Molecular electro- and photocatalytic approach to artificial nitrogen fixation for the synthesis of green ammonia

Ottavia Bettucci , Giorgia Salerno , Norberto Manfredi , Alessandro Abbotto
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Abstract

Ammonia (NH3) stands as a cornerstone compound across industries, pivotal in agriculture, chemicals, and energy sectors. However, the conventional Haber-Bosch process demands high pressures, temperatures, and fossil fuels, calling for sustainable alternatives. Electrocatalytic Nitrogen Reduction Reactions (E-NRRs) and Photocatalytic Nitrogen Reduction Reactions (Photo-NRRs) present innovative routes, leveraging electricity and direct sunlight to convert nitrogen (N2) to NH3 under mild conditions, reducing emissions and softening energy requirements. Catalysts play a strategic role in these approaches, overcoming activation barriers and enhancing efficiency. However, some challenges still need to be addressed. Indeed, noble metals exhibit limits and their scarcity, geopolitical involvement, and often fluctuating costs inhibit large-scale use. Non-noble metals offer promise but require optimization and face durability concerns. Finally, carbon-based catalysts present challenges in optimization and doping. In this scenario, a molecular-based approach, comprising both specific single coordination-based molecules with transition metal centres and either metal centre coordination-based or fully organic multi-dimensional networks originating from direct molecular organic precursors, overcomes these issues while keeping the benefits of the previously mentioned classes of compounds. This mini-review explores the molecular approach to E-NRRs and Photo-NRRs from coordination compounds carrying porphyrins and phthalocyanines as organic ligands to polymeric networks based on coordination compounds between metallic centres and organic ligands (Metal-Organic Frameworks), and to networks of molecular organic units into multi-dimensional structures (Covalent Organic Frameworks). Mechanistic insights into E-NRRs and Photo-NRRs pathways elucidate N2 conversion to NH3. A critical comparative evaluation of reported catalysts has been carried out to highlight the limits and the possibilities of each class of compounds. Although challenges persist in terms of stability, cost and complexity of the synthesis, the use of a molecular approach in NRRs represents one of the most promising routes towards the sustainable preparation of ammonia.

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利用分子电催化和光催化方法进行人工固氮以合成绿色氨气
氨(NH3)是各行各业的基石化合物,在农业、化工和能源领域举足轻重。然而,传统的哈伯-博施工艺需要高压、高温和化石燃料,因此需要可持续的替代品。电催化氮还原反应(E-NRRs)和光催化氮还原反应(Photo-NRRs)提出了创新路线,利用电力和直射阳光在温和条件下将氮气(N2)转化为 NH3,从而减少排放并降低能源需求。催化剂在这些方法中发挥着战略性作用,可以克服活化障碍并提高效率。然而,一些挑战仍有待解决。事实上,贵金属有其局限性,它们的稀缺性、地缘政治问题和经常波动的成本阻碍了其大规模使用。非贵金属前景广阔,但需要优化并面临耐久性问题。最后,碳基催化剂在优化和掺杂方面面临挑战。在这种情况下,以分子为基础的方法,既包括带有过渡金属中心的特定单一配位分子,也包括以金属中心配位为基础的或源自直接分子有机前体的完全有机多维网络,既克服了这些问题,又保持了前面提到的化合物类别的优点。本微型综述探讨了 E-NRR 和 Photo-NRR 的分子方法,从携带卟啉和酞菁作为有机配体的配位化合物,到基于金属中心和有机配体之间配位化合物的聚合物网络(金属有机框架),再到多维结构的分子有机单元网络(共价有机框架)。对 E-NRRs 和 Photo-NRRs 途径的机理研究阐明了 N2 向 NH3 的转化。我们对已报道的催化剂进行了严格的比较评估,以突出每一类化合物的局限性和可能性。尽管在合成的稳定性、成本和复杂性方面仍存在挑战,但在 NRRs 中使用分子方法是实现可持续制备氨的最有前途的途径之一。
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