The nonlinear rheology of a concentrated lithium-ion battery anode slurry was examined under large amplitude oscillatory shear and interpreted with a sequence of physical process (SPP) analysis. A complex interplay of three anode slurry components—graphite (Gr) as an active material, carbon black (CB) as a conductive additive, and carboxymethyl cellulose (CMC) as a binder—leads to a two-step yielding behavior, represented as the secondary plateau in dynamic strain and stress sweep tests. We demonstrate that a two-step yielding behavior is manifested as double deltoids in SPP analysis through the study of intra-cycle rheological transition under oscillatory shear flow. Slurries of Gr-CMC exhibit the two-step yielding behavior; slurries of CB-CMC do not, suggesting that Gr and CMC are the primary causes of two-step yielding in an anode slurry. A sedimentation test on a dilute Gr-CMC solution yielded phase separation between graphite particles, with CMC adsorbed on their surface and graphite particles aggregated via hydrophobic attraction. This indicates two possible types of interactions in a concentrated slurry: a hydrophobic interaction between graphite particles and a physicochemical interaction caused by CMC adsorbed on graphite particles. The first yielding step relates to the hydrophobic attraction between graphite particles, resulting in a network structure that is expected to be brittle and rupture at a small strain. The second yielding step is attributed to the interaction between concentrated CMC, which is corroborated by the overlap of the secondary deltoid of the anode slurry and the single deltoid of the concentrated CMC solution in SPP analysis.

This soft machine can pick up and release an ultrathin “living” cell sheet and electronics without crumpling.

Ferrocene-based nanoparticles have garnered interest as reactive oxygen species (ROS)-responsive nanocarriers of anticancer drugs and imaging agents. However, their biomedical applications remain limited due to their poor physiological stability. PEGylation of nanocarriers improves their stability and biocompatibility. In this study, we aimed to develop novel PEG-ferrocene nanoparticles (PFNPs) with enhanced stability and ROS responsiveness for the delivery of paclitaxel (PTX) and imaging agents. PEGylation improved the stability of ferrocene nanoparticles, inhibiting their ROS-responsive destruction. Several PEG-ferrocene polymers containing different molar ratios of methacrylic acid and poly (ethylene glycol) methyl ether methacrylate was designed for optimization. ROS-responsive polymers with optimal monomer ratios were self-assembled into PFNPs with enhanced stability. The PFNPs distended, effectively releasing encapsulated PTX and imaging agents within 8 h in the presence of ROS. Furthermore, they remained stable, with no changes in their hydrodynamic diameters or polydispersity indexes after storage in an aqueous solution and biological buffer. The accumulation of PFNPs in a tumor model in vivo was 15-fold higher than a free dye. PTX-loaded PFNPs showed a substantial tumor-suppression effect, reducing tumor size to approximately 18% of that in the corresponding control group. These findings suggest a promising application of ROS-responsive PFNPs in tumor treatment as biocompatible nanocarriers of anticancer drugs and imaging agents.