Xian is now a postdoc researcher in the Group of Jian Qin, Department of Chemical Engineering. His research is focused on the theoretical and simulation studies of polymer in applications of battery.
Bachelor of Engineering, Tsinghua University (2010)
Doctor of Philosophy, Tsinghua University (2016)
Potentiometric Measurement to Probe Solvation Energy and Its Correlation to Lithium Battery Cyclability.
Journal of the American Chemical Society
The electrolyte plays a critical role in lithium-ion batteries, as it impacts almost every facet of a battery's performance. However, our understanding of the electrolyte, especially solvation of Li+, lags behind its significance. In this work, we introduce a potentiometric technique to probe the relative solvation energy of Li+ in battery electrolytes. By measuring open circuit potential in a cell with symmetric electrodes and asymmetric electrolytes, we quantitatively characterize the effects of concentration, anions, and solvents on solvation energy across varied electrolytes. Using the technique, we establish a correlation between cell potential (Ecell) and cyclability of high-performance electrolytes for lithium metal anodes, where we find that solvents with more negative cell potentials and positive solvation energies-those weakly binding to Li+-lead to improved cycling stability. Cryogenic electron microscopy reveals that weaker solvation leads to an anion-derived solid-electrolyte interphase that stabilizes cycling. Using the potentiometric measurement for characterizing electrolytes, we establish a correlation that can guide the engineering of effective electrolytes for the lithium metal anode.
View details for DOI 10.1021/jacs.1c03868
View details for PubMedID 34184873
- Weakening of Solvation-Induced Ordering by Composition Fluctuation in Salt-Doped Block Polymers ACS MACRO LETTERS 2021; 10 (5): 545-550
Dual-Solvent Li-Ion Solvation Enables High-Performance Li-Metal Batteries
Novel electrolyte designs to further enhance the lithium (Li) metal battery cyclability are highly desirable. Here, fluorinated 1,6-dimethoxyhexane (FDMH) is designed and synthesized as the solvent molecule to promote electrolyte stability with its prolonged -CF2 - backbone. Meanwhile, 1,2-dimethoxyethane is used as a co-solvent to enable higher ionic conductivity and much reduced interfacial resistance. Combining the dual-solvent system with 1 m lithium bis(fluorosulfonyl)imide (LiFSI), high Li-metal Coulombic efficiency (99.5%) and oxidative stability (6 V) are achieved. Using this electrolyte, 20 µm Li||NMC batteries are able to retain ≈80% capacity after 250 cycles and Cu||NMC anode-free pouch cells last 120 cycles with 75% capacity retention under ≈2.1 µL mAh-1 lean electrolyte conditions. Such high performances are attributed to the anion-derived solid-electrolyte interphase, originating from the coordination of Li-ions to the highly stable FDMH and multiple anions in their solvation environments. This work demonstrates a new electrolyte design strategy that enables high-performance Li-metal batteries with multisolvent Li-ion solvation with rationally optimized molecular structure and ratio.
View details for DOI 10.1002/adma.202008619
View details for Web of Science ID 000648495100001
View details for PubMedID 33969571
Physical networks from entropy-driven non-covalent interactions.
2021; 12 (1): 746
Physical networks typically employ enthalpy-dominated crosslinking interactions that become more dynamic at elevated temperatures, leading to network softening. Moreover, standard mathematical frameworks such as time-temperature superposition assume network softening and faster dynamics at elevated temperatures. Yet, deriving a mathematical framework connecting the crosslinking thermodynamics to the temperature-dependent viscoelasticity of physical networks suggests the possibility for entropy-driven crosslinking interactions to provide alternative temperature dependencies. This framework illustrates that temperature negligibly affects crosslink density in reported systems, but drastically influences crosslink dynamics. While the dissociation rate of enthalpy-driven crosslinks is accelerated at elevated temperatures, the dissociation rate of entropy-driven crosslinks is negligibly affected or even slowed under these conditions. Here we report an entropy-driven physical network based on polymer-nanoparticle interactions that exhibits mechanical properties that are invariant with temperature. These studies provide a foundation for designing and characterizing entropy-driven physical crosslinking motifs and demonstrate how these physical networks access thermal properties that are not observed in current physical networks.
View details for DOI 10.1038/s41467-021-21024-7
View details for PubMedID 33531475
- Molecular design for electrolyte solvents enabling energy-dense and long-cycling lithium metal batteries NATURE ENERGY 2020
A New Class of Ionically Conducting Fluorinated Ether Electrolytes with High Electrochemical Stability.
Journal of the American Chemical Society
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.
View details for DOI 10.1021/jacs.9b11056
View details for PubMedID 32233433
- Dendrite Suppression by a Polymer Coating: A Coarse-Grained Molecular Study ADVANCED FUNCTIONAL MATERIALS 2020
Electrochemical generation of liquid and solid sulfur on two-dimensional layered materials with distinct areal capacities.
It has recently been shown that sulfur, a solid material in its elementary form S8, can stay in a supercooled state as liquid sulfur in an electrochemical cell. We establish that this newly discovered state could have implications for lithium-sulfur batteries. Here, through in situ studies of electrochemical sulfur generation, we show that liquid (supercooled) and solid elementary sulfur possess very different areal capacities over the same charging period. To control the physical state of sulfur, we studied its growth on two-dimensional layered materials. We found that on the basal plane, only liquid sulfur accumulates; by contrast, at the edge sites, liquid sulfur accumulates if the thickness of the two-dimensional material is small, whereas solid sulfur nucleates if the thickness is large (tens of nanometres). Correlating the sulfur states with their respective areal capacities, as well as controlling the growth of sulfur on two-dimensional materials, could provide insights for the design of future lithium-sulfur batteries.
View details for DOI 10.1038/s41565-019-0624-6
View details for PubMedID 31988508
Transient Voltammetry with Ultramicroelectrodes Reveals the Electron Transfer Kinetics of Lithium Metal Anodes
Adv. Energy Lett.
2020; 5: 701-709
View details for DOI 10.1021/acsenergylett.0c00031
'Chromatic' neuronal jamming in a primitive brain
View details for DOI 10.1038/s41567-020-0809-9
Electrochemical generation of liquid and solid sulfur on two-dimensional layered materials with distinct areal capacities
View details for DOI 10.1038/s41565-019-0624-6
- Nonpolar Alkanes Modify Lithium-Ion Solvation for Improved Lithium Deposition and Stripping ADVANCED ENERGY MATERIALS 2019
- Geometric structure-guided photo-driven ion current through asymmetric graphene oxide membranes JOURNAL OF MATERIALS CHEMISTRY A 2019; 7 (35): 20182–86
- An Atomistic Simulation Study on POC/PIM Mixed-Matrix Membranes for Gas Separation JOURNAL OF PHYSICAL CHEMISTRY C 2019; 123 (24): 15113–21
Ultrathin, flexible, solid polymer composite electrolyte enabled with aligned nanoporous host for lithium batteries.
The urgent need for safer batteries is leading research to all-solid-state lithium-based cells. To achieve energy density comparable to liquid electrolyte-based cells, ultrathin and lightweight solid electrolytes with high ionic conductivity are desired. However, solid electrolytes with comparable thicknesses to commercial polymer electrolyte separators (~10mum) used in liquid electrolytes remain challenging to make because of the increased risk of short-circuiting the battery. Here, we report on a polymer-polymer solid-state electrolyte design, demonstrated with an 8.6-mum-thick nanoporous polyimide (PI) film filled with polyethylene oxide/lithium bis(trifluoromethanesulfonyl)imide (PEO/LiTFSI) that can be used as a safe solid polymer electrolyte. The PI film is nonflammable and mechanically strong, preventing batteries from short-circuiting even after more than 1,000h of cycling, and the vertical channels enhance the ionic conductivity (2.3*10-4Scm-1 at 30°C) of the infused polymer electrolyte. All-solid-state lithium-ion batteries fabricated with PI/PEO/LiTFSI solid electrolyte show good cycling performance (200 cycles at C/2 rate) at 60°C and withstand abuse tests such as bending, cutting and nail penetration.
View details for DOI 10.1038/s41565-019-0465-3
View details for PubMedID 31133663
Flow effects on silicate dissolution and ion transport at an aqueous interface.
Physical chemistry chemical physics : PCCP
Flow effects on chemical reactions at a solid-liquid interface are fundamental to diverse technological applications but remain poorly understood from a molecular perspective. In this work, we demonstrate that the coupling between laminar flow and surface chemistry can be adequately described using classical density functional theory for ion distributions near the surface in conjunction with kinetics modeling and the Navier-Stokes equation. In good agreement with recent experiments, we find that flowing of fresh water over a silica surface may result in drastic changes in the rate of silica dissolution and, consequently, the surface charge density and the interfacial structure. A nonlinear streaming current is predicted when the surface reactions are disturbed by a laminar flow.
View details for DOI 10.1039/c9cp00640k
View details for PubMedID 30869104
Light-Powered Directional Nanofluidic Ion Transport in Kirigami-Made Asymmetric Photonic-Ionic Devices.
Small (Weinheim an der Bergstrasse, Germany)
Nacre-mimetic 2D nanofluidic materials with densely packed sub-nanometer-height lamellar channels find widespread applications in water-, energy-, and environment-related aspects by virtue of their scalable fabrication methods and exceptional transport properties. Recently, light-powered nanofluidic ion transport in synthetic materials gained considerable attention for its remote, noninvasive, and active control of the membrane transport property using the energy of light. Toward practical application, a critical challenge is to overcome the dependence on inhomogeneous or site-specific light illumination. Here, asymmetric photonic-ionic devices based on kirigami-tailored graphene oxide paper are fabricated, and directional nanofluidic ion transport properties therein powered by full-area light illumination are demonstrated. The in-plane asymmetry of the graphene oxide paper is essential to the generation of photoelectric driving force under homogeneous illumination. This light-powered ion transport phenomenon is explained based on a modified carrier diffusion model. In asymmetric nanofluidic structures, enhanced recombination of photoexcited charge carriers at the membrane boundary breaks the electric potential balance in the horizontal direction, and thus drives the ion transport in that direction under symmetric illumination. The kirigami-based strategy provides a facile and scalable way to fabricate paper-like photonic-ionic devices with arbitrary shapes, working as fundamental elements for large-scale light-harvesting nanofluidic circuits.
View details for DOI 10.1002/smll.201905557
View details for PubMedID 31805218