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JOURNAL OF MATERIALS SCIENCE-MATERIALS IN ELECTRONICS · 2021 ·Vol. 32 ·期 15 ·20104-20114 · IF 2.478

Ag nanoparticle-decorated SiO2@TiO2 hierarchical microspheres improve the efficiency of dye-sensitized solar cells

Sun Junchen,Fang Min,Zhu Weiju,Wu Zhenyu,Li Cun

SiO 2 @TiO 2 -Ag (STA) microspheres decorated with Ag nanoparticles (Ag NPs) were prepared and assembled into the photoanode. The photoanode composed of STA microspheres and TiO 2 nanoparticles (P25) was prepared by doctor blade method. UV–vis measurement indicates that the introduction of a few STA microspheres observably enhances the light scattering and capturing ability of the photoanode. The photoelectric conversion efficiency of the DSSCs with 2wt% STA photoanode increased to 7.4% from 4.3% comparing with pure P25 TiO 2 nanoparticles. The configuration DSSCs have the maximum short circuit current density ( J sc ) of 16.0 mA cm −2 and open-circuit voltage ( V oc ) of 0.780 V, which are significantly higher than the pure TiO 2 DSSCs. The significant improvement of the DSSCs performance can be due to the synergistic effect of the superior light scattering of STA and the localized surface plasma resonance (LSPR) effect of Ag NPs modified on the microspheres surface.

CAS / MDL: 13463-67-7 546-68-9
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ChemCatChem · 2021 ·Vol. 13 ·期 14 ·3312-3318 · IF 5.686

Fabrication of h-BN/SiO2 Nanofibers Showing High Olefins Productivity in Oxidative Dehydrogenation of Propane

Ding Ding,Bing Yan,Yang Wang,An-Hui Lu

Graphical Nanofiber Catalysis : Hexagonal boron nitride has been regarded as a potential inorganic nonmetallic catalyst for the oxidative dehydrogenation of propane. Herein, a novel nanofiber catalyst consisting of hexagonal boron nitride/silica oxide ( h -BN/SiO 2 ) was prepared via electrospinning method, which exhibited remarkable 24.9 g olefins ⋅ g BN −1 ⋅ h −1 productivity of olefins in oxidative dehydrogenation of propane. Fibrous nanomaterials have drawn considerable attention in the field of catalysis due to the promoted utilization of the surface and facilitated mass transfer process. In this study, we prepared one-dimensional nanofiber catalysts consisting of hexagonal boron nitride/silica oxide ( h -BN/SiO 2 ) via electrospinning method. The key is to prepare uniform sols consisting of exfoliated h -BN. The diameters of the nanofiber catalysts can be tuned in the range of 150–300 nm through h -BN loading change. When used in oxidative dehydrogenation of propane (ODHP), the obtained nanofibrous catalysts exhibited a 12.4 % conversion of propane and 85.1 % selectivity towards propylene, with remarkable olefins productivity of 24.9 g olefins ⋅ g BN −1 ⋅ h −1 , which is more than 5 times higher than that of bulk ODHP catalysts reported to date. This study shines light on the specific one-dimensional fibrous structure containing dispersed h -BN as well as a new strategy of preparing more efficient boron-based catalysts in the ODHP process.

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JOURNAL OF SOLID STATE CHEMISTRY · 2021 · IF 3.498

A facile synthesis method of TiO2@SiO2 porous core shell structure for photocatalytic hydrogen evolution

Xian Yue,Huaxin Li,Yunsheng Qiu,Zhou Xiao,Xianbo Yu,Chao Xue,Junhui Xiang

Limited by low specific surface area and complex synthesis methods, it is laborious to realize wide utilization of photocatalytic materials. Although various photocatalytic materials have been reported constantly, as a vital prototype of photocatalytic materials with the advantages of low cost, no-toxicity, and high stability, TiO 2 still reveals great research potential. Nevertheless, pure TiO 2 usually present small specific surface area and low photocatalytic activity . Besides, the preparation process of composite photocatalysts based on TiO 2 remain inconvenient. Hence, to enhance the photocatalytic activity of TiO 2 , this work proposed a facile synthesis method to fabricate a TiO 2 @SiO 2 porous core shell structure materials based on our previous research. Specifically, silica microspheres were prepared by one-step method with atmospheric pressure drying. And TiO 2 @SiO 2 composite gel was fabricated by a primitive liquid phase deposition . The whole process retains simple and green and the obtained porous core shell materials display extraordinary specific surface area (over 400 ​m 2 /g) with high photocatalytic efficiency. Under optimized conditions, the H 2 production rates are roughly 3 times higher than that of P25 powder, which shows great application potential. This study confirms that the photocatalytic performance can be enhanced by improvement of active site area and provides some insights in convenient preparation of TiO 2 based photocatalysts as well.

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JOURNAL OF APPLIED POLYMER SCIENCE · 2021 ·Vol. 138 ·期 37 ·50943 · IF 3.125

Core-shell structured BaTiO3@SiO2@PDA for high dielectric property nanocomposites with ultrahigh energy density

Rui Wang,Congzhen Xie,Bin Gou,Huasong Xu,Shoukang Luo,Yan Du,Jiangang Zhou,Hao Yang

Flexible nanocomposite dielectrics with high dielectric constant and discharge energy density have broad application prospects in the field of energy storage. However, dielectrics with high dielectric constant tend to have a high dielectric loss. Herein, we prepared a dielectric composite material with ultra-high discharge energy density by modifying the interface between nanoparticles and poly(vinylidene fluoride-co-hexafluoropropylene) (P[VDF-HFP]). After coating a shell of insulating amorphous SiO 2 (~7 nm) outside the barium titanate (BT), the electric field concentration and current density inside BT particles can be significantly reduced. In addition, coating the SiO 2 shell with a polydopamine (PDA) shell (~7 nm) not only enhances the interface interaction between the nanoparticles and the polymer matrix, but also can form lots of microcapacitors in the composite. As a result, an ultra-high discharge energy density of 13.78 J/cm 3 at the expense of relatively inconspicuous efficiency (~59.8%) in the BT@SiO 2 @PDA/P (VDF-HFP) with 2.5 wt% loading has been achieved under 460 kV/mm. This is mainly attributed to the increases of dielectric constant from 12.1 to 14.2 and the relatively low dielectric loss (0.086) at 100 Hz. Moreover, compared with the pure P (VDF-HFP) (400 kV/mm), the breakdown voltage of the composite with 2.5 wt% loading is surged to 460 kV/mm, which benefited from the hindrance of nanoparticles on carrier migration at low content. This work has realized a thin-film dielectric with ultra-high discharge energy density through a novel design of the nanoparticle structure, providing a theoretical direction for the development of polymer dielectric capacitors.

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JOURNAL OF HAZARDOUS MATERIALS · 2021 · IF 10.588

Self-assembling of versatile Si3N4@SiO2 nanofibre sponges by direct nitridation of photovoltaic silicon waste

Nannan Zhang,Daoping Xiang

Solar cells based on crystalline silicon wafers have dominated the global photovoltaic market for many years. Unfortunately, a large amount of photovoltaic silicon waste (PSW) also was produced during the process of cutting silicon ingot into silicon wafer. The improperly discarded PSW will bring about serious environmental hazardous problems, so it is highly necessary to safely and effectively recover and utilize PSW. Here, we report self-assembled 3D Si 3 N 4 @SiO 2 nanofibre sponges utilising PSW as silicon sources for the first time. This kind of ceramic sponge displays excellent compression resilience under a maximum strain of 67% due to the flexibility of the Si 3 N 4 @SiO 2 nanofibres. The Si 3 N 4 @SiO 2 nanofibre sponges can withstand high temperatures beyond 1200 °C with negligible weight loss and demonstrates favourable thermal insulation properties. Furthermore, the porous Si 3 N 4 @SiO 2 nanofibre sponges possess ultra-low dielectric properties , with the minimum dielectric constant and dielectric loss approaching 1 and 0, respectively. In short, a simple and low-cost technology using industrial waste to fabricate versatile Si 3 N 4 @SiO 2 nanofibre sponges with prominent performance is of great significance for the development and application of 3D ceramic architectures in various industry fields including aerospace, electronic devices and thermal insulation.

CAS / MDL: 12033-89-5
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INTERNATIONAL JOURNAL OF HYDROGEN ENERGY · 2021 · IF 5.816

New gas chromatographic packing ZIF-67@NH2–SiO2 for separation of hydrogen isotope H2/D2

Xiaoxiao Chen,Mengyao Liu,Lijuan Zhang,Yunshan Zhou,Enming Ping,Chunyan Ding

ZIF-67@NH 2 –SiO 2 composites were prepared by loading the metal-organic frameworks ZIF-67 on amino modified SiO 2 gel particles (NH 2 –SiO 2 , 80–100 mesh) through layer-by-layer self-assembly method. Systematic investigation on the effects of ZIF-67 loading amounts on NH 2 –SiO 2 packed stainless steel chromatographic column (specification 1.0 m×2.0 mm I.D.), the flow rate of He as carrier gas and the injection amount of mixed gas (H 2 /D 2 ) on the hydrogen isotope H 2 /D 2 separation performance at liquid nitrogen temperature, unraveled the optimal conditions for H 2 /D 2 isotope separation . The results showed that the optimal stationary phase materials under the optimized conditions can effectively separate H 2 and D 2 with separation resolution R = 1.52 and the separation time t = 10.15 min. The superior performance of the ZIF-67 is tentatively thought to be due to kinetic quantum sieving (pore size 3.3 Å) effect and chemical affinity sieving effect of Co ion in ZIF-67.

CAS / MDL: 112926-00-8
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JOURNAL OF SOL-GEL SCIENCE AND TECHNOLOGY · 2021 ·Vol. 98 ·期 1 ·224-237 · IF 2.326

Fabrication of superhydrophobic PET filter material with fluorinated SiO2 nanoparticles via simple sol–gel process

Dong Wei,Qian Fuping,Li Qing,Tang Gang,Xiang Tengfei,Chun Tiejun,Lu Jinli,Han Yunlong,Xia Yongjun,Hu Jia

A high moisture content in the flue gas of iron and steel sintering process causes the issue of filter material pasting, which leads to a decrease in the filtration effect and service life of the filter material. Surface modification of the filter materials is a useful strategy for their hydrophobicity enhancement. Therefore, the Sol–gel method was employed to modify the polyethylene glycol terephthalate (PET) filter with tetraethyl orthosilicate(TEOS) as precursor and perfluorodecyl triethoxysilane (PFDTES) as modifier. Field emission scanning electron microscope (FESEM), Fourier transform infrared spectrometer (FT-IR), and contact angle tester were used to characterize the PET filter materials before and after modification, and exhaustive filter efficiency was evaluated by the comprehensive performance test machine. The particle size and distribution of SiO 2 nanoparticles were analyzed using a nanometer particle size analyzer, the effects of TEOS/PFDTES loading on the hydrophobic performance and filtration performance of the filter material have been discussed. Based on the results of these studies, superhydrophobic stability of the filter material was evaluated. The results show that the microscopic pore structure of PET filter materials was retained after modification. TEOS modified PET (T-PET) filter materials were completely wetted with static contact angle (WCA) of 0°. The surface energy of PFDTES modified PET (F-PET) filter materials was reduced, the WCA was 144.6 ± 1.6° and WSA was 7.6 ± 4.5°. For TEOS/PFDTES co-modified PET (TF-PET), the SiO 2 nanoparticles was modified by the long fluorine chain -CH 2 CH 2 (CF 2 ) 7 CF 3 groups, endowing TF-PET with superhydrophobic property. With the increasing of TEOS loading, TF-PET fiber presented significant enhancement of roughness, while average particle size of SiO 2 nanoparticles on the fiber surface gradually decreased. The particle size distribution first increased sharply, and then, slowly decreased when TEOS addition was enhanced. TF-PET filter material possessed WCA of 163.2 ± 2.3°, while when TEOS: PFDTES mass ratio was 2.5:2, WSA was 6.2 ± 1.9° with filtration efficiency (0.3 μm) of 68.61%.

CAS / MDL: 78-10-4
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METALLURGICAL AND MATERIALS TRANSACTIONS B-PROCESS METALLURGY AND MATERIALS PROCESSING SCIENCE · 2020 ·Vol. 52 ·期 1 ·314-321 · IF 2.035

The Distribution of Cobalt Between Co-Cu Alloys and Alumina-Saturated MnO-SiO2-Al2O3 Slags

Ren Guoxing,Xiao Songwen,Xia Longgong,Liao Caibin,Liu Zhihong

To obtain fundamental information on the dissolution of cobalt into alumina-saturated MnO-SiO 2 -Al 2 O 3 slags in the smelting reduction of spent lithium-ion batteries, the equilibrium distribution of cobalt between Co-Cu alloys and alumina-saturated MnO-SiO 2 -Al 2 O 3 slags was measured at 1573 K and 1623 K under a controlled CO-CO 2 atmosphere. The results show that (i) the solubility of cobalt in the slag increased with increasing concentration of cobalt in the alloy and increasing oxygen partial pressure in the atmosphere at a fixed concentration of cobalt in the alloy, and (ii) the activity coefficient of CoO in the slag increased with increasing cobalt oxide in the slag. The activity coefficient of CoO in the slag, γ CoO, referred to as solid CoO, can be described as a function of the concentration of CoO in slag as follows: γ CoO  = 11.2957(wt pct CoO in slag) + 12.0944 (1573 K, (wt pct MnO)/(wt pct SiO 2 )= 0.76–0.83); γ CoO  = 2.2286(wt pct CoO in slag) + 4.5232 (1623 K, (wt pct MnO)/(wt pct SiO 2 )= 0.78–0.85).

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LANGMUIR · 2020 · IF 3.557

pH-Responsive Non-Pickering Emulsion Stabilized by Dynamic Covalent Bond Surfactants and Nano-SiO2 Particles

Ying Zhang,Hongsheng Lu,Baogang Wang,Na Wang,Dongfang Liu

A novel stimulus-responsive non-Pickering emulsion stabilized by nano-SiO2 particles was prepared in our recent study. 4-formylbenzoic acid and hexylamine through a dynamic covalent bond form a surface-active substance, which was confirmed by Fourier transform infrared (FTIR) and 1H NMR. Through optimization experiments, it was proved that a stable emulsion can be formed by low surfactant concentration (below cmc) and low nano-SiO2 particle concentration (0.5 wt %). In this emulsion, nano-SiO2 particles are not located at the interface of oil–water but dispersed in the continuous phase of the emulsion, which is different from the Pickering emulsion. The negatively charged nano-SiO2 particles and anionic surfactants repel each other, thereby synergistically stabilizing the emulsion so that the concentrations of surfactants and nanoparticles required to stabilize the emulsion are reduced. In addition, the system can also control the formation and fracture of dynamic covalent bonds by changing pH, thereby controlling the stability and demulsification of the emulsion. At the same time, this non-Pickering emulsion could be used as a microreactor for chemical synthesis and still had a high yield after three cycles. This study provides a new application direction for this environmentally friendly emulsion.

CAS / MDL: 111-26-2 81-88-9
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SEPARATION AND PURIFICATION TECHNOLOGY · 2020 · IF 5.774

Constructing superhydrophobic surface of PES/PES-SiO2 mixed matrix membrane contactors for efficient SO2 capture

Qingping Xin,Chao Zhang,Yu Zhang,Qingqing Liang,Lei Zhang,Shaofei Wang,Hui Ye,Xiaoli Ding,Yuzhong Zhang

Obtaining high SO 2 absorption flux for membrane contactor is noticeably vital for fule gas desulfurization, and superhydrophobic surface is essential to reach excellent desulfurization performance. The development of a generic and low budget strategy for membrane contactors preparation is important in indisturial application. In this study, a superhydrophobic polyethersulfone-silica (PES/PES-SiO 2 ) gas-liquid membrane contactor is fabricated using a facile spin coating method. PES substrate is prepared by a facile non-solvent induced phase separation (NIPS), and then the superhydrophobic surface of PES/PES-SiO 2 is formed on the PES substrate by spin coating method. The solubility parameters of mixed solvent, PES concentration, and SiO 2 content are regulated to investigate the morphology of membrane contactors. On one hand, the surface structure of MMMCs is regulated, and constructs lotus-leaf like morphology, which noticeably elevate surface roughness. On the other hand, SiO 2 nanoparticles enhance hydrophobic characteristic with water contact angle 159° and anti wetting resistance with liquid entry pressure of water (LEP w ) 1.389 bar. Moreover, the SiO 2 nanoparticles help to significantly improve the stability of desulfurization performance, which is much higher than PES control membrane after 12 h test. The SO 2 absorption fluxes and SO 2 removal efficiencies are 1.24 × 10 −3 mol·m −2 ·s −1 and 63.8%, respectively. Besides, the membrane phase transfer coefficient ( K m ) and membrane phase transfer resistance ( H / K m ) are explored.

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ACS Applied Materials & Interfaces · 2020 · IF 8.758

MOF-Assisted Synthesis of Highly Mesoporous Cr2O3/SiO2 Nanohybrids for Efficient Lewis-Acid-Catalyzed Reactions

Fengfeng Chen,Kui Shen,Yitao Yang,Haigen Huang,Yingwei Li

The facile fabrication of porous solid acids is highly desired for replacing hazardous liquid acids for many acid-catalyzed reactions in the industry. Herein, we present a bottom-up strategy to construct ultrastable mesoporous Cr2O3/SiO2 nanohybrids (denoted as Meso-Cr–Si–O) with highly dispersed Lewis acid sites by pyrolysis of a SiO2@MIL-101 precursor prepared via nanocasting by a reverse double-solvent approach, which can guarantee the efficient encapsulation of SiO2 nanoparticles (NPs) inside the MIL-101 pores. The pore environment of Meso-Cr–Si–O can be well tuned by simply controlling the amount of silica within the MIL-101 pores and the pyrolysis temperature. Pyridine adsorption experiments demonstrate that the density of Lewis acidic sites in the obtained Meso-Cr–Si–O is much higher than that of MIL-101-derived Cr2O3 NPs. Benefitting from its highly mesoporous nanostructure with abundant acid sites, the optimal Meso-Cr–Si–O exhibits a significantly improved catalytic activity for the Lewis-acid-catalyzed Meerwein–Ponndorf–Verley reduction of cyclohexanone with 4.5 times higher yield of cyclohexanol than that of the MIL-101-derived Cr2O3 NPs, representing the first efficient Cr2O3-based catalytic system for this reaction.

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Biomaterials Science · 2020 ·Vol. 9 ·期 5 ·1795-1804 · IF 6.183

Antibacterial activity and reinforcing effect of SiO2–ZnO complex cluster fillers for dental resin composites

Dan-Lei Yang,Ya-Nan Cui,Qian Sun,Mei Liu,Hao Niu,Jie-Xin Wang

The accumulation of bacteria at the margin of dental resin composites is the main reason for secondary caries, which may further cause failure of prosthodontics. Therefore, antibacterial activity is highly required. However, the addition of antibacterial agents or fillers weakens the mechanical or aesthetic properties of composites. In this work, regular-shaped SiO2–ZnO complex clusters (CCs) constructed by spray-drying technology can enhance the antibacterial activity while maintaining the mechanical and aesthetic properties of dental resin composites. The results show that the regular shape and closely packed structure of nanoparticle clusters were not corrupted by the introduction of ZnO particles. As compared to resin composites filled with SiO2 nanoparticle clusters, the comprehensive performances of composites containing SiO2–ZnO CCs were further improved, and the composites filled with 70 wt% Si66Zn4 (CCs composed of 66/70 SiO2 and 4/70 of ZnO) exhibited superior antibacterial capability (antibacterial ratio >99.9%) and acceptable depth of cure, degree of conversion, and biocompatibility. The cooperation of different fillers is highly essential for resin composites to achieve enhanced multifunctional performance.

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