J
Joel Reid
Researcher at Canadian Light Source
Publications - 44
Citations - 1489
Joel Reid is an academic researcher from Canadian Light Source. The author has contributed to research in topics: Powder diffraction & Silicon. The author has an hindex of 14, co-authored 42 publications receiving 1331 citations. Previous affiliations of Joel Reid include Queen's University.
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Silicon substitution in the calcium phosphate bioceramics
TL;DR: Silicon (Si) substitution in the crystal structures of calcium phosphate (CaP) ceramics such as hydroxyapatite (HA) and tricalcium phosphate (TCP) generates materials with superior biological performance to stoichiometric counterparts.
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Structure and composition of silicon-stabilized tricalcium phosphate
M. Sayer,A. D. Stratilatov,Joel Reid,Lazaro Calderin,Malcolm J. Stott,Xilin Yin,M MacKenzie,Timothy J. N. Smith,Jason A. Hendry,S. Langstaff +9 more
TL;DR: A composition range and crystallographic structure for Si-TCP is proposed and it is proposed that Si(4+) substitutes for P(5+)in the TCP lattice with the average chemical composition of Si- TCP set primarily by the mechanisms available for charge compensation.
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Synthesis and characterization of single-phase silicon-substituted α-tricalcium phosphate
TL;DR: In this article, the lattice parameters of single-phase Si- α -TCP prepared with 0.87% silicon are a = 1 2.8 7 4 (1 ) A, b = 2 7.3 7 2 (2 ) A, c = 1 5.2 2 5 (1) A, and β = 12 6.3 8 ( 1 ) °.
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Phase formation and evolution in the silicon substituted tricalcium phosphate/apatite system.
TL;DR: The sintering of silicon doped calcium phosphate ceramics prepared from a basic colloidal hydroxyapatite precipitate mixed with silica over 800 degrees C yields a phase mixture of tricalcium phosphate phases (TCP) designated Si-TCP, beta- TCP and a silicon substituted dehydrated apatite (Si-Ap).
Journal ArticleDOI
Capacity Fade Mechanism of Li4Ti5O12 Nanosheet Anode
Hsien-Chieh Chiu,Xia Lu,Xia Lu,Jigang Zhou,Lin Gu,Joel Reid,Raynald Gauvin,Karim Zaghib,George P. Demopoulos +8 more
TL;DR: In this article, the authors considered the issue of nanostructure-induced relaxation in 2D LTO nanosheets which profoundly modifies their Li storage properties and structural stability.