CoP2/Fe-CoP2 yolk-shell nanoboxes as efficient electrocatalysts for the oxygen evolution reaction.
TL;DR: In this article, the authors synthesized CoP2/Fe-CoP2 yolk-shell nanoboxes (YSBs) as efficient electrocatalysts for the oxygen evolution reaction (OER).
Abstract: The development of an efficient electrocatalyst is an important requirement for water splitting systems to produce clean and sustainable hydrogen fuel Herein, we synthesized CoP2/Fe-CoP2 yolk–shell nanoboxes (YSBs) as efficient electrocatalysts for the oxygen evolution reaction (OER) Initially, zeolitic imidazolate framework-67/CoFe-Prussian blue analogue (ZIF-67/CoFe-PBA) YSBs were prepared by the reaction of ZIF-67 and [Fe(CN)6]3− ions in the presence of a small amount of water as an etching agent The size of the CoP2 yolk depends on the amount of water The heteronanostructure composed of the CoP2 yolk and the FexCo1−xP2 shell with a cubic shape was obtained by phosphidation of ZIF-67/CoFe-PBA YSBs Benefiting from the unique structure and chemical composition, the CoP2/Fe-CoP2 YSB electrocatalyst has a large specific surface area of 114 m2 g−1 and shows superior electrocatalytic performances for the OER such as a low overpotential of 266 mV, a small Tafel slope value of 681 mV dec−1, and excellent cyclic stability
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TL;DR: In this article, a review summarizes the up-to-date advances of P-rich metal phosphides (MPs) in energy storage and conversion from typical structures, main synthetic methods and diversified advanced applications.
32 citations
TL;DR: In this paper, the morphological engineering of the original ZIF-67 and its derivatives (core-shell, hollow, and array structures) through doping (cation doping, anion doping, and co-doping), derivative composition engineering (metal oxide, phosphide, sulfide, selenide, and telluride), and corresponding single-atom catalysis.
Abstract: As a new type of crystalline porous material, the imidazole zeolite framework (ZIF) has attracted widespread attention due to its ultra-high surface area, large pore volume, and unique advantage of easy functionalization. Developing different methods to control the shape and composition of ZIF is very important for its practical application as catalyst. In recent years, nano-ZIF has been considered an electrode material with excellent oxygen evolution reaction (OER) performance, which provides a new way to research electrolyzed water. This review focuses on the morphological engineering of the original ZIF-67 and its derivatives (core-shell, hollow, and array structures) through doping (cation doping, anion doping, and co-doping), derivative composition engineering (metal oxide, phosphide, sulfide, selenide, and telluride), and the corresponding single-atom catalysis. Besides, combined with DFT calculations, it emphasizes the in-depth understanding of actual active sites and provides insights into the internal mechanism of enhancing the OER and proposes the challenges and prospects of ZIF-67 based electrocatalysts. We summarize the application of ZIF-67 and its derivatives in the OER for the first time, which has significantly guided research in this field.
31 citations
TL;DR: In this paper, a yolk-shell structure of Fe2 O3 nanotube@hollow Co9 S8 nanocage@C is rationally prepared, and a prearranged sequence is followed by coating of zeolitic imidazolate framework (ZIF-67) layer, chemical etching of ZIF -67 by thioacetamide, and eventual annealing treatment.
Abstract: The development of high-efficiency, robust, and available electrode materials for oxygen evolution reaction (OER) and lithium-ion batteries (LIBs) is critical for clean and sustainable energy system but remains challenging. Herein, a unique yolk-shell structure of Fe2 O3 nanotube@hollow Co9 S8 nanocage@C is rationally prepared. In a prearranged sequence, the fabrication of Fe2 O3 nanotubes is followed by coating of zeolitic imidazolate framework (ZIF-67) layer, chemical etching of ZIF-67 by thioacetamide, and eventual annealing treatment. Benefiting from the hollow structures of Fe2 O3 nanotubes and Co9 S8 nanocages, the conductivity of carbon coating and the synergy effects between different components, the titled sample possesses abundant accessible active sites, favorable electron transfer rate, and exceptional reaction kinetics in the electrocatalysis. As a result, excellent electrocatalytic activity for alkaline OER is achieved, which delivers a low overpotential of 205 mV at the current density of 10 mA cm-2 along with the Tafel slope of 55 mV dec-1 . Moreover, this material exhibits excellent high-rate capability and excellent cycle life when employed as anode material of LIBs. This work provides a novel approach for the design and the construction of multifunctional electrode materials for energy conversion and storage.
18 citations
TL;DR: In this paper, the authors summarized current advances in the synthesis of low-cost earth-abundant electrocatalysts for overall water splitting, with a particular focus on how to be linked with photoelectrocatalytic water splitting devices.
Abstract: Of all the available resources given to mankind, the sunlight is perhaps the most abundant renewable energy resource, providing more than enough energy on earth to satisfy all the needs of humanity for several hundred years. Therefore, it is transient and sporadic that poses issues with how the energy can be harvested and processed when the sun does not shine. Scientists assume that electro/photoelectrochemical devices used for water splitting into hydrogen and oxygen may have one solution to solve this hindrance. Water electrolysis-generated hydrogen is an optimal energy carrier to store these forms of energy on scalable levels because the energy density is high, and no air pollution or toxic gas is released into the environment after combustion. However, in order to adopt these devices for readily use, they have to be low-cost for manufacturing and operation. It is thus crucial to develop electrocatalysts for water splitting based on low-cost and land-rich elements. In this review, I will summarize current advances in the synthesis of low-cost earth-abundant electrocatalysts for overall water splitting, with a particular focus on how to be linked with photoelectrocatalytic water splitting devices. The major obstacles that persist in designing these devices. The potential future developments in the production of efficient electrocatalysts for water electrolysis are also described.
17 citations
TL;DR: In this article , a review focusing on the topic of "etching MOFs" is presented, which can be broadly classified into four categories including pore engineering, surface/facet modification, defect modification and self-templated conversion to layered metal hydroxides (LDHs).
17 citations
References
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TL;DR: This review acquaints some materials for performing OER activity, in which the metal oxide materials build the basis of OER mechanism while non-oxide materials exhibit greatly promising performance toward overall water-splitting.
Abstract: There is still an ongoing effort to search for sustainable, clean and highly efficient energy generation to satisfy the energy needs of modern society. Among various advanced technologies, electrocatalysis for the oxygen evolution reaction (OER) plays a key role and numerous new electrocatalysts have been developed to improve the efficiency of gas evolution. Along the way, enormous effort has been devoted to finding high-performance electrocatalysts, which has also stimulated the invention of new techniques to investigate the properties of materials or the fundamental mechanism of the OER. This accumulated knowledge not only establishes the foundation of the mechanism of the OER, but also points out the important criteria for a good electrocatalyst based on a variety of studies. Even though it may be difficult to include all cases, the aim of this review is to inspect the current progress and offer a comprehensive insight toward the OER. This review begins with examining the theoretical principles of electrode kinetics and some measurement criteria for achieving a fair evaluation among the catalysts. The second part of this review acquaints some materials for performing OER activity, in which the metal oxide materials build the basis of OER mechanism while non-oxide materials exhibit greatly promising performance toward overall water-splitting. Attention of this review is also paid to in situ approaches to electrocatalytic behavior during OER, and this information is crucial and can provide efficient strategies to design perfect electrocatalysts for OER. Finally, the OER mechanism from the perspective of both recent experimental and theoretical investigations is discussed, as well as probable strategies for improving OER performance with regards to future developments.
3,976 citations
TL;DR: This study shows that these r-RuO2 and r-IrO2 NPs can serve as a benchmark in the development of active OER catalysts for electrolyzers, metal-air batteries, and photoelectrochemical water splitting applications.
Abstract: The activities of the oxygen evolution reaction (OER) on iridium-oxide- and ruthenium-oxide-based catalysts are among the highest known to date. However, the OER activities of thermodynamically stable rutile iridium oxide (r-IrO2) and rutile iridium oxide (r-RuO2), normalized to catalyst mass or true surface area are not well-defined. Here we report a synthesis of r-IrO2 and r-RuO2 nanoparticles (NPs) of ∼6 nm, and examine their OER activities in acid and alkaline solutions. Both r-IrO2 and r-RuO2 NPs were highly active for OER, with r-RuO2 exhibiting up to 10 A/goxide at 1.48 V versus reversible hydrogen electrode. When comparing the two, r-RuO2 NPs were found to have slightly higher intrinsic and mass OER activities than r-IrO2 in both acid and basic solutions. Interestingly, these oxide NPs showed higher stability under OER conditions than commercial Ru/C and Ir/C catalysts. Our study shows that these r-RuO2 and r-IrO2 NPs can serve as a benchmark in the development of active OER catalysts for electrol...
2,762 citations
TL;DR: In this article, the intrinsic catalytic activity and durability of carbon supported Ru, Ir, and Pt nanoparticles and corresponding bulk materials for the electrocatalytic oxygen evolution reaction (OER) were examined by surface-sensitive cyclic voltammetry.
Abstract: A comparative investigation was performed to examine the intrinsic catalytic activity and durability of carbon supported Ru, Ir, and Pt nanoparticles and corresponding bulk materials for the electrocatalytic oxygen evolution reaction (OER). The electrochemical surface characteristics of nanoparticles and bulk materials were studied by surface-sensitive cyclic voltammetry. Although basically similar voltammetric features were observed for nanoparticles and bulk materials of each metal, some differences were uncovered highlighting the changes in oxidation chemistry. On the basis of the electrochemical results, we demonstrated that Ru nanoparticles show lower passivation potentials compared to bulk Ru material. Ir nanoparticles completely lost their voltammetric metallic features during the voltage cycling, in contrast to the corresponding bulk material. Finally, Pt nanoparticles show an increased oxophilic nature compared to bulk Pt. With regard to the OER performance, the most pronounced effects of nanosca...
1,885 citations
TL;DR: In this article, the hydrogen (H2) and oxygen (O2) fuel cell is the one with zero carbon emission and water as the only byproduct, which is essential to ensure higher life cycle and less decay in cell efficiency.
Abstract: Increasing demand for finding eco-friendly and everlasting energy sources is now totally depending on fuel cell technology. Though it is an eco-friendly way of producing energy for the urgent requirements, it needs to be improved to make it cheaper and more eco-friendly. Although there are several types of fuel cells, the hydrogen (H2) and oxygen (O2) fuel cell is the one with zero carbon emission and water as the only byproduct. However, supplying fuels in the purest form (at least the H2) is essential to ensure higher life cycles and less decay in cell efficiency. The current large-scale H2 production is largely dependent on steam reforming of fossil fuels, which generates CO2 along with H2 and the source of which is going to be depleted. As an alternate, electrolysis of water has been given greater attention than the steam reforming. The reasons are as follows: the very high purity of the H2 produced, the abundant source, no need for high-temperature, high-pressure reactors, and so on. In earlier days,...
1,757 citations
TL;DR: The unique properties and niche applications of the hollow structures in diverse fields, including micro-/nanocontainers and reactors, optical properties and applications, magnetic properties, energy storage, catalysis, biomedical applications, environmental remediation, and sensors are discussed.
Abstract: In this Review, we aim to provide an updated summary of the research related to hollow micro- and nanostructures, covering both their synthesis and their applications. After a brief introduction to the definition and classification of the hollow micro-/nanostructures, we discuss various synthetic strategies that can be grouped into three major categories, including hard templating, soft templating, and self-templating synthesis. For both hard and soft templating strategies, we focus on how different types of templates are generated and then used for creating hollow structures. At the end of each section, the structural and morphological control over the product is discussed. For the self-templating strategy, we survey a number of unconventional synthetic methods, such as surface-protected etching, Ostwald ripening, the Kirkendall effect, and galvanic replacement. We then discuss the unique properties and niche applications of the hollow structures in diverse fields, including micro-/nanocontainers and rea...
1,135 citations