In Situ Spectroscopic Examination of a Low Overpotential Pathway for Carbon Dioxide Conversion to Carbon Monoxide

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• 作者：Brian A. Rosen ; John L. Haan ; Prabuddha Mukherjee ; Bj枚rn Braunschweig ; Wei Zhu ; Amin Salehi-Khojin ; Dana D. Dlott ; Richard I. Masel
• 刊名：The Journal of Physical Chemistry C
• 出版年：2012
• 出版时间：July 26, 2012
• 年：2012
• 卷：116
• 期：29
• 页码：15307-15312
• 全文大小：275K
• 年卷期：v.116,no.29(July 26, 2012)
• ISSN：1932-7455

文摘

Lowering the overpotential for the electrochemical conversion of CO₂ to useful products is one of the grand challenges in the Department Of Energy report, 鈥淐atalysis for Energy鈥? In a previous paper, we showed that CO₂ conversion occurs at low overpotential on a 1-ethyl-3-methylimidazolium tetrafluoroborate (EMIM-BF₄)-coated silver catalyst in an aqueous solution of EMIM-BF4. One of the surprises in the previous paper was that the selectivity to CO was better than 96% on silver, compared with 80% in the absence of ionic liquid. In this article, we use sum frequency generation (SFG) to explore the mechanism of the enhancement of selectivity. The study used platinum rather than silver because previous workers had found that platinum is almost inactive for CO production from CO₂. The results show that EMIM-BF₄ has two effects: it suppresses hydrogen formation and enhances CO₂ conversion. SFG shows that there is a layer of EMIM on the platinum surface that inhibits hydrogen formation. CO₂, however, can react with the EMIM layer to form a complex such as CO₂-EMIM at potentials more negative than 鈭?.1 V with respect to a standard hydrogen electrode (SHE). That complex is converted to adsorbed CO at cathodic potentials of 鈭?.25 V with respect to SHE. These results demonstrate that adsorbed monolayers can substantially lower the barrier for CO₂ conversion on platinum and inhibit hydrogen formation, opening the possibility of a new series of metal/organic catalysts for this reaction.