碳量子点@MOF-808 纳米复合材料作为生物相容性光催化剂在可见光下降解酸性蓝 41

IF 4.1 3区 化学 Q2 CHEMISTRY, PHYSICAL Journal of Photochemistry and Photobiology A-chemistry Pub Date : 2024-08-22 DOI:10.1016/j.jphotochem.2024.115984
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引用次数: 0

摘要

采用船瓶法合成了作为生物相容性光催化剂的CQDs@MOF-808客体@宿主纳米复合材料,包括浸渍法将葡萄糖分子作为碳量子点(CQDs)前体固定到MOF-808孔隙中形成Glucose@MOF-808,以及通过原位热解法将葡萄糖分子负载到MOF-808孔隙中进一步制备碳量子点(CQDs)。在可见光照射下,CQDs@MOF-808 纳米复合材料在 120 分钟内对酸性蓝 41 的光催化降解效率为 86.62%,这归功于 MOF-808 孔隙中 CQDs 的存在。CQDs 的优异特性包括出色的上转换光致发光(UCPL)效应、光诱导电子转移、电子贮存特性和电子-空穴分离,这些特性都有助于酸性蓝 41 的光催化降解。合成样品的表征方法包括 PXRD、FT-IR、EDX、N2 吸附-解吸等温线、TEM、DRS、PL、EIS 和 Mott - Sckottky 测量。
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Degradation of acid blue 41 with carbon quantum dots@MOF-808 nanocomposite as a biocompatible photocatalyst under visible light

CQDs@MOF-808 guest@host nanocomposite as a biocompatible photocatalyst has been synthesized using a ship-bottle approach involving the impregnation method for immobilization of glucose molecules as carbon quantum dots (CQDs) precursor into the MOF-808 pores to form Glucose@MOF-808 and further fabrication of carbon quantum dots (CQDs) via in-situ thermolysis route of glucose molecules loaded into the pores of MOF-808. The photocatalytic degradation efficiency of 86.62 % was calculated for CQDs@MOF-808 nanocomposite for degradation of Acid Blue 41 in 120 min under visible light irradiation, that was attributed to the presence of CQDs inside MOF-808 pores. The exceptional characteristics of CQDs include outstanding up-converted photoluminescence (UCPL) effects, photo-induced electron transfer, electron reservoir properties, and electron-hole separations, all contributing to the photocatalytic degradation of Acid Blue 41. The synthesized samples were characterized by PXRD, FT-IR, EDX, N2 adsorption–desorption isotherm, TEM, DRS, PL, EIS and Mott − Sckottky measurements.

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来源期刊
CiteScore
7.90
自引率
7.00%
发文量
580
审稿时长
48 days
期刊介绍: JPPA publishes the results of fundamental studies on all aspects of chemical phenomena induced by interactions between light and molecules/matter of all kinds. All systems capable of being described at the molecular or integrated multimolecular level are appropriate for the journal. This includes all molecular chemical species as well as biomolecular, supramolecular, polymer and other macromolecular systems, as well as solid state photochemistry. In addition, the journal publishes studies of semiconductor and other photoactive organic and inorganic materials, photocatalysis (organic, inorganic, supramolecular and superconductor). The scope includes condensed and gas phase photochemistry, as well as synchrotron radiation chemistry. A broad range of processes and techniques in photochemistry are covered such as light induced energy, electron and proton transfer; nonlinear photochemical behavior; mechanistic investigation of photochemical reactions and identification of the products of photochemical reactions; quantum yield determinations and measurements of rate constants for primary and secondary photochemical processes; steady-state and time-resolved emission, ultrafast spectroscopic methods, single molecule spectroscopy, time resolved X-ray diffraction, luminescence microscopy, and scattering spectroscopy applied to photochemistry. Papers in emerging and applied areas such as luminescent sensors, electroluminescence, solar energy conversion, atmospheric photochemistry, environmental remediation, and related photocatalytic chemistry are also welcome.
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