Mishra Amit K, Belgamwar Rajesh, Jana Rajkumar, Datta Ayan, Polshettiwar Vivek
Department of Chemical Sciences, Tata Institute of Fundamental Research, Mumbai 400005, India.
School of Chemical Sciences, Indian Association for the Cultivation of Science, Kolkata 700032, India.
Proc Natl Acad Sci U S A. 2020 Mar 24;117(12):6383-6390. doi: 10.1073/pnas.1917237117. Epub 2020 Mar 10.
Active and stable metal-free heterogeneous catalysts for CO fixation are required to reduce the current high level of carbon dioxide in the atmosphere, which is driving climate change. In this work, we show that defects in nanosilica (E' centers, oxygen vacancies, and nonbridging oxygen hole centers) convert CO to methane with excellent productivity and selectivity. Neither metal nor complex organic ligands were required, and the defect alone acted as catalytic sites for carbon dioxide activation and hydrogen dissociation and their cooperative action converted CO to methane. Unlike metal catalysts, which become deactivated with time, the defect-containing nanosilica showed significantly better stability. Notably, the catalyst can be regenerated by simple heating in the air without the need for hydrogen gas. Surprisingly, the catalytic activity for methane production increased significantly after every regeneration cycle, reaching more than double the methane production rate after eight regeneration cycles. This activated catalyst remained stable for more than 200 h. Detailed understanding of the role of the various defect sites in terms of their concentrations and proximities as well as their cooperativity in activating CO and dissociating hydrogen to produce methane was achieved.
为了降低当前大气中导致气候变化的高水平二氧化碳,需要活性和稳定的无金属多相催化剂来固定一氧化碳。在这项工作中,我们表明纳米二氧化硅中的缺陷(E' 中心、氧空位和非桥连氧空穴中心)能以优异的生产率和选择性将一氧化碳转化为甲烷。既不需要金属也不需要复杂的有机配体,仅缺陷就充当了二氧化碳活化和氢解离的催化位点,它们的协同作用将一氧化碳转化为甲烷。与随时间失活的金属催化剂不同,含缺陷的纳米二氧化硅表现出明显更好的稳定性。值得注意的是,该催化剂可以通过在空气中简单加热进行再生,无需氢气。令人惊讶的是,每次再生循环后甲烷生产的催化活性都显著提高,八个再生循环后甲烷生产率达到两倍以上。这种活化催化剂在200多小时内保持稳定。我们详细了解了各种缺陷位点在其浓度、邻近性以及它们在活化一氧化碳和氢解离以产生甲烷方面的协同作用中的作用。