Tongji University

About: Tongji University is a education organization based out in Shanghai, China. It is known for research contribution in the topics: Computer science & Population. The organization has 76116 authors who have published 81176 publications receiving 1248911 citations. The organization is also known as: Tongji & Tóngjì Dàxué.

Hydrophilic microporous membranes for selective ion separation and flow-battery energy storage

Abstract: Membranes with fast and selective ion transport are widely used for water purification and devices for energy conversion and storage including fuel cells, redox flow batteries and electrochemical reactors. However, it remains challenging to design cost-effective, easily processed ion-conductive membranes with well-defined pore architectures. Here, we report a new approach to designing membranes with narrow molecular-sized channels and hydrophilic functionality that enable fast transport of salt ions and high size-exclusion selectivity towards small organic molecules. These membranes, based on polymers of intrinsic microporosity containing Troger’s base or amidoxime groups, demonstrate that exquisite control over subnanometre pore structure, the introduction of hydrophilic functional groups and thickness control all play important roles in achieving fast ion transport combined with high molecular selectivity. These membranes enable aqueous organic flow batteries with high energy efficiency and high capacity retention, suggesting their utility for a variety of energy-related devices and water purification processes. Ion-selective membranes are widely used for water purification and electrochemical energy devices but designing their pore architectures is challenging. Membranes with narrow channels and hydrophilic functionality are shown to exhibit salt ions transport and selectivity towards small organic molecules.

Direct reprogramming of mouse fibroblasts into cardiomyocytes with chemical cocktails

Abstract: The direct conversion, or transdifferentiation, of non-cardiac cells into cardiomyocytes by forced expression of transcription factors and microRNAs provides promising approaches for cardiac regeneration. However, genetic manipulations raise safety concerns and are thus not desirable in most clinical applications. The discovery of full chemically induced pluripotent stem cells suggest the possibility of replacing transcription factors with chemical cocktails. Here, we report the generation of automatically beating cardiomyocyte-like cells from mouse fibroblasts using only chemical cocktails. These chemical-induced cardiomyocyte-like cells (CiCMs) express cardiomyocyte-specific markers, exhibit sarcomeric organization, and possess typical cardiac calcium flux and electrophysiological features. Genetic lineage tracing confirms the fibroblast origin of these CiCMs. Further studies show the generation of CiCMs passes through a cardiac progenitor stage instead of a pluripotent stage. Bypassing the use of viral-derived factors, this proof of concept study lays a foundation for in vivo cardiac transdifferentiation with pharmacological agents and possibly safer treatment of heart failure.

Zeolitic Imidazolate Framework-8 with High Efficiency in Trace Arsenate Adsorption and Removal from Water

Abstract: The development of highly efficient adsorbents, especially those aimed at the capture of trace (ppb, 10–9) arsenate, is one of the principal challenges in the water treatment field. In this article, zeolitic imidazolate framework-8 (ZIF-8) was explored for the removal of trace arsenate from water. Results showed that ZIF-8 outperformed some other adsorbents and owned the first and highest reported adsorption capacity (76.5 mg g–1) at a low equilibrium concentration (9.8 μg L–1). Satisfactory adsorption properties (adsorption capacity, adsorption rate, adaptability to water environment, regeneration capacity) demonstrated the feasibility of using ZIF-8 as an efficient adsorbent for the removal of aquatic trace arsenate. In addition, Fourier transform infrared (FTIR) and X-ray photoelectron spectroscopy (XPS) spectra revealed the proposed mechanism of As(V) adsorption onto ZIF-8: producing large amounts of external active sites (Zn–OH) through the dissociative adsorption of water and subsequently forming an...

Excellent energy density of polymer nanocomposites containing BaTiO3@Al2O3 nanofibers induced by moderate interfacial area

Abstract: Inorganic/polymer nanocomposites, using one-dimensional (1D) core–shell structure BaTiO3@Al2O3 nanofibers (BT@Al2O3 nfs) as fillers and poly(vinylidene fluoride) (PVDF) as the polymer matrix, have been prepared. The core–shell structure BT@Al2O3 nfs have been synthesized via coaxial electrospinning. The breakdown strength (Eb) and discharged energy density of the nanocomposites can be significantly improved by creating an insulating Al2O3 shell layer with moderate dielectric constant on the surfaces of BT nanofibers to form a moderate interfacial area. The Al2O3 shell layer could effectively confine the mobility of charge carriers, which reduces energy loss by reducing the Maxwell–Wagner–Sillars (MWS) interfacial polarization and space charge polarization between the fillers and the polymer matrix. As a result, the nanocomposite films filled with 5 vol% BT@Al2O3 nfs exhibit a excellent discharge energy density of 12.18 J cm−3 at 400 MV m−1, which is ≈254% over bare PVDF (4.8 J cm−3 at 350 MV m−1) and ≈1015% greater than the biaxially oriented polypropylenes (BOPP) (≈1.2 J cm−3 at 640 MV m−1). The work here indicates that this promising state-of-the-art method of preparing high energy density nanocomposites can be used in the next generation of dielectric capacitors.