Scott Evers

Bio: Scott Evers is an academic researcher from University of Waterloo. The author has contributed to research in topics: Sulfur & Lithium–sulfur battery. The author has an hindex of 7, co-authored 7 publications receiving 3384 citations.

New approaches for high energy density lithium-sulfur battery cathodes.

Abstract: The goal of replacing combustion engines or reducing their use presents a daunting problem for society. Current lithium-ion technologies provide a stepping stone for this dramatic but inevitable change. However, the theoretical gravimetric capacity (∼300 mA h g–1) is too low to overcome the problems of limited range in electric vehicles, and their cost is too high to sustain the commercial viability of electrified transportation. Sulfur is the one of the most promising next generation cathode materials. Since the 1960s, researchers have studied sulfur as a cathode, but only recently have great strides been made in preparing viable composites that can be used commercially. Sulfur batteries implement inexpensive, earth-abundant elements at the cathode while offering up to a five-fold increase in energy density compared with present Li-ion batteries.Over the past few years, researchers have come closer to solving the challenges associated with the sulfur cathode. Using carbon or conducting polymers, research...

Stabilizing lithium-sulphur cathodes using polysulphide reservoirs

Abstract: The possibility of achieving high-energy, long-life storage batteries has tremendous scientific and technological significance. An example is the Li-S cell, which can offer a 3-5-fold increase in energy density compared with conventional Li-ion cells, at lower cost. Despite significant advances, there are challenges to its wide-scale implementation, which include dissolution of intermediate polysulphide reaction species into the electrolyte. Here we report a new concept to mitigate the problem, which relies on the design principles of drug delivery. Our strategy employs absorption of the intermediate polysulphides by a porous silica embedded within the carbon-sulphur composite that not only absorbs the polysulphides by means of weak binding, but also permits reversible desorption and release. It functions as an internal polysulphide reservoir during the reversible electrochemical process to give rise to long-term stabilization and improved coulombic efficiency. The reservoir mechanism is general and applicable to Li/S cathodes of any nature.

Understanding the Nature of Absorption/Adsorption in Nanoporous Polysulfide Sorbents for the Li–S Battery

Abstract: The possibility of achieving high-energy, long-life storage batteries has tremendous scientific and technological significance. A prime example is the Li–S cell, which can offer a 3–5-fold increase in energy density compared with conventional Li-ion cells, at lower cost. Despite significant recent advances, there are challenges to its wide-scale implementation. Upon sulfur reduction, intermediate soluble lithium polysulfides readily diffuse into the electrolyte, causing capacity fading and poor Coulombic efficiency in the cell. Herein, we increase the capacity retention and cycle life of the Li–S cell through the use of nanocrystalline and mesoporous titania additives as polysulfide reservoirs and examine the role of surface adsorption vs pore absorption. We find that the soluble lithium polysulfides are preferentially absorbed within the pores of the nanoporous titania at intermediate discharge/charge. This provides the major factor in stabilizing capacity although surface binding (adsorption) also plays...

Sulfur Speciation in Li–S Batteries Determined by Operando X-ray Absorption Spectroscopy

Abstract: Among the most challenging issues in electrochemical energy storage is developing insightful in situ probes of redox processes for a working cell. This is particularly true for cells that operate on the basis of chemical transformations such as Li–S and Li–O2, where the factors that govern capacity and cycling stability are difficult to access owing to the amorphous nature of the intermediate species. Here, we investigate cathodes for the Li–S cell comprised of sulfur-imbibed robust spherical carbon shells with tailored porosity that exhibit excellent cycling stability. Their highly regular nanoscale dimensions and thin carbon shells allow highly uniform electrochemical response and further enable direct monitoring of sulfur speciation within the cell over the entire redox range by operando X-ray absorption spectroscopy on the S K-edge. The results reveal the first detailed evidence of the mechanisms of sulfur redox chemistry on cycling, showing how sulfur fraction (under-utilization) and sulfide precipit...

Tailoring Porosity in Carbon Nanospheres for Lithium–Sulfur Battery Cathodes

Abstract: Porous hollow carbon spheres with different tailored pore structures have been designed as conducting frameworks for lithium-sulfur battery cathode materials that exhibit stable cycling capacity. By deliberately creating shell porosity and utilizing the interior void volume of the carbon spheres, sufficient space for sulfur storage as well as electrolyte pathways is guaranteed. The effect of different approaches to develop shell porosity is examined and compared in this study. The most highly optimized sulfur-porous carbon nanosphere composite, created using pore-formers to tailor shell porosity, exhibits excellent cycling performance and rate capability. Sulfur is primarily confined in 4-5 nm mesopores in the carbon shell and inner lining of the shells, which is beneficial for enhancing charge transfer and accommodating volume expansion of sulfur during redox cycling. Little capacity degradation (∼0.1% /cycle) is observed over 100 cycles for the optimized material.

Li-O2 and Li-S batteries with high energy storage.

Abstract: Li-ion batteries have transformed portable electronics and will play a key role in the electrification of transport. However, the highest energy storage possible for Li-ion batteries is insufficient for the long-term needs of society, for example, extended-range electric vehicles. To go beyond the horizon of Li-ion batteries is a formidable challenge; there are few options. Here we consider two: Li-air (O(2)) and Li-S. The energy that can be stored in Li-air (based on aqueous or non-aqueous electrolytes) and Li-S cells is compared with Li-ion; the operation of the cells is discussed, as are the significant hurdles that will have to be overcome if such batteries are to succeed. Fundamental scientific advances in understanding the reactions occurring in the cells as well as new materials are key to overcoming these obstacles. The potential benefits of Li-air and Li-S justify the continued research effort that will be needed.

Promise and reality of post-lithium-ion batteries with high energy densities

Abstract: Energy density is the main property of rechargeable batteries that has driven the entire technology forward in past decades. Lithium-ion batteries (LIBs) now surpass other, previously competitive battery types (for example, lead–acid and nickel metal hydride) but still require extensive further improvement to, in particular, extend the operation hours of mobile IT devices and the driving mileages of all-electric vehicles. In this Review, we present a critical overview of a wide range of post-LIB materials and systems that could have a pivotal role in meeting such demands. We divide battery systems into two categories: near-term and long-term technologies. To provide a realistic and balanced perspective, we describe the operating principles and remaining issues of each post-LIB technology, and also evaluate these materials under commercial cell configurations. Post-lithium-ion batteries are reviewed with a focus on their operating principles, advantages and the challenges that they face. The volumetric energy density of each battery is examined using a commercial pouch-cell configuration to evaluate its practical significance and identify appropriate research directions.

Challenges Facing Lithium Batteries and Electrical Double‐Layer Capacitors

Abstract: Energy-storage technologies, including electrical double-layer capacitors and rechargeable batteries, have attracted significant attention for applications in portable electronic devices, electric vehicles, bulk electricity storage at power stations, and “load leveling” of renewable sources, such as solar energy and wind power. Transforming lithium batteries and electric double-layer capacitors requires a step change in the science underpinning these devices, including the discovery of new materials, new electrochemistry, and an increased understanding of the processes on which the devices depend. The Review will consider some of the current scientific issues underpinning lithium batteries and electric double-layer capacitors.

Lithium–Sulfur Batteries: Electrochemistry, Materials, and Prospects

Abstract: With the increasing demand for efficient and economic energy storage, Li-S batteries have become attractive candidates for the next-generation high-energy rechargeable Li batteries because of their high theoretical energy density and cost effectiveness. Starting from a brief history of Li-S batteries, this Review introduces the electrochemistry of Li-S batteries, and discusses issues resulting from the electrochemistry, such as the electroactivity and the polysulfide dissolution. To address these critical issues, recent advances in Li-S batteries are summarized, including the S cathode, Li anode, electrolyte, and new designs of Li-S batteries with a metallic Li-free anode. Constructing S molecules confined in the conductive microporous carbon materials to improve the cyclability of Li-S batteries serves as a prospective strategy for the industry in the future.