Kern Ho Park

Solution-Processable Glass LiI-Li4SnS4 Superionic Conductors for All-Solid-State Li-Ion Batteries

A new, highly conductive (4.1 × 10(-4) S cm(-1) at 30 °C), highly deformable, and dry-air-stable glass 0.4LiI-0.6Li4 SnS4 is prepared using a homogeneous methanol solution. The solution process enables the wetting of any exposed surface of the active materials with highly conductive solidified electrolytes (0.4LiI-0.6Li4 SnS4), resulting in considerable improvements in the electrochemical performance of these electrodes over conventional mixture electrodes.

Na3SbS4: A Solution Processable Sodium Superionic Conductor for All‐Solid‐State Sodium‐Ion Batteries

All-solid-state sodium-ion batteries that operate at room temperature are attractive candidates for use in large-scale energy storage systems. However, materials innovation in solid electrolytes is imperative to fulfill multiple requirements, including high conductivity, functional synthesis protocols for achieving intimate ionic contact with active materials, and air stability. A new, highly conductive (1.1 mS cm(-1) at 25 °C, Ea =0.20 eV) and dry air stable sodium superionic conductor, tetragonal Na3 SbS4 , is described. Importantly, Na3 SbS4 can be prepared by scalable solution processes using methanol or water, and it exhibits high conductivities of 0.1-0.3 mS cm(-1) . The solution-processed, highly conductive solidified Na3 SbS4 electrolyte coated on an active material (NaCrO2 ) demonstrates dramatically improved electrochemical performance in all-solid-state batteries.

Infiltration of Solution-Processable Solid Electrolytes into Conventional Li-Ion-Battery Electrodes for All-Solid-State Li-Ion Batteries

Bulk-type all-solid-state lithium-ion batteries (ASLBs) have the potential to be superior to conventional lithium-ion batteries (LIBs) in terms of safety and energy density. Sulfide SE materials are key to the development of bulk-type ASLBs because of their high ionic conductivity (max of ∼10-2 S cm-1) and deformability. However, the severe reactivity of sulfide materials toward common polar solvents and the particulate nature of these electrolytes pose serious complications for the wet-slurry process used to fabricate ASLB electrodes, such as the availability of solvent and polymeric binders and the formation of ionic contacts and networks. In this work, we report a new scalable fabrication protocol for ASLB electrodes using conventional composite LIB electrodes and homogeneous SE solutions (Li6PS5Cl (LPSCl) in ethanol or 0.4LiI-0.6Li4SnS4 in methanol). The liquefied LPSCl is infiltrated into the tortuous porous structures of LIB electrodes and solidified, providing intimate ionic contacts and favorable ionic percolation. The LPSCl-infiltrated LiCoO2 and graphite electrodes show high reversible capacities (141 and 364 mA h g-1) at 0.14 mA cm-2 (0.1 C) and 30 °C, which are not only superior to those for conventional dry-mixed and slurry-mixed ASLB electrodes but also comparable to those for liquid electrolyte cells. Good electrochemical performance of ASLBs employing the LPSCl-infiltrated LiCoO2 and graphite electrodes at 100 °C is also presented, highlighting the excellent thermal stability and safety of ASLBs.

Coatable Li4SnS4 solid electrolytes prepared from aqueous solutions for all-solid-state lithium-ion batteries

Bulk-type all-solid-state lithium-ion batteries (ASLBs) for large-scale energy-storage applications have emerged as a promising alternative to conventional lithium-ion batteries (LIBs) owing to their superior safety. However, the electrochemical performance of bulk-type ASLBs is critically limited by the low ionic conductivity of solid electrolytes (SEs) and poor ionic contact between the active materials and SEs. Herein, highly conductive (0.14 mS cm-1 ) and dry-air-stable SEs (Li4 SnS4 ) are reported, which are prepared using a scalable aqueous-solution process. An active material (LiCoO2 ) coated by solidified Li4 SnS4 from aqueous solutions results in a significant improvement in the electrochemical performance of ASLBs. Side-effects of the exposure of LiCoO2 to aqueous solutions are minimized by using predissolved Li4 SnS4 solution.

Aqueous-solution synthesis of Na3SbS4 solid electrolytes for all-solid-state Na-ion batteries

Room-temperature-operable all-solid-state Na-ion batteries (ASNBs) using sulfide Na-ion solid electrolytes (SEs) are promising because of their potential for greater safety, lower cost, and acceptable performance. Despite extensive developments in the area of sulfide Na-ion SEs, their poor chemical stability and prospects for wet-chemical synthesis have been overlooked to date. Herein, the scalable synthesis of Na3SbS4via aqueous-solution routes using precursors of Na2S, Sb2S3, and elemental sulfur for ASNBs is described. With no concerns about the evolution of toxic H2S gas, the aqueous-solution-synthesized Na3SbS4 exhibits high ionic conductivities (0.1–0.2 mS cm−1 at 25 °C). Importantly, the homogeneity of the aqueous solutions enables the creation of uniform Na3SbS4 coatings on FeS2. Fe2S/Na–Sn ASNBs, employing the aqueous-solution-synthesized Na3SbS4 and the Na3SbS4-coated FeS2 for the SE layer and positive electrode, respectively, demonstrate a high charge capacity of 256 or 346 mA h g−1 with good reversibility at 30 °C, highlighting their potential for practical applications.

Diagnosis of failure modes for all-solid-state Li-ion batteries enabled by three-electrode cells

Bulk-type all-solid-state Li-ion batteries have emerged as the enabler to achieve better safety and to use Li metal negative electrodes for higher energy density. However, all-solid-state half-cells fabricated using In or Li–In counter electrodes (CEs) have been routinely tested to assess working electrodes (WEs) without any verification. Moreover, there have been few reports on the in-depth analysis of all-solid-state full-cells, which is imperative for practical applications. In this work, for the first time, we report novel bulk-type all-solid-state three-electrode cells that enable successful deconvolution and diagnosis of the voltages of positive and negative electrodes even for cells having thin solid electrolyte (SE) layers. In the first case study, that of Sn/Li–In half-cells, earlier termination of Li–In CEs than Sn WEs, which results in unexpectedly low capacity, is measured. This problem is solved by percolating Li–In with SEs. For the second case, namely, that of LiNi0.6Co0.2Mn0.2O2/graphite full-cells having only 50–60 μm-thick SE layers (which are fabricated by a scalable wet-slurry process), internal short circuits by penetrating growth of Li metal during charging at high C-rates are revealed for the first time. Further, a unique dischargeability to 0 V for LiNi0.6Co0.2Mn0.2O2/graphite or LiNi0.6Co0.2Mn0.2O2/Si–C full-cells is described.

Solution-derived glass-ceramic NaI·Na3SbS4 superionic conductors for all-solid-state Na-ion batteries

Bulk-type all-solid-state Na-ion batteries (ASNBs) employing inorganic Na-ion conductors and operating at room temperature are considered as promising candidates for large-scale energy storage systems. However, their realization has been impeded by low ionic conductivity, instability in air of the solid electrolytes, and poor ionic contacts among the constituents of the electrodes. Here, we report novel glass-ceramic xNaI·(1 − x)Na3SbS4 superionic conductors (maximum Na+ conductivity of 0.74 mS cm−1 at 30 °C, for x = 0.10) obtained from scalable methanol solutions. Comprehensive spectroscopic evidence, density functional theory calculations, and electrochemical analysis suggest the decisive role of I− incorporated in the disordered domains at the nanoscale in the overall Na+ transport. Furthermore, the solution-derived NaI·Na3SbS4 forms uniform coating layers on the surface of the active material FeS2, providing unobstructed ionic transport pathways in the electrodes. The good electrochemical performance of FeS2/Na–Sn ASNBs at 30 °C is demonstrated.

Coordination Polymers for High-Capacity Li-Ion Batteries: Metal-Dependent Solid-State Reversibility

Electrode materials exploiting multielectron-transfer processes are essential components for large-scale energy storage systems. Organic-based electrode materials undergoing distinct molecular redox transformations can intrinsically circumvent the structural instability issue of conventional inorganic-based host materials associated with lattice volume expansion and pulverization. Yet, the fundamental mechanistic understanding of metal-organic coordination polymers toward the reversible electrochemical processes is still lacking. Herein, we demonstrate that metal-dependent spatial proximity and binding affinity play a critical role in the reversible redox processes, as verified by combined 13C solid-state NMR, X-ray absorption spectroscopy, and transmission electron microscopy. During the electrochemical lithiation, in situ generated metallic nanoparticles dispersed in the organic matrix generate electrically conductive paths, synergistically aiding subsequent multielectron transfer to π-conjugated ligands. Comprehensive screening on 3d-metal-organic coordination polymers leads to a high-capacity electrode material, cobalt-2,5-thiophenedicarboxylate, which delivers a stable specific capacity of ∼1100 mA h g-1 after 100 cycles.