Effect of growth dynamics on the structural, photophysical and pseudocapacitance properties of famatinite copper antimony sulphide colloidal nanostructures (including nanosheets)†

IF 3.3 3区 化学 Q2 CHEMISTRY, INORGANIC & NUCLEAR Dalton Transactions Pub Date : 2025-01-17 DOI:10.1039/D4DT02826K
Kimberly Weston, Richard A. Taylor, Kim Kisslinger and Shobha Mantripragada
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Abstract

Facile phase selective synthesis of copper antimony sulphide (CAS) nanostructures is important because of their tunable photoconductive and electrochemical properties. In this study, off-stoichiometric famatinite phase CAS (fCAS) quasi-spherical and quasi-hexagonal colloidal nanostructures (including nanosheets) of sizes, 2.4–18.0 nm were grown under variable conditions of temperature (60–200 °C), time and oleylamine capping ligand concentration using copper(II) acetylacetonate and antimony(III) diethyldithiocarbamate precursors. Data from powder X-ray diffraction, Raman spectroscopy and high-resolution scanning/transmission electron microscopy confirm the tetragonal structure of the famatinite phase. X-ray photoelectron spectroscopy, transmission electron microscopy and scanning electron microscopy-energy dispersive X-ray spectroscopy data suggest a correlation of particle size, morphology and composition of the off-stoichiometric fCAS nanostructures with growth temperature and time, and oleylamine concentration. The off-stoichiometric Cu3−aSb1+bS4±c (a, b, c – mole fractions) nanostructures being severely copper-deficient and antimony-rich, exhibit shallow-lying acceptor copper vacancy states, deep-lying donor states of antimony interstitials, sulphur vacancies and antimony-copper antisites and shallow-lying acceptor surface trapping states. These electronic states are likely implicated in tunable UV-visible absorption and bandgaps between 2.3 and 2.8 eV, and broad visible-NIR photoluminescence with fast recombination of radiative lifetimes between 0.2 and 6.2 ns, confirmed from absorption, steady-state and time-resolved photoluminescence spectroscopies. Additionally, cyclic voltammetry and electrochemical impedance spectroscopy confirm that electrodes of the fCAS nanostructures display slightly variable pseudocapacitance of charge-storage primarily via possible sodium ion intercalation with a high specific capacitance of ∼84 F g−1 obtained at a scan rate of 5 mV s−1. Overall, these results show the influence of composition, in particular point defects, phase quality and morphology on the optical and pseudocapacitance properties of fCAS nanostructures, suitable as solar absorbers or electrodes for energy storage devices.

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生长动力学对黄褐铁矿硫化铜锑胶体纳米结构(包括纳米片)结构、光物理和赝电容性能的影响
易相选择性合成硫化铜锑纳米结构具有可调的光导和电化学性能。在本研究中,以乙酰丙酮铜(II)和二乙基二硫代氨基甲酸锑(III)为前驱体,在温度(60-200℃)、时间和油胺覆盖配体浓度的不同条件下,制备了尺寸为2.4-18.0 nm的非化学测量法法黄铁矿相CAS (fCAS)准球形和准六角形胶体纳米结构(包括纳米片)。粉末x射线衍射、拉曼光谱和高分辨率扫描/透射电子显微镜的数据证实了黄铁矿相的四方结构。x射线光电子能谱、透射电镜和扫描电镜-能量色散x射线能谱数据表明,非化学计量fCAS纳米结构的粒径、形貌和组成与生长温度、生长时间和胺浓度有关。非化学计量Cu3−aSb1+bS4±c (a, b, c -摩尔分数)纳米结构是严重缺铜和富锑的,表现为浅层受体铜空位态、深部锑间隙、硫空位和锑-铜反位的供体态和浅层受体表面俘获态。吸收光谱、稳态光谱和时间分辨光谱证实,这些电子态可能与可调谐的紫外-可见吸收和带隙在2.3至2.8 eV之间,以及辐射寿命在0.2至6.2 ns之间快速重组的宽可见-近红外光致发光有关。此外,循环伏安法和电化学阻抗谱证实,fCAS纳米结构的电极主要通过可能的钠离子插入显示出略微可变的电荷存储伪电容,在5 mV s−1的扫描速率下获得了高达84 F g−1的高比电容。总的来说,这些结果表明,组成,特别是点缺陷,相位质量和形貌对fCAS纳米结构的光学和赝电容性能的影响,适合作为太阳能吸收器或储能装置的电极。
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来源期刊
Dalton Transactions
Dalton Transactions 化学-无机化学与核化学
CiteScore
6.60
自引率
7.50%
发文量
1832
审稿时长
1.5 months
期刊介绍: Dalton Transactions is a journal for all areas of inorganic chemistry, which encompasses the organometallic, bioinorganic and materials chemistry of the elements, with applications including synthesis, catalysis, energy conversion/storage, electrical devices and medicine. Dalton Transactions welcomes high-quality, original submissions in all of these areas and more, where the advancement of knowledge in inorganic chemistry is significant.
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