Quantum geometric spin frustration of antiferromagnetic CuFeO2 enables photocatalytic applications

Photocatalysis, containing a potential solution to the global crises of energy shortage and the greenhouse effect, has been studied extensively in recent years. The CuFeO2 (abbreviated as CFO) is a material with a Delafossite structure, and has also been widely studied because of its triangular lattice antiferromagnets. The triangular lattice composed of Fe3+ ions, along with strong antiferromagnetic spin coupling between the Fe3+ ions, leads to a geometric spin frustration. Furthermore, CFO is also a potential candidate for the photocatalytic material due to its narrow band gap of 1.1–1.6 eV, electrochemical stability in an aqueous environment, high charge carrier mobility, flat-band potential positioned at ∼ 1 eV, and contains an abundance of raw materials in the earth. In this study, we successfully grew the size and highly-quality CFO single crystals using the optical floating-zone technique. Powder x-ray diffraction (XRD) and Rietveld refinement indicate that the CFO is a rhombohedral structure with a space group of R3̅m, consisting of edge-shared FeO6 octahedron to form the FeO2 layer, and the Cu cations occupied between the two FeO2 layers. The core-level electron energy loss (EEL) spectra found the valence of Fe and Cu in CFO is +3 and +1, respectively. The low-loss EEL spectrum observed two volume plasmons at ∼5 eV and ∼23 eV contributed from the collective oscillation of Cu-O antibonding states σCu−O* and mixed nonbonding Cu 3dxy, σCu−O bonding states, and Fe-O, respectively, based on the density function theory calculation. The optical absorption spectrum measured the energy bandgap for CFO is about 1.5 eV. The Raman spectrum shows significant Eg and A1 g vibration modes corresponding to the in-plane Fe-O and out-of-plane Cu-O vibrations, respectively. Both magnetic susceptibility, χ(T), with the applied magnetic field along the c-axis and specific heat capacity reveal the two magnetic phase transition temperatures at low temperatures: TN1 = 13.5 K when transition from paramagnetic (PM) phase to partially disordered antiferromagnetic, and TN2 = 10.5 K when complete transition from partially disordered antiferromagnetic to antiferromagnetic phase. The additional calculation of magnetic entropy change is 0.15, which is roughly close to 0.2, meaning that only 1/5 of the Fe3+ spins are disordered when transforming from PM states to partially disordered at T < TN1 in this study. The presence of instantaneous ferromagnetic spin arrangement (↑↑↓) extends the residence time of H2O on the surface of CFO, facilitating electron exchange with CFO and promoting photocatalytic water splitting reactions.