Enhancement in thermal, mechanical and electrical properties of novel PVA nanocomposite embedded with SrO nanofillers and the analysis of its thermal degradation behavior by nonisothermal approach
Abstract:Effect of SrO nanofillers on the physical and chemical properties of newly prepared PVA nanocomposites was investigated in‐depth in this article. The structure of SrO nanopowder and PVA nanocomposites were analyzed using FTIR for surface chemistry and XRD for crystallographic nature. The extent of dispersion and particle size of SrO nanopowders were obtained from TEM micrographs. The average particle size of the SrO nanopowder was 57 nm. The uniformly dispersed SrO nanofillers in the host PVA matrix were obser… Show more
“…The SAED pattern for particle 1 in Figure 4a can be assigned to (), (), and () planes of tetragonal RuO 2 (the Joint Committee on Powder Diffraction Standards (JCPDS) # 00‐040‐1290) (Figure 4b), [ 50 ] while the electron diffraction rings recorded from the adjacent particles can be assigned to cubic SrO phase (JCPDS # 00‐006‐0520) (Figure 4c). [ 51 ] TEM image on a selected rod clearly indicates the existence of a thin SrO layer on the {110} planes of RuO 2 (Figure 4d). The configuration of RuO 2 coated by SrO is also verified by the EDS elemental maps (Figure 4e,f and Figure S12, Supporting Information).…”
Section: Resultsmentioning
confidence: 99%
“…Figure 4h shows the HRTEM images of RuO 2 [ 50 ] on the bottom and the cubic SrO phase on the top‐right part of the picture. [ 51 ] Interestingly, we occasionally observed the in situ exsolution process during the electron beam illumination. A crystallite was newly formed between RuO 2 and SrO phases as exhibited in Figure 4i.…”
Elemental vacancies are proposed as an effective approach to tuning the electronic structure of catalysts that are critical for energy conversion. However, for reactions such as the sluggish oxygen evolution reaction, the excess of oxygen vacancies (VO) is inevitable and detrimental to catalysts’ electrochemical stability and activities, e.g., in the most active RuO2. While significant work is carried out to hinder the formation of VO, the development of a fast and efficient strategy is limited. Herein, a protection SrO layer produced successfully at the surface of RuO2 with the in situ exsolution method with perovskite SrRuO3 as the precatalyst, which could significantly hinder the generation of VO. Benefited from the suppression of VO, the surface‐modified RuO2 requires a low overpotential of 290 mV at 100 mA cm−2, accompanied by remarkably high electrochemical stability (100 h) and Faraday efficiency (≈100%). Theoretical investigation reveals that the formation energy of VO in RuO2 is almost doubled in the exsolved RuO2 phase as a result of the weakened RuO bond covalency. This work not only provides insight into the structural evolution of perovskite oxide catalysts but also demonstrates the feasibility of controlling vacancy formation via in situ exsolution.
“…The SAED pattern for particle 1 in Figure 4a can be assigned to (), (), and () planes of tetragonal RuO 2 (the Joint Committee on Powder Diffraction Standards (JCPDS) # 00‐040‐1290) (Figure 4b), [ 50 ] while the electron diffraction rings recorded from the adjacent particles can be assigned to cubic SrO phase (JCPDS # 00‐006‐0520) (Figure 4c). [ 51 ] TEM image on a selected rod clearly indicates the existence of a thin SrO layer on the {110} planes of RuO 2 (Figure 4d). The configuration of RuO 2 coated by SrO is also verified by the EDS elemental maps (Figure 4e,f and Figure S12, Supporting Information).…”
Section: Resultsmentioning
confidence: 99%
“…Figure 4h shows the HRTEM images of RuO 2 [ 50 ] on the bottom and the cubic SrO phase on the top‐right part of the picture. [ 51 ] Interestingly, we occasionally observed the in situ exsolution process during the electron beam illumination. A crystallite was newly formed between RuO 2 and SrO phases as exhibited in Figure 4i.…”
Elemental vacancies are proposed as an effective approach to tuning the electronic structure of catalysts that are critical for energy conversion. However, for reactions such as the sluggish oxygen evolution reaction, the excess of oxygen vacancies (VO) is inevitable and detrimental to catalysts’ electrochemical stability and activities, e.g., in the most active RuO2. While significant work is carried out to hinder the formation of VO, the development of a fast and efficient strategy is limited. Herein, a protection SrO layer produced successfully at the surface of RuO2 with the in situ exsolution method with perovskite SrRuO3 as the precatalyst, which could significantly hinder the generation of VO. Benefited from the suppression of VO, the surface‐modified RuO2 requires a low overpotential of 290 mV at 100 mA cm−2, accompanied by remarkably high electrochemical stability (100 h) and Faraday efficiency (≈100%). Theoretical investigation reveals that the formation energy of VO in RuO2 is almost doubled in the exsolved RuO2 phase as a result of the weakened RuO bond covalency. This work not only provides insight into the structural evolution of perovskite oxide catalysts but also demonstrates the feasibility of controlling vacancy formation via in situ exsolution.
“…The second stage of degradation origination from 200 C is may be related to the complete carbonization and condensation of water molecules of the PVA sample. 46 In case of nanocomposites, the first transition were observed near 180 C which may be caused by the dehydration of the LDH interlayer whereas the second major transition occurs at 250 C in the nanocomposites, which can be attributed to decomposition of polymeric chains and anionic species present at the interlayer of LDH nanosheets. 47 Above 500 C, the mixed metal oxides were formed by the decomposition of LDH and total loss of polymer takes place.…”
In this work, we have synthesized the zinc‐aluminum layered double hydroxide (ZnAl LDH) nanostructures using cost‐effective hydrothermal technique. The ZnAl LDH and graphene‐based poly(vinyl alcohol) (PVA) nanocomposites are fabricated. The crystal structure, morphology, thermal, and dielectric properties of pristine PVA and ZnAl LDH and graphene‐based PVA nanocomposites films were investigated using X‐ray diffraction, HR‐transmission electron microscopy, thermo gravimetric analysis, and impedance analyzer. HRTEM analysis reveals the hexagonal nanoplates shape‐like morphology of Zn‐Al layered double hydroxides with an average thickness of 40–50 nm and size of 400–600 nm. High thermal stability was observed from ZnAl LDH and graphene‐reinforced nanocomposite. Enhanced thermal stability of 250°C and low weight loss was observed from ZnAl LDH reinforced PVA‐based nanocomposites compared to pristine PVA. Zn‐Al LDH nanoplates‐graphene‐PVA based nanocomposites showed ultra‐high dielectric constant (ɛ′) of 794 as compared to the ZnAl LDH‐PVA nanocomposites (ɛ′ ~ 334) and pristine PVA sample (ɛ′ ~ 35). Low dielectric loss of 0.27, 0.18, 0.38 was observed for pristine PVA, ZnAl‐LDH‐PVA and ZnAl‐LDH‐graphene‐PVA nanocomposites. The large enhancement of the dielectric constant and thermal stability were discussed in terms of improved crystallinity, interfacial polarization and formation of nanodipoles in the matrix. This study reveals a significant role of LDH‐graphene‐based hybrid nanocomposites in optoelectronics, energy storage, sensors, energy conversion and thermally stable devices.Highlights
Growth of highly crystalline zinc‐aluminum layered double hydroxide nanostructures.
Improved thermal stability for Zn‐Al LDH‐graphene‐PVA nanocomposites.
High thermal stability from ZnAl LDH‐based PVA nanocomposites.
Ultra‐high dielectric constant of 794 is observed from Zn‐Al LDH nanoplates‐graphene‐nanocomposites.
“…An effective and simple method to obtain metal oxide NPs is the route of chemical oxidation. In this method, Sr salt, usually SrCl 2 , is dissolved in a strongly basic solution (achieved by the addition of NaOH up to a pH value of 12). , Hydrothermal synthesis is another method usually employed that combines pressure as a driving force for the forward reaction. In this method, a Sr salt, for example, Sr(OH) 2 , is reacted with a strong reducing agent in a strongly basic solution.…”
Section: Methods Of Synthesis Of Sro Npsmentioning
Biodiesel
is a renewable and environmentally friendly alternative
to fossil fuels. Despite nearly 3 decades of research in the field
of biodiesel, there remains major obstacles for large-scale production.
In the search for an active, selective, and reusable solid base catalyst,
strontium oxide (SrO) is emerging out as a preferred choice for the
transesterification reaction under various methods of activation.
SrO exhibits the highest activity among processable alkaline earth
metal oxides as a result of its strong basicity. SrO nanoparticles
(NPs) and hybrids showed improved performance. Recent progress achieved
in the development of synthetic methods of SrO NPs is reviewed. Advantages
of SrO-based nanocomposites for biodiesel production are discussed.
Finally, potential support materials for enhancing the catalytic performance
of SrO NPs with commercial implications are elaborated.
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