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Electrocatalytic Hydrogen Evolution by a Uranium(VI) Polyoxometalate: an Environmental Toxin for Sustainable Energy Generation

铀酰 化学 拉曼光谱 多金属氧酸盐 光致发光 结晶学 红外光谱学 离子 分析化学(期刊) 无机化学 催化作用 生物化学 物理 材料科学 有机化学 色谱法 光学 冶金
作者
Sateesh Mulkapuri,Asha Siddikha,Athira Ravi,Pinki Saha,Avulu Vinod Kumar,Sathyanarayana Boodida,M. Vithal,Samar K. Das
出处
期刊:Inorganic Chemistry [American Chemical Society]
卷期号:62 (48): 19664-19676 被引量:7
标识
DOI:10.1021/acs.inorgchem.3c03018
摘要

The uranyl ion (UO2)2+, a uranium nuclear waste, is one of the serious contaminants in our ecosystem because of its radioactivity, relevant human activities, and highly mobile and complex nature of living cells. In this article, we have reported the synthesis and structural characterization of an uranyl cation-incorporated polyoxometalate (POM) compound, K10[{K4(H2O)6}{UO2}2(α-PW9O34)2]·13H2O (1), in which the uranyl cations are complexed with an in situ generated [α-PW9O34]9– cluster. Single-crystal X-ray diffraction (SCXRD) analysis of compound 1 reveals that the uranyl–potassium complex cationic species, [{K4(H2O)6}{UO2}2]8+, is sandwiched by two [α-PW9O34]9– clusters resulting in a Dawson type of POM. Compound 1 was further characterized by inductively coupled plasma optical emission spectroscopy (ICP-OES) analysis and infrared (IR), Raman, electronic absorption, and solid-state photoluminescence spectral studies. IR stretching vibrations at 895 and 856 cm–1 and the Raman signature peak at 792 cm–1 in the IR and Raman spectra of compound 1 primarily confirm the presence of a trans-[O═U═O]2+ ion. The solid-state photoluminescence spectrum of 1 exhibits a typical vibronic structure, resulting from symmetrical vibrations of [O═U═O]2+ bands, corresponding to the electronic transitions of S11 → S10 and S10 → S0υ (υ = 0–3). Interestingly, title compound 1 shows efficient electrocatalytic hydrogen evolution by water reduction with low Tafel slope values of 186.59 and 114.83 mV dec–1 at 1 mA cm–2 along with optimal Faradaic efficiency values of 82 and 87% at neutral pH and in acidic pH 3, respectively. Detailed electrochemical analyses reveal that the catalytic hydrogen evolution reaction (HER) activity mediated by compound 1 is associated with the UVI/UV redox couple of the POM. The microscopic as well as routine spectral analyses of postelectrode samples and controlled experiments have confirmed that compound 1 behaves like a true molecular electrocatalyst for the HER. To our knowledge, this is the first paradigm of a uranium-containing polyoxometalate that exhibits electrocatalytic water reduction to molecular H2. In a nutshell, an environmental toxin (a uranium-oxo compound) has been demonstrated to be utilized as an efficient electrocatalyst for hydrogen generation from water, a green approach of sustainable energy production.
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