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The adaptability of conductive rubber in SO2/salt spray environment was studied by using graphene-filled conductive fluoroether rubber and alloy nickel powder-filled conductive silicone rubber in“SO2/salt spray” test. The macro morphology，Shore A hardness，tensile strength，elongation at break，tear strength and volume resistivity were tested to analyze the influence of the “SO2/salt spray” environment on the properties of conductive rubber. The results show before the test，the Shore A hardness of conductive fluoroether rubber and conductive silicone rubber are equivalent，the tensile strength of conductive fluoroether rubber is higher than that of conductive silicone rubber，and the volume resistivity is lower than that of conductive silicone rubber. After 8 cycles of “SO2/salt spray” test，the macro morphology of conductive fluoroether rubber does not change，Shore A hardness decreases by 3，tensile strength increases by 0.8 MPa（5%），elongation at break decreases by 18%， the volume resistivity increases by 2.1 Ω·cm（65.8%）and there is no change in tear strength；while the conductive silicone rubber has obvious corrosion，with green corrosion products appeared on the surface，Shore A hardness gradually decreases，and the tensile strength decreases by 1.2 MPa（16.4%），the elongation at break decreases by 2%，the volume resistivity decreases by 3.00 Ω·cm（52.4%）and there is no change in tear strength. The analysis of the comprehensive performances obtained by the study shows that the adaptability of conductive fluoroether rubber in “SO2/salt spray” environment is superior to that of conductive silicone rubber.

Surface-enhanced Raman spectroscopy (SERS), with high sensitivity to a broad range of molecules, can detect molecular "fingerprints" in a complex substance and thereby offers a promising solution for noninvasive medical diagnostics and personal healthcare monitoring. The eventual realization of such applications relies on SERS substrates with dense and uniform hot spots, good chemical stability, and high mechanical durability. With these criteria in mind, we developed a flexible nanoporous SERS substrate via the in situ synthesis of gold nanostars (AuNSs) on an ion-track-etched polycarbonate membrane. The nanoporous SERS substrate can realize analyte enrichment and exhibit excellent Raman performance by taking the advantage of hot spots on AuNSs. The SERS substrate yields highly repeatable and uniform signals for analytes (e.g., methylene blue) over a wide concentration range from 10–4 to 10–13 M. The flexible SERS substrate even can work well after 2000 times bending and exhibit excellent stability for long-term use. It can be prepared on a large scale with a low-cost and simple fabrication process and can be used repeatedly after cleaning to reduce the use-cost further. On-body experiments prove that the sweat SERS substrate allows effective identification of sweat contents, such as lactic acid and uric acid (UA), and the monitoring of diet-induced variation in sweat UA. The potential of the wearable nanoporous SERS substrates in sweat analysis thus has been demonstrated, opening possibilities for autonomous and noninvasive medical health monitoring. [ABSTRACT FROM AUTHOR]

Lithium (Li) metal anodes have received sustained attention due to their remarkable theoretical specific capacities and low electrochemical potentials. However, the nucleation and growth of Li dendrites during cycling have hindered their application in Li metal batteries (LMBs). As an indispensable battery component, separators offer an ideal platform for mitigating Li dendrites. Herein, an ion‐management membrane (IMM) concept utilizing polydopamine (PDA)‐modified polyetherimide track‐etched membranes (PEITEMs) is proposed. The PDA@PEITEM‐based IMM features vertically aligned uniform electronegative nanochannels, serving as ion distributors and “Li‐ion guides” to simultaneously smooth ion concentration fluctuations and accelerate Li+ selective conduction. The IMM's unique structural and chemical properties yield exceptional ionic conductivity (0.73 mS cm−1) and high Li+ transfer number (0.80) while minimizing Li+ concentration fluctuations. When employed in Li/Cu cells, the IMM facilitates a Coulombic efficiency exceeding 96% over 100 cycles at 0.5 mA cm−2. Moreover, it extends the cycle lifespan of Li/Li cells to 1 200 h at 1.0 mA cm−2. For Li/LiFePO4 cells, this approach enables a specific capacity of 146 mAh g−1, maintaining capacity retention of 79.84% after 1 000 cycles. This novel strategy for constructing free‐standing functional separators is convenient, efficient, and scalable, providing valuable insights into multifunctional separators for dendrite‐free LMBs. [ABSTRACT FROM AUTHOR]