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.

Fast parallel algorithms for short-range molecular dynamics

다중혈관 관상동맥 환자에서 y-문합을 이용하여 양쪽 내흉동맥만을 사용한 우회술의 조기 성적

BACKGROUND With a rising global population, increasing energy demands, and impending climate change, major concerns have been raised over the security of our energy future. Developing sustainable, fossil-free pathways to produce fuels and chemicals of global importance could play a major role in reducing carbon dioxide emissions while providing the feedstocks needed to make the products we use on a daily basis. One prospective goal is to develop electrochemical conversion processes that can convert molecules in the atmosphere (e.g., water, carbon dioxide, and nitrogen) into higher-value products (e.g., hydrogen, hydrocarbons, oxygenates, and ammonia) by coupling to renewable energy. Electrocatalysts play a key role in these energy conversion technologies because they increase the rate, efficiency, and selectivity of the chemical transformations involved. Today’s electrocatalysts, however, are inadequate. The grand challenge is to develop advanced electrocatalysts with the enhanced performance needed to enable widespread penetration of clean energy technologies. ADVANCES Over the past decade, substantial progress has been made in understanding several key electrochemical transformations, particularly those that involve water, hydrogen, and oxygen. The combination of theoretical and experimental studies working in concert has proven to be a successful strategy in this respect, yielding a framework to understand catalytic trends that can ultimately provide rational guidance toward the development of improved catalysts. Catalyst design strategies that aim to increase the number of active sites and/or increase the intrinsic activity of each active site have been successfully developed. The field of hydrogen evolution, for example, has seen important breakthroughs over the years in the development of highly active non–precious metal catalysts in acid. Notable advancements have also been made in the design of oxygen reduction and evolution catalysts, although there remains substantial room for improvement. The combination of theory and experiment elucidates the remaining challenges in developing further improved catalysts, often involving scaling relations among reactive intermediates. This understanding serves as an initial platform to design strategies to circumvent technical obstacles, opening up opportunities and approaches to develop higher-performance electrocatalysts for a wide range of reactions. OUTLOOK A systematic framework of combining theory and experiment in electrocatalysis helps to uncover broader governing principles that can be used to understand a wide variety of electrochemical transformations. These principles can be applied to other emerging and promising clean energy reactions, including hydrogen peroxide production, carbon dioxide reduction, and nitrogen reduction, among others. Although current paradigms for catalyst development have been helpful to date, a number of challenges need to be successfully addressed in order to achieve major breakthroughs. One important frontier, for example, is the development of both experimental and computational methods that can rapidly elucidate reaction mechanisms on broad classes of materials and in a wide range of operating conditions (e.g., pH, solvent, electrolyte). Such efforts would build on current frameworks for understanding catalysis to provide the deeper insights needed to fine-tune catalyst properties in an optimal manner. The long-term goal is to continue improving the activity and selectivity of these catalysts in order to realize the prospects of using renewable energy to provide the fuels and chemicals that we need for a sustainable energy future.

/pdf/combining-theory-and-experiment-in-electrocatalysis-insights-3l4yblici7.pdf

Combining theory and experiment in electrocatalysis: Insights into materials design

A fundamental change has been achieved in understanding surface electrochemistry due to the profound knowledge of the nature of electrocatalytic processes accumulated over the past several decades and to the recent technological advances in spectroscopy and high resolution imaging. Nowadays one can preferably design electrocatalysts based on the deep theoretical knowledge of electronic structures, via computer-guided engineering of the surface and (electro)chemical properties of materials, followed by the synthesis of practical materials with high performance for specific reactions. This review provides insights into both theoretical and experimental electrochemistry toward a better understanding of a series of key clean energy conversion reactions including oxygen reduction reaction (ORR), oxygen evolution reaction (OER), and hydrogen evolution reaction (HER). The emphasis of this review is on the origin of the electrocatalytic activity of nanostructured catalysts toward the aforementioned reactions by correlating the apparent electrode performance with their intrinsic electrochemical properties. Also, a rational design of electrocatalysts is proposed starting from the most fundamental aspects of the electronic structure engineering to a more practical level of nanotechnological fabrication.

Design of electrocatalysts for oxygen- and hydrogen-involving energy conversion reactions

The pace of materials discovery for heterogeneous catalysts and electrocatalysts could, in principle, be accelerated by the development of efficient computational screening methods. This would require an integrated approach, where the catalytic activity and stability of new materials are evaluated and where predictions are benchmarked by careful synthesis and experimental tests. In this contribution, we present a density functional theory-based, high-throughput screening scheme that successfully uses these strategies to identify a new electrocatalyst for the hydrogen evolution reaction (HER). The activity of over 700 binary surface alloys is evaluated theoretically; the stability of each alloy in electrochemical environments is also estimated. BiPt is found to have a predicted activity comparable to, or even better than, pure Pt, the archetypical HER catalyst. This alloy is synthesized and tested experimentally and shows improved HER performance compared with pure Pt, in agreement with the computational screening results.

Computational high-throughput screening of electrocatalytic materials for hydrogen evolution

The electrochemical behavior of hydrogen peroxide, which is a possible intermediate of the oxygen reduction reaction (ORR), has been investigated on platinum single crystal electrodes containing terraces with (111) symmetry separated by monoatomic steps with either (110) or (100) symmetry in different pH solutions [1]. On these electrodes, a decrease, in absolute value, of the reduction current at low potentials is observed. The potential at which the decrease is observed, can be correlated with the potential of maximum entropy (pme) of the double layer formation on the terraces. In addition, it is possible to relate the peak appearing at potentials below 0.3 V (RHE) to the local pme in the steps.
 By performing experiments at different pH values, up to pH ≈ 5, it is observed that the inhibition potential on the terraces shifts 59 mV per pH unit towards more positive potentials, in line with what was observed for the pme in laser-induced temperature jump experiments. For the possible explanation of this phenomenon, it must be taken into account that OH adsorption may influence this trend when the pme values are close to the potentials corresponding to OH adsorption. From results obtained in alkaline medium, it is clear that the surface charge plays an important role in this inhibition of the limiting diffusion current.
 Finally, the comparison of the results obtained under similar conditions for the hydrogen peroxide and oxygen reduction reactions suggests that the formation of hydrogen peroxide as an ORR intermediate is less favored with increasing pH. As a consequence, there must be a bifurcation in the ORR mechanism prior to peroxide formation. These results agree with previous results [2], which indicate that ORR involves different steps in which several bifurcation points may exist. Depending on the experimental conditions, the reaction may follow a different reaction pathway [3].
 
 References.
 
 (1) Briega-Martos, V.; Herrero, E.; Feliu, J.M. Electrochimica Acta 
 2020
 , 334, 135452.
 (2) Gomez-Marin, A.M.; Feliu, J.M. ChemSusChem 
 2013, 6, 172-176.
 (3) Briega-Martos, V.; Herrero, E.; Feliu, J.M. Chinese J. Catal. 
 2020, 41, 732-738.

(Keynote) Effect of the Surface Charge on the Oxygen and Hydrogen Peroxide Reduction Reactions

/pdf/increased-sensitivity-and-selectivity-for-as-iii-detection-2i1kubts.pdf

Increased Sensitivity and Selectivity for As(III) Detection at the Au(111) Surface: Single Crystals and Ultraflat Thin Films Comparison

Electrodeposition technique allows depositing nanoparticles of metals and alloys with variable size as a function of the deposition conditions, the deposition charge, and the nature of the substrate In this work, the possibility of obtaining electrochemically core-shell submicrometric particles with a platinum shell has been tested; in order to design a preparationmethod of particles of different size, the general purpose is to approach the surface properties of platinum but with lower amounts than those in a massive platinum particle Cobalt nanoparticles in the range 100–600 nm of diameter have been electrodeposited on vitreous carbon The size of the particles and the average distance between them varies as a function of the deposition potential and the transferred charge Low overpotentials have been selected to obtain isolated cobalt particles of similar size (around 140 nm) These particles have been covered with a skin layer of platinum by galvanic displacement reaction by immersion in a platinum-containing solution The control of the total recovery of the particles (to obtain core-shell cobalt-platinum particles) has been performed electrochemically by recording the voltammetric profile of the samples in a blank solution The electrocatalytic activity of the prepared particles for methanol oxidation has been tested

http://link.springer.com/content/pdf/10.1007/978-3-319-15207-3_36-1.pdf

Juan M. Feliu

Papers

(Keynote) Effect of the Surface Charge on the Oxygen and Hydrogen Peroxide Reduction Reactions

Increased Sensitivity and Selectivity for As(III) Detection at the Au(111) Surface: Single Crystals and Ultraflat Thin Films Comparison

Electrochemical Control of the Core-Shell Cobalt-Platinum Nanoparticles

Formic Acid Oxidation on Different Coverages of Bismuth-Modified Pt(100): A Detailed Voltammetric and FTIR Study

Experimental assessment of the interfacial properties of well-defined Cu single crystalline electrodes.