Publications by authors named "Guanghu He"

Improving the high-temperature performance of polymer dielectrics is critical for the development of advanced electrical systems. The deterioration of the capacitive performance of polymer dielectrics at high electric fields and elevated temperatures is attributable to the exponentially increased conduction loss. Herein, a synergistic strategy of molecular trap and aggregation structure optimization is developed to suppress the conduction loss of polymer dielectrics.

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Electrostatic capacitors, with the advantages of high-power density, fast charging-discharging, and outstanding cyclic stability, have become important energy storage devices for modern power electronics. However, the insulation performance of the dielectrics in capacitors will significantly deteriorate under the conditions of high temperatures and electric fields, resulting in limited capacitive performance. In this paper, we report a method to improve the high-temperature energy storage performance of a polymer dielectric for capacitors by incorporating an extremely low loading of 0.

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Conventional methods for fabricating multilayered ceramic membranes with ion conducting dense thin layers are often cumbersome, costly, and limited by poor adhesion between layers. Inspired by the architectural structure of the rooted grasses in soil, here, we report an interface-reaction-induced reassembly approach for the direct fabrication of Ce Gd O (CGO) thin layers rooted in the parent multilayered ceramic membranes by only one firing step. The CGO dense layers are very thin, and adhered strongly to the parent support layer, ensuring low ionic transport resistance and structural integrity of the multilayered membranes.

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Polymer dielectrics are attracting increasing attention for electrical energy storage owing to their advantages of mechanical flexibility, corrosion resistance, facile processability, light weight, great reliability, and high operating voltages. However, the dielectric constants of most dielectric polymers are less than 10, which results in low energy densities and limits their applications in electrostatic capacitors for advanced electronics and electrical power systems. Therefore, intensive efforts have been placed on the development of high-energy-density polymer dielectrics.

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Using oxygen permeable membranes (OPMs) to upgrade low-purity hydrogen is a promising concept for high-purity H production. At high temperatures, water dissociates into hydrogen and oxygen. The oxygen permeates through OPM and oxidizes hydrogen in a waste stream on the other side of the membrane.

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Coupling of two oxygen-involved reactions at the opposite sides of an oxygen transport membrane (OTM) has demonstrated great potential for process intensification. However, the current cobalt- or iron-containing OTMs suffer from poor reduction tolerance, which are incompetent for membrane reactor working in low oxygen partial pressure (pO). Here, we report for the first time a both Co- and Fe-free SrMgZrTiO (SMZ-Ti) membrane that exhibits both superior reduction tolerance for 100 h in 20 vol.

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Article Synopsis
  • A new method of doping the perovskite PrBaCoO with calcium (Ca) has been shown to enhance its durability and electrocatalytic activity for the oxygen evolution reaction (OER).
  • The calcium-doped version, PrBaCaCoO, exhibited a roughly 90% increase in electrocatalytic activity compared to the original perovskite.
  • Additionally, the durability of the material improved significantly after the calcium doping process.
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