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Overcharge is a hazardous abuse condition that has dominant influences on cell performance and safety. This work, for the first time, comprehensively investigates the impact of different overcharge degrees on degradation and thermal runaway behavior of lithium-ion batteries. The results indicate that single overcharge has little influence on cell capacity, while it severely degrades thermal stability. Degradation mechanisms are investigated by utilizing the incremental capacity-differential voltage and relaxation voltage analyses. During the slight overcharge process, the conductivity loss and the loss of lithium inventory always occur; the loss of active material starts happening only when the cell is overcharged to a certain degree. Lithium plating is the major cause for the loss of lithium inventory, and an interesting phenomenon that the arrival time of the dV/dt peak decreases linearly with the increase of the overcharge degree is found. The cells with different degrees of overcharge exhibit a similar behavior during adiabatic thermal runaway. Meanwhile, the relationship between sudden voltage drop and thermal runaway is further established. More importantly, the characteristic temperature of thermal runaway, especially the self-heating temperature (T1), decreases severely along with overcharging, which means that a slight overcharge severely decreases the cell thermal stability. Further, post-mortem analysis is conducted to investigate the degradation mechanisms. The mechanism of the side reactions caused by a slight overcharge on the degradation performance and thermal runaway characteristics is revealed.

Electromechanical impedance (EMI) technique coupled with the piezoelectric sensor has been explored as a promising non-destructive testing (NDT) method to determine the quality of cementitious materials. Among the piezoelectric sensors, Lead Zirconate Titanate (PZT) is the most commonly used piezo-ceramic materials for conducting the EMI because of the high sensitivity and high piezoelectric constant. However, the inherent brittleness of PZT limited their potential application as embedded sensors for in-situ monitoring of materials/structure properties. To improve the durability and flexibility of the PZT sensor, we have systematically investigated the effect of different polymer coating methods of PZT on their sensitivity and effectiveness of EMI sensors. Specifically, two polymer coating agents were used to encapsulate the PZT sensor including the flexible organic polymer compound - Polydimethylsiloxane (PDMS) and the rigid polymer compound- Polyepoxides (Epoxy) We have also investigated the feasibility of EMI technique with the surface bonded sensor and embedded sensor to test the compressive strength gain of mortars. The compressive strength test of samples was also conducted using conventional mechanical methods per ASTM C109 as a baseline at the first 5th to 8th hour. The EMI signatures were collected for all the samples at the same time. Our preliminary results have shown a high correlation of EMI methods’ results with the compressive testing results for two different polymers coated PZT sensors, which indicated the polymer-coated PZT sensors can be used as an effective NDT method for in-situ monitoring of concrete compressive strength gain at the very early age.

Occurrence of lithium plating on the anode is a severe side reaction in the lithium-ion batteries, which brings cell capacity degradation and reduces the cell safety. This paper focuses on 37Ah commercial lithium-ion batteries and clarifies the evolution of lithium plating during long-term low temperature (−10 °C) cycling. The tested cells are analyzed at different degradation stages, named “fixed-point analysis”, to evaluate the evolution process of lithium plating. It is found that the capacity fade and the internal resistance increase exhibit a decelerated trend with a turning point around 450 cycles. The loss of cyclable lithium caused by lithium plating is deemed to be the main reason behind the battery degradation. Post-mortem analysis including scanning electron microscope (SEM) and X-ray photoelectron spectroscopy (XPS) is conduced to reveal the mechanism. The thickness and morphology change of plated lithium, and the plated lithium covered by solid electrolyte interface film, are disclosed by the surface and cross-section SEM images from the fixed-point analysis. XPS analysis further reveals the composition of solid electrolyte interface film, and the plated lithium existing. In a nutshell, lithium plating is inhomogeneous and has high spatial dependence.

A novel phenol–formaldehyde carbon with ordered/disordered bimodal mesoporous structure is synthesized by the facile evaporation induced self-assembly strategy under a basic aqueous condition with SiO2 particles as template. The prepared bimodal mesoporous carbons (BMCs) are composed of ordered mesoporous and disordered mesoporous with diameter of about 3.5 nm and 7.0 nm, respectively. They can be employed as supercapacitor electrodes in H2SO4 aqueous electrolyte after the simple acid-treatment. BMC exhibits an exceptional specific capacitance of 344 F g−1 at the current density of 0.1 A g−1, although it has a relatively low surface area of 722 m2 g−1. And the BMC electrode displays an excellent cycling stability over 10,000 cycles.

Highly ordered, body-centered cubic mesoporous phenol–formaldehyde carbon C-FDU-16 is prepared by a facile evaporation induced self-assembly strategy under a basic aqueous condition. Afterwards, in order to increase the active site of surface electrochemical reactions and promote the wettability in aqueous electrolyte, a simple chemical surface modification is carried out on the C-FDU-16 by nitric acid treatment. The C-FDU-16 and the acid-modified C-FDU-16 (N-FDU-16) are used as the active materials for supercapacitors. Although C-FDU-16 has unique 3D mesoporous network combined with high specific surface area, it do not show well supercapacitor properties for its bad wettability with the aqueous electrolyte. However, the N-FDU-16 with acid treatment exhibits the largest specific capacitance of 219 F g−1 at a current density of 0.1 A g−1 in 1 M H2SO4 electrolyte which is 7 times larger than that of the C-FDU-16 and it also shows good cycling stability as well. Therefore, based on the above investigations, ordered mesoporous phenol–formaldehyde carbon such as C-FDU-16 can be a potential candidate for supercapacitors after the simply acid treatment.