Anodic oxygen evolution reaction (OER) is recognized as kinetic bottleneck in water electrolysis. Transition metal sites with high valence states can accelerate the reaction kinetics to offer highly intrinsic activity, but suffer from thermodynamic formation barrier. Here, we show subtle engineering of highly oxidized Ni⁴⁺ species in surface reconstructed (oxy)hydroxides on multicomponent FeCoCrNi alloy film through interatomically electronic interplay. Our spectroscopic investigations with theoretical studies uncover that Fe component enables the formation of Ni⁴⁺ species, which is energetically favored by the multistep evolution of Ni²⁺→Ni³⁺→Ni⁴⁺. The dynamically constructed Ni⁴⁺ species drives holes into oxygen ligands to facilitate intramolecular oxygen coupling, triggering lattice oxygen activation to form Fe-Ni dual-sites as ultimate catalytic center with highly intrinsic activity. As a result, the surface reconstructed FeCoCrNi OER catalyst delivers outstanding mass activity and turnover frequency of 3601 A g_metal⁻¹ and 0.483 s⁻¹ at an overpotential of 300 mV in alkaline electrolyte, respectively.

The sp² nature of graphene endows the hexagonal lattice with very high theoretical stiffness, strength and resilience, all well-documented. However, the ultimate stretchability of graphene has not yet been demonstrated due to the difficulties in experimental design. Here, directly performing in situ tensile tests in a scanning electron microscope after developing a protocol for sample transfer, shaping and straining, we report the elastic properties and stretchability of free-standing single-crystalline monolayer graphene grown by chemical vapor deposition. The measured Young’s modulus is close to 1 TPa, aligning well with the theoretical value, while the representative engineering tensile strength reaches ~50-60 GPa with sample-wide elastic strain up to ~6%. Our findings demonstrate that single-crystalline monolayer graphene can indeed display near ideal mechanical performance, even in a large area with edge defects, as well as resilience and mechanical robustness that allows for flexible electronics and mechatronics applications.

Small, smooth, and bendable diamonds: If you manage to deform a diamond, it usually means you have broken it. Diamonds have very high hardness, but they do not deform elastically. This limits their usefulness for some applications. However, Banerjee et al. discovered that diamond nanoneedles can deform elastically after all (see the Perspective by LLorca). The key was in their small size (300 nm), which allowed for very smooth-surfaced, defect-free diamonds. The deformation was close to the theoretical limit for diamond, which opens up the potential for applications in microelectronics and drug delivery. Science , this issue p. 300 ; see also p. 264