GPAW: An open Python package for electronic structure calculations.

We review the GPAW open-source Python package for electronic structure calculations. GPAW is based on the projector-augmented wave method and can solve the self-consistent density functional theory (DFT) equations using three different wave-function representations, namely real-space grids, plane waves, and numerical atomic orbitals. The three representations are complementary and mutually independent and can be connected by transformations via the real-space grid. This multi-basis feature renders GPAW highly versatile and unique among similar codes. By virtue of its modular structure, the GPAW code constitutes an ideal platform for the implementation of new features and methodologies. Moreover, it is well integrated with the Atomic Simulation Environment (ASE), providing a flexible and dynamic user interface. In addition to ground-state DFT calculations, GPAW supports many-body GW band structures, optical excitations from the Bethe-Salpeter Equation, variational calculations of excited states in molecules and solids via direct optimization, and real-time propagation of the Kohn-Sham equations within time-dependent DFT. A range of more advanced methods to describe magnetic excitations and non-collinear magnetism in solids are also now available. In addition, GPAW can calculate non-linear optical tensors of solids, charged crystal point defects, and much more. Recently, support for graphics processing unit (GPU) acceleration has been achieved with minor modifications to the GPAW code thanks to the CuPy library. We end the review with an outlook, describing some future plans for GPAW.

Nanoporous MoS2 Membrane for Water Desalination: A Molecular Dynamics Study.

Molybdenum disulfide (MoS2), a two-dimensional (2D) material, promises better desalination efficiency, benefiting from the small diffusion length. While the monolayer nanoporous MoS2 membrane has great potential in the reverse osmosis (RO) desalination membrane, multilayer MoS2 membranes are more feasible to synthesize and economical than the monolayer MoS2 membrane. Building on the monolayer MoS2 membrane knowledge, the effects of the multilayer MoS2 membrane in water desalination were explored, and the results showed that increasing the pore size from 3 to 6 Å resulted in higher permeability but with lower salt rejection. The salt rejection increases from 85% in a monolayer MoS2 membrane to about 98% in a trilayer MoS2 membrane. When averaged over all three types of membranes studied, the ions rejection follows the trend of trilayer > bilayer > monolayer. Besides, a narrow layer separation was found to play an important role in the successful rejection of salt ions in bilayer and trilayer membranes. This study aims to provide a collective understanding of this high permiselective MoS2 membrane's realization for water desalination, and the findings showed that the water permeability of the MoS2 monolayer membrane was in the order of magnitude greater than that of the conventional RO membrane and the nanoporous MoS2 membrane can have an important place in the purification of water.

About the Implementation of Frequency Conversion Processes in Solar Cell Device Simulations.

Solar cells are electrical devices that can directly convert sunlight into electricity. While solar cells are a mature technology, their efficiencies are still far below the theoretical limit. The major losses in a typical semiconductor solar cell are due to the thermalization of electrons in the UV and visible range of the solar spectrum, the inability of a solar cell to absorb photons with energies below the electronic band gap, and losses due to the recombination of electrons and holes, which mainly occur at the contacts. These prevent the realization of the theoretical efficiency limit of 85% for a generic photovoltaic device. A promising strategy to harness light with minimum thermal losses outside the typical frequency range of a single junction solar cell could be frequency conversion using rare earth ions, as suggested by Trupke. In this work, we discuss the modelling of generic frequency conversion processes in the context of solar cell device simulations, which can be used to supplement experimental studies. In the spirit of a proof-of-concept study, we limit the discussion to up-conversion and restrict ourselves to a simple rare earth model system, together with a basic diode model for a crystalline silicon solar cell. The results of this show that these simulations are very useful for the development of new types of highly efficient solar cells.

Ab initio potential energy surface of CH and reaction dynamics of H + CH+.

This work presents a new ground state potential energy surface (PES) for CH. The potential is tested using quasi classical trajectory (QCT) and quantum reactive scattering methods for the H + CH(+) reaction. Cross sections and rate coefficients for all reaction channels up to 300 K are calculated. The abstraction rate coefficients follow the expected slightly decreasing behaviour above 90 K, but have a positive gradient with lower temperatures. The inelastic collision and exchange reaction rate constants are increasing monotonically with temperature. The rate coefficients of the exchange reaction differ significantly between QCT and quantum reactive scattering, due to intrinsic shortcomings of the QCT final state distributions.

Modeling the ion transfer and polarization of ion exchange membranes in bioelectrochemical systems.

An explicit numerical model for the charge balancing ion transfer across monopolar ion exchange membranes under conditions of bioelectrochemical systems is presented. Diffusion and migration equations have been solved according to the Nernst-Planck Equation and the resulting ion concentrations, pH values and the resistance values of the membrane for different conditions were computed. The modeling results underline the principle limitations of the application of ion exchange membranes in biological fuel cells and electrolyzers, caused by the inherent occurrence of a pH-gradient between anode and cathode compartment, and an increased ohmic membrane resistance at decreasing electrolyte concentrations. Finally, the physical and numerical limitations of the model are discussed.