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Journal of Colloid and Interface Science
Academic Press
Journal of Colloid and Interface Science

Academic Press

0021-9797

Journal of Colloid and Interface Science/Journal Journal of Colloid and Interface ScienceSCIAHCIISTPEI
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    Insight into the aqueous Laponite? nanodispersions for self-assembled poly(itaconic acid) nanocomposite hydrogels: The effect of multivalent phosphate dispersants

    Bujok S.Konefal M.Konefal R.Nevoralova M....
    12页
    查看更多>>摘要:? 2021 Elsevier Inc.Hypothesis: We hypothesize, that physical network between Laponite? nanoparticles and high molecular weight polyelectrolyte formed by mixing of Laponite? nanodispersion (containing multivalent phosphate dispersant) and polyelectrolyte solution is strongly influenced by the type and content of dispersant, which forms electric double layer (EDL) closely to the Laponite? edges. Thus, optimum dispersant concentration is necessary to overcome clay-clay interactions (excellent clay delamination), but should not be exceeded, what would result in the EDL compression and weakening of attractions forming clay-polyelectrolyte network. Thus, deeper investigation of Laponite? nanodispersions is highly demanded since it would enable to better design the self-assembled clay-polyelectrolyte hydrogels. Experiments: To study clay interparticle interactions in the presence of various multivalent phosphates, complementary methods providing wide nanodispersion characterization have been applied: zeta potential measurement and SAXS technique (electrostatic interactions), oscillatory rheology (nanodispersion physical state) and NMR experiments (ion immobilization degree). Findings: It was found that multivalent phosphates induce and tune strength of clay-polyelectrolyte interactions forming hydrogel network in terms of varying EDL on the Laponite? edges. Moreover, phosphate dispersing efficiency depends on the molecular size, chemical structure, and valence of the anion; its potential as efficient dispersant for hydrogel preparation can be evaluated by estimation of anion charge density.

    In situ configuration of dual S-scheme BP/(Ti3C2Tx@TiO2) heterojunction for broadband spectrum solar-driven photocatalytic H2 evolution in pure water

    Ai Z.Shao Y.Shen J.Wu Y....
    11页
    查看更多>>摘要:? 2021Artificial photocatalysis with high-efficiency is a promising route for storing sustainable energy from water splitting. Whereas it is challenging to broaden the solar-spectrum responsive window for harvesting high level of conversion. Herein, based on the band-matching engineering theory, a design of dual S-Scheme heterojunction system is proposed and established in a BP/(Ti3C2Tx@TiO2) composite photocatalyst. The complementary light response region between TiO2 and BP realizes the extension of solar energy utilization over a broad absorption window. Furthermore, this specific band-matching configuration endows spatially long-lived charge carriers with greater accumulation on the divided sub-systems, thereby maintaining the sufficient potential energy capacity associated with excellent photocatalytic properties (H2 evolution rate of 564.8 μmol h?1 g?1 and AQE of 2.7% at 380 nm in pure water). This work describes a promising protocol of designing advanced broadband light-activated photocatalytic systems for solar-chemical energy conversion applications.

    Insights into enhanced peroxydisulfate activation with S doped Fe@C catalyst for the rapid degradation of organic pollutants

    Lin C.Ye X.Shi Y.Liu M....
    11页
    查看更多>>摘要:? 2021 Elsevier Inc.In this study, the S modified iron-based catalyst (S-Fe@C) for activating peroxydisulfate (PDS) was fabricated by heating the S-MIL-101 (Fe) precursor at 800 °C. The resulted S-Fe@C composite mainly consisted of carbon, Fe0, FeS, FeS2, and Fe3O4, and showed strong magnetism. Compared with Fe@C obtained from MIL-101 (Fe), the S-Fe@C exhibited much higher performance (1.5 times larger) on PDS activation and the S-Fe@C/PDS could rapidly degrade various organic pollutants in 5 min under the attack of the species of SO4-·, 1O2, electro-transfer and Fe(IV). The S element in enhancing the PDS activation mainly involved two mechanisms. Firstly, the doped S could speed up the electron transfer efficiency, resulting in a promotion on PDS decomposition; secondly, the S2- S22- or S0 could achieve the circulation of Fe2+ and Fe3+, leading to the formation of non-radicals Fe(IV) and 1O2.

    High performance flexible asymmetric supercapacitor constructed by cobalt aluminum layered double hydroxide @ nickel cobalt layered double hydroxide heterostructure grown in-situ on carbon cloth

    Wang Y.Yang H.Lv H.Zhou Z....
    14页
    查看更多>>摘要:? 2021 Elsevier Inc.Hypothesis: Three-dimensional layered layered double hydroxide (LDH) nanostructure materials grow in-situ on excellent conductive and flexible carbon cloth (CC) substrate not only reduce the ability of binders in resisting ions transfer, but also make them to be quasi-vertically arranged well on substrates without aggregation. This would result in enough electroactive sites, to obtain superior electrochemical performance. Experiments: A hierarchical CoAl-LDH@NiCo-LDH composite was prepared on a surface-modified carbon cloth by a simple two-step hydrothermal process. In this process, CoAl-LDH nanosheets (NSs)/CC acting as the inner core were wrapped up in NiCo-LDH nanoneedle arrays (NNAs) evenly. Also, a flexible quasi-solid-state supercapacitor device was constructed using CoAl-LDH@NiCo-LDH/CC and activated carbon (AC) as a positive electrode and a negative electrode, respectively. Findings: The CoAl-LDH@NiCo-LDH/CC developed had an excellent specific capacitance (2633.6F/g at 1 A/g) with remarkable cyclic performance (92.5% retention of its incipient over 5000 cycles at 4 A/g). The flexible quasi-solid-state supercapacitor device CoAl-LDH@NiCo-LDH/CC//AC/CC yielded a splendid energy density of 57.8 Wh/kg at a power density of 0.81 kW/kg and a brilliant power density of 16.09 kW/kg at 38.0 Wh/kg in a broad potential window of 1.55 V. Furthermore, the exceptional cyclic stability and excellent flexibility of the device show it can be applied in flexible energy storage systems.

    Novel N,C,S-TiO2/WO3/rGO Z-scheme heterojunction with enhanced visible-light driven photocatalytic performance

    Vu T.-P.-T.Tran D.-T.Dang V.-C.
    12页
    查看更多>>摘要:? 2021 Elsevier Inc.Novel N,C,S-TiO2/WO3/rGO Z scheme photocatalyst was successfully synthesized from graphite, TIOT, and ammonium metatungstate precursors. Material characteristics such as crystal structure, surface morphology, functional groups, specific surface area, elemental composition, band gap energy, and electron-hole recombination were characterized by XRD, TEM, BET, SEM/EDX, FT-IR, UV–VIS, and PL methods. The as-synthesized novel N,C,S-TiO2/WO3/rGO Z-scheme heterojunction photocatalyst exhibited visible light-driven photocatalytic activity (the band gap energy = 2.24 eV), could generate both effective electrons and holes, and presented the lowest electron-hole recombination rate compared to all individual components. Different factors impacting the photocatalytic decomposition of Direct Blue 71 (DB 71) by the N,C,S-TiO2/WO3/rGO system were studied. The results showed that pH of the solution, catalyst load, DB 71 initial concentration, and reaction time affected the DB 71 photocatalytic degradation efficiency. The DB 71 degradation completed after 100 min with a typical efficiency of over 91%, which was much better than other photocatalytic systems. The DB 71 degradation process followed the pseudo-first-order kinetics model with coefficients of determination > 0.95 for all conditions. The photocatalyst was easily regenerated, and exhibited a very good stability, with a photocatalytic degradation efficiency of over 83.0% after 3 cycles.

    Solid lipid nanoparticles and nanoemulsions with solid shell: Physical and thermal stability

    Kolik-Shmuel L.Danino D.Koroleva M.Mischenko E....
    9页
    查看更多>>摘要:? 2021 Elsevier Inc.Hypothesis: Nanoemulsions (NE) and solid lipid nanoparticles (SLN) used for drug delivery should have a solid shell to be stable during long shelf life and become liquid at human body temperature. The core components of lipid nanoparticles can be partially incorporated into the shell and affect the physical and thermal stability. Experiments: We prepared NE and SLN by the phase inversion temperature (PIT) method. Solidification of the surfactants Tween 60 and Span 60 on the surface of NE droplets with paraffin oil resulted in the formation of the solid shell. SLN contained stearic acid in the core and the same surfactants in the solid shell. The size, structure and stability of the NE and SLN were studied by DLS and cryo-TEM. Their crystallization and melting were analyzed using DSC. Findings: The lipid nanoparticles were resistant to aggregation and sedimentation and hold up to at least two cycles of heating to 50–60 °C and subsequent cooling to 5 °C, even though the upper temperatures were higher than the melting point of the surfactant shell. The expected liquid core/solid shell morphology of NE was confirmed. SLN were composed of a semi-liquid core of supercooled stearic acid melt and coated with a solid surfactant shell, so they can be treated as NE. Stearic acid molecules penetrated the shell, leading to an increase in its melting point.

    Regulation of morphology and electronic configuration of NiCo2O4 by aluminum doping for high performance supercapacitors

    Chen X.Song L.Zeng M.Tong L....
    10页
    查看更多>>摘要:? 2021 Elsevier Inc.Morphology engineering and element doping are two effective strategies to boost the capacitive performance of electroactive materials. The morphology control through doping process is conducive to simplifying the preparation process. Herein, an aluminum-doped (Al-doped) strategy was used to prepare Al-doped NiCo2O4 nanosheet-wire structure (Al-NiCo2O4 NSW) by hydrothermal method and subsequent calcination. The nanosheet-wire structure was composed of one-dimensional (1D) nanowires and two-dimensional (2D) ultrathin nanosheets. 1D nanowires can provide efficient pathways for the electrons/ions transport. 2D nanosheets can enlarge the specific surface area and expose more active sites. The Al doping can change the electronic structure of NiCo2O4 with enhanced electrical conductivity as revealed by density functional theory (DFT) calculations. Meanwhile, a strong adsorption capacity of OH– was obtained on Al-NiCo2O4 NSW for redox reactions. The Al-NiCo2O4 NSW electrode demonstrated a high specific capacity of 1441C g?1 (2446F g?1) at 1 A g?1 and excellent cycling stability (87.6% capacity retention at 10 A g?1 for 5000 charge-discharge cycles). The assembled asymmetric supercapacitor manifested a superior energy density of 46.2 Wh Kg?1 at a power density of 800 W kg?1.

    First-principles identification of interface effect on Li storage capacity of C3N/graphene multilayer heterostructure

    Gavali D.S.Thapa R.Kawazoe Y.
    9页
    查看更多>>摘要:? 2021 Elsevier Inc.The design and development of new and light weight two-dimensional (2D) heterostructures as anode materials to enhance the electrochemical properties for Li-ion batteries (LIB's) is a challenge. In this work, using first-principles study, we have demonstrated that the ratio of two-dimensional polyaniline (C3N) and graphene in the multilayer heterostructures plays a major role to define the Li storage properties and to provide metallicity for easy conduction of electrons. We have found that charge transfer between Li and the host depends on the interface and site, which helps in the improvement in specific capacity. The proposed heterostructures shows specific capacity varies from 558 mAh/gm to 423 mAh/gm. The specific capacity is high for heterostructures with more graphene in ratio which is correlated to higher charge accumulation in the host. Also, graphene helps to minimize the open-circuit voltage (OCV) of C3N and maintained an average of 0.4 V. The volume expansion for fully lithiated heterostructures is within 22 %. Li diffusion barrier energy varies in the range of 0.57 to 0.25 eV. The proposed 2D heterostructures could be a future material for anode in LIB's and the description of the interface effect on Li storage properties will help for further development of 2D heterostructure materials.

    Gold nanorod@void@polypyrrole yolk@shell nanostructures: Synchronous regulation of photothermal and drug delivery performance for synergistic cancer therapy

    Sun X.Wang J.Wang Z.Fan L....
    9页
    查看更多>>摘要:? 2021 Elsevier Inc.Synergistic therapy has been emerging as new trend for effective tumor treatment due to synchronous function and cooperative reinforcement of multi therapeutic modalities. Herein, gold nanorods (GNRs) encapsulated into polypyrrole (PPy) shell with tunable void space (GNRs@Void@PPy) showing yolk@shell nanostructures were innovatively designed. The exploitation of dual near-infrared (NIR) absorptive species offered synergistic enhancement of photothermal performance. In addition, the manipulation of the void space between them provided additional benefits of high drug encapsulation efficiency (92.6%) and, interestingly, tumor microenvironment and NIR irradiation triggered targeted drug releasing. Moreover, the GNRs@Void@PPy exhibited excellent biocompatibility, and optimal curative effect by chemo-photothermal synergistic therapy was achieved through both in vitro and in vivo antitumor activity investigation.

    ZIF-8 derived porous carbon to mitigate shuttle effect for high performance aqueous zinc–iodine batteries

    Xu J.Wang J.Ge L.Sun J....
    8页
    查看更多>>摘要:? 2021 Elsevier Inc.Rechargeable aqueous zinc–iodine batteries (ZIBs) with low environmental impacts and abundant natural reserves have emerged as promising electrochemical energy storage devices. However, the shuttle effect and low conductivity of the iodine species cause poor electrochemical performance and hinder their practical application. Herein, we propose a ZIF-8 derived porous carbon (ZPC) for iodine species immobilization in ZIBs. The rich porous structure and highly conductive framework of ZPC provide efficient iodine loading and allow the fast transmission of electrons. In addition, the presence of N, Zn and ZnO in the carbon framework can build chemical anchoring with the iodine species to mitigate the shuttle effect. Thus, the ZPC/I2 cathode exhibits a reversible capacity of 156 mAh g?1 after 100 cycles at 100 mA g?1 and a long-term stability of 1000 cycles at a high rate. This study will open a new paradigm for devolving highly reversible ZIBs.