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In this manuscript, the graphite/resin composite plates were prepared via a facile ball milling strategy. The needle coke (NC) as a conductive additive was studied on effects of treated by ball milling on the electrical conductivity, mechanical property of the composite plates. All the characterizations showed that after ball milling, the NC particles have smaller particle size, and more uniform particle size distribution, which enhanced the interfacial adhesion between particles and resin. Due to the difference in shape and size between the auxiliary conductive filler and flake graphite, the addition of NC particles can easily fill the gap between flake‐like graphite and phenolic resin. The uniform distribution of these fillers improves the cross‐linking density, and the conductive path was added between the flake‐like graphite and the resin, which improved the electric conductivity of composit plate from 26.32 S cm−1 to 149.23 S cm−1. Such a prominent performance was attributed to the synergistic effects between the uniformly incorporated NC and the graphite/resin composite adhesive system. [ABSTRACT FROM AUTHOR]

Highly active Pt‐based intermetallic nanoparticles (i‐NPs) loaded on stable supports have garnered considerable interest as promising oxygen reduction reaction (ORR) catalysts for proton‐exchange‐membrane fuel cells (PEMFCs). Herein, thermostable tellurium (Te) is vapor‐deposited onto commercial conductive carbon to anchor high‐temperature‐synthesized Pt3Co i‐NPs. Advanced characterization and density functional theory (DFT) calculations demonstrate that the binding energy of Pt 4f and Co 2p shift positively by 0.12 and 0.95 eV after the introduction of Te in carbon support, promoting the formation of Pt─Te bonds, which enhances the metal–support interactions (MSIs) in Pt3Co/Te‐C (with a more negative binding energy of −10.28 eV). The average size of well‐dispersed Pt3Co i‐NPs (≈3.9 nm) on Te─C is considerably smaller than that of Pt3Co i‐NPs (≈9.1 nm) on commercial carbon. The specific activity of Pt3Co/Te‐C decreases by only 1.5% after 100,000 ultra‐long voltage‐accelerated cycles, while the morphology remains almost unchanged. The membrane electrode assembly using Pt3Co/Te‐C as a cathode demonstrates impressive activity (power density of 2.32 W cm−2@4 A cm−2 and mass activity of 0.50 A mgPt−1@0.9 V) and robust durability (mass activity@0.9 V loss of 26% after 30,000 cycles with intact L12 ordered structure) in H2–O2 operation, significantly exceeding the DOE 2025 requirements. [ABSTRACT FROM AUTHOR]