Analysis of matter - rupa - in Theravada Buddhism with special reference to the Abhidhamma.

This study constitutes an inquiry into the analysis of matter as expressed in the sources of Theravada Buddhism, specially in the later systematizations known as the Abhi-dhamma. The introductory chapter is devoted to an examination of the many senses, and contexts in which rupa - a term often used in the sense of matter - occurs; the definition of rupa in the sense of matter; and the general nature of the rupa-dhammas, i.e., the ultimate factors into which matter is analysed. These rupa-dhammas, twenty eight in all, are classified into two categories as primary and secondary. Chapter II deals with those that constitute the primary category and shows how they represent four properties of matter; solidity and extension; viscidity and cohesion; the temperature of cold and heat; distension and mobility. Chapter III examines the position of the secondary rupa-dhammas in relation to the primary and indicates how some of the former category stand for certain facts intimately connected with matter. Chapter IV deals with those secondary rupa-dhammas which in the Abhidhammic commentaries came to be recognised as real entities. This involves a discussion of five material sense-organs, four varieties of sense-objects, two faculties of sex, the material faculty of life, the nutritive "quality" of matter, and the physical basis of mental activity. Chapter V deals with those secondary rupa-dhararnas which in the Abhidhamrnic commentaries came to be recogniaed as nominal entities with no autonomous objective counterparts. This involves a discussion of two modes of self-expression, three characteristics and four phases of the matter of the body, and the space delimited by matter. Chapter VI introduces the many ways in which the rupa-dhammas are sought to be classified, and Chapter VII explains how their inter-dependence and inter-connection are sought to be established with reference to laws of causation and conditionality. Chapter VIII introduces the theory of rupaKalapas - the Theravada form of atomism - and shows how it presents a close analogy to the atomic theories of the schools of Sanskrit Buddhism. The concluding Chapter endeavours to determine the philosophical and the ethical basis of the Buddhist analysis of matter, and to understand the whole subject in the context of Buddhism as a religion

Low Temperature Spin Freezing in Dy2Ti2O7 Spin Ice

We report a study of the low temperature bulk magnetic properties of the spin ice compound Dy2Ti2O7 with particular attention to the (T < 4 K) spin freezing transition. While this transition is superficially similar to that in a spin glass, there are important qualitative differences from spin glass behavior: the freezing temperature increases slightly with applied magnetic field, and the distribution of spin relaxation times remains extremely narrow down to the lowest temperatures. Furthermore, the characteristic spin relaxation time increases faster than exponentially down to the lowest temperatures studied. These results indicate that spin-freezing in spin ice materials represents a novel form of magnetic glassiness associated with the unusual nature of geometrical frustration in these materials.Comment: 24 pages, 8 figure

Electrocatalytic hydrogen evolution by an iron complex containing a nitro-functionalized polypyridyl ligand

Iron polypyridyl complexes have recently been reported to electrocatalytically reduce protons to hydrogen gas at -1.57 V versus Fc(+)/Fc. A new iron catalyst with a nitro-functionalized polypyridyl ligand has been synthesized and found to be active for proton reduction. Interestingly, catalysis occurs at -1.18 V versus Fc(+)/Fc for the nitro-functionalized complex, resulting in an overpotential of 300 mV. Additionally, the complex is active with a turnover frequency of 550 s(-1). Catalysis is also observed in the presence of water with a 12% enhancement in activity. (C) 2015 Elsevier Ltd. All rights reserved

Magnetisation Studies of Geometrically Frustrated Antiferromagnets SrLn2O4, with Ln = Er, Dy and Ho

We present the results of susceptibility \chi(T) and magnetisation M(H) measurements performed on single crystal samples of the rare-earth oxides SrLn2O4 (Ln = Er, Dy and Ho). The measurements reveal the presence of magnetic ordering transition in SrHo2O4 at 0.62 K and confirm that SrEr2O4 orders magnetically at 0.73 K, while in SrDy2O4 such a transition is absent down to at least 0.5 K. The observed ordering temperatures are significantly lower than the Curie-Weiss temperatures, \theta_{CW}, obtained from the high-temperature linear fits to the 1/\chi(T) curves, which implies that these materials are subject to geometric frustration. Strong anisotropy found in the \chi(T) curves for a field applied along the different crystallographic directions is also evident in the M(H) curves measured both above and below the ordering temperatures. For all three compounds the magnetisation plateaux at approximately one third of the magnetisation saturation values can be seen for certain directions of applied field, which is indicative of field-induced stabilisation of a collinear {\it two-up one-down} structure.Comment: 6 pages, 6 figure

Recent advances in unveiling active sites in molybdenum sulfide-based electrocatalysts for the hydrogen evolution reaction

Hydrogen has received significant attention as a promising future energy carrier due to its high energy density and environmentally friendly nature. In particular, the electrocatalytic generation of hydrogen fuel is highly desirable to replace current fossil fuel-dependent hydrogen production methods. However, to achieve widespread implementation of electrocatalytic hydrogen production technology, the development of highly active and durable electrocatalysts based on Earth-abundant elements is of prime importance. In this context, nanostructured molybdenum sulfides (MoS x ) have received a great deal of attention as promising alternatives to precious metal-based catalysts. In this focus review, we summarize recent efforts towards identification of the active sites in MoS x -based electrocatalysts for the hydrogen evolution reaction (HER). We also discuss recent synthetic strategies for the engineering of catalyst structures to achieve high active site densities. Finally, we suggest ongoing and future research challenges in the design of advanced MoS x -based HER electrocatalysts

Self-optimizing, highly surface-active layered metal dichalcogenide catalysts for hydrogen evolution

Low-cost, layered transition-metal dichalcogenides (MX_2) based on molybdenum and tungsten have attracted substantial interest as alternative catalysts for the hydrogen evolution reaction (HER). These materials have high intrinsic per-site HER activity; however, a significant challenge is the limited density of active sites, which are concentrated at the layer edges. Here we unravel electronic factors underlying catalytic activity on MX_2 surfaces, and leverage the understanding to report group-5 MX_2 (H-TaS_2 and H-NbS_2) electrocatalysts whose performance instead mainly derives from highly active basal-plane sites, as suggested by our first-principles calculations and performance comparisons with edge-active counterparts. Beyond high catalytic activity, they are found to exhibit an unusual ability to optimize their morphology for enhanced charge transfer and accessibility of active sites as the HER proceeds, offering a practical advantage for scalable processing. The catalysts reach 10 mA cm^(−2) current density at an overpotential of ∼50–60 mV with a loading of 10–55 μg cm^(−2), surpassing other reported MX2 candidates without any performance-enhancing additives