Conveying Advanced Li‐ion Battery Materials into Practice The Impact of Electrode Slurry Preparation Skills

Li‐ion batteries (LIB's) are of the greatest practical utility for portable electronics and electric vehicles (EV's). LIB energy, power and cycle life performances depend on cathode and anode compositions and morphology, electrolyte composition and the overall cell design. Electrode morphology is influenced by the shape and size of the active material (AM), conductive additive (CA) particles, the polymeric binder properties, and also on the AM/CA/binder mass ratio. At the same time, it also substantially depends on the electrode preparation process. This process is usually comprised of mixing a solvent, a binder, AM and CA powders, and casting the resulting slurry onto a current collector foil followed by a drying process. Whereas the problems of electrode morphology and their influence on the LIB‐electrode performance always receive a proper attention, the influence of slurry properties and slurry preparation techniques on the electrode morphology is often overlooked or at least underrated. The present work summarizes the current state‐of‐the‐art in the field of LIB‐electrode precursor slurries preparation, characterized by multicomponent compounds and large variations in sizes and shapes of the solid components. Approaches to LIB‐electrode slurry preparation are outlined and discussed in the context of the ultimate LIB‐electrode morphology and performance.     

Stable Li–Organic Batteries with Nafion‐Based Sandwich‐Type Separators

Similar to Li–S batteries, Li–organic batteries have also been plagued by the dissolution of active materials and the resulting shuttle effect for many years. An effective strategy to eliminate the shuttle effect is adopting solid electrolytes or Li–ion permselective separators to prohibit the dissolved electroactive species from migrating to the Li anode. A polypropylene/Nafion/polypropylene (PNP) sandwich‐type separator is reported with many advantages in comparison with previously reported LISICON, polymer electrolyte, and other Nafion utilization forms. The physical and chemical properties of PNP separators are studied in detail by cross‐section scanning electron microscopy (SEM), infrared spectroscopy (IR), and electrochemical impedance spectroscopy. 1,1′‐Iminodianthraquinone (IDAQ), a novel organic cathode, is taken as an example to quantitatively investigate the function of PNP separators. In the presence of PNP5 with the most appropriate Nafion loading of 0.5 mg cm^–2, IDAQ is able to achieve dramatically improved cycling stability with capacity retention of 76% after 400 cycles and Coulombic efficiency above 99.6%, which reaches the highest level for reported soluble organic electrode materials. Besides Li–organic batteries, such kind of Nafion‐based sandwich‐type separators are also promising for Li–S batteries and other new battery designs involving dissolved electroactive species.     

Nanoscale Elastic Changes in 2D Ti3C2Tx (MXene) Pseudocapacitive Electrodes

Designing sustainable electrodes for next generation energy storage devices relies on the understanding of their fundamental properties at the nanoscale, including the comprehension of ions insertion into the electrode and their interactions with the active material. One consequence of ion storage is the change in the electrode volume resulting in mechanical strain and stress that can strongly affect the cycle life. Therefore, it is important to understand the changes of dimensions and mechanical properties occurring during electrochemical reactions. While the characterization of mechanical properties via macroscopic measurements is well documented, in situ characterization of their evolution has never been achieved at the nanoscale. It is reported here with in situ imaging, combined with density functional theory of the elastic changes of a 2D titanium carbide (Ti₃C₂T_x) based electrode in direction normal to the basal plane (electrode surface) during alkaline cation intercalation/extraction. 2D carbides, known as MXenes, are promising new materials for supercapacitors and various kinds of batteries, and understanding the coupling between their mechanical and electrochemical properties is therefore necessary. The results show a strong correlation between the cations content and the out‐of‐plane elastic modulus. This strategy enables identifying the preferential intercalation pathways within a single particle, which is important for understanding ionic transport in these materials.     

Two‐Dimensional Materials for Beyond‐Lithium‐Ion Batteries

Lithium‐ion batteries (LIBs) have dominated the portable electronics industry and solid‐state electrochemical research and development for the past two decades. In light of possible concerns over the cost and future availability of lithium, sodium‐ion batteries (SIBs) and other new technologies have emerged as candidates for large‐scale stationary energy storage. Research in these technologies has increased dramatically with a focus on the development of new materials for both the positive and negative electrodes that can enhance the cycling stability, rate capability, and energy density. Two‐dimensional (2D) materials are showing promise for many energy‐related applications and particularly for energy storage, because of the efficient ion transport between the layers and the large surface areas available for improved ion adsorption and faster surface redox reactions. Recent research highlights on the use of 2D materials in these future ‘beyond‐lithium‐ion’ battery systems are reviewed, and strategies to address challenges are discussed as well as their prospects.     

Xylene‐Bridged Phosphaviologen Oligomers and Polymers as High‐Performance Electrode‐Modifiers for Li‐Ion Batteries

Lithium‐ion batteries are one of the most common forms of energy storage devices used in society today. Due to the inherent limitations of conventional Li‐ion batteries, organic materials have surfaced as potentially suitable electrode alternatives with improved performance and sustainability. Viologens and phosphaviologens in particular, are strong electron‐accepting materials with excellent kinetic properties, making them suitable candidates for battery applications. In this paper, new polymeric species of the latter moieties are reported that lead to improved electrode stability and device performance. The performance of the phosphaviologen is further enhanced through the utilization of both redox steps, allowing for good performance proof‐of‐concept hybrid organic/Li‐ion batteries. This opens the potential for more sustainable and improved battery performance for use in current energy applications.     

An amperometric lactate biosensor based on lactate dehydrogenase immobilized onto graphene oxide nanoparticles‐modified pencil graphite electrode

A novel amperometric lactate biosensor was developed based on immobilization of lactate dehydrogenase onto graphene oxide nanoparticles‐decorated pencil graphite electrode. The enzyme electrode was characterized by scanning electron microscopy, Fourier transform infrared spectroscopy (FTIR), and cyclic voltammetry at different stages of its construction. The biosensor showed optimum response within 5 s at pH 7.3 (0.1 M sodium phosphate buffer) and 35°C, when operated at 0.7 V. The biosensor exhibited excellent sensitivity (detection limit as low as 0.1 μM), fast response time (5 s), and wider linear range (5–50 mM). Analytical recovery of added lactic acid in serum was between 95.81–97.87% and within‐batch and between‐batch coefficients of variation were 5.04 and 5.40%, respectively. There was a good correlation between serum lactate values obtained by standard colorimetric method and the present biosensor (r = 0.99). The biosensor measured lactate levels in sera of apparently healthy subjects and persons suffering from lactate acidosis and other biological materials (milk, curd, yogurt, beer, white wine, and red wine). The enzyme electrode lost 25% of its initial activity after 60 days of its regular uses, when stored dry at 4°C.     

A methodology to estimate national REDD+ reference levels using the Zero-Sum-Gains DEA approach

REDD+ reference levels directly impact the benefits which a country may receive. However, the existing “Compensation Reduction” (CR) and “Compensated Successful Efforts” (CSE) are only considered from a unilateral perspective of outputs or inputs. The combination of these two approaches is considered to estimate the REDD+ reference levels through the Zero-Sum-Gains Data Envelopment Analysis in this paper. The agricultural labor force and agricultural land area are used as input variables, and the gross agricultural production and carbon emissions from deforestation are considered as output variables. The REDD+ reference levels of 89 countries are calculated and classified through the Zero-Sum-Gains DEA model. The results demonstrate that the REDD+ reference levels are estimated efficiently through the Zero-Sum-Gains DEA model, and all countries with deforestation are in the Zero-Sum-Gains DEA frontier, indicating the overall Pareto optimality has been achieved. The empirical results also indicate that the use of Zero-Sum-Gains DEA model is more beneficial for Latin American and the Caribbean, while the countries that may see a revenue drop in REDD+ are in Africa, Asia and Oceania. Consequently, the final REDD+ reference levels should take into account both efficiency and fairness by selecting the appropriate fairness-efficiency weighting factor.     

Will income inequality affect environmental quality? Analysis based on China's provincial panel data

During the last two decades of China's rapid economic growth, the gap in citizens’ income has widened and environmental quality has deteriorated. Using Gini coefficients as the measure of income inequality, this study investigated the impacts of income inequality on carbon emissions per capita in China. To control for potential endogeneity and allow for dynamics, the Generalized Method of Moments (GMM) technique is utilized. Moreover, the influential factors that can affect carbon emissions per capita in China have been examined. The empirical results indicate that carbon emissions per capita increase as the income gap expands for nationwide and in the eastern and non-eastern regions of China. Among all factors that may affect carbon emissions per capita, a “U” shaped relationship exists between per capita income and per capita carbon emissions, and increasing the value-added share of secondary industry in the GDP would significantly increase carbon emissions per capita.     

Drought-induced dynamics of carbon and water use efficiency of global grasslands from 2000 to 2011

Drought is frequently recorded as a result of climate warming and elevated concentration of greenhouse gases, which affect the carbon and water cycles in terrestrial ecosystems, particularly in arid and semi-arid regions. To identify the drought in grassland ecosystems and to determine how such drought affects grassland ecosystems in terms of carbon and water cycles across the globe, this study evaluated the drought conditions of global grassland ecosystems from 2000 to 2011 on the basis of the remotely sensed Drought Severity Index (DSI) data. The temporal dynamics of grassland carbon use efficiency (CUE) and water use efficiency (WUE), as well as their correlations with DSI, were also investigated at the global scale. Results showed that 57.04% of grassland ecosystems experienced a dry trend over this period. In general, most grassland ecosystems in the northern hemisphere (N.H.) were in near normal condition, whereas those in the southern hemisphere (S.H.) experienced a clear drying and wetting trend, with the year 2005 regarded as the turning point. Grassland CUE increased continually despite the varied drought conditions over this period. By contrast, WUE increased in the closed shrublands and woody savannas but decreased in all the other grassland types. The drought conditions affected the carbon and water use mainly by influencing the primary production and evapotranspiration of grass through photosynthesis and transpiration process. The CUE and WUE of savannas was most sensitive to droughts among all the grassland types. The areas of grassland DSI that showed significant correlations with CUE and WUE were 52.92% and 22.11% of the total grassland areas, respectively. Overall, droughts sufficiently explained the dynamics of grassland CUE, especially in the S.H. In comparison with grassland CUE, the grassland WUE was less sensitive to drought conditions at the global scale.