Search

Enhancing catalytic activity through modulating the interaction between N-doped carbon and metal phosphides clusters is an effective approach. Herein, the electronic structure modulation of CoP2 supported N-modified carbon (CoP2/NC) has been designed and prepared as efficient electrocatalysts for oxygen reduction reaction (ORR), oxygen evolution reaction (OER), and hydrogen evolution reaction (HER). Notably, CoP2/NC-1 catalyst exhibits impressive performance in alkaline media, with an ORR half-wave potential of 0.84 V, as well as OER and HER overpotentials of 290 and 129 mV (at 10 mA·cm−2), respectively. In addition, CoP2/NC-1 produces a power density as high as 172.9 mW·cm−2, and excellent reversibility of 100 h at 20 mA·cm−2 in home-made Zn-air batteries. The experimental results demonstrate that the synergistic interactions between N modified carbon substrate and CoP2 material significantly enhance the kinetics of ORR, OER, and HER. Density functional theory (DFT) calculations reveal the strong electrons redistribution of CoP2 induced by high-density N atoms at the interface, thus optimizing the key intermediates and significantly lower the energy barrier of reactions. These electronic adjustments of CoP2 greatly enhance its kinetics of ORR/OER/HER, leading to faster reactions. This study provides profound insights into the specific modification of CoP2 by N-doped carbon, enabling the construction of efficient catalysts. [ABSTRACT FROM AUTHOR]

Cost‐effective, non‐fluorinated polymer proton exchange membranes (PEMs) are highly desirable in emerging hydrogen fuel cells (FCs) technology; however, their low proton conductivities and poor chemical and dimension stabilities hinder their further development as alternatives to commercial Nafion®. Here, we report the inorganic‐organic hybridization strategy by facilely complexing commercial polymers, polyvinyl butyral (PVB), with inorganic molecular nanoparticles, H3PW12O40 (PW) via supramolecular interaction. The strong affinity among them endows the obtained nanocomposites amphiphilicity and further lead to phase separation for bi‐continuous structures with both inter‐connected proton transportation channels and robust polymer scaffold, enabling high proton conductivities, mechanical/dimension stability and barrier performance, and the H2/O2 FCs equipped with the composite PEM show promising power densities and long‐term stability. Interestingly, the hybrid PEM can be fabricated continuously in large scale at challenging ~10 μm thickness via typical tape casting technique originated from their facile complexing strategy and the hybrids' excellent mechanical properties. This work not only provides potential material systems for commercial PEMs, but also raises interest for the research on hybrid composites for PEMs. [ABSTRACT FROM AUTHOR]

The explosive growth of binder industry spurs the development of strong adhesives with the integration of multi‐functionalities as well as cost‐effective and eco‐friendly processability. Here, polyvinyl alcohol (PVA) and sub‐nanoscale metal oxide cluster, phosphotungstic acid (PTA), both with broad commercial availability, are complexed through hydrogen bonding in water. The obtained nanocomposites demonstrate promising light transmittance and proton conductivity, and most importantly, unprecedentedly high adhesive strengths as ≈4 kN m–1 for peeling strength and 8.2 ± 1.7 MPa for single lap shear strength on typical glass substrate. The supramolecular complexation of PVA with PTA can significantly reduce its crystallinity and accelerate PVA chain dynamics for negligible internal stress and membrane shrinkage upon drying, leading to close contact with glass substrates for strong adhesion. Meanwhile, the supramolecular interaction between PVA and PTA contributes to the nanocomposites' enhanced mechanical strength and resolves the issue of cohesion failure to ensure high adhesive strengths. The fast chain dynamics also benefit rapid proton transportation, contributing to the high proton conductivities. The binder design protocol can be extended to general polymer systems integrated with desired functionalities and allows scale up processing, providing great opportunities for functional adhesives for safety glass and electronic industry. [ABSTRACT FROM AUTHOR]