Search citation statements
Paper Sections
Citation Types
Year Published
Publication Types
Relationship
Authors
Journals
Electrochemically active hollow nanostructured materials hold great promise in diverse energy conversion and storage applications, however, intricate synthesis steps and poor control over compositions and morphologies have limited the realization of delicate hollow structures with advanced functional properties. In this study, we demonstrate a one-step wet-chemical strategy for co-engineering the hollow nanostructure and anion intercalation of nickel cobalt layered double hydroxide (NiCo-LDH) to attain highly electrochemical active energy conversion and storage functionalities. Self-templated pseudomorphic transformation of cobalt acetate hydroxide solid nanoprisms using nickel nitrate leads to the construction of well-defined NiCo-LDH hollow nanoprisms (HNPs) with multi-anion intercalation. The unique hierarchical nanosheet-assembled hollow structure and efficiently expanded interlayer spacing offer an increased surface area and exposure of active sites, reduced mass and charge transfer resistance, and enhanced stability of the materials. This leads to a significant improvement in the pseudocapacitive and electrocatalytic properties of NiCo-LDH HNP with respect to specific capacitance, rate and cycling performance, and OER overpotential, outperforming most of the recently reported NiCo-based materials. This work establishes the potential of manipulating sacrificial template transformation for the design and fabrication of novel classes of functional materials with well-defined nanostructures for electrochemical applications and beyond.
Electrochemically active hollow nanostructured materials hold great promise in diverse energy conversion and storage applications, however, intricate synthesis steps and poor control over compositions and morphologies have limited the realization of delicate hollow structures with advanced functional properties. In this study, we demonstrate a one-step wet-chemical strategy for co-engineering the hollow nanostructure and anion intercalation of nickel cobalt layered double hydroxide (NiCo-LDH) to attain highly electrochemical active energy conversion and storage functionalities. Self-templated pseudomorphic transformation of cobalt acetate hydroxide solid nanoprisms using nickel nitrate leads to the construction of well-defined NiCo-LDH hollow nanoprisms (HNPs) with multi-anion intercalation. The unique hierarchical nanosheet-assembled hollow structure and efficiently expanded interlayer spacing offer an increased surface area and exposure of active sites, reduced mass and charge transfer resistance, and enhanced stability of the materials. This leads to a significant improvement in the pseudocapacitive and electrocatalytic properties of NiCo-LDH HNP with respect to specific capacitance, rate and cycling performance, and OER overpotential, outperforming most of the recently reported NiCo-based materials. This work establishes the potential of manipulating sacrificial template transformation for the design and fabrication of novel classes of functional materials with well-defined nanostructures for electrochemical applications and beyond.
2D materials have demonstrated good chemical, optical, electrical, and magnetic characteristics, and offer great potential in numerous applications. Corresponding synthesis technologies of 2D materials that are highquality, high-yield, low-cost, and time-saving are highly desired. Salt-assisted methods are emerging technologies that can meet these requirements for the fabrication of 2D materials. Herein, the recent process for the salt-assisted synthesis of 2D materials and their typical applications are summarized. First, the properties of salt crystals and molten salts are briefly introduced, and then some examples of 2D materials synthesis with the assistance of salt as well as their representative applications are presented. The underlying mechanisms of salts with different states on the formation of 2D morphology are discussed to aid in the rational design of synthetic route of 2D materials. At last, the challenges and future perspectives for salt-assisted methods are briefly described. This review provides guidance for the controllable synthesis of 2D materials based on the salt-assisted approaches.The ORCID identification number(s) for the author(s) of this article can be found under https://doi.org/10.1002/adfm.201908486.MoO 3 , and LaNb 2 O 7 ), [14][15][16] layered double hydroxides (LDHs, e.g., Mg 6 Al 2 (OH) 16 CO 3 •4H 2 O), [17] hexagonal-boron nitride (h-BN), [2,18] transition metal halides (such as MoCl 2 and CrCl 3 ), [19] black phosphorus, [20] graphitic carbon nitride (g-C 3 N 4 ), [5] MXene (such as Ti 2 C and Ti 3 CN), [21][22][23][24][25] and clays (for instance, [(Mg 3 )(Si 2 O 5 ) 2 (OH) 2 ] and [(Al 2 )(Si 3 Al) O 10 (OH) 2 ]K). [19] Notably, many nonlayered structure species can also form 2D morphology with specific synthetic methods, largely expanding the 2D family (such as hexagonal-MoO 3 (h-MoO 3 ), hexagonal-WO 3 (h-WO 3 ), [15] transition metal nitrides (TMNs), [26,27] and transition metal phosphides (TMPs)). [28] To exploit the applications of 2D materials, the development of a synthetic method should be prioritized. Currently, synthesis processes of 2D materials could be divided into two categories, naming the top-down and bottom-up approaches. [29][30][31] Generally, exfoliation is the most common top-down method to produce monolayer or few-layer 2D materials. [19,32] Graphene was first prepared by mechanical exfoliation of highly oriented pyrolytic graphite with sellotape in 2004. [33] The exfoliation can weaken the interlayer Van der Waals force for bulk materials with layered crystal structures while maintain the covalent bonding in plane to produce monolayer or few-layer nanosheets. Although the productivity based on this method is limited due to the low efficiency, the exfoliation approach provides a new synthesis methodology for 2D materials. A series of studies on liquid exfoliation have been conducted by Coleman and co-workers. [19,34,35] By sonicating the bulk material in an appropriate solvent with similar interface energy, 2D material ink can be prepared. After the liq...
Layered double hydroxides (LDHs), as classic 2D materials, have received worldwide attention in electrochemical energy storage devices due to its superior ion insertion rate and ultrahigh specific capacitance. However, the poor conductivity, severe aggregation limited capacitance, and unsatisfied internal stability have become the main factors hinder its further development as the electrode of supercapacitor. In recent years, various strategies on the modification of the LDHs’ structure, composition, properties, and fabrication have been demonstrated to effectively improve their electrochemical performance, and fruitful achievements have been made. However, there is a lack of systematic summary on the functional mechanisms and effects of various modification strategies. Herein, this review gives a comprehensive introduction of the modification strategies based on LDHs for superior supercapacitor, including active metal ions adjustment, intercalated ions adjustment, morphology optimization, conductivity enhancement and internal stability enhancement. Particularly, an in‐depth and fundamental understanding on the effects and mechanisms of modification on LDHs’ electrochemical properties and performance. Furthermore, the general performance metrics of above strategies, the potential directions and perspectives for further research are proposed.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.
hi@scite.ai
10624 S. Eastern Ave., Ste. A-614
Henderson, NV 89052, USA
Copyright © 2024 scite LLC. All rights reserved.
Made with 💙 for researchers
Part of the Research Solutions Family.