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CdS 纳米粒子的原位生长和固定在功能化 MoS 上:光电化学电池的制备、表征和制造。

In-Situ Growth and Immobilization of CdS Nanoparticles onto Functionalized MoS : Preparation, Characterization and Fabrication of Photoelectrochemical Cells.

机构信息

Theoretical and Physical Chemistry Institute, National Hellenic Research Foundation, 48 Vassileos Constantinou Avenue, Athens, 11635, Greece.

Instituto de Carboquimica (ICB-CSIC), C/Miguel Luesma Castan 4, 50018, Zaragoza, Spain.

出版信息

Chem Asian J. 2020 Aug 3;15(15):2350-2356. doi: 10.1002/asia.201901371. Epub 2019 Dec 12.

Abstract

A facile strategy for the controllable growth of CdS nanoparticles at the periphery of MoS en route the preparation of electron donor-acceptor nanoensembles is developed. Precisely, the carboxylic group of α-lipoic acid, as addend of the modified MoS obtained upon 1,2-dithiolane functionalization, was employed as anchor site for the in situ preparation and immobilization of the CdS nanoparticles in an one-pot two-step process. The newly prepared MoS /CdS hybrid material was characterized by complementary spectroscopic, thermal and microscopy imaging means. Absorption spectroscopy was employed to register the formation of MoS /CdS, by observing a broad shoulder centered at 420 nm due to CdS nanoparticles, while the excitonic bands of MoS were also evident. Moreover, based on the efficient quenching of the characteristic fluorescence emission of CdS at 725 nm by the presence of MoS , strong electronic interactions at the excited state between the two species within the ensemble were identified. Photoelectrochemical assays of MoS /CdS thin-film electrodes revealed a prompt, steady and reproducible anodic photoresponse during repeated on-off cycles of illumination. A significant zero-current photopotential of -540 mV and an anodic photocurrent of 1 μA were observed, underlining improved charge-separation and electron transport from CdS to MoS . The superior performance of the charge-transfer processes in MoS /CdS is of direct interest for the fabrication of photoelectrochemical and optoelectronic devices.

摘要

一种可控生长 CdS 纳米粒子的简便策略,用于制备电子给体-受体纳米组装体,是在 MoS 外围进行的。具体而言,1,2-二硫杂环戊烷功能化得到的修饰 MoS 的羧酸基团,作为原位制备和固定 CdS 纳米粒子的锚定位点,在一步两步法中进行。采用互补光谱、热和显微镜成像手段对新制备的 MoS/CdS 杂化材料进行了表征。吸收光谱用于注册 MoS/CdS 的形成,通过观察到由于 CdS 纳米粒子而位于 420nm 的宽肩,而 MoS 的激子带也很明显。此外,基于 MoS 存在时 CdS 的特征荧光发射的有效猝灭,确定了在组装体中两种物质在激发态下的强电子相互作用。MoS/CdS 薄膜电极的光电化学分析表明,在反复光照关闭循环期间,存在快速、稳定和可重复的阳极光响应。观察到-540mV 的零电流光电压和 1μA 的阳极光电流,突出了 CdS 到 MoS 的电荷分离和电子传输的改善。在 MoS/CdS 中,电荷转移过程的优异性能直接关系到光电化学和光电设备的制造。

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