A Perovskite Nanorod as Bifunctional Electrocatalyst for Overall Water Splitting
TL;DR: In this article, a nanostructured perovskite oxide (SNCF-NR) was used as a bifunctional electrocatalyst for overall water splitting, achieving a current density of 10 mA cm(-2) at a cell voltage of merely approximate 1.68 V.
Abstract: The development of highly efficient and low-cost electrocatalysts for oxygen evolution reaction (OER) and hydrogen evolution reaction (HER) is paramount for water splitting associated with the storage of clean and renewable energy. Here, this study reports its findings in the development of a nanostructured perovskite oxide as OER/HER bifunctional electrocatalyst for overall water splitting. Prepared by a facile electrospinning method, SrNb0.1Co0.7Fe0.2O3- perovskite nanorods (SNCF-NRs) display excellent OER and HER activity and stability in an alkaline solution, benefiting from the catalytic nature of perovskites and unique structural features. More importantly, the SNCF-NR delivers a current density of 10 mA cm(-2) at a cell voltage of merely approximate to 1.68 V while maintaining remarkable durability when used as both anodic and cathodic catalysts in an alkaline water electrolyzer. The performance of this bifunctional perovskite material is among the best ever reported for overall water splitting, offering a cost-effective alternative to noble metal based electrocatalysts.
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TL;DR: In this paper, a template-engaged strategy followed by sequential etching and phosphorization treatments is demonstrated to fabricate open and hierarchical Ni-Co-P hollow nanobricks (HNBs) via the assembly of oriented 2D nanosheets.
Abstract: Complex nano-architectures with ordered two-dimensional (2D) building blocks are a class of promising electrocatalysts for different electrochemical technologies. In this work, a novel template-engaged strategy followed by sequential etching and phosphorization treatments is demonstrated to fabricate open and hierarchical Ni–Co–P hollow nanobricks (HNBs) via the assembly of oriented 2D nanosheets. Benefiting from the unique nano-architectures with large electrolyte-accessible surface and abundant mass diffusion pathways, the as-prepared Ni–Co–P HNBs exhibit high electrocatalytic activity, which affords the current density of 10 mA cm−2 at low overpotentials of 270 mV and 107 mV for oxygen and hydrogen evolution reactions respectively, and excellent stability in an alkaline medium. Remarkably, when used as both the anode and cathode, a low cell voltage of 1.62 V is required to reach the current density of 10 mA cm−2, making the Ni–Co–P HNBs an efficient bifunctional electrocatalyst for overall water splitting.
704 citations
03 Jan 2020
TL;DR: The metal oxides have been of great importance to the development of energy conversion and storage technologies including heterojunction solar cells, Li-ion batteries, and electrocatalysts/photocatalys.
Abstract: Metal oxides have been of great importance to the development of energy conversion and storage technologies including heterojunction solar cells, Li-ion batteries, and electrocatalysts/photocatalys...
408 citations
TL;DR: In this article, the mass and energy circulation in the solar-hydrogen-electricity circle are delineated, and different strategies for light-driven water splitting proposed in laboratories are introduced, the progress of electrocatalytic hydrogen and oxygen evolution reactions are reviewed, and finally, the reactions in hydrogen fuel cells are briefly discussed.
Abstract: Artificial photosynthesis provides a blueprint to harvest solar energy to sustain the future energy demands. Solar-driven water splitting, converting solar energy into hydrogen energy, is the prototype of photosynthesis. Various systems have been designed and evaluated to understand the reaction pathways and/or to meet the requirements of potential applications. In solar-to-hydrogen conversion, electrocatalytic hydrogen and oxygen evolution reactions are key research areas that are meaningful both theoretically and practically. To utilize hydrogen energy, fuel cell technology has been extensively investigated because of its high efficiency in releasing chemical energy. In this review, general concepts of the photosynthesis in green plants are discussed, different strategies for the light-driven water splitting proposed in laboratories are introduced, the progress of electrocatalytic hydrogen and oxygen evolution reactions are reviewed, and finally, the reactions in hydrogen fuel cells are briefly discussed. Overall, the mass and energy circulation in the solar-hydrogen-electricity circle are delineated. The authors conclude that attention from scientists and engineers of relevant research areas is still highly needed to eliminate the wide disparity between the aspirations and realities of artificial photosynthesis.
395 citations
TL;DR: In this article, a general description about water splitting is presented to understand the reaction mechanism and proposed scaling relations toward activities, and key stability issues for Ru-based materials are further given.
Abstract: As a highly appealing technology for hydrogen generation, water electrolysis including oxygen evolution reaction (OER) at the anode and hydrogen evolution reaction (HER) at the cathode largely depends on the availability of efficient electrocatalysts. Accordingly, over the past years, much effort has been made to develop various electrocatalysts with superior performance and reduced cost. Among them, ruthenium (Ru)-based materials for OER and HER are very promising because of their prominent catalytic activity, pH-universal application, the cheapest price among the precious metal family, and so on. Herein, recent advances in this hot research field are comprehensively reviewed. A general description about water splitting is presented to understand the reaction mechanism and proposed scaling relations toward activities, and key stability issues for Ru-based materials are further given. Subsequently, various Ru-involving electrocatalysts are introduced and classified into different groups for improving or optimizing electrocatalytic properties, with a special focus on several significant bifunctional electrocatalysts along with a simulated water electrolyzer. Finally, a perspective on the existing challenges and future progress of Ru-based catalysts toward OER and HER is provided. The main aim here is to shed some light on the design and construction of emerging catalysts for energy storage and conversion technologies.
388 citations
TL;DR: In this paper, the synthesis of CoP nanoparticles encapsulated in ultrathin nitrogen-doped porous carbon (CoP@NC) through a metal-organic framework (MOF) is reported.
Abstract: Searching for non-noble-metal-based electrocatalysts with high efficiency and durability toward the hydrogen evolution reaction (HER) is vitally necessary for the upcoming clean and renewable energy systems. Here we report the synthesis of CoP nanoparticles encapsulated in ultrathin nitrogen-doped porous carbon (CoP@NC) through a metal–organic framework (MOF) route. This hybrid exhibits remarkable electrocatalytic activity toward the HER in both acidic and alkaline media, with good stability. Experiments and theoretical calculations reveal that the carbon atoms adjacent to N dopants on the shells of CoP@NC are active sites for hydrogen evolution and that CoP and N dopants synergistically optimize the binding free energy of H* on the active sites, which results in a higher electrocatalytic activity in comparison to its counterparts without nitrogen doping and/or CoP encapsulation.
379 citations
References
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TL;DR: The biggest challenge is whether or not the goals need to be met to fully utilize solar energy for the global energy demand can be met in a costeffective way on the terawatt scale.
Abstract: Energy harvested directly from sunlight offers a desirable approach toward fulfilling, with minimal environmental impact, the need for clean energy. Solar energy is a decentralized and inexhaustible natural resource, with the magnitude of the available solar power striking the earth’s surface at any one instant equal to 130 million 500 MW power plants.1 However, several important goals need to be met to fully utilize solar energy for the global energy demand. First, the means for solar energy conversion, storage, and distribution should be environmentally benign, i.e. protecting ecosystems instead of steadily weakening them. The next important goal is to provide a stable, constant energy flux. Due to the daily and seasonal variability in renewable energy sources such as sunlight, energy harvested from the sun needs to be efficiently converted into chemical fuel that can be stored, transported, and used upon demand. The biggest challenge is whether or not these goals can be met in a costeffective way on the terawatt scale.2
8,037 citations
TL;DR: This Perspective provides a snapshot of the current energy landscape and discusses several research and development opportunities and pathways that could lead to a prosperous, sustainable and secure energy future for the world.
Abstract: Access to clean, affordable and reliable energy has been a cornerstone of the world's increasing prosperity and economic growth since the beginning of the industrial revolution. Our use of energy in the twenty–first century must also be sustainable. Solar and water–based energy generation, and engineering of microbes to produce biofuels are a few examples of the alternatives. This Perspective puts these opportunities into a larger context by relating them to a number of aspects in the transportation and electricity generation sectors. It also provides a snapshot of the current energy landscape and discusses several research and development opportunities and pathways that could lead to a prosperous, sustainable and secure energy future for the world.
7,721 citations
TL;DR: Solar energy is by far the largest exploitable resource, providing more energy in 1 hour to the earth than all of the energy consumed by humans in an entire year, and if solar energy is to be a major primary energy source, it must be stored and dispatched on demand to the end user.
Abstract: Global energy consumption is projected to increase, even in the face of substantial declines in energy intensity, at least 2-fold by midcentury relative to the present because of population and economic growth. This demand could be met, in principle, from fossil energy resources, particularly coal. However, the cumulative nature of CO2 emissions in the atmosphere demands that holding atmospheric CO2 levels to even twice their preanthropogenic values by midcentury will require invention, development, and deployment of schemes for carbon-neutral energy production on a scale commensurate with, or larger than, the entire present-day energy supply from all sources combined. Among renewable energy resources, solar energy is by far the largest exploitable resource, providing more energy in 1 hour to the earth than all of the energy consumed by humans in an entire year. In view of the intermittency of insolation, if solar energy is to be a major primary energy source, it must be stored and dispatched on demand to the end user. An especially attractive approach is to store solar-converted energy in the form of chemical bonds, i.e., in a photosynthetic process at a year-round average efficiency significantly higher than current plants or algae, to reduce land-area requirements. Scientific challenges involved with this process include schemes to capture and convert solar energy and then store the energy in the form of chemical bonds, producing oxygen from water and a reduced fuel such as hydrogen, methane, methanol, or other hydrocarbon species.
7,076 citations
TL;DR: In this paper, the authors report a protocol for evaluating the activity, stability, and Faradaic efficiency of electrodeposited oxygen-evolving electrocatalysts for water oxidation.
Abstract: Objective evaluation of the activity of electrocatalysts for water oxidation is of fundamental importance for the development of promising energy conversion technologies including integrated solar water-splitting devices, water electrolyzers, and Li-air batteries. However, current methods employed to evaluate oxygen-evolving catalysts are not standardized, making it difficult to compare the activity and stability of these materials. We report a protocol for evaluating the activity, stability, and Faradaic efficiency of electrodeposited oxygen-evolving electrocatalysts. In particular, we focus on methods for determining electrochemically active surface area and measuring electrocatalytic activity and stability under conditions relevant to an integrated solar water-splitting device. Our primary figure of merit is the overpotential required to achieve a current density of 10 mA cm–2 per geometric area, approximately the current density expected for a 10% efficient solar-to-fuels conversion device. Utilizing ...
4,808 citations
TL;DR: 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 eg symmetry of surface transition metal cations in an oxide.
Abstract: 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.
3,876 citations