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Fabrication of strong bifunctional electrocatalytically active hybrid Cu–Cu2O nanoparticles in a carbon matrix†
Catalysis Science & Technology ( IF 4.4 ) Pub Date : 2018-01-09 00:00:00 , DOI: 10.1039/c7cy02048a
Pandi Muthukumar 1, 2, 3, 4, 5 , Vadivel Vinod Kumar 1, 2, 3, 4, 5 , Gajjala Rajendra Kumar Reddy 1, 2, 3, 4, 5 , P. Suresh Kumar 1, 2, 3, 4, 5 , Savarimuthu Philip Anthony 1, 2, 3, 4, 5
Affiliation  

Herein, earth-abundant cost-effective hybrid copper–cuprous oxide nanoparticles have been fabricated in a carbon matrix (Cu–Cu2ONPs@C) and used as bifunctional electrocatalysts for the oxygen evolution reaction (OER) and hydrogen evolution reaction (HER). At a 0.1 mg loading, OER studies of Cu–Cu2ONPs@C showed a significantly low overpotential of 530 mV @ 10 mA cm−2 with the applied potential of 2.07 V in 0.4 M KOH. HER studies showed an overpotential of −672 mV @ 10 mA cm−2 with the applied potential of −1.058 V in 0.4 M H2SO4. Cu–Cu2ONPs@C showed a good electrocatalytic current density of 57.7 mA cm−2 for OER and −125 mA cm−2 for HER at a significantly low catalyst loading. For controlled studies, Cu2ONPs and CuNPs in carbon matrix have also been synthesized, and their catalytic activities (OER and HER) have been compared with those of the hybrid Cu–Cu2ONPs@C. The comparative studies indicated that the presence of conducting metal CuNPs along with Cu2ONPs in the carbon matrix enhanced the electrocatalytic activity for both OER and HER as compared to that of pure Cu2ONPs and CuNPs in the carbon matrix. Interestingly, the solvent used for fabricating different NP electrodes has also shown significant influence on the electrocatalytic current density. The synthesized hybrid Cu–Cu2ONPs@C, Cu2ONPs@C, and CuNPs@C were characterized using powder X-ray diffraction (PXRD), X-ray photoelectron spectroscopy (XPS), high resolution transmission electron microscopy (HR-TEM), and BET analysis. To the best of our knowledge, the fabricated hybrid Cu–Cu2ONP@C exhibited a strong bifunctional electrocatalytic response at a high current density with a low catalyst loading (0.1 mg) among the different Cu-based nanostructured catalysts explored for the water splitting reactions.

中文翻译:

在碳基质中 制备强双功能电催化活性杂化Cu–Cu 2 O纳米粒子

在此,已在碳基质(Cu-Cu 2 ONPs @ C)中制备了地球上富于成本效益的杂化铜-亚铜氧化物纳米颗粒,并用作氧气逸出反应(OER)和氢气逸出反应(HER)的双功能电催化剂。 。在0.1 mg负载下,Cu–Cu 2 ONPs @ C的OER研究显示,在10 mA cm -2时,530 mV的过低电势非常低,在0.4 M KOH中的施加电势为2.07V。HER研究表明,在10 mA cm -2处的过电势为-672 mV ,在0.4 MH 2 SO 4中的施加电势为-1.058V 。Cu–Cu 2 ONPs @ C对OER和-125 mA cm均显示出良好的电催化电流密度,为57.7 mA cm -2对于HER -2,催化剂负载量非常低。为了进行对照研究,还合成了碳基质中的Cu 2 ONPs和CuNPs,并将它们的催化活性(OER和HER)与杂化Cu-Cu 2 ONPs @ C进行了比较。比较研究表明,与碳基质中纯Cu 2 ONP和CuNPs相比,碳基质中导电金属CuNPs与Cu 2 ONPs的存在增强了对OER和HER的电催化活性。有趣的是,用于制造不同NP电极的溶剂也已显示出对电催化电流密度的显着影响。合成的杂化Cu–Cu 2 ONPs @ C,Cu 2使用粉末X射线衍射(PXRD),X射线光电子能谱(XPS),高分辨率透射电子显微镜(HR-TEM)和BET分析对ONPs @ C和CuNPs @ C进行了表征。据我们所知,在探索用于水分解的不同铜基纳米结构催化剂中,合成的Cu–Cu 2 ONP @ C在高电流密度下具有很强的双功能电催化响应,催化剂负载量低(0.1 mg)。反应。
更新日期:2018-01-09
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