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  • Royal Society of Chemistry (RSC)  (84)
  • 2020-2024  (84)
Type of Medium
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  • Royal Society of Chemistry (RSC)  (84)
Language
Years
  • 2020-2024  (84)
Year
  • 1
    Online Resource
    Online Resource
    Royal Society of Chemistry (RSC) ; 2020
    In:  Inorganic Chemistry Frontiers Vol. 7, No. 15 ( 2020), p. 2753-2758
    In: Inorganic Chemistry Frontiers, Royal Society of Chemistry (RSC), Vol. 7, No. 15 ( 2020), p. 2753-2758
    Type of Medium: Online Resource
    ISSN: 2052-1553
    Language: English
    Publisher: Royal Society of Chemistry (RSC)
    Publication Date: 2020
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  • 2
    In: Journal of Materials Chemistry C, Royal Society of Chemistry (RSC), Vol. 9, No. 42 ( 2021), p. 15026-15033
    Abstract: To achieve efficient photocatalysis for producing hydrogen and oxygen from dissociated water molecules using solar energy, all steps in the process – the photon absorption, exciton dissociation, carrier transfer and redox reactions – must be optimized because the overall efficiency is a product of all these fundamental efficiencies. However, most photocatalysts that have been investigated fulfil some but not all of these requirements, resulting in bottle necks in the process and a low overall solar-to-hydrogen efficiency. Here, we carry out a comprehensive investigation of the photocatalytic water-splitting performance of monolayer Janus platinum dichalcogenide materials, i.e. , PtSSe, PtSTe and PtSeTe, using first-principles and GW calculations. It is found that the narrow-band gap PtSTe and PtSeTe materials exhibit excellent solar light absorption, covering a wide range of the solar spectrum, down to the near-infrared region. The unique feature of a strong internal vertical electric field in the Janus platinum dichalcogenides polarizes the electrons and holes in opposite chalcogen layers, leading to a reduced electron–hole recombination rate. These, combined with the large difference in the electron and hole mobilities, allow efficient carrier generation and transfer. The overpotential of PtSTe is 0.75 and 0.22 eV for the oxygen-evolution reaction and the hydrogen-evolution reaction, respectively, and its solar-to-hydrogen efficiency can reach up to 24.7%, breaking the conventional theoretical limit. Overall, our computations not only predict the promising photocatalytic application potential for water splitting of Janus platinum dichalcogenides but also suggest a valuable strategy for optimizing and improving the photocatalytic performance by utilizing the intrinsic polarizations of 2D polar materials.
    Type of Medium: Online Resource
    ISSN: 2050-7526 , 2050-7534
    Language: English
    Publisher: Royal Society of Chemistry (RSC)
    Publication Date: 2021
    detail.hit.zdb_id: 2702245-6
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  • 3
    Online Resource
    Online Resource
    Royal Society of Chemistry (RSC) ; 2022
    In:  Catalysis Science & Technology Vol. 12, No. 11 ( 2022), p. 3614-3621
    In: Catalysis Science & Technology, Royal Society of Chemistry (RSC), Vol. 12, No. 11 ( 2022), p. 3614-3621
    Abstract: Using direct Z-scheme heterojunction photocatalysts has been regarded as one of the most effective methods to separate photogenerated carriers for photocatalytic redox reactions of water splitting. However, their unique band alignment results in small driving photovoltages, significantly limiting the overall photocatalytic efficiency. In this work, we propose two practical methods to address this problem in Z-scheme heterojunction photocatalysts. One is to introduce a large interfacial polarization. The other is to take wide-bandgap components. Nonpolar wide-bandgap PtO 2 and GeC are chosen in this work, because these two nonpolar materials have a large difference in the work function to fulfil the requirement of their large interfacial polarization. Besides, it is convenient to make an effective comparison between our work and the previous works on the direct Z-scheme heterojunctions based on MoSe 2 and WSe 2 . Therefore, PtO 2 /MoSe 2 and PtO 2 /WSe 2 are also investigated in this work. Therefore, the material realization of such rational design is achieved and demonstrated in three van der Waals (vdW) two-dimensional (2D) polar heterojunctions: PtO 2 /MoSe 2 , PtO 2 /WSe 2 , and PtO 2 /GeC. Our first-principles calculations show that the polar heterojunctions have an extended light absorption range (covering the near-infrared spectrum), small exciton binding energy, small global band gap, and large interfacial electric field, indicating a high efficiency of light utilization and carrier separation. The most important feature is their large driving photovoltages, up to 4 V for the oxidation evolution reaction (OER) and 2 V for the hydrogen evolution reaction (HER), induced by the large interfacial polarization and wide band gaps of 2D monolayer materials. The calculated Gibbs free energies demonstrate that such high photovoltages can smoothly drive both the OER and HER, implying a high redox efficiency for the proposed Z-scheme polar heterojunctions. Our work provides a significant strategy for designing the direct Z-scheme heterojunctions with high photocatalytic performance.
    Type of Medium: Online Resource
    ISSN: 2044-4753 , 2044-4761
    Language: English
    Publisher: Royal Society of Chemistry (RSC)
    Publication Date: 2022
    detail.hit.zdb_id: 2595090-3
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  • 4
    Online Resource
    Online Resource
    Royal Society of Chemistry (RSC) ; 2023
    In:  Energy & Environmental Science
    In: Energy & Environmental Science, Royal Society of Chemistry (RSC)
    Abstract: Searching for high-performance thermoelectric (TE) materials has long been a focused theme. Here, the intrinsic conductivity σ0 is proposed as a simple indicator to evaluate the intrinsic electrical performance of potential TE materials and instruct the exploration of better thermoelectrics. Under the framework of the single parabolic band (SPB) model, σ0 is proved exactly to be the electrical conductivity of a TE material when its power factor (PF) reaches the maximum value. Moreover, a simplified SPB model is developed, with which simpler mathematical equations can be employed for instructing the optimization of the TE performance, enabling the rapid screening and development of new TE materials. The upper limit of the dimensionless TE figure of merit zT at different temperatures can be easily predicted. Further beyond, aiming at the enhancement of σ0, the carrier selective scattering engineering is theoretically proposed, with which the σ0 and PFmax could possibly be significantly improved through the selective scattering of low-energy carriers. The experimental routes to realize the carrier selective scattering are also suggested. Finally, a roadmap towards higher σ0 and zT is summarized, which could provide an insightful understanding and instruction for the future development of thermoelectrics.
    Type of Medium: Online Resource
    ISSN: 1754-5692 , 1754-5706
    Language: English
    Publisher: Royal Society of Chemistry (RSC)
    Publication Date: 2023
    detail.hit.zdb_id: 2439879-2
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  • 5
    In: Environmental Science: Nano, Royal Society of Chemistry (RSC), Vol. 9, No. 3 ( 2022), p. 911-953
    Abstract: Global warming due to greenhouse gases (GHGs), mainly CO 2 , has become a serious concern globally. Accordingly, electrocatalytic CO 2 conversion provides an environment-friendly approach to reduce CO 2 emissions and achieve carbon neutrality. Copper (Cu) is one of the few metal catalysts that can convert CO 2 to high-value multi-carbon products (C 2+ ), and thus has received significant attention. In this review, we discuss the manipulation strategies to promote C–C coupling to form C 2+ from the intermediate product CO* in terms of adsorption capability and configuration, surface coverage, and re-coupling efficiency on copper-based catalysts. In addition, some advanced characterization techniques to investigate the mechanism of C–C coupling in the CO 2 reduction reaction (CO 2 RR) are summarized. Finally, the outlooks and future development directions of CO 2 RR are highlighted.
    Type of Medium: Online Resource
    ISSN: 2051-8153 , 2051-8161
    Language: English
    Publisher: Royal Society of Chemistry (RSC)
    Publication Date: 2022
    detail.hit.zdb_id: 2758235-8
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  • 6
    Online Resource
    Online Resource
    Royal Society of Chemistry (RSC) ; 2020
    In:  Inorganic Chemistry Frontiers Vol. 7, No. 19 ( 2020), p. 3548-3554
    In: Inorganic Chemistry Frontiers, Royal Society of Chemistry (RSC), Vol. 7, No. 19 ( 2020), p. 3548-3554
    Type of Medium: Online Resource
    ISSN: 2052-1553
    Language: English
    Publisher: Royal Society of Chemistry (RSC)
    Publication Date: 2020
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  • 7
    In: Dalton Transactions, Royal Society of Chemistry (RSC), Vol. 52, No. 35 ( 2023), p. 12244-12252
    Abstract: The catalytic oxidative desulfurization (ODS) technique is able to remove sulfur compounds from fuels, conducive to achieving deep desulfurization for the good of the ecological environment. Ti-based metal–organic frameworks (Ti-MOFs) possessing good affinity to organic reactants and considerable numbers of Ti active sites are promising catalysts for ODS. However, current Ti-MOFs suffer from severe diffusion limitations caused by the size mismatch between sole micropores and bulky sulfur compounds, leading to poor ODS performance. Here, a facile method of intraparticle ripening without any additive is developed to obtain hierarchically meso–microporous Ti-MIL-125 single crystals (Meso-Ti-MIL-125) for the first time. Such Meso-Ti-MIL-125 shows a BET surface area of 1401 m 2 g −1 and a mesoporous volume that is 1.7 times as high as that of the conventional Ti-MIL-125. Our novel Meso-Ti-MIL-125 exhibits excellent catalytic performance in the ODS of a series of bulky thiophenic sulfur compounds, completely removing benzothiophene (BT), dibenzothiophene (DBT), and 4,6-dimethyldibenzothiophene (DMDBT) from model fuels, which is, respectively, 2.4 times, 1.5 times, and 6.7 times higher than the removal achieved with conventional Ti-MIL-125. Such a facile synthetic strategy is envisioned to be applied in many kinds of crystalline materials, such as zeolites, for industrial production.
    Type of Medium: Online Resource
    ISSN: 1477-9226 , 1477-9234
    Language: English
    Publisher: Royal Society of Chemistry (RSC)
    Publication Date: 2023
    detail.hit.zdb_id: 1472887-4
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  • 8
    In: Biomaterials Science, Royal Society of Chemistry (RSC), Vol. 11, No. 3 ( 2023), p. 1013-1030
    Abstract: Multiple gastrointestinal barriers (mucus clearance and epithelium barrier) are the main challenges in the oral administration of nanocarriers. To achieve efficient mucus penetration and epithelial absorption, a novel strategy based on mesoporous silica nanoparticles with dendritic superstructure, hydrophilicity, and nearly neutral-charged modification was designed. The mPEG covalently grafted dendritic mesoporous silica nanoparticles (mPEG-DMSNs) had a particle size of about 200 nm and a loading capacity of up to 50% andrographolide (AG) as a nanocrystal cluster in the mesoporous structure. This dual strategy of combining with the surface topography structure and hydrophilic modification maintained a high mucus permeability and showed an increase in cell absorption. The mPEG-DMSN formulation also exhibited effective transepithelial transport and intestinal tract distribution. The pharmacokinetics study demonstrated that compared with other AG formulations, the andrographolide nanocrystals-loaded mPEG-DMSN (AG@mPEG-DMSN) exhibited much higher bioavailability. Also, AG@mPEG-DMSN could significantly improve the in vitro and in vivo anti-inflammatory efficacy of AG. In summary, mPEG-DMSN offers an interesting strategy to overcome the mucus clearance and epithelium barriers of the gastrointestinal tract.
    Type of Medium: Online Resource
    ISSN: 2047-4830 , 2047-4849
    Language: English
    Publisher: Royal Society of Chemistry (RSC)
    Publication Date: 2023
    detail.hit.zdb_id: 2693928-9
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  • 9
    Online Resource
    Online Resource
    Royal Society of Chemistry (RSC) ; 2022
    In:  Journal of Materials Chemistry B Vol. 10, No. 33 ( 2022), p. 6328-6337
    In: Journal of Materials Chemistry B, Royal Society of Chemistry (RSC), Vol. 10, No. 33 ( 2022), p. 6328-6337
    Abstract: Nanozymes, as a unique class of nanomaterials with enzyme-like properties, have attracted significant interest due to their potential applications in many significant fields. Great endeavours have been made to improve the catalytic activities of nanozymes; however, it is still a challenging issue to develop nanozymes that can functionally mimic multiplex enzymes with broader application prospects. Here, we develop a simple hydrothermal method to construct “three-in-one” nanocomposites as multifunctional nanozymes for the ultrasensitive ratiometric fluorescence detection of alkaline phosphatase (ALP). The prepared flower-like Fe 3 O 4 nanocomposites (Fef NCs) are composed of ternary components, in which hierarchical MnO 2 nanosheets (NSs) are assembled on Fe 3 O 4 nanoparticles (NPs), followed by the decoration of CeO 2 NPs. Fef NCs present tetra-enzyme-like activities, i.e. , oxidase-, peroxidase-, catalase-, and superoxide dismutase-like activity. More importantly, Fef NCs can effectively catalyze the oxidation of phenolic compounds ( i.e. , 3,5-DTBC and dopamine) to produce the corresponding o-quinones, demonstrating specific catechol oxidase-like activity. Based on the excellent catalytic oxidation and fluorescence quenching abilities of Fef NCs, we established a ratiometric fluorescence strategy using two fluorogenic substrates for label-free, ultrasensitive, and selective detection of ALP. The fluorescence bioassay exhibits a linear relationship between the fluorescence ratio and the ALP concentration ranging from 0.2 to 1.0 mU mL −1 , with a detection limit down to be 0.19 mU mL −1 . Furthermore, this bioassay can detect ALP in mixture and human serum samples, presenting good selectivity as well as real-world applicability. This work not only provides a novel approach for the preparation of a multiple-enzyme-like nanozyme but also offers an advanced ratiometric fluorescence sensing platform for ultrasensitive bioanalysis.
    Type of Medium: Online Resource
    ISSN: 2050-750X , 2050-7518
    Language: English
    Publisher: Royal Society of Chemistry (RSC)
    Publication Date: 2022
    detail.hit.zdb_id: 2702241-9
    detail.hit.zdb_id: 2705149-3
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  • 10
    Online Resource
    Online Resource
    Royal Society of Chemistry (RSC) ; 2022
    In:  Journal of Materials Chemistry C Vol. 10, No. 5 ( 2022), p. 1850-1861
    In: Journal of Materials Chemistry C, Royal Society of Chemistry (RSC), Vol. 10, No. 5 ( 2022), p. 1850-1861
    Abstract: In spite of the great success of all-polymer solar cells (all-PSCs) in terms of device efficiency mainly owing to the vigorous development of polymer donors ( P D s) and polymer acceptors ( P A s), the synergistic effects of the molecular structure and molecular weight ( M w ) of P D and P A materials as well as P D – P A pair miscibility on device performance are still unclear and rarely reported. Herein, we introduced PBDB-T and its congener materials (PM6 and PM7) as P D s with comparable M w s and two PYT batches as P A s with different M w s (PYT-M and PYT-H) to deeply investigate the effects of molecular mechanisms on the device efficiency and stability in these six systems. Benefiting from proper P D – P A miscibility owing to the matched molecular structure and M w s, both PBDB-T:PYT-H and PM6:PYT-M systems with suitable phase separation show comparable device efficiencies, which are much better than those of the other four all-polymer systems. Impressively, further investigation demonstrates that the PBDB-T:PYT-H active layer is more stable than the PM6:PYT-M one, resulting from the trade-offs between molecular miscibility and M w . This work not only employs the synergetic effect of the molecular structure and molecular weight on device efficiency and stability but also provides a promising strategy to simultaneously improve the device performance of all-PSCs.
    Type of Medium: Online Resource
    ISSN: 2050-7526 , 2050-7534
    Language: English
    Publisher: Royal Society of Chemistry (RSC)
    Publication Date: 2022
    detail.hit.zdb_id: 2702245-6
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