Enhancing Performance and Stability of High-Temperature Proton Exchange Membranes through Multiwalled Carbon Nanotube Incorporation into Self-Cross-Linked Fluorenone-Containing Polybenzimidazole.

Addressing critical challenges in enhancing the oxidative stability and proton conductivity of high-temperature proton exchange membranes (HT-PEMs) is pivotal for their commercial viability. This study uncovers the significant capacity of multiwalled carbon nanotubes (MWNTs) to absorb a substantial amount of phosphoric acid (PA). The investigation focuses on incorporating long-range ordered hollow MWNTs into self-cross-linked fluorenone-containing polybenzimidazole (FPBI) membranes. The absorbed PA within MWNTs and FPBI forms dense PA networks within the membrane, effectively enhancing the proton conductivity. Moreover, the exceptional inertness of MWNTs plays a vital role in reinforcing the oxidation resistance of the composite membranes. The proton conductivity of the 1.5% CNT-FPBI membrane is measured at 0.0817 S cm-1 at 160 °C. Under anhydrous conditions at the same temperature, the power density of the 1.5% CNT-FPBI membrane reaches 831.3 mW cm-2. Notably, the power density remains stable even after 200 h of oxidation testing and 250 h of operational stability in a single cell. The achieved power density and long-term stability of the 1.5% CNT-FPBI membrane surpass the recently reported results. This study introduces a straightforward approach for the systematic design of high-performance and robust composite HT-PEMs for fuel cells.

Intrinsically Self-Healable and Wearable All-Organic Thermoelectric Composite with High Electrical Conductivity for Heat Harvesting.

The development of wearable electronics has led to the growing demand for the self-powered and maintenance-free power sources. Under these circumstances, thermoelectric generators are considered promising candidates, which can directly convert body heat into electricity to power wearable electronics. However, most of the thermoelectric materials are either brittle or unrecoverable under external physical damage. It is urgent to develop thermoelectric materials that possess both stretchability and intrinsic self-healing property, and the remaining challenge is to combine the high mechanical robustness and excellent electrical conductivity. Herein, a self-healing and wearable all-organic thermoelectric composite is reported. The composite film exhibits high electrical conductivity of 238 S cm-1, high flexibility of up to 119% strain, and a maximum tensile strength of 23 MPa. When the composite film is subjected to external physical damage, most functionalities can be maintained after self-healing, 78% recovery in electrical conductivity, and 80% recovery in tensile strength. Using the self-healing composite, we fabricated a thermoelectric generator with a power output of 85.5 nW at a temperature difference of 48 K, which is a significant advance over the recently reported thermoelectric generators based on intrinsic self-healing thermoelectric materials. This work represents a crucial step toward achieving intrinsic self-healing all-organic thermoelectric materials with high electrical conductivity.