TY - JOUR
T1 - MgH2 nanoparticles confined in reduced graphene oxide pillared with organosilica
T2 - a novel type of hydrogen storage material
AU - Yan, Feng
AU - Moretón Alfonsín, Estela
AU - Ngene, Peter
AU - de Graaf, Sytze
AU - De Luca, Oreste
AU - Cao, Huatang
AU - Spyrou, Konstantinos
AU - Lu, Liqiang
AU - Thomou, Eleni
AU - Pei, Yutao
AU - Kooi, Bart J.
AU - Gournis, Dimitrios P.
AU - de Jongh, Petra E.
AU - Rudolf, Petra
N1 - Publisher Copyright:
© 2024 The Royal Society of Chemistry.
PY - 2024/6/20
Y1 - 2024/6/20
N2 - Hydrogen is a promising alternative fuel that can push forward the energy transition because of its high energy density (142 MJ kg−1), variety of potential sources, low weight and low environmental impact, but its storage for automotive applications remains a formidable challenge. MgH2, with its high gravimetric and volumetric density, presents a compelling platform for hydrogen storage; however, its utilization is hindered by the sluggish kinetics of hydrogen uptake/release and high temperature operation. Herein we show that a novel layered heterostructure of reduced graphene oxide and organosilica with high specific surface area and narrow pore size distribution can serve as a scaffold to host MgH2 nanoparticles with a narrow diameter distribution around ∼2.5 nm and superior hydrogen storage properties to bulk MgH2. Desorption studies showed that hydrogen release starts at relatively low temperature, with a maximum at 348 °C and kinetics dependent on particle size. Reversibility tests demonstrated that the dehydrogenation kinetics and re-hydrogenation capacity of the system remains stable at 1.62 wt% over four cycles at 200 °C. Our results prove that MgH2 confinement in a nanoporous scaffold is an efficient way to constrain the size of the hydride particles, avoid aggregation and improve kinetics for hydrogen release and recharging.
AB - Hydrogen is a promising alternative fuel that can push forward the energy transition because of its high energy density (142 MJ kg−1), variety of potential sources, low weight and low environmental impact, but its storage for automotive applications remains a formidable challenge. MgH2, with its high gravimetric and volumetric density, presents a compelling platform for hydrogen storage; however, its utilization is hindered by the sluggish kinetics of hydrogen uptake/release and high temperature operation. Herein we show that a novel layered heterostructure of reduced graphene oxide and organosilica with high specific surface area and narrow pore size distribution can serve as a scaffold to host MgH2 nanoparticles with a narrow diameter distribution around ∼2.5 nm and superior hydrogen storage properties to bulk MgH2. Desorption studies showed that hydrogen release starts at relatively low temperature, with a maximum at 348 °C and kinetics dependent on particle size. Reversibility tests demonstrated that the dehydrogenation kinetics and re-hydrogenation capacity of the system remains stable at 1.62 wt% over four cycles at 200 °C. Our results prove that MgH2 confinement in a nanoporous scaffold is an efficient way to constrain the size of the hydride particles, avoid aggregation and improve kinetics for hydrogen release and recharging.
UR - http://www.scopus.com/inward/record.url?scp=85201121288&partnerID=8YFLogxK
U2 - 10.1039/d4nr01524j
DO - 10.1039/d4nr01524j
M3 - Article
AN - SCOPUS:85201121288
SN - 2040-3364
JO - Nanoscale
JF - Nanoscale
ER -