SIMES Publications

Abstract

Solid-state Li−S batteries are attractive due to their high energy density and safety. However, it is unclear whether the concepts from liquid electrolytes are applicable in the solid state to improve battery performance. Here, we demonstrate that the nanoscale encapsulation concept based on Li₂S@TiS₂ core−shell particles, originally developed in liquid electrolytes, is effective in solid polymer electrolytes. Using in situ optical cell and sulfur Kedge X-ray absorption, we find that polysulfides form and are welltrapped inside individual particles by the nanoscale TiS₂ encapsulation. This TiS₂ encapsulation layer also functions to catalyze the oxidation reaction of Li₂S to sulfur, even in solid-state electrolytes, proven by both experiments and density functional theory calculations. A high cell-level specific energy of 427 W·h· kg⁻¹ is achieved by integrating the Li₂S@TiS₂ cathode with a poly(ethylene oxide)-based electrolyte and a lithium metal anode. This study points to the fruitful direction of borrowing concepts from liquid electrolytes into solid-state batteries.

Abstract

We propose an exotic scenario in which topological superconductivity can emerge by doping strongly interacting fermionic systems whose spin degrees of freedom form a bosonic symmetry protected topological (SPT) state. Specifically, we study a one-dimensional (1D) example where the spin degrees of freedom form a spin-1 Haldane phase. Before doping, the charge and spin degrees of freedom are both gapped. Upon doping, the charge channel becomes gapless and is described by a c =1 compactified bosonic conformal field theory (CFT), while the spin channel remains gapped and still form a bosonic SPT state. Interestingly, an instability toward p-wave topological superconductivity is induced, coexisting with the symmetry protected spin edge modes that are inherited from the Haldane phase. This scenario is confirmed by density-matrix renormalization group simulation of a concrete lattice model, where we find that topological superconductivity is robust against interactions. We further show that by stacking doped Haldane phases an exotic 2D anisotropic superconductor can be realized, where the boundaries transverse to the chain direction are either gapless or spontaneously symmetry broken due to the Lieb-Schultz-Mattis (LSM) anomaly.

Abstract

Practical applications of Li-S batteries are hindered by the dissolution/diffusion loss of sulfur-related active materials in cathode and dendrite growth in Li metal anode. Here we present an integrated sulfur cathode design on tortuosity and sulfur-binding affinity parameters for mitigating diffusion loss of sulfur-based active materials. The high sulfur-philicity property (from oxygen functional groups, 16% in concentration) in reduced graphene oxide (rGO) host favors bonding with sulfur species to mitigate their diffusion/dissolution loss, while the high tortuosity (13.24, from horizontal arrangement of rGO sheets) can localize the soluble active materials within the host rather than outward diffusion loss with subsequent uneven redeposition. With this integrated concept, we achieved ultrahigh cathode areal capacities of 21 mAh cm⁻² with 98.1% retention after 160 cycles, surpassing those electrodes with lower tortuosity and sulfur-philicity. In addition, same rGO host suppresses dendrite growth in Li anode, enabling 278% prolonged cycle life in the full cell.

Abstract

Microsized battery anodes such as silicon offer cost advantages over nanosized counterparts but suffer from poor cycling stability. Now, an electrolyte design is reported to enable a LiF-rich solid–electrolyte interphase that stabilizes microsized silicon over a reasonably long cycle life.

Abstract

Increasing battery energy density is greatly desired for applications such as portable electronics and transportation. However, many next-generation batteries are limited by electrolyte selection because high ionic conductivity and poor electrochemical stability are typically observed in most electrolytes. For example, ether-based electrolytes have high ionic conductivity but are oxidatively unstable above 4 V, which prevents the use of high-voltage cathodes that promise higher energy densities. In contrast, hydrofluoroethers (HFEs) have high oxidative stability but do not dissolve lithium salt. In this work, we synthesize a new class of fluorinated ether electrolytes that combine the oxidative stability of HFEs with the ionic conductivity of ethers in a single compound. We show that conductivities of up to 2.7 × 10^–4 S/cm (at 30 °C) can be obtained with oxidative stability up to 5.6 V. The compounds also show higher lithium transference numbers compared to typical ethers. Furthermore, we use nuclear magnetic resonance (NMR) and molecular dynamics (MD) to study their ionic transport behavior and ion solvation environment, respectively. Finally, we demonstrate that this new class of electrolytes can be used with a Ni-rich layered cathode (NMC 811) to obtain over 100 cycles at a C/5 rate. The design of new molecules with high ionic conductivity and high electrochemical stability is a novel approach for the rational design of next-generation batteries.

Abstract

Collective excitations contain rich information about photoinduced transient states in correlated systems. In a Mott insulator, charge degrees of freedom are frozen, but can be activated by photodoping. The energymomentum distribution of the charge excitation spectrum reflects the propagation of charge degrees of freedom and provides information about the interplay among various intertwined instabilities on the timescale set by the pump. To reveal charge excitations out of equilibrium, we simulate time-resolved x-ray absorption and resonant inelastic x-ray scattering using a Hubbard model. After pumping, the former resolves photodoping, while the latter characterizes the formation, dispersion, weight, and nonlinear effects of collective excitations. Intermediate-state information from time-resolved resonant inelastic x-ray scattering (trRIXS) can be used to decipher the origin of these excitations, including bimagnons, Mott-gap excitations, doublon and single-electron in-gap states, and anti-Stokes relaxation during an ultrafast pump. This paper provides a theoretical foundation for existing and future trRIXS experiments.

Abstract

Lithium (Li) metal is the ultimate anode material for Li batteries because of its highest capacity among all candidates. Recent research has focused on stable interphase and host materials to address its low stability and reversibility. Here, we discover that tortuosity is a critical parameter affecting the morphology and electrochemical performances of hosted Li anodes. In three types of hosts—vertically aligned, horizontally aligned, and random reduced graphene oxide (rGO) electrodes with tortuosities of 1.25, 4.46, and 1.76, respectively—we show that high electrode tortuosity causes locally higher current density on the top surface of electrodes, resulting in thick Li deposition on the surface and degraded cycling performance. Low electrode tortuosity in the vertically aligned rGO host enables homogeneous Li transport and uniform Li deposition across the host, realizing greatly improved cycling stability. Using this principle of low tortuosity, the designed electrode shows through-electrode uniform morphology with anodic Coulombic efficiency of ∼99.1% under high current and capacity cycling conditions.

Abstract

The spin-1/2 kagome antiferromagnet is considered an ideal host for a quantum spin liquid (QSL) ground state. We find that when the bonds of the kagome lattice are modulated with a periodic pattern, new quantum ground states emerge. Newly synthesized crystalline barlowite (Cu₄(OH)₆FBr) and Zn-substituted barlowite demonstrate the delicate interplay between singlet states and spin order on the spin-1/2 kagome lattice. Comprehensive structural measurements demonstrate that our new variant of barlowite maintains hexagonal symmetry at low temperatures with an arrangement of distorted and undistorted kagome triangles, for which numerical simulations predict a pinwheel valence bond crystal (VBC) state instead of a QSL. The presence of interlayer spins eventually leads to an interesting pinwheel q=0 magnetic order. Partially Zn-substituted barlowite (Cu_3.44Zn_0.56(OH)₆FBr) has an ideal kagome lattice and shows QSL behavior, indicating a surprising robustness of the QSL against interlayer impurities. The magnetic susceptibility is similar to that of herbertsmithite, even though the Cu²⁺ impurities are above the percolation threshold for the interlayer lattice and they couple more strongly to the nearest kagome moment. This system is a unique playground displaying QSL, VBC, and spin order, furthering our understanding of these highly competitive quantum states.

Abstract

Metallic lithium (Li) anodes are crucial for the development of high specific energy batteries yet are plagued by their poor cycling efficiency. Electrode architecture engineering is vital for maintaining a stable anode volume and suppressing Li corrosion during cycling. In this paper, a reduced graphene oxide “host” framework for Li metal anodes is further optimized by embedding silicon (Si) nanoparticles between the graphene layers. They serve as Li nucleation seeds to promote Li deposition within the framework even without prestored Li. Meanwhile, the Li_xSi alloy particles serve as supporting “pillars” between the graphene layers, enabling a minimized thickness shrinkage after full stripping of metallic Li. Combined with a Li compatible electrolyte, a 99.4% Coulombic efficiency over ∼600 cycles is achieved, and stable cycling of a Li||NMC532 full cell for ∼380 cycles with negligible capacity decay is realized.

Abstract

Nanoporous silicon is a promising anode material for high energy density batteries due to its high cycling stability and high tap density compared to other nanostructured anode materials. However, the high cost of synthesis and low yield of nanoporous silicon limit its practical application. Here, we develop a scalable, low-cost top-down process of controlled oxidation of Mg₂Si in the air, followed by HCl removal of MgO to generate nanoporous silicon without the use of HF. By controlling the synthesis conditions, the oxygen content, grain size and yield of the porous silicon are simultaneously optimized from commercial standpoints. In situ environmental transmission electron microscopy reveals the reaction mechanism; the Mg₂Si microparticle reacts with O₂ to form MgO and Si, while preventing SiO₂ formation. Owing to the low oxygen content and microscale secondary structure, the nanoporous silicon delivers a higher initial reversible capacity and initial Coulombic efficiency compared to commercial Si nanoparticles (3,033 mAh/g vs. 2,418 mAh/g, 84.3% vs. 73.1%). Synthesis is highly scalable, and a yield of 90.4% is achieved for the porous Si nanostructure with the capability to make an excess of 10 g per batch. Our synthetic nanoporous silicon is promising for practical applications in next generation lithium-ion batteries.