Reichert Robert, Zambrzycki Christian, Jusys Zenonas, Behm R Jürgen
Institute of Surface Chemistry and Catalysis, Ulm University, 89069, Ulm, Germany.
Institute of Chemical Engineering, Ulm University, 89069, Ulm, Germany.
ChemSusChem. 2015 Nov;8(21):3677-87. doi: 10.1002/cssc.201500800. Epub 2015 Sep 18.
To better understand organic-molecule-assisted photo-electrochemical water splitting, photo-electrochemistry and on-line mass spectrometry measurements are used to investigate the photo-electrochemical oxidation of the C1 molecules methanol, formaldehyde, and formic acid over WO3 film anodes in aqueous solution and its competition with O2 evolution from water oxidation O2 (+) and CO2 (+) ion currents show that water oxidation is strongly suppressed by the organic species. Photo-electro-oxidation of formic acid is dominated by formation of CO2 , whereas incomplete oxidation of formaldehyde and methanol prevails, with the selectivity for CO2 formation increasing with increasing potential and light intensity. The mechanistic implications for the photo-electro-oxidation of the organic molecules and its competition with water oxidation, which could be derived from this novel approach, are discussed.
为了更好地理解有机分子辅助的光电化学水分解过程,采用光电化学和在线质谱测量方法,研究了水溶液中WO3薄膜阳极上C1分子甲醇、甲醛和甲酸的光电化学氧化及其与水氧化产生O2的竞争。O2(+)和CO2(+)离子电流表明,有机物种强烈抑制了水氧化。甲酸的光电氧化主要以生成CO2为主,而甲醛和甲醇的不完全氧化占主导,随着电位和光强的增加,生成CO2的选择性增加。讨论了这种新方法对有机分子光电氧化及其与水氧化竞争的机理意义。