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JOURNAL OF ALLOYS AND COMPOUNDS · 2024 · IF 5.8

Tuning the thermal conductivity of organic-inorganic double-shell thermal storage microcapsules triggered by atomic layer deposition

Linfeng Li,Yaoqi Huang,Yuanyuan Li,Xiaomin Cheng

The regulation of the thermal conductivity of thermal energy storage materials has become a primary challenge to expand the range of utilization for different application scenarios. In this study, organic-shell microcapsule (paraffin@melamine formaldehyde) was initially prepared by in situ polymerization, followed by the deposition of anatase TiO 2 on the organic-shell microcapsule using atomic layer deposition (ALD) to form organic-inorganic double-shell microcapsule. The effect of the thickness of the TiO 2 shell on the equivalent thermal conductivity of the microcapsules was investigated by utilizing ALD's precise and controllable characteristics for the coating thickness. The obtained double-shell microcapsules indicated a drop in thermal storage capacity, but a substantial boost in thermal stability. Moreover, the thermal conductivity of microcapsules can be tuned in the range between 0.1837 and 0.7529 W m −1 K −1 within 1500 ALD cycle treatment. Furthermore, the parameters of ALD, such as reaction temperature and exposure time, were varied to obtain an amorphous TiO 2 shell, and the impacts of different crystal form of TiO 2 on the heat transfer properties of microcapsules were concluded by comparison. Double-shell microcapsules exhibited superior mechanical properties compared to single-shell structure. The findings can stimulate significant research interest in broadening the applications of thermal storage microcapsules.

CAS / MDL: 546-68-9
研究领域: 材料科学 · 能源存储
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ELECTROCHIMICA ACTA · 2013 · IF 3.777

Effect of TiO2 shell layer prepared by wet-chemical method on the photovoltaic performance of ZnO nanowires arrays-based quantum dot sensitized solar cells

Xingtian Yin,Wenxiu Que,Duan Fei,Haixia Xie,Zuoli He

TiO 2 shell layer on the surface of ZnO nanowires (NWs) was synthesized by a layer by layer adsorption and reaction (LBLAR) method. Scanning electron microscopy image shows that the prepared ZnO–TiO 2 core–shell NW arrays have a similar morphology with the well-aligned ZnO core NW arrays, providing the LBLAR cycles is controlled within a certain number. The prepared ZnO–TiO 2 core–shell NW arrays were sensitized with CdS quantum dots to assemble quantum dots sensitized solar cells. Results indicate that a dramatic increase in open-circuit voltage and fill factor is achieved with an introduction of the TiO 2 shell layer with a thickness of about 7   nm, resulting in a substantial improvement of the overall energy conversion efficiency. A rapid electron transfer from the CdS QDs to the ZnO NWs and a reduced electron recombination rate due to the energy barrier occurred at the interface between the ZnO core and the TiO 2 shell are believed to contribute to the improved performance of the solar cells based on the ZnO–TiO 2 core–shell NW arrays. In addition, effects of the TiO 2 shell thickness on the performance of the as-fabricated devices are also discussed in detail.

CAS / MDL: 9002-98-6
研究领域: 材料科学 · 能源技术 · 纳米技术
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Crystals · 2020 ·Vol. 10 ·期 4 ·325 · IF 2.404

ZnO@TiO2 Core/Shell Nanowire Arrays with Different Thickness of TiO2 Shell for Dye-Sensitized Solar Cells

Liqing Liu,Hui Wang,Dehao Wang,Yongtao Li,Xuemin He,Hongguang Zhang,Jianping Shen

The ZnO@TiO2core/shell nanowire arrays with different thicknesses of the TiO2shell were synthesized, through depositing TiO2on the ZnO nanowire arrays using the pulsed laser deposition process. Scanning electron microscopy (SEM) and transmission electron microscopy (TEM) images show that these core/shell nanowires were homogeneously coated with TiO2nanoparticles with high crystallinity, appearing to be a rather rough surface compared to pure ZnO nanowires. The efficiency of ZnO@TiO2core/shell structure-based dye-sensitized solar cells (DSSCs) was improved compared with pure ZnO nanowires. This is mainly attributed to the enlarged internal surface area of the core/shell structures, which increases dye adsorption on the anode to improve the light harvest. In addition, the energy barrier which formed at the interface between ZnO and TiO2promoted the charge separation and suppressed the carrier recombination. Furthermore, the efficiency of DSSCs was further improved by increasing the thickness of the TiO2shell. This work shows an efficient method to achieve high power conversion efficiency in core/shell nanowire-based DSSCs.

研究领域: 材料科学 · 能源技术
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CHEMISTRY-A EUROPEAN JOURNAL · 2014 ·Vol. 20 ·期 43 ·14012-14017 · IF 5.696

Upconverting Nanoparticles with a Mesoporous TiO2 Shell for Near-Infrared-Triggered Drug Delivery and Synergistic Targeted Cancer Therapy

Meili Yin,Enguo Ju,Zhaowei Chen,Zhenhua Li,Jinsong Ren,Xiaogang Qu

Graphical Better together : Upconverting nanoparticles with a mesoporous TiO 2 shell (MTUNs) have been synthesized for light-triggered drug delivery and synergistic cancer therapy. Cytotoxicity experiments demonstrated that combined therapy mediated the highest rate of death of breast carcinoma cells compared with that of single chemotherapy or photodynamic therapy (see figure; Dox=doxorubicin, HA=hyaluronic acid, Hyal=hyaluronidase). Malignant tumors remain a major health burden throughout the world and effective therapeutic strategies are urgently needed. Herein, we report the synthesis of upconverting nanoparticles with a mesoporous TiO 2 (mTiO 2 ) shell for near-infrared (NIR)-triggered drug delivery and synergistic targeted cancer therapy. The NaGdF 4 :Yb,Tm could convert NIR light to UV light, which activated the mTiO 2 to produce reactive oxygen species for photodynamic therapy (PDT). Due to the large surface area and porous structure, the mTiO 2 shell endowed the nanoplatform with another functionality of anticancer drug loading for chemotherapy. The hyaluronic acid modified on the surface not only promised controlled drug release but also conferred targeted ability of the system toward cluster determinant 44 overexpressed cancer cells. More importantly, cytotoxicity experiments demonstrated that combined therapy mediated the highest rate of death of breast carcinoma cells compared with that of single chemotherapy or PDT.

研究领域: 生物医学工程 · 肿瘤学 · 纳米医学
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APPLIED SURFACE SCIENCE · 2018 · IF 4.439

A novel bi-functional SiO2@TiO2/CDs nanocomposite with yolk-shell structure as both efficient SERS substrate and photocatalyst

Xinna Gao,Xueyan Wang,Zheng Yang,Yuhua Shen,Anjian Xie

A novel multi-functional yolk-shell SiO 2 @TiO 2 /CDs(y-STCs) nanocomposite with interesting structure of SiO 2 cores, porous TiO 2 shell, and cavities was synthesized by using a simple method. The experimental results indicate that the yolk-shell structure and modification of carbon dots (CDs) play important roles in the enhancement of SERS signals and photocatalytic performance. The y-STCs nanocomposite used as the SERS substrate showed excellent efficiency and reproducibility for the detection of rhodamine 6G (R6G). The detection limit of R6G was shown to be as low as 6 × 10 −8 M. Furthermore, the fabricated y-STCs nanocomposite utilized as the photocatalytst for the degradation of dinitraphenols (DNP) can greatly shorten reaction time to 120 min compared with previous studies, and the DNP degradation rate could reach 96% under simulated sunlight irradiation. The y-STCs nanospheres also possessed excellent cycle stability for the photocatalytic degradation of DNP. Thus, the bi-functional y-STCs nanocomposite may have potential applications in the detection and photocatalytic degradation of organic pollutants.

研究领域: 材料科学 · 环境科学
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CHEMICAL ENGINEERING JOURNAL · 2019 · IF 8.355

Synthesis of CoSe2 nanoparticles embedded in N-doped carbon with conformal TiO2 shell for sodium-ion batteries

Bo Zhao,Qianqian Liu,Guijuan Wei,Jianghao Wang,Xin-Yao Yu,Xiang Li,Hao Bin Wu

CoSe 2 is a potential anode material for sodium-ion batteries in terms of their high sodium storage capacity and tunable properties. However, structural degradation and unstable interphase during the reversible sodiation and de-sodiation lead to fast capacity decay. In this work, we develop a nanocomposite architecture based on CoSe 2 nanoparticles embedded in N-doped carbon matrix with conformal TiO 2 coating (CoSe 2 @NC@TiO 2 ) by using a metal-organic framework-assisted strategy. The small CoSe 2 nanoparticles and N-doped carbon matrix facilitate charge transport and suppress the structural degradation, while the redox-active TiO 2 shell further strengthens the structural and interfacial stability without decreasing the capacity. The as-prepared CoSe 2 @NC@TiO 2 nanocomposite particles deliver a reversible sodium storage capacity of 520 mAh g −1 at 0.1 A g −1 with a capacity retention of 78% after 200 cycles, in contrast to the rapid capacity fading after 50 cycles of the pristine CoSe 2 @NC particles without TiO 2 shell.

CAS / MDL: 10026-22-9 7782-49-2
研究领域: 材料科学 · 电化学 · 能源存储
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