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Author

Yi Cui

Other affiliations: KAIST, University of California, Berkeley, Harvard University  ...read more
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.


Papers
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TL;DR: In this article, a rechargeable manganese-hydrogen battery was proposed, where the cathode is cycled between soluble Mn2+ and solid MnO2 with a two-electron reaction.
Abstract: Batteries including lithium-ion, lead–acid, redox-flow and liquid-metal batteries show promise for grid-scale storage, but they are still far from meeting the grid's storage needs such as low cost, long cycle life, reliable safety and reasonable energy density for cost and footprint reduction. Here, we report a rechargeable manganese–hydrogen battery, where the cathode is cycled between soluble Mn2+ and solid MnO2 with a two-electron reaction, and the anode is cycled between H2 gas and H2O through well-known catalytic reactions of hydrogen evolution and oxidation. This battery chemistry exhibits a discharge voltage of ~1.3 V, a rate capability of 100 mA cm−2 (36 s of discharge) and a lifetime of more than 10,000 cycles without decay. We achieve a gravimetric energy density of ~139 Wh kg−1 (volumetric energy density of ~210 Wh l−1), with the theoretical gravimetric energy density of ~174 Wh kg−1 (volumetric energy density of ~263 Wh l−1) in a 4 M MnSO4 electrolyte. The manganese–hydrogen battery involves low-cost abundant materials and has the potential to be scaled up for large-scale energy storage.

269 citations

Journal ArticleDOI
TL;DR: Li2S is an attractive prelithiated cathode material with a high theoretical capacity of 1166 mA h g−1, which is far above that of its transition metal oxide/phosphate counterparts.
Abstract: Li2S is an attractive prelithiated cathode material with a high theoretical capacity of 1166 mA h g−1, which is far above that of its transition metal oxide/phosphate counterparts. Here, we demonstrate facile, in situ synthesis of Li2S–polypyrrole composites for use as high-performance Li2S cathodes. The N atoms in polypyrrole were found to possess favorable Li–N interaction with Li2S, which enables polypyrrole to bind strongly onto and cover the surface of Li2S to constrain intermediate polysulfides during cycling. Polypyrrole, being a conducting polymer, also helps to facilitate electronic conduction. Using the Li2S–polypyrrole composites as a cathode material, we demonstrate a high discharge capacity of 785 mA h g−1 of Li2S (∼1126 mA h g−1 of S) with stable cycling over prolonged 400 charge/discharge cycles.

267 citations

Journal ArticleDOI
15 Apr 2020-Joule
TL;DR: In this paper, the authors reviewed recent progress on advanced textiles for personal thermal management and its significance in energy efficiency, and discussed textiles with engineered properties targeting at passively controlling human body heat dissipation routes, the active warming and/or cooling textiles, and the responsive textiles that offer adaptive personal temperature management ability according to the external stimuli.

264 citations

Journal ArticleDOI
TL;DR: A Li-ion conductive framework was developed as a stable “host” and efficient surface protection to address the multifaceted problems, which is a significant step forward compared with previous host concepts and sheds light on the effectiveness of the design principle for developing safe and stable Li metal anodes.
Abstract: Rechargeable batteries based on lithium (Li) metal chemistry are attractive for next-generation electrochemical energy storage. Nevertheless, excessive dendrite growth, infinite relative dimension change, severe side reactions, and limited power output severely impede their practical applications. Although exciting progress has been made to solve parts of the above issues, a versatile solution is still absent. Here, a Li-ion conductive framework was developed as a stable “host” and efficient surface protection to address the multifaceted problems, which is a significant step forward compared with previous host concepts. This was fulfilled by reacting overstoichiometry of Li with SiO. The as-formed LixSi–Li2O matrix would not only enable constant electrode-level volume, but also protect the embedded Li from direct exposure to electrolyte. Because uniform Li nucleation and deposition can be fulfilled owing to the high-density active Li domains, the as-obtained nanocomposite electrode exhibits low polarization, stable cycling, and high-power output (up to 10 mA/cm2) even in carbonate electrolytes. The Li–S prototype cells further exhibited highly improved capacity retention under high-power operation (∼600 mAh/g at 6.69 mA/cm2). The all-around improvement on electrochemical performance sheds light on the effectiveness of the design principle for developing safe and stable Li metal anodes.

263 citations

Journal ArticleDOI
TL;DR: The resulting semitransparent phthalocyanine/fullerene organic solar cell has a power conversion efficiency that is 57% of that of a device with a conventional metal cathode due to differences in optical absorption.
Abstract: We demonstrate semitransparent small molecular weight organic photovoltaic cells using a laminated silver nanowire mesh as a transparent, conductive cathode layer. The lamination process does not damage the underlying solar cell and results in a transparent electrode with low sheet resistance and high optical transmittance without impacting photocurrent collection. The resulting semitransparent phthalocyanine/fullerene organic solar cell has a power conversion efficiency that is 57% of that of a device with a conventional metal cathode due to differences in optical absorption.

263 citations


Cited by
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08 Dec 2001-BMJ
TL;DR: There is, I think, something ethereal about i —the square root of minus one, which seems an odd beast at that time—an intruder hovering on the edge of reality.
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 …

33,785 citations

01 May 1993
TL;DR: 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.
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.

29,323 citations

28 Jul 2005
TL;DR: PfPMP1)与感染红细胞、树突状组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�ly.
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。

18,940 citations