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首页> 外文期刊>Advanced Functional Materials >Supported Metal Oxide Nanosystems for Hydrogen Photogeneration: Quo Vadis?
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Supported Metal Oxide Nanosystems for Hydrogen Photogeneration: Quo Vadis?

机译:支持氢光生的金属氧化物纳米系统:Vadis吗?

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摘要

Hydrogen has attracted a great share of attention both as an energy carrier and as an irreplaceble reagent for many industrial processes. Photoactivated routes, ranging from photocatalytic and photo-electrochemical water splitting to photoreforming of suitable oxygenates, appear to be attractive long-term solutions among possible strategies for hydrogen production. However, the success of such processes depends on the efficient use of solar energy and on the identification of active and stable catalysts, which, in addition, should be eco-friendly and available in large amounts at accessible costs. Researchers are exploring the use of supported oxide nanomaterials, which enable an easy catalyst recovery and exhibit unique advantages due to their peculiar nano-organization. In this Feature Article, the potential of such systems towards photoinduced hydrogen evolution is discussed based on selected case studies that highlight the relations between structure, morphology, composition, and functional performances of oxide nanomaterials. In addition, potential limitations of oxide-based nanomaterials as well as unexplored key aspects that require special attention in future investigations are discussed.
机译:氢作为能量载体和许多工业过程中不可替代的试剂已引起了广泛的关注。从光催化和光电化学水分解到合适的含氧化合物的光重整的光活化途径似乎是可能的制氢策略中的有吸引力的长期解决方案。然而,这种方法的成功取决于太阳能的有效利用以及活性和稳定催化剂的鉴定,此外,这些催化剂应该是生态友好的并且可以以可承受的成本大量获得。研究人员正在探索使用负载型氧化物纳米材料的方法,该方法能够轻松回收催化剂,并且由于其独特的纳米组织而具有独特的优势。在本专题文章中,将基于选定的案例研究来讨论此类系统对光致氢释放的潜力,这些案例研究突出了氧化物纳米材料的结构,形态,组成和功能性能之间的关系。此外,讨论了基于氧化物的纳米材料的潜在局限性以及在未来的研究中需要特别注意的未探索的关键方面。

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  • 来源
    《Advanced Functional Materials》 |2011年第14期|p.2611-2623|共13页
  • 作者单位

    CNR-ISTM, INSTM, and Department of Chemistry Padova University via F. Marzolo, 1-35131 Padova, Italy;

    INSTM and Department of Chemistry Padova University via F. Marzolo, 1-35131 Padova, Italy;

    Department of Chemical and Pharmaceutical Sciences ICCOM-CNR Trieste Research Unit, and INSTM Research Unit Trieste University via L Giorgieri, 1-34127 Trieste, Italy;

    INSTM and Department of Chemistry Padova University via F. Marzolo, 1-35131 Padova, Italy;

    INSTM and Department of Chemistry Padova University via F. Marzolo, 1-35131 Padova, Italy;

    Department of Chemical and Pharmaceutical Sciences ICCOM-CNR Trieste Research Unit, and INSTM Research Unit Trieste University via L Giorgieri, 1-34127 Trieste, Italy;

    INSTM and Department of Chemistry Padova University via F. Marzolo, 1-35131 Padova, Italy;

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