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Abstract. We report an attenuation of hiss wave intensity in theduskside of the outer plasmasphere in response to enhanced convection anda substorm based on Van Allen Probe observations. Using test particle codes,we simulate the dynamics of energetic electron fluxes based on a realisticmagnetospheric electric field model driven by solar wind and subauroralpolarization stream. We suggest that the enhanced magnetospheric electricfield causes the outward and sunward motion of energetic electrons,corresponding to the decrease of energetic electron fluxes on the duskside,leading to the subsequent attenuation of hiss wave intensity. The resultsindicate that the enhanced electric field can significantly change theenergetic electron distributions, which provide free energy for hiss waveamplification. This new finding is critical for understanding the generationof plasmaspheric hiss and its response to solar wind and substorm activity. 

Formaldehyde is an essential building block for hundreds of chemicals and a promising liquid organic hydrogen carrier (LOHC), yet its indirect energy-intensive synthesis process prohibits it from playing a more significant role. Here we report a direct CO reduction to formaldehyde (CORTF) process that utilizes hydrogen underpotential deposition to overcome the thermodynamic barrier and the scaling relationship restriction. This is the first time that this reaction has been realized under ambient conditions. Using molybdenum phosphide as a catalyst, formaldehyde was produced with nearly a 100% faradaic efficiency in aqueous KOH solution, with its formation rate being one order of magnitude higher compared with the state-of-the-art thermal catalysis approach. Simultaneous tuning of the current density and reaction temperature led to a more selective and productive formaldehyde synthesis, indicating the electrochemical and thermal duality of this reaction. DFT calculations revealed that the desorption of the *H 2 CO intermediate likely served as the rate-limiting step, and the participation of H 2 O made the reaction thermodynamically favorable. Furthermore, a full-cell reaction set-up was demonstrated with CO hydrogenation to HCHO achieved without any energy input, which fully realized the spontaneous potential of the reaction. Our study shows the feasibility of combining thermal and electrochemical approaches for realizing the thermodynamics and for scaling relationship-confined reactions, which could serve as a new strategy in future reaction design. 

Very-Low-Frequency (VLF) transmitters operate worldwide mostly at frequencies of 10–30 kilohertz for submarine communications. While it has been of intense scientific interest and practical importance to understand whether VLF transmitters can affect the natural environment of charged energetic particles, for decades there remained little direct observational evidence that revealed the effects of these VLF transmitters in geospace. Here we report a radially bifurcated electron belt formation at energies of tens of kiloelectron volts (keV) at altitudes of ~0.8–1.5 Earth radii on timescales over 10 days. Using Fokker-Planck diffusion simulations, we provide quantitative evidence that VLF transmitter emissions that leak from the Earth-ionosphere waveguide are primarily responsible for bifurcating the energetic electron belt, which typically exhibits a single-peak radial structure in near-Earth space. Since energetic electrons pose a potential danger to satellite operations, our findings demonstrate the feasibility of mitigation of natural particle radiation environment.

 

Active sites play an essential role in heterogeneous catalysis and largely determine the reaction properties. Yet identification and study of the active sites remain challenging owing to their dynamic behaviors during catalysis process and issues with current characterization techniques. This article provides a short review of research progresses in active sites of metal and metal oxide catalysts, which covers the past achievements, current research status, and perspectives in this research field. In particular, the concepts and theories of active sites are introduced. Major experimental and computational approaches that are used in active site study are summarized, with their applications and limitations being discussed. An outlook of future research direction in both experimental and computational catalysis research is provided.