Fast carrier diffusion via synergistic effects between lithium-ions and polarons in rutile TiO2.

Carrier mobility in titanium dioxide (TiO2) systems is a key factor for their application as energy materials, especially in solar cells and lithium-ion batteries. Studies on the diffusion of Li-ions and polarons in rutile TiO2 systems have attracted extensive attention. However, how their interaction affects the diffusion of Li-ions and electron polarons is largely unclear and related studies are relatively lacking. By using first-principles calculations, we systematically investigate the interaction between the intercalated Li-ions and electron polarons in rutile TiO2 materials. Our analysis shows that the diffusion barrier of the electron polarons decreases around the Li-ion. The interaction between the Li-ions and polarons would benefit their synergistic diffusion both in the pristine and defective rutile TiO2 systems. Our study reveals the synergistic effects between the ions and polarons, which is important for understanding the carrier properties in TiO2 systems and in further improving the performance of energy materials.

Nuclear Quantum Effects on the Charge-Density Wave Transition in NbX2 (X = S, Se).

Understanding the origin of charge-density wave (CDW) instability is important for manipulating novel collective electronic states. Many layered transition metal dichalcogenides (TMDs) share similarity in the structural and electronic instability, giving rise to diverse CDW phases and superconductivity. It is still puzzling that even isostructural and isoelectronic TMDs show distinct CDW features. For instance, bulk NbSe2 exhibits CDW order at low temperature, while bulk NbS2 displays no CDW instability. The CDW transitions in single-layer NbS2 and NbSe2 are also different. In the classic limit, we investigate the electron correlation effects on the dimensionality dependence of the CDW ordering. By performing ab initio path integral molecular dynamics simulations and comparative analyses, we further revealed significant nuclear quantum effects in these systems. Specifically, the quantum motion of sulfur anions significantly reduces the CDW transition temperature in both bulk and single-layer NbS2, resulting in distinct CDW features in the NbS2 and NbSe2 systems.

A first-principles study of exciton self-trapping and electric polarization in one-dimensional organic lead halide perovskites.

Revealing the origin of self-trapped excitons is a prerequisite for further improving the photoluminescence efficiency of low-dimensional organic perovskites. Here, the microscopic formation mechanism of intrinsic self-trapped excitons in one-dimensional (1D) C4N2H14PbX4 (X = Cl, Br and I) systems is investigated, and the polarization-luminescence relationship is established. Our results show that 1D-C4N2H14PbX4 has a low electronic dimension (flat band characteristics), which facilitates the formation of intrinsic self-trapped excitons. The potential well formed by local distortion of the [PbX6] octahedron is the origin of exciton self-trapping. Combined with the electronic density of states and partial charge density, we further confirmed the existence of intrinsic self-trapping excitons in 1D-C4N2H14PbX4. In addition, we found that the breaking of the central inversion symmetry will induce electric polarization, which greatly improves the transition probability of electrons. These results could potentially offer a new direction for improving the luminescence properties of 1D organic lead halide perovskites.

Ab initio study of the miscibility for solid hydrogen-helium mixtures at high pressure.

Understanding the behavior of H2-He binary mixtures at high pressure is of great importance. Two more recent experiments [J. Lim and C. S. Yoo, Phys. Rev. Lett. 120, 165301 (2018) and R. Turnbull et al., ibid. 121, 195702 (2018)] are in conflict, regarding the miscibility between H2 and He in solids at high pressure. On the basis of first-principles calculations combined with the structure prediction method, we investigate the miscibility for solid H2-He mixtures at pressures from 0 GPa to 200 GPa. It is found that there is no sign of miscibility and chemical reactivity in H2-He mixtures with any H:He ratio. Moreover, instead of H2-He mixtures, the calculated Raman modes of the N-H mixtures can better explain the characteristic peaks observed experimentally, which were claimed to be the H-He vibrational modes. These calculation results are more in line with the experimental findings by Turnbull et al. [Phys. Rev. Lett. 121, 195702 (2018)].

Prediction of erbium-nitrogen compounds as high-performance high-energy-density materials.

To explore high-energy-density materials, intense attention has been focused on how to stabilize the N-N bond in nitrogen-rich compounds. Here, we report several stable phases of erbium-nitrogen compounds ErNxas high-energy-density materials. Specifically, the phase diagrams of stable high-pressure structuresImmm-ErN2,C2-ErN3,P1--ErN4, andP1--ErN6, are theoretically studied by combining first-principles calculation with particle swarm optimization algorithm. In these erbium-nitrogen compounds, the N-N bonds are stabilized as diatomic quasi-molecule N2, helical-like nitrogen chains, armchair nitrogen chains, and armchair-anti-armchair nitrogen chains, respectively. Among them, theP1--ErN6harbors excellent stability at high thermal up to 1000 K. More importantly, theP1--ErN6has outstanding explosive performance with high-energy-density of 1.30 kJ g-1, detonation velocity of 10.87 km s-1, and detonation pressure of 812.98 kbar, which shows its promising application prospect as high-energy-density materials.

Origin of Broadband Emission and Large Stokes Shift in Antimony Trisulfide.

The antimony trisulfide (Sb2S3) has been theoretically predicted to have various merits in exploiting high-performance thin-film solar cells and attracted intense attention. However, the power conversion efficiency of Sb2S3-based solar cells is yet to be satisfactory in experiments and the origin of large open circuit voltage (VOC) loss is still a controversial question. Based on first-principles calculations, we have systematically analyzed the excited state behavior and dynamics images of carriers in Sb2S3 materials. Our calculations showed that intrinsic defects like vacancy (VSb and VS) and antisites (SbS and SSb) are energetically accessible. More importantly, we found that the sulfide vacancy-bound excitons can produce a large Stokes shift of ∼0.66 eV, which could well rationalize the experimental observations like the reduction of VOC. These new findings suggest that the performance of Sb2S3-based solar cells might be largely enhanced by avoiding sulfide vacancy defects.

Predicted stable high-pressure phases of copper-nitrogen compounds.

The nitrogen-rich compounds are promising candidates for high-energy-density applications, owing to the large difference in the bonding energy between triple and single/double nitrogen bonds. The exploration of stable copper-nitrogen (Cu-N) compounds with high-energy-density has been challenging for a long time. Recently, through a combination of high temperatures and pressures, a new copper diazenide compound (P63/mmc-CuN2) has been synthesized (Binnset al2019J. Phys. Chem. Lett.101109-1114). But the pressure-composition phase diagram of Cu-N compounds at different temperatures is still highly unclear. Here, by combining first-principles calculations with crystal structure prediction method, the Cu-N compounds with different stoichiometric ratios were searched within the pressure range of 0-150 GPa. Four Cu-N compounds are predicted to be thermodynamically stable at high pressures,Pnnm-CuN2, two CuN3compounds with theP-1 space group (named as I-CuN3and II-CuN3) andP21/m-CuN5containing cyclo-N5-. Finite temperature effects (vibrational energies) play a key role in stabilizing experimentally synthesizedP63/mmc-CuN2at ∼55 GPa, compared to our predictedPnnm-CuN2. These new Cu-N compounds show great promise for potential applications as high-energy-density materials with the energy densities of 1.57-2.74 kJ g-1.

Bimetallic and postsynthetically alloyed PtCu nanostructures with tunable reactivity for the methanol oxidation reaction.

Designing effective catalysts by controlling morphology and structure is key to improving the energy efficiency of fuel cells. A good understanding of the effects of specific structures on electrocatalytic activity, selectivity, and stability is needed. Here, we propose a facile method to synthesize PtCu bimetallic nanostructures with controllable compositions by using Cu nanowires as a template and ascorbic acid as a reductant. A further annealing process provided the alloy PtCu with tunable crystal structures. The combination of distinct structures with tunable compositions in the form of PtCu nanowires provides plenty of information for better understanding the reaction mechanism during catalysis. HClO4 cyclic voltammetry (CV) tests confirmed that various phase transformations occurred in bimetallic and alloy samples, affecting morphology and unit cell structures. Under a bifunctional synergistic effect and the influence of the insertion of a second metal, the two series of structures show superior performance toward methanol electrooxidation. Typically, the post-product alloy A-Pt14Cu86 with a cubic structure (a = 3.702 Å) has better methanol oxidation reaction (MOR) catalysis performance. Density functional theory (DFT) calculations were performed to determine an optimal pathway using the Gibbs free energy and to verify the dependence of the electrocatalytic performance on the lattice structure via overpotential changes. Bimetallic PtCu has high CO tolerance, maintaining high stability. This work provides an approach for the systematic design of novel catalysts and the exploration of electrocatalytic mechanisms for fuel cells and other related applications.