Superior performance of ordered macroporous TiNb2O7 anodes for lithium ion batteries: Understanding from the structural and pseudocapacitive insights on achieving high rate capability
TL;DR: In this paper, a three-dimensional ordered macroporous (3DOM) TiNb2O7 composed of interconnected single-crystalline nanoparticles was prepared using polystyrene (PS) colloidal crystals as a hard template.
About: This article is published in Nano Energy.The article was published on 2017-04-01. It has received 318 citations till now. The article focuses on the topics: Lithium & Anode.
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TL;DR: In this paper, bimetallic sulfide (Co9S8/ZnS) nanocrystals embedded in hollow nitrogen-doped carbon nanosheets are demonstrated with a high sodium diffusion coefficient, pseudocapacitive effect, and excellent reversibility.
Abstract: Lithium-ion batteries (LIBs) have permeated energy storage market from portable electronics to electric vehicles in view of their high energy density and long cycle life.[1] Nevertheless, it is still expensive to scale up due to the limited Li sources.[2] In contrast, sodium-ion batteries (SIBs), with similar energy Sodium-ion batteries (SIBs) are promising next-generation alternatives due to the low cost and abundance of sodium sources. Yet developmental electrodes in SIBs such as transition metal sulfides have huge volume expansion, sluggish Na+ diffusion kinetics, and poor electrical conductivity. Here bimetallic sulfide (Co9S8/ZnS) nanocrystals embedded in hollow nitrogen-doped carbon nanosheets are demonstrated with a high sodium diffusion coefficient, pseudocapacitive effect, and excellent reversibility. Such a unique composite structure is designed and synthesized via a facile sulfidation of the CoZn-MOFs followed by calcination and is highly dependant on the reaction time and temperature. The optimized Co1Zn1-S(600) electrode exhibits excellent sodium storage performance, including a high capacity of 542 mA h g−1 at 0.1 A g−1, good rate capability at 10 A g−1, and excellent cyclic stability up to 500 cycles for half-cell. It also shows potential in full-cell configuration. Such capabilities will accelerate the adoption of sodium-ion batteries for electrical energy applications.
397 citations
TL;DR: In this article, nano-TiNb2O7 and its carbon nanotube (CNT) nanocomposites were prepared by direct hydrolysis of TiNb10O29-type crystal structure with O2− vacancies and lower-valence cations, leading to improved Li+-ion diffusion coefficient and increased electronic conductivity.
252 citations
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TL;DR: 3D porous MXene foam with developed porous structure is established via a simple sulfur-template method, which is freestanding, flexible, and highly conductive, and can be directly used as the electrode in lithium-ion batteries.
Abstract: 2D transition-metal carbides and nitrides, named MXenes, are promising materials for energy storage, but suffer from aggregation and restacking of the 2D nanosheets, which limits their electrochemical performance. In order to overcome this problem and realize the full potential of MXene nanosheets, a 3D MXene foam with developed porous structure is established via a simple sulfur-template method, which is freestanding, flexible, and highly conductive, and can be directly used as the electrode in lithium-ion batteries. The 3D porous architecture of the MXene foam offers massive active sites to enhance the lithium storage capacity. Moreover, its foam structure facilitates electrolyte infiltration for fast Li+ transfer. As a result, this flexible 3D porous MXene foam exhibits significantly enhanced capacity of 455.5 mAh g-1 at 50 mA g-1 , excellent rate performance (101 mAh g-1 at 18 A g-1 ), and superior ultralong-term cycle stability (220 mAh g-1 at 1 A g-1 after 3500 cycles). This work not only demonstrates the great superiority of the 3D porous MXene foam but also proposes the sulfur-template method for controllable constructing of the 3D foam from 2D nanosheets at a relatively low temperature.
196 citations
TL;DR: This work successfully achieves the growth of single-crystalline metal-organic frameworks in three-dimensional (3D) ordered macroporous template voids by saturated solution-based double-solvent-assisted strategy with precise control over the nucleation process.
Abstract: Constructing ordered hierarchical porous structures while maintaining their overall crystalline order is highly desirable but remains an arduous challenge. Herein, we successfully achieve the growt...
194 citations
TL;DR: Wang et al. as mentioned in this paper summarized recent advancements in 3D ordered porous (3DOP) electrode materials and their unusual electrochemical properties endowed by their intrinsic and geometric structures.
Abstract: The past decade has witnessed substantial advances in the synthesis of various electrode materials with three-dimensional (3D) ordered macroporous or mesoporous structures (the so-called “inverse opals”) for applications in electrochemical energy storage devices. This review summarizes recent advancements in 3D ordered porous (3DOP) electrode materials and their unusual electrochemical properties endowed by their intrinsic and geometric structures. The 3DOP electrode materials discussed here mainly include carbon materials, transition metal oxides (such as TiO2, SnO2, Co3O4, NiO, Fe2O3, V2O5, Cu2O, MnO2, and GeO2), transition metal dichalcogenides (such as MoS2 and WS2), elementary substances (such as Si, Ge, and Au), intercalation compounds (such as Li4Ti5O12, LiCoO2, LiMn2O4, LiFePO4), and conductive polymers (polypyrrole and polyaniline). Representative applications of these materials in Li ion batteries, aqueous rechargeable lithium batteries, Li-S batteries, Li-O2 batteries, and supercapacitors are presented. Particular focus is placed on how ordered porous structures influence the electrochemical performance of electrode materials. Additionally, we discuss research opportunities as well as the current challenges to facilitate further contributions to this emerging research frontier. Three-dimensional ordered porous materials can improve the electrochemical storage of energy. Jing Wang and Yuping Wu from Nanjing Tech University, China and co-workers review the development of these materials for use as electrodes in devices such as batteries and supercapacitors. Three-dimensional ordered porous materials are created by inserting the desired raw material into a template made from an array of spheres. The spheres are removed to leave a hole-filled material ideal for storage. The authors describe how this ordered porous structure influences the electrochemical performance of electrodes made from elementary materials, transition metal oxides, conductive polymers, or carbon-based materials, among others. The challenges for the future are discussed, including developing a better fundamental understanding of charge transport, improving efficiency, scaling-up production, and lowering production costs. The past decade has witnessed substantial advances in the synthesis of various electrode materials with three-dimensional (3D) ordered macroporous or mesoporous structures (the so-called “inverse opals”) for applications in electrochemical energy storage devices. Yuping Wu from Nanjing Tech University anchored recent advancements in 3D ordered porous (3DOP) electrode materials and their unusual electrochemical properties bound by their intrinsic and geometric structures. The team introduces various 3DOP electrode materials and their representative applications as electrode materials. Additionally, the team also provides research opportunities as well as the challenges to facilitate further contributions to this emerging research frontier.
194 citations
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TL;DR: A brief historical review of the development of lithium-based rechargeable batteries is presented, ongoing research strategies are highlighted, and the challenges that remain regarding the synthesis, characterization, electrochemical performance and safety of these systems are discussed.
Abstract: Technological improvements in rechargeable solid-state batteries are being driven by an ever-increasing demand for portable electronic devices. Lithium-ion batteries are the systems of choice, offering high energy density, flexible and lightweight design, and longer lifespan than comparable battery technologies. We present a brief historical review of the development of lithium-based rechargeable batteries, highlight ongoing research strategies, and discuss the challenges that remain regarding the synthesis, characterization, electrochemical performance and safety of these systems.
17,496 citations
TL;DR: Electrochemical measurements can distinguish between different types of energy storage materials and their underlying mechanisms, used to recover power in cars and electric mass transit vehicles that would otherwise lose braking energy as heat.
Abstract: Electrochemical measurements can distinguish between different types of energy storage materials and their underlying mechanisms.
4,394 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: The latest progress in supercapacitors in charge storage mechanisms, electrode materials, electrolyte materials, systems, characterization methods, and applications are reviewed and the newly developed charge storage mechanism for intercalative pseudocapacitive behaviour is clarified for comparison.
Abstract: Electrochemical capacitors (i.e. supercapacitors) include electrochemical double-layer capacitors that depend on the charge storage of ion adsorption and pseudo-capacitors that are based on charge storage involving fast surface redox reactions. The energy storage capacities of supercapacitors are several orders of magnitude higher than those of conventional dielectric capacitors, but are much lower than those of secondary batteries. They typically have high power density, long cyclic stability and high safety, and thus can be considered as an alternative or complement to rechargeable batteries in applications that require high power delivery or fast energy harvesting. This article reviews the latest progress in supercapacitors in charge storage mechanisms, electrode materials, electrolyte materials, systems, characterization methods, and applications. In particular, the newly developed charge storage mechanism for intercalative pseudocapacitive behaviour, which bridges the gap between battery behaviour and conventional pseudocapacitive behaviour, is also clarified for comparison. Finally, the prospects and challenges associated with supercapacitors in practical applications are also discussed.
2,698 citations