Michael Grätzel

Bio: Michael Grätzel is an academic researcher from École Polytechnique Fédérale de Lausanne. The author has contributed to research in topics: Dye-sensitized solar cell & Perovskite (structure). The author has an hindex of 248, co-authored 1423 publications receiving 303599 citations. Previous affiliations of Michael Grätzel include University of California, Berkeley & Siemens Energy Sector.

Hydrothermally processed CuCrO2 nanoparticles as an inorganic hole transporting material for low-cost perovskite solar cells with superior stability

Abstract: Despite the impressive photovoltaic performances of perovskite solar cells (PSCs) with a power conversion efficiency (PCE) beyond 22%, intensive studies are still required to overcome ongoing issues such as cost, stability, and hysteresis. Here, for the first time, we report a cesium-containing triple-cation mixed-halide perovskite solar cell (n–i–p structure) by using hydrothermally synthesized inorganic CuCrO2 (CCO) delafossite nanoparticles as a hole transporting material (HTM). After optimization of the concentration, a fully homogeneous and completely covered CCO layer that facilitates fast carrier extraction and collection was obtained on the surface of the perovskite. Our CCO-based cells achieved the best PCE of 16.7% (average 16.04 ± 0.40) with negligible hysteresis. More importantly, it was found that our cells showed a significant improvement in stability in ambient air compared with Spiro-OMeTAD HTM-based cells. After 60 days of storage in air without encapsulation, PCE remained at ∼83% of the initial value with the CCO-based cells, whereas it decreased to ∼24% of the initial value with devices based on the Spiro-OMeTAD HTM. Furthermore, cost estimation results indicated that the current prospect of CCO has an affordable cost/device ratio (∼180-fold cheaper than Spiro-OMeTAD). This work not only reveals the importance of air-stable inorganic HTMs, but also provides a low-cost HTM for highly efficient and stable PSCs.

Globularity-Selected Large Molecules for a New Generation of Multication Perovskites.

Abstract: Perovskite solar cells (PSCs) use perovskites with an APbX3 structure, where A is a monovalent cation and X is a halide such as Cl, Br, and/or I. Currently, the cations for high-efficiency PSCs are Rb, Cs, methylammonium (MA), and/or formamidinium (FA). Molecules larger than FA, such as ethylammonium (EA), guanidinium (GA), and imidazolium (IA), are usually incompatible with photoactive "black"-phase perovskites. Here, novel molecular descriptors for larger molecular cations are introduced using a "globularity factor", i.e., the discrepancy of the molecular shape and an ideal sphere. These cationic radii differ significantly from previous reports, showing that especially ethylammonium (EA) is only slightly larger than FA. This makes EA a suitable candidate for multication 3D perovskites that have potential for unexpected and beneficial properties (suppressing halide segregation, stability). This approach is tested experimentally showing that surprisingly large quantities of EA get incorporated, in contrast to most previous reports where only small quantities of larger molecular cations can be tolerated as "additives". MA/EA perovskites are characterized experimentally with a band gap ranging from 1.59 to 2.78 eV, demonstrating some of the most blue-shifted PSCs reported to date. Furthermore, one of the compositions, MA0.5 EA0.5 PbBr3 , shows an open circuit voltage of 1.58 V, which is the highest to date with a conventional PSC architecture.

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.

A low-cost, high-efficiency solar cell based on dye-sensitized colloidal TiO2 films

Abstract: THE large-scale use of photovoltaic devices for electricity generation is prohibitively expensive at present: generation from existing commercial devices costs about ten times more than conventional methods1. Here we describe a photovoltaic cell, created from low-to medium-purity materials through low-cost processes, which exhibits a commercially realistic energy-conversion efficiency. The device is based on a 10-µm-thick, optically transparent film of titanium dioxide particles a few nanometres in size, coated with a monolayer of a charge-transfer dye to sensitize the film for light harvesting. Because of the high surface area of the semiconductor film and the ideal spectral characteristics of the dye, the device harvests a high proportion of the incident solar energy flux (46%) and shows exceptionally high efficiencies for the conversion of incident photons to electrical current (more than 80%). The overall light-to-electric energy conversion yield is 7.1-7.9% in simulated solar light and 12% in diffuse daylight. The large current densities (greater than 12 mA cm-2) and exceptional stability (sustaining at least five million turnovers without decomposition), as well as the low cost, make practical applications feasible.

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。

Environmental Applications of Semiconductor Photocatalysis

Abstract: The civilian, commercial, and defense sectors of most advanced industrialized nations are faced with a tremendous set of environmental problems related to the remediation of hazardous wastes, contaminated groundwaters, and the control of toxic air contaminants. For example, the slow pace of hazardous waste remediation at military installations around the world is causing a serious delay in conversion of many of these facilities to civilian uses. Over the last 10 years problems related to hazardous waste remediation have emerged as a high national and international priority.