Journal : Electronic Materials Letters 
Volume : 19 
issue :
page : 1-18 
year : 2023 
authors : Soon Hyeong So, Sae Jin Sung, Seung Jae Yang, Chong Rae Park 
DOI: : 10.1007/s13391-022-00388-y 
pubdate : 2022-09-26 
region : International 
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Hydrogen is expected to overcome energy resource depletion because it is the most abundant element in the universe and because an ideal hydrogen energy cycle has the potential to exploit energy infinitely. Conventionally, hydrogen storage utilizes compression under high pressure (350-700 bar) into a tank and liquefaction in the cryotemperature regime (20 K). To mitigate the impractical operating conditions researchers have conducted adsorption-dependent research to increase the specific surface area (SSA) in physisorption and to decrease the H2 binding energy in chemisorption. Nevertheless, these strategies are still unlikely to reach the required the U.S. Department of Energy (DOE) targets. To this end, researchers have tried to find hydrogen storage material to fit the H2 binding energy between the physisorption region and chemisorption region. Previous governing parameters, the SSA, and the H2 binding energy show no correlation to gravimetric H2 storage capacity (GHSC). In addition, no correlation between the H2 densification index (HDI) and the H2 binding energy is found as well, which means the latter cannot describe the H2-adsorbent interaction thoroughly. The several notable findings presented here suggest that the development of high-performance H2 storage materials can be realized through the optimal modulation of an underlying parameter that dominates the H2-adsorbent interaction. This paper highlights the necessity of research on what the underlying parameter that dominates the H2-adsorbent interaction is and on how it affects GHSC to develop H2 storage materials that meet the DOE targets.

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