TY - JOUR
T1 - Hydrogen in Palladium and Storage Properties of Related Nanomaterials
T2 - Size, Shape, Alloying, and Metal-Organic Framework Coating Effects
AU - Dekura, Shun
AU - Kobayashi, Hirokazu
AU - Kusada, Kohei
AU - Kitagawa, Hiroshi
N1 - Funding Information:
This research was supported by Core Research for Evolutional Science and Technology (CREST) and ACCEL (JPMJAC1501) from the Japan Science and Technology Agency (JST).
Publisher Copyright:
© 2019 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim
PY - 2019/5/16
Y1 - 2019/5/16
N2 - One of the key issues for an upcoming hydrogen energy-based society is to develop highly efficient hydrogen-storage materials. Among the many hydrogen-storage materials reported, transition-metal hydrides can reversibly absorb and desorb hydrogen, and have thus attracted much interest from fundamental science to applications. In particular, the Pd−H system is a simple and classical metal-hydrogen system, providing a platform suitable for a thorough understanding of ways of controlling the hydrogen-storage properties of materials. By contrast, metal nanoparticles have been recently studied for hydrogen storage because of their unique properties and the degrees of freedom which cannot be observed in bulk, i. e., the size, shape, alloying, and surface coating. In this review, we overview the effects of such degrees of freedom on the hydrogen-storage properties of Pd-related nanomaterials, based on the fundamental science of bulk Pd−H. We shall show that sufficiently understanding the nature of the interaction between hydrogen and host materials enables us to control the hydrogen-storage properties though the electronic-structure control of materials.
AB - One of the key issues for an upcoming hydrogen energy-based society is to develop highly efficient hydrogen-storage materials. Among the many hydrogen-storage materials reported, transition-metal hydrides can reversibly absorb and desorb hydrogen, and have thus attracted much interest from fundamental science to applications. In particular, the Pd−H system is a simple and classical metal-hydrogen system, providing a platform suitable for a thorough understanding of ways of controlling the hydrogen-storage properties of materials. By contrast, metal nanoparticles have been recently studied for hydrogen storage because of their unique properties and the degrees of freedom which cannot be observed in bulk, i. e., the size, shape, alloying, and surface coating. In this review, we overview the effects of such degrees of freedom on the hydrogen-storage properties of Pd-related nanomaterials, based on the fundamental science of bulk Pd−H. We shall show that sufficiently understanding the nature of the interaction between hydrogen and host materials enables us to control the hydrogen-storage properties though the electronic-structure control of materials.
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U2 - 10.1002/cphc.201900109
DO - 10.1002/cphc.201900109
M3 - Review article
C2 - 30887646
AN - SCOPUS:85064076184
VL - 20
SP - 1158
EP - 1176
JO - ChemPhysChem
JF - ChemPhysChem
SN - 1439-4235
IS - 10
ER -