Symmetry breaking is a characteristic to determine which branch of a bifurcation system follows upon crossing a critical point. Specifically, in spin–orbit torque (SOT) devices, a fundamental question arises: how can the symmetry of the perpendicular magnetic moment be broken by the in-plane spin polarization? Here, we show that the chiral symmetry breaking by the antisymmetric Dzyaloshinskii–Moriya interaction (DMI) can induce the deterministic SOT switching of the perpendicular magnetization. By introducing a gradient of saturation magnetization or magnetic anisotropy, the dynamic noncollinear spin textures are formed under the current-driven SOT, and thus, the chiral symmetry of these dynamic spin textures is broken by the DMI, resulting in the deterministic magnetization switching. We introduce a strategy to induce an out-of-plane (z) gradient of magnetic properties as a practical solution for the wafer-scale manufacture of SOT devices.
Giant spin-orbit torque (SOT) from topological insulators (TIs) provides an energy efficient writing method for magnetic memory, which, however, is still premature for practical applications due to the challenge of the integration with magnetic tunnel junctions (MTJs). Here, we demonstrate a functional TI-MTJ device that could become the core element of the future energy-efficient spintronic devices, such as SOT-based magnetic random-access memory (SOT-MRAM). The state-of-the-art tunneling magnetoresistance (TMR) ratio of 102% and the ultralow switching current density of 1.2 × 105 A cm−2 have been simultaneously achieved in the TI-MTJ device at room temperature, laying down the foundation for TI-driven SOT-MRAM. The charge-spin conversion efficiency θSH in TIs is quantified by both the SOT-induced shift of the magnetic switching field (θSH = 1.59) and the SOT-induced ferromagnetic resonance (ST-FMR) (θSH = 1.02), which is one order of magnitude larger than that in conventional heavy metals. These results inspire a revolution of SOT-MRAM from classical to quantum materials, with great potential to further reduce the energy consumption.
In transport, the topological Hall effect (THE) presents itself as nonmonotonic features (or humps and dips) in the Hall signal and is widely interpreted as a sign of chiral spin textures, like magnetic skyrmions. However, when the anomalous Hall effect (AHE) is also present, the coexistence of two AHEs could give rise to similar artifacts, making it difficult to distinguish between genuine THE with AHE and two-component AHE. Here, we confirm genuine THE with AHE by means of transport and magneto-optical Kerr effect (MOKE) microscopy, in which magnetic skyrmions are directly observed, and find that genuine THE occurs in the transition region of the AHE. In sharp contrast, the artifact “THE” or two-component AHE occurs well beyond the saturation of the “AHE component” (under the false assumption of THE + AHE). Furthermore, we distinguish artifact “THE” from genuine THE by three methods: (1) minor loops, (2) temperature dependence, and (3) gate dependence. Minor loops of genuine THE with AHE are always within the full loop, while minor loops of the artifact “THE” may reveal a single loop that cannot fit into the “AHE component”. In addition, the temperature or gate dependence of the artifact “THE” may also be accompanied by a polarity change of the “AHE component”, as the nonmonotonic features vanish, while the temperature dependence of genuine THE with AHE reveals no such change. Our work may help future researchers to exercise caution and use these methods for careful examination in order to ascertain the genuine THE.
We demonstrate that atomically thin Pt shells deposited on transition metal carbide or nitride cores induce up to a 4-fold enhancement in C2H4 selectivity during the partial hydrogenation of acetylene compared with commercial carbon-supported Pt (Ptcomm) nanoparticles. While Pt typically catalyzes the complete hydrogenation of alkynes to alkanes, a catalyst comprising a nominal one monolayer (ML) Pt shell on titanium tungsten nitride cores (Pt/TiWN) is capable of net C2H4 generation under industrial front-end reaction conditions featuring a large excess of C2H4 and H2. Microcalorimetry measurements are consistent with a change in the Pt electronic structure that decreases C2H4 binding strength, thus increasing partial hydrogenation selectivity. Density functional theory (DFT) calculations and X-ray absorption near edge structure (XANES) both indicate broadening of the Pt d-band and concomitant down-shifting of the d-band center. The ability to control shell coverage and core composition opens up extensive opportunities to modulate the electronic and catalytic properties of noble metal-based catalysts.
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