separated with good resolution even if there were no buffer salts in the eluent. In reversed-phase liquid chromatography, the column indicated satisfactory separation abilities for positional isomers, alkylbenzenes as well as polycyclic aromatic hydrocarbons (PAHs). The selectivity and retention of the new column for PAHs were higher than those for alkylbenzene, which may be affected by the π–π forces between the PAH analytes and naphthalene ring from the surface of the silica. Depending on the retention mode, the elution order can be reversed using this column. Thus, the stationary phase was intended as a novel mixed-mode column. Meanwhile, the retention and selectivity can be adjusted very flexibly by changing the chromatographic conditions.

高碳含量新型亚微米无孔二氧化硅材料的修饰方法及其在反相加压毛细管电色谱平台上的应用

亚微米无孔二氧化硅(NPS)材料具有小粒径及表面光滑形状规整等特点,是一种性能优异的色谱材料,但其存在比表面积小、修饰效率低的问题。针对此设计了一种具有高碳含量的修饰方法:以3-缩水甘油基氧基丙基三甲氧基硅烷(GPTS)作为硅烷偶联剂,聚乙烯亚胺(PEI)作为聚合物包覆层,并以硬脂酰氯修饰得到一种氨基包覆的具有C18碳链结构的新型亚微米无孔二氧化硅材料(C18-NH2-GPTS-SiO2)。利用元素分析、傅里叶变换红外光谱、Zeta电势等进行表征,证明C18-NH2-GPTS-SiO2固定相的成功制备。该修饰方法将NPS的碳含量从0.55%提高到了8.29%,解决了过往NPS材料采用十八烷基氯硅烷等传统C18修饰方法时碳含量较低的问题。此外,29Si固体核磁显示:NPS与多孔二氧化硅(PS)微球相比不仅存在孔结构与比表面积区别,且表面硅羟基种类也不同。16%的PS微球硅原子带有一个硅羟基(孤立硅羟基,Q3)、19%带有两个硅羟基(偕硅羟基,Q2);而NPS微球不存在偕硅羟基,仅有30%硅原子处于孤立硅羟基状态。实验发现NPS微球存在硅羟基数量低且缺少偕硅羟基的特点,导致NPS材料表面修饰活性低,难以通过简单一步反应获得高碳含量。采用不同疏水物质如苯系物、多环芳烃对色谱性能及保留机理进行研究,结果表明C18-NH2-GPTS-SiO2色谱柱符合反相作用机理。氨基的包覆改变硅球表面电性,提高了NPS材料运用于加压毛细管电色谱平台(pCEC)时的电渗流大小,施加+15 kv时,显示出良好的分离能力,证实了C18-NH2-GPTS-SiO2材料通过多步反应提高碳含量的修饰方法在pCEC平台上应用的优异性。

Carbene-Co2 Adducts Grafted Hierarchical Porous Silica Microspheres as Heterogeneous Catalyst for Efficient Conversion of Co2 into Cyclic Carbonates

Carbene-Co2 Adducts Grafted Hierarchical Porous Silica Microspheres as Heterogeneous Catalyst for Efficient Conversion of Co2 into Cyclic Carbonates

Pseudomorphic synthesis of bimodal porous silica microspheres for size-exclusion chromatography of small molecules

In this work, mesoporous silica microspheres with bimodal porous structures for size exclusion chromatography (SEC) supports were synthesized via a pseudomorphic transformation method by using 3.5 and 5 μm commercial silica particles as sources and cetyltrimethylammonium bromide (CTAB) as a template. The effects of the synthetic conditions on the pore size distribution were examined, including the temperature, reaction time and the molar ratio of SiO2:NaOH. Bimodal porous silicas (BPSs) with pore sizes of 3.01 and 12.80 nm were obtained with SiO2:NaOH:CTAB:H2O=1:0.1:0.1:20 at 80 °C for 24 h. The BPSs were bonded with diol groups to produce a stationary phase for SEC. The column performance was evaluated with three types of samples, namely, dextran (70 KDa-62 Da), polyethene glycol (PEG) (20 KDa-32 Da) and three biomolecules (36 KDa-1.36 KDa). The column that was packed with a 3.5 μm stationary phase showed excellent resolution for molecular weights of less than 1 KDa with high column efficiency. Carbohydrate samples (dextran (MW=1296), dextran (MW=972), sucrose (MW=342), glucose (MW=180) and glycerol (MW=92)) were separated. Heptaethylene glycol, hexaethylene glycol, pentaethylene glycol, tetraethylene glycol, triethylene glycol, and diethylene glycol were resolved in a PEG200 sample. In summary, this work shows the advantages of bimodal mesopores in SEC for small molecules less than 1 kDa. In the pseudomorphic synthesis, the pore size can be regulated by template micelles. Thus, the development SEC supports with high accuracy for a specified molecular weight range is expected since the pore size can be regulated by the surfactant template.

Highly Porous, Molecularly Imprinted Core–Shell Type Boronate Affinity Sorbent with a Large Surface Area for Enrichment and Detection of Sialic Acid Isomers

Molecularly imprinted, core–shell type boronate affinity sorbents for isolation and detection of sialic acid (SA) isoforms, N-acetylneuraminic acid (Neu5Ac) and N-glycolylneuraminic acid (Neu5Gc), were synthesized. The monomer mixture containing a phenylboronic acid functionalized monomer was polymerized on highly porous silica microspheres 5.5 μm in size, in the presence of a SA isomer. The selection of highly porous silica microspheres as the core material eliminated the risk of agglomeration during the formation of polymer shell and resulted in the synthesis of a boronate affinity sorbent with a large surface area available for parking of high number of SA molecules. Neu5Ac was extracted from human serum with high isolation yield and successfully determined in the elution medium by LC-MS/MS. The sorbent is a promising stationary phase for precolumn purification of SA isoforms before LC-MS/MS due to its suitable particle size and high porosity.

Porous Silica Microspheres with Immobilized Titania Nanoparticles for In-Flow Solar-Driven Purification of Wastewater.

In this paper, inorganic silica microspheres with interconnected macroporosity are tested as a platform for designing robust and efficient photocatalytic systems for a continuous flow reactor, enabling a low cost and straightforward purification of wastewater through solar‐driven photocatalysis. The photocatalytically active microspheres are prepared by wet impregnation of porous silica scaffolds with Trizma‐functionalized anatase titania (TiO2) nanoparticles (NPs). NPs loading of 22 wt% is obtained in the form of a thin and well‐attached layer, covering the external surface of the microspheres as well as the internal surface of the pores. The TiO2 loading leads to an increase of the specific surface area by 26%, without impacting the typically interconnected macroporosity (≈60%) of the microspheres, which is essential for an efficient flow of the pollutant solution during the photocatalytic tests. These are carried out in a liquid medium for the decomposition of methyl orange and paracetamol. In addition to photocatalytic activity under continuous flow, the microspheres offer the advantage that they can be easily removed from the reaction medium, which is an appealing aspect for industrial applications. In this work, the typical issues of TiO2 NPs photocatalysts are circumvented, without the need for elaborate chemistries, and for low availability and expensive raw materials.

Interface Chemical Modification between All-Inorganic Perovskite Nanocrystals and Porous Silica Microspheres for Composite Materials with Improved Emission.

In recent years, there has been rapid progress in the development of photonic devices based on lead halide perovskite nanocrystals since they possess a set of unique optical and charge transport properties. However, the main limiting factor for their subsequent application is poor stability against exposure to adverse environmental conditions. In this work, a study of a composite material based on perovskite CsPbBr3 nanocrystals embedded in porous silica microspheres is presented. We developed two different approaches to change the interface between nanocrystals and the surface of the microsphere pores: surface treatment of (i) nanocrystals or (ii) microspheres. The surface modification with tetraethylorthosilicate molecules not only increased stability but also improved the optical responses of the composite material. The position of the emission band remained almost unchanged, but its lifetime increased significantly compared to the initial value. The improvement of the optical performance via surface modification with tetraethylorthosilicate molecules also works for the lead-free Bi-doped Cs2AgInCl6 double perovskite nanocrystals leading to increased stability of their optical responses at ambient conditions. These results clearly demonstrate the advantage of a composite material that can be used in novel photonic devices with improved performance.