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      Water electrolysis for hydrogen production: from hybrid systems to self-powered/catalyzed devices

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          Abstract

          This perspective highlights recent advancements in innovative strategies to provide valuable insights into the potential for energy-saving hydrogen production through water electrolysis.

          Abstract

          The electrocatalytic splitting of water holds great promise as a sustainable and environmentally friendly technology for hydrogen production. However, the sluggish kinetics of the oxygen evolution reaction (OER) at the anode significantly hampers the efficiency of this process. In this comprehensive perspective, we outline recent advancements in innovative strategies aimed at improving the energy and economic efficiency of conventional water electrolysis, thereby facilitating efficient hydrogen generation. These novel strategies mainly include: (i) sacrificial-agent-assisted water electrolysis, which integrates thermodynamically favorable small molecules to replace the OER while simultaneously degrading pollutants; (ii) organic upgrading-assisted water electrolysis, wherein thermodynamically and kinetically favorable organic oxidation reactions replace the OER, leading to the production of high-value chemicals alongside hydrogen; (iii) self-powered electrolysis systems, achieved by coupling water splitting with metal-based batteries or fuel cells, enabling hydrogen production without the need for additional electricity input; and (iv) self-catalyzed electrolysis systems driven by the spontaneous metal oxidation at the anode, which provides electrons for hydrogen evolution at the cathode. In particular, we emphasize the design of electrocatalysts using non-noble metal elements, elucidate the underlying reaction mechanisms, and explore the construction of efficient electrolyzers. Additionally, we discuss the prevailing challenges and future prospects, aiming to foster the development of electrocatalytic systems for highly efficient hydrogen production from water in the future.

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          Combining theory and experiment in electrocatalysis: Insights into materials design

          Electrocatalysis plays a central role in clean energy conversion, enabling a number of sustainable processes for future technologies. This review discusses design strategies for state-of-the-art heterogeneous electrocatalysts and associated materials for several different electrochemical transformations involving water, hydrogen, and oxygen, using theory as a means to rationalize catalyst performance. By examining the common principles that govern catalysis for different electrochemical reactions, we describe a systematic framework that clarifies trends in catalyzing these reactions, serving as a guide to new catalyst development while highlighting key gaps that need to be addressed. We conclude by extending this framework to emerging clean energy reactions such as hydrogen peroxide production, carbon dioxide reduction, and nitrogen reduction, where the development of improved catalysts could allow for the sustainable production of a broad range of fuels and chemicals.
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            A perovskite oxide optimized for oxygen evolution catalysis from molecular orbital principles.

            The efficiency of many energy storage technologies, such as rechargeable metal-air batteries and hydrogen production from water splitting, is limited by the slow kinetics of the oxygen evolution reaction (OER). We found that Ba(0.5)Sr(0.5)Co(0.8)Fe(0.2)O(3-δ) (BSCF) catalyzes the OER with intrinsic activity that is at least an order of magnitude higher than that of the state-of-the-art iridium oxide catalyst in alkaline media. The high activity of BSCF was predicted from a design principle established by systematic examination of more than 10 transition metal oxides, which showed that the intrinsic OER activity exhibits a volcano-shaped dependence on the occupancy of the 3d electron with an e(g) symmetry of surface transition metal cations in an oxide. The peak OER activity was predicted to be at an e(g) occupancy close to unity, with high covalency of transition metal-oxygen bonds.
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              Recent advances in transition metal phosphide nanomaterials: synthesis and applications in hydrogen evolution reaction.

              The urgent need of clean and renewable energy drives the exploration of effective strategies to produce molecular hydrogen. With the assistance of highly active non-noble metal electrocatalysts, electrolysis of water is becoming a promising candidate to generate pure hydrogen with low cost and high efficiency. Very recently, transition metal phosphides (TMPs) have been proven to be high performance catalysts with high activity, high stability, and nearly ∼100% Faradic efficiency in not only strong acidic solutions, but also in strong alkaline and neutral media for electrochemical hydrogen evolution. In this tutorial review, an overview of recent development of TMP nanomaterials as catalysts for hydrogen generation with high activity and stability is presented. The effects of phosphorus (P) on HER activity, and their synthetic methods of TMPs are briefly discussed. Then we will demonstrate the specific strategies to further improve the catalytic efficiency and stability of TMPs by structural engineering. Making use of TMPs as cocatalysts and catalysts in photochemical and photoelectrochemical water splitting is also discussed. Finally, some key challenges and issues which should not be ignored during the rapid development of TMPs are pointed out. These strategies and challenges of TMPs are instructive for designing other high-performance non-noble metal catalysts.

                Author and article information

                Contributors
                (View ORCID Profile)
                Journal
                EESNBY
                Energy & Environmental Science
                Energy Environ. Sci.
                Royal Society of Chemistry (RSC)
                1754-5692
                1754-5706
                January 02 2024
                2024
                : 17
                : 1
                : 49-113
                Affiliations
                [1 ]National Institute for Advanced Materials, School of Materials Science and Engineering, Smart Sensing Interdisciplinary Science Center, Nankai University, Tianjin 300350, China
                [2 ]Key Laboratory of Advanced Energy Materials Chemistry (Ministry of Education), Nankai University, Tianjin 300071, China
                Article
                10.1039/D3EE02467A
                d46482d4-6f20-44d6-884e-48bbd396e398
                © 2024

                http://rsc.li/journals-terms-of-use

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