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      Tandem catalysis in electrocatalytic nitrate reduction: Unlocking efficiency and mechanism

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          Abstract

          The electrochemical nitrate reduction reaction (NO 3RR) holds promise for ecofriendly nitrate removal. However, the challenge of achieving high selectivity and efficiency in electrocatalyst systems still significantly hampers the mechanism understanding and the large‐scale application. Tandem catalysts, comprising multiple catalytic components working synergistically, offer promising potential for improving the efficiency and selectivity of the NO 3RR. This review highlights recent progress in designing tandem catalysts for electrochemical NO 3RR, including the noble metal‐related system, transition metal electrocatalysts, and pulsed electrocatalysis strategies. Specifically, the optimization of active sites, interface engineering, synergistic effects between catalyst components, various in situ technologies, and theory simulations are discussed in detail. Challenges and opportunities in the development of tandem catalysts for scaling up electrochemical NO 3RR are further discussed, such as stability, durability, and reaction mechanisms. By outlining possible solutions for future tandem catalyst design, this review aims to open avenues for efficient nitrate reduction and comprehensive insights into the mechanisms for energy sustainability and environmental safety.

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          Nitrogen cycle electrocatalysis.

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            Unveiling the Activity Origin of a Copper‐based Electrocatalyst for Selective Nitrate Reduction to Ammonia

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              Current and future role of Haber–Bosch ammonia in a carbon-free energy landscape

              The future of green ammonia as long-term energy storage relies on the replacement of the conventional CO 2 intensive methane-fed Haber–Bosch process by distributed and agile ones aligned to the geographically isolated and intermittent renewable energy. The future of a carbon-free society relies on the alignment of the intermittent production of renewable energy with our continuous and increasing energy demands. Long-term energy storage in molecules with high energy content and density such as ammonia can act as a buffer versus short-term storage ( e.g. batteries). In this paper, we demonstrate that the Haber–Bosch ammonia synthesis loop can indeed enable a second ammonia revolution as energy vector by replacing the CO 2 intensive methane-fed process with hydrogen produced by water splitting using renewable electricity. These modifications demand a redefinition of the conventional Haber–Bosch process with a new optimisation beyond the current one which was driven by cheap and abundant natural gas and relaxed environmental concerns during the last century. Indeed, the switch to electrical energy as fuel and feedstock to replace fossil fuels ( e.g. methane) will lead to dramatic energy efficiency improvements through the use of high efficiency electrical motors and complete elimination of direct CO 2 emissions. Despite the technical feasibility of the electrically-driven Haber–Bosch ammonia, the question still remains whether such revolution will take place. We reveal that its success relies on two factors: increased energy efficiency and the development of small-scale, distributed and agile processes that can align to the geographically isolated and intermittent renewable energy sources. The former requires not only higher electrolyser efficiencies for hydrogen production but also a holistic approach to the ammonia synthesis loop with the replacement of the condensation separation step by alternative technologies such as absorption and catalysis development. Such innovations will open the door to moderate pressure systems, the development and deployment of novel ammonia synthesis catalysts, and even more importantly, the opportunity for integration of reaction and separation steps to overcome equilibrium limitations. When realised, green ammonia will reshape the current energy landscape by directly replacing fossil fuels in transportation, heating, electricity, etc. , and as done in the last century, food.
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                Author and article information

                Contributors
                (View ORCID Profile)
                Journal
                Interdisciplinary Materials
                Interdisciplinary Materials
                Wiley
                2767-441X
                2767-441X
                March 2024
                February 28 2024
                March 2024
                : 3
                : 2
                : 245-269
                Affiliations
                [1 ] State Key Laboratory for Modification of Chemical Fibers and Polymer Materials College of Materials Science and Engineering Donghua University Shanghai China
                [2 ] Key Laboratory of Interface Science and Engineering in Advanced Materials Ministry of Education Taiyuan University of Technology Taiyuan China
                [3 ] Helmholtz‐Institute Ulm (HIU) Ulm Germany
                Article
                10.1002/idm2.12152
                9b1ceaa9-173b-4699-b37c-771e24b9099f
                © 2024

                http://creativecommons.org/licenses/by/4.0/

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