TY - JOUR
T1 - Scalable nanoporous carbon films allow line-of-sight 3D atomic layer deposition of Pt
T2 - Towards a new generation catalyst layer for PEM fuel cells
AU - Atwa, Marwa
AU - Li, Xiaoan
AU - Wang, Zhaoxuan
AU - Dull, Samuel
AU - Xu, Shicheng
AU - Tong, Xia
AU - Tang, Rui
AU - Nishihara, Hirotomo
AU - Prinz, Fritz
AU - Birss, Viola
N1 - Funding Information:
V. I. B. acknowledges the Natural Sciences and Engineering Research Council of Canada (NSERC) for financial support, as well as support from the Canada Research Chairs program. H. N. acknowledges partial support from the Cooperative Research Program of Five-star Alliance and NJRC Mater. & Dev. of Japan. M. A. extends her acknowledgements to the Egyptian Cultural Affairs and Missions Sector and NSERC for scholarship support. We also thank Drs. Robert Marriott and Ruohong Sui for their help with the gas sorption measurements. We also thank Dr Scott Paulson for useful discussions, Bin Pan for contact angle measurements and Arlene Ai for a SEM image. Z. W., S. D., S. X., and F. P. thank the Volkswagen Group of America for financial support and extend their acknowledgments to the Stanford Nano-Shared Facilities (SNSF) where part of the work was performed, supported by the National Science Foundation under award ECCS-1542152. Finally, V. I. B. and M. A. would like to thank Drs. Haoyang Yu and Peng Li from the nanoFAB Center at the University of Alberta for collecting the HR-TEM images.
Publisher Copyright:
© The Royal Society of Chemistry.
PY - 2021/9
Y1 - 2021/9
N2 - Although nanoporous carbons are ubiquitous materials that are used in many clean energy and environmental applications, most are in powder form, thus requiring binders to hold particles together. This results in uncontrolled and complex pathways between particles, potentially exacerbating mass transport issues. To overcome these problems, we have developed an unprecedented binderless, self-supported, nanoporous carbon scaffold (NCS) with tunable and monodisperse pores (5-100+ nm), high surface area (ca. 200-575 m2 g-1), and 3-dimensional scalability (1-150+ cm2, 1-1000 μm thickness). Here, it is shown that NCS85 membranes (85 nm pores) are particularly promising as a host for the homogeneous and efficient 3-D atomic layer deposition (ALD) of Pt nanoparticles, due to the facile penetration of gas phase Pt precursor throughout the homogeneous, low tortuosity internal structure. Furthermore, the high density of surface defects of the as-synthesized NCS promotes uniform Pt nucleation with minimal agglomeration. These advantageous features are key to the rapid oxygen reduction kinetics observed under polymer electrolyte membrane (PEM) fuel cell MEA testing conditions. Cells constructed with an optimal ALD Pt loading of 30 cycles are shown to exhibit a specific activity of ≥0.4 mA cm-2Pt which is exemplary when compared to two commercial catalyst layers with comparable Pt mass loadings and tested under the same conditions. Furthermore, a maximum power density of 1230 mW cm-2 (IR-corrected) is obtained, with the limiting current densities approaching a very respectable 3 A cm-2.
AB - Although nanoporous carbons are ubiquitous materials that are used in many clean energy and environmental applications, most are in powder form, thus requiring binders to hold particles together. This results in uncontrolled and complex pathways between particles, potentially exacerbating mass transport issues. To overcome these problems, we have developed an unprecedented binderless, self-supported, nanoporous carbon scaffold (NCS) with tunable and monodisperse pores (5-100+ nm), high surface area (ca. 200-575 m2 g-1), and 3-dimensional scalability (1-150+ cm2, 1-1000 μm thickness). Here, it is shown that NCS85 membranes (85 nm pores) are particularly promising as a host for the homogeneous and efficient 3-D atomic layer deposition (ALD) of Pt nanoparticles, due to the facile penetration of gas phase Pt precursor throughout the homogeneous, low tortuosity internal structure. Furthermore, the high density of surface defects of the as-synthesized NCS promotes uniform Pt nucleation with minimal agglomeration. These advantageous features are key to the rapid oxygen reduction kinetics observed under polymer electrolyte membrane (PEM) fuel cell MEA testing conditions. Cells constructed with an optimal ALD Pt loading of 30 cycles are shown to exhibit a specific activity of ≥0.4 mA cm-2Pt which is exemplary when compared to two commercial catalyst layers with comparable Pt mass loadings and tested under the same conditions. Furthermore, a maximum power density of 1230 mW cm-2 (IR-corrected) is obtained, with the limiting current densities approaching a very respectable 3 A cm-2.
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U2 - 10.1039/d1mh00268f
DO - 10.1039/d1mh00268f
M3 - Article
C2 - 34846397
AN - SCOPUS:85114211844
SN - 2051-6347
VL - 8
SP - 2451
EP - 2462
JO - Materials Horizons
JF - Materials Horizons
IS - 9
ER -