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05 Mar 00:59

Improved electrical conductivity and thermoelectric performance of ZnO by doping with NaCl and CdO

Publication date: Available online 16 December 2020

Source: Chemical Engineering Journal

Author(s): Chhatrasal Gayner

17 Apr 10:33

Aqueous Stable Gold Nanostar/ZIF‐8 Nanocomposites for Light‐Triggered Release of Active Cargo Inside Living Cells

by Carolina Carrillo‐Carrión, Raquel Martínez, María F. Navarro Poupard, Beatriz Pelaz, Ester Polo, Ana Arenas‐Vivo, Alessandro Olgiati, Pablo Taboada, Mahmoud G. Soliman, Úrsula Catalán, Sara Fernández‐Castillejo, Rosa Solà, Wolfgang J. Parak, Patricia Horcajada, Ramon A. Alvarez‐Puebla, Pablo del Pino
Angewandte Chemie International Edition Aqueous Stable Gold Nanostar/ZIF‐8 Nanocomposites for Light‐Triggered Release of Active Cargo Inside Living Cells

Triggered release: A thermoresponsive carrier comprising gold nanostars coated with ZIF‐8 stabilized with an amphiphilic polymer was developed for the light‐triggered release of encapsulated cargo inside cells. This nanocomposite, which is stable in aqueous solution (even when stored in cells), combines thermoplasmonic and high drug‐loading capabilities.


Abstract

A plasmonic core–shell gold nanostar/zeolitic‐imidazolate‐framework‐8 (ZIF‐8) nanocomposite was developed for the thermoplasmonic‐driven release of encapsulated active molecules inside living cells. The nanocomposites were loaded, as a proof of concept, with bisbenzimide molecules as functional cargo and wrapped with an amphiphilic polymer that prevents ZIF‐8 degradation and bisbenzimide leaking in aqueous media or inside living cells. The demonstrated molecule‐release mechanism relies on the use of near‐IR light coupled to the plasmonic absorption of the core gold nanostars, which creates local temperature gradients and thus, bisbenzimide thermodiffusion. Confocal microscopy and surface‐enhanced Raman spectroscopy (SERS) were used to demonstrate bisbenzimide loading/leaking and near‐IR‐triggered cargo release inside cells, thereby leading to DNA staining.

29 Oct 00:58

Full spectrum light driven photocatalytic in-situ epitaxy of one-unit-cell Bi2O2CO3 layers on Bi2O4 nanocrystals for highly efficient photocatalysis and mechanism unveiling

Publication date: April 2019

Source: Applied Catalysis B: Environmental, Volume 243

Author(s): Jun Li, Xiaoyong Wu, Zhen Wan, Hong Chen, Gaoke Zhang

Abstract

In-situ epitaxial growth is a fascinating strategy to nicely couple two low dimensional semiconductors as highly efficient composite photocatalysts. Meanwhile, organic contaminants in the photocatalytic process are usually decomposed into greenhouse gas (CO2) that can’t be reused. Herein, we reported a green full spectrum light (UV, visible and NIR lights) induced epitaxial growth strategy to synthesize highly efficient Bi2O4/Bi2O2CO3 heterostructure photocatalyst by reusing waste carbon source, in which one-unit-cell Bi2O2CO3 layers (1.0 nm) in-situ grew on the surface of Bi2O4 nanocrystals during the photocatalytic degradation of rhodamine B (RhB) or phenol. More importantly, 13C nuclear magnetic resonance (NMR) spectroscopy confirmed that the carbon element in Bi2O2CO3 was from the photocatalytic degradation of organic contaminations. Furthermore, density functional theory (DFT) calculations confirm that the Bi2O4 nanocrystals with exposed {-101} facets have the larger percentage of undercoordinated Bi atoms, which provided favorable conditions for the in-situ epitaxy of Bi2O2CO3 during the photocatalytic reaction. Additionally, the increased charge density near the Fermi level resulted in improved photoresponsivity of Bi2O4/Bi2O2CO3 composite and the coalescence of Bi2O4 and Bi2O2CO3 could favor the travel of photogenerated carriers from one to another owing to the close work functions for Bi2O4 (4.295 eV) and Bi2O2CO3 (4.410 eV). As we expected, the Bi2O4/Bi2O2CO3 composite presented higher photocatalytic activity for phenol and ciprofloxacin (CIP) degradation than pure Bi2O4 nanocrystals. The possible degradation pathway of CIP in aqueous solution and photocatalytic mechanism of Bi2O4/Bi2O2CO3 composite were also proposed based on liquid chromatography mass spectrometer (LC–MS) analysis and experimental results. This work provides a green strategy for designing highly efficient photocatalysts.

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Graphical abstract for this article