Yi Cui

Bio: Yi Cui is an academic researcher from Stanford University. The author has contributed to research in topics: Anode & Lithium. The author has an hindex of 220, co-authored 1015 publications receiving 199725 citations. Previous affiliations of Yi Cui include KAIST & University of California, Berkeley.

Uniform High Ionic Conducting Lithium Sulfide Protection Layer for Stable Lithium Metal Anode

Abstract: DOI: 10.1002/aenm.201900858 dendrites,[6] guided lithium plating,[7] and nanostructured electrode design.[8] Among all the methods, the focus on solidelectrolyte interphase (SEI) between anode materials and electrolyte is one of the most critical issues. During LMB operation, the SEI that primarily originated from electrolyte decomposition, is easily cracked. This will locally enhance ion flux and promote nonuniform lithium depositing/stripping,[9] resulting in Li dendrites that can trigger internal short circuit and compromise battery safety. Repeated breakdown and repair of SEI during cycling create a vicious cycle which alternates between “uneven stripping/plating and SEI fracture,” brings about continuous loss of active materials and limited battery cycle life. Therefore, an ideal SEI should continuously passivate the anode and prevent the parasitic reactions between reactive anode and electrolyte to address the aforementioned problems in principle.[3] Previous studies have demonstrated several effective artificial SEI to protect lithium metal anode such as polymer,[10] inorganic conductive compounds,[11,12] electrolyte additives,[13,14] and carbonbased materials.[7,15] However, the evolution of SEI during cycling and key mechanisms such as impact of SEI quality on its stability need to be further explored.[16] Herein, we demonstrate a “simultaneous homogeneous and high ionic conductivity” strategy by developing a method of forming a uniform lithium sulfide (Li2S) protective layer for suppressing dendrite growth and stabilizing the lithium metal anode. Although Li2S interfacial layers through soluble electrolyte additives have been studied before,[14,17–20] the work here demonstrates that the elevated temperature (170 °C) and gas phase reaction are critical for the synthesis of a homogenous Li2S coating, which importantly can be used as SEI in carbonate electrolyte system. We reveal the evolution of thus formed Li2S artificial SEI component distribution during battery operation: the uniform and high ionic conductivity protective layer turns into a layered SEI that preserves protective function, rather than into a disordered, broken SEI mainly made up of parasitic reaction products. Simulation results also confirm the critical importance of compositional homogeneity and high ionic conductivity in stabilizing SEI. With this strategy, stable cycles in both high capacity symmetric cells and Li–LiFePO4 full cells were realized. We believe that this practical fabrication method, fundamental design strategy, and understanding on Artificial solid-electrolyte interphase (SEI) is one of the key approaches in addressing the low reversibility and dendritic growth problems of lithium metal anode, yet its current effect is still insufficient due to insufficient stability. Here, a new principle of “simultaneous high ionic conductivity and homogeneity” is proposed for stabilizing SEI and lithium metal anodes. Fabricated by a facile, environmentally friendly, and low-cost lithium solidsulfur vapor reaction at elevated temperature, a designed lithium sulfide protective layer successfully maintains its protection function during cycling, which is confirmed by both simulations and experiments. Stable dendritefree cycling of lithium metal anode is realized even at a high areal capacity of 5 mAh cm−2, and prototype Li–Li4Ti5O12 cell with limited lithium also achieves 900 stable cycles. These findings give new insight into the ideal SEI composition and structure and provide new design strategies for stable lithium metal batteries.

Efficient electrocatalytic CO 2 reduction on a three-phase interface

Abstract: Electrochemical CO2 reduction is a critical approach to reducing the globally accelerating CO2 emission and generating value-added products. Despite great efforts to optimize catalyst activity and selectivity, facilitating the catalyst accessibility to high CO2 concentrations while maintaining electrode durability remains a significant challenge. Here, we designed a catalytic system that mimics the alveolus structure in mammalian lungs with high gas permeability but very low water diffusibility, enabling an array of three-phase catalytic interfaces. Flexible, hydrophobic, nanoporous polyethylene membranes with high gas permeability were used to enable efficient CO2 access and a high local alkalinity on the catalyst surface at different CO2 flow rates. Such an alveolus-mimicking structure generates a high CO production Faradaic efficiency of 92% and excellent geometric current densities of CO production (25.5 mA cm−2) at −0.6 V versus the reversible hydrogen electrode, with a very thin catalyst thickness of 20−80 nm. The efficient design of electrochemical CO2 reduction catalysts requires high CO2 concentrations on the catalyst surface. Here, Cui and co-workers make use of flexible, hydrophobic, nanoporous polyethylene membranes with good gas permeability to design a catalytic set-up that mimics the alveolus structure in mammalian lungs, achieving high activity and selectivity to CO.

Batteries for efficient energy extraction from a salinity difference

Abstract: An electrochemical system includes: (1) a battery including an anode and a cathode; (2) a first source of a first electrolyte having a first concentration of ions; (3) a second source of a second electrolyte having a second concentration of the ions, wherein the second concentration is greater than the first concentration; and (4) a fluid conveyance mechanism connected between the battery and each of the first source and the second source. During charging of the battery, the anode and the cathode are at least partially immersed in the first electrolyte, and, during discharging of the battery, the anode and the cathode are at least partially immersed in the second electrolyte. The fluid conveyance mechanism exchanges the first electrolyte with the second electrolyte between charging and discharging of the battery, and exchanges the second electrolyte with the first electrolyte between discharging and charging of the battery.

Improving the cycling stability of silicon nanowire anodes with conducting polymer coatings

Abstract: For silicon nanowires (Si NWs) to be used as a successful high capacity lithium-ion battery anode material, improvements in cycling stability are required. Here we show that a conductive polymer surface coating on the Si NWs improves cycling stability; coating with PEDOT causes the capacity retention after 100 charge–discharge cycles to increase from 30% to 80% over bare NWs. The improvement in cycling stability is attributed to the conductive coating maintaining the mechanical integrity of the cycled Si material, along with preserving electrical connections between NWs that would otherwise have become electrically isolated during volume changes.

Improved Lithium Ionic Conductivity in Composite Polymer Electrolytes with Oxide-Ion Conducting Nanowires

Abstract: Solid Li-ion electrolytes used in all-solid-state lithium-ion batteries (LIBs) are being considered to replace conventional liquid electrolytes that have leakage, flammability, and poor chemical stability issues, which represents one major challenge and opportunity for next-generation high-energy-density batteries. However, the low mobility of lithium ions in solid electrolytes limits their practical applications. Here, we report a solid composite polymer electrolyte with Y2O3-doped ZrO2 (YSZ) nanowires that are enriched with positive-charged oxygen vacancies. The morphologies and ionic conductivities have been studied systemically according to concentration of Y2O3 dopant in the nanowires. In comparison to the conventional filler-free electrolyte with a conductivity of 3.62 × 10–7 S cm–1, the composite polymer electrolytes with the YSZ nanowires show much higher ionic conductivity. It indicates that incorporation of 7 mol % of Y2O3-doped ZrO2 nanowires results in the highest ionic conductivity of 1.07 × ...

I and i

Abstract: There is, I think, something ethereal about i —the square root of minus one. I remember first hearing about it at school. It seemed an odd beast at that time—an intruder hovering on the edge of reality. Usually familiarity dulls this sense of the bizarre, but in the case of i it was the reverse: over the years the sense of its surreal nature intensified. It seemed that it was impossible to write mathematics that described the real world in …

Fast parallel algorithms for short-range molecular dynamics

Abstract: Three parallel algorithms for classical molecular dynamics are presented. The first assigns each processor a fixed subset of atoms; the second assigns each a fixed subset of inter-atomic forces to compute; the third assigns each a fixed spatial region. The algorithms are suitable for molecular dynamics models which can be difficult to parallelize efficiently—those with short-range forces where the neighbors of each atom change rapidly. They can be implemented on any distributed-memory parallel machine which allows for message-passing of data between independently executing processors. The algorithms are tested on a standard Lennard-Jones benchmark problem for system sizes ranging from 500 to 100,000,000 atoms on several parallel supercomputers--the nCUBE 2, Intel iPSC/860 and Paragon, and Cray T3D. Comparing the results to the fastest reported vectorized Cray Y-MP and C90 algorithm shows that the current generation of parallel machines is competitive with conventional vector supercomputers even for small problems. For large problems, the spatial algorithm achieves parallel efficiencies of 90% and a 1840-node Intel Paragon performs up to 165 faster than a single Cray C9O processor. Trade-offs between the three algorithms and guidelines for adapting them to more complex molecular dynamics simulations are also discussed.

疟原虫var基因转换速率变化导致抗原变异[英]／Paul H, Robert P, Christodoulou Z, et al//Proc Natl Acad Sci U S A

Abstract: 抗原变异可使得多种致病微生物易于逃避宿主免疫应答。表达在感染红细胞表面的恶性疟原虫红细胞表面蛋白1（PfPMP1）与感染红细胞、内皮细胞、树突状细胞以及胎盘的单个或多个受体作用，在黏附及免疫逃避中起关键的作用。每个单倍体基因组var基因家族编码约60种成员，通过启动转录不同的var基因变异体为抗原变异提供了分子基础。