Covalent-organic-frameworks derived N-doped porous carbon materials as anode for superior long-life cycling lithium and sodium ion batteries
TL;DR: In this paper, N-doped porous carbon materials (NPCs) were used as anodes for lithium and sodium ion batteries (LIBs and SIBs) for the first time.
About: This article is published in Carbon.The article was published on 2017-05-01. It has received 240 citations till now. The article focuses on the topics: Dielectric spectroscopy & Lithium.
Citations
More filters
TL;DR: In this article, a review of nitrogen-doped carbon materials is presented, focusing on their preparation and applications, in the order of graphene, carbon nanotube and fibers, porous carbons and carbon blacks.
482 citations
TL;DR: A new strategy to construct CTFs (CTF‐HUSTs) via a polycondensation approach, which allows the synthesis of CTFS under mild conditions from a wide array of building blocks, and Interestingly, these C TFs display a layered structure.
Abstract: Covalent triazine frameworks (CTFs) are normally synthesized by ionothermal methods. The harsh synthetic conditions and associated limited structural diversity do not benefit for further development and practical large-scale synthesis of CTFs. Herein we report a new strategy to construct CTFs (CTF-HUSTs) via a polycondensation approach, which allows the synthesis of CTFs under mild conditions from a wide array of building blocks. Interestingly, these CTFs display a layered structure. The CTFs synthesized were also readily scaled up to gram quantities. The CTFs are potential candidates for separations, photocatalysis and for energy storage applications. In particular, CTF-HUSTs are found to be promising photocatalysts for sacrificial photocatalytic hydrogen evolution with a maximum rate of 2647 μmol h-1 g-1 under visible light. We also applied a pyrolyzed form of CTF-HUST-4 as an anode material in a sodium-ion battery achieving an excellent discharge capacity of 467 mAh g-1 .
371 citations
TL;DR: This review focuses on the systematic design of the materials from MOF and control over their inherent properties to enhance the electrochemical performances.
Abstract: Exploring new materials with high efficiency and durability is the major requirement in the field of sustainable energy conversion and storage systems Numerous techniques have been developed in last three decades to enhance the efficiency of the catalyst systems, control over the composition, structure, surface area, pore size, and moreover morphology of the particles In this respect, metal organic framework (MOF) derived catalysts are emerged as the finest materials with tunable properties and activities for the energy conversion and storage Recently, several nano- or microstructures of metal oxides, chalcogenides, phosphides, nitrides, carbides, alloys, carbon materials, or their hybrids are explored for the electrochemical energy conversion like oxygen evolution, hydrogen evolution, oxygen reduction, or battery materials Interest on the efficient energy storage system is also growing looking at the practical applications Though, several reviews are available on the synthesis and application of MOF and MOF derived materials, their applications for the electrochemical energy conversion and storage is totally a new field of research and developed recently This review focuses on the systematic design of the materials from MOF and control over their inherent properties to enhance the electrochemical performances
332 citations
TL;DR: It is demonstrated that the enhancement of ORR performance is associated with favorably well‐designed porous structure, large surface area, and high‐tensity active sites.
Abstract: The oxygen reduction reaction (ORR) is the core reaction of numerous sustainable energy-conversion technologies such as fuel cells and metal-air batteries. It is crucial to develop a cost-effective, highly active, and durable electrocatalysts for ORR to overcome the sluggish kinetics of four electrons pathway. In recent years, the carbon-based electrocatalysts derived from metal-organic frameworks (MOFs) have attracted tremendous attention and have been shown to exhibit superior catalytic activity and excellent intrinsic properties such as large surface area, large pore volume, uniform pore distribution, and tunable chemical structure. Here in this review, the development of MOF-derived heteroatom-doped carbon-based electrocatalysts, including non-metal (such as N, S, B, and P) and metal (such as Fe and Co) doped carbon materials, is summarized. It furthermore, it is demonstrated that the enhancement of ORR performance is associated with favorably well-designed porous structure, large surface area, and high-tensity active sites. Finally, the future perspectives of carbon-based electrocatalysts for ORR are provided with an emphasis on the development of a clear mechanism of MOF-derived non-metal-doped electrocatalysts and certain metal-doped electrocatalysts.
282 citations
References
More filters
TL;DR: Li-ion battery technology has become very important in recent years as these batteries show great promise as power sources that can lead us to the electric vehicle (EV) revolution as mentioned in this paper.
Abstract: Li-ion battery technology has become very important in recent years as these batteries show great promise as power sources that can lead us to the electric vehicle (EV) revolution. The development of new materials for Li-ion batteries is the focus of research in prominent groups in the field of materials science throughout the world. Li-ion batteries can be considered to be the most impressive success story of modern electrochemistry in the last two decades. They power most of today's portable devices, and seem to overcome the psychological barriers against the use of such high energy density devices on a larger scale for more demanding applications, such as EV. Since this field is advancing rapidly and attracting an increasing number of researchers, it is important to provide current and timely updates of this constantly changing technology. In this review, we describe the key aspects of Li-ion batteries: the basic science behind their operation, the most relevant components, anodes, cathodes, electrolyte solutions, as well as important future directions for R&D of advanced Li-ion batteries for demanding use, such as EV and load-leveling applications.
5,531 citations
4,311 citations
TL;DR: This work quantifies the kinetics of charge storage in T-Nb2O5: currents that vary inversely with time, charge-storage capacity that is mostly independent of rate, and redox peaks that exhibit small voltage offsets even at high rates.
Abstract: Pseudocapacitance is commonly associated with surface or near-surface reversible redox reactions, as observed with RuO2·xH2O in an acidic electrolyte. However, we recently demonstrated that a pseudocapacitive mechanism occurs when lithium ions are inserted into mesoporous and nanocrystal films of orthorhombic Nb2O5 (T-Nb2O5; refs 1, 2). Here, we quantify the kinetics of charge storage in T-Nb2O5: currents that vary inversely with time, charge-storage capacity that is mostly independent of rate, and redox peaks that exhibit small voltage offsets even at high rates. We also define the structural characteristics necessary for this process, termed intercalation pseudocapacitance, which are a crystalline network that offers two-dimensional transport pathways and little structural change on intercalation. The principal benefit realized from intercalation pseudocapacitance is that high levels of charge storage are achieved within short periods of time because there are no limitations from solid-state diffusion. Thick electrodes (up to 40 μm thick) prepared with T-Nb2O5 offer the promise of exploiting intercalation pseudocapacitance to obtain high-rate charge-storage devices.
3,725 citations
TL;DR: In this paper, the capacitive effects of nanostructured materials for electrochemical energy storage have been investigated over a dimensional regime where both capacitive and lithium intercalation processes contribute to the total stored charge.
Abstract: The advantages in using nanostructured materials for electrochemical energy storage have largely focused on the benefits associated with short path lengths. In this paper, we consider another contribution, that of the capacitive effects, which become increasingly important at nanoscale dimensions. Nanocrystalline TiO2 (anatase) was studied over a dimensional regime where both capacitive and lithium intercalation processes contribute to the total stored charge. An analysis of the voltammetric sweep data was used to distinguish between the amount of charge stored by these two processes. At particle sizes below 10 nm, capacitive contributions became increasingly important, leading to greater amounts of total stored charge (gravimetrically normalized) with decreasing TiO2 particle size. The area normalized capacitance was determined to be well above 100 μF/cm2, confirming that the capacitive contribution was pseudocapacitive in nature. Moreover, reducing the particle size to the nanoscale regime led to faster...
3,572 citations
TL;DR: Findings place COFs among the most porous and the best adsorbents for hydrogen, methane, and carbon dioxide.
Abstract: Dihydrogen, methane, and carbon dioxide isotherm measurements were performed at 1−85 bar and 77−298 K on the evacuated forms of seven porous covalent organic frameworks (COFs). The uptake behavior and capacity of the COFs is best described by classifying them into three groups based on their structural dimensions and corresponding pore sizes. Group 1 consists of 2D structures with 1D small pores (9 A for each of COF-1 and COF-6), group 2 includes 2D structures with large 1D pores (27, 16, and 32 A for COF-5, COF-8, and COF-10, respectively), and group 3 is comprised of 3D structures with 3D medium-sized pores (12 A for each of COF-102 and COF-103). Group 3 COFs outperform group 1 and 2 COFs, and rival the best metal−organic frameworks and other porous materials in their uptake capacities. This is exemplified by the excess gas uptake of COF-102 at 35 bar (72 mg g−1 at 77 K for hydrogen, 187 mg g−1 at 298 K for methane, and 1180 mg g−1 at 298 K for carbon dioxide), which is similar to the performance of COF...
2,102 citations