Michael F. Toney

Michael F. Toney

Top Cited Scholar 2023
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Michael F. Toney


Research Focus & Metrics

Academic Career Length

29Years (1998-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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25 February 2019 in Nature Energy
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Journal Article
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JLJun Liu
Jun Liu
ZBZhenan Bao
Zhenan Bao
YCYi Cui
Yi Cui
EDEric J. Dufek
Eric J. Dufek
JGJohn B. Goodenough
John B. Goodenough
JZJi-Guang Zhang
Ji-Guang Zhang

4 August 2017 in Journal of the American Chemical Society
Verified
Journal Article
Closed access
RPRohit Prasanna
Rohit Prasanna
AGAryeh Gold-Parker
Aryeh Gold-Parker
TLTomas Leijtens
Tomas Leijtens
BCBert Conings
Bert Conings
ABAslihan Babayigit
Aslihan Babayigit
MMMichael D. McGehee
Michael D. McGehee

12 December 2017 in Nature Communications
Verified
Journal Article
Open access
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WGWilliam E. Gent
William E. Gent
KLKipil Lim
Kipil Lim
YLYufeng Liang
Yufeng Liang
QLQinghao Li
Qinghao Li
TBTaylor Barnes
Taylor Barnes
WCWilliam C. Chueh
William C. Chueh
Lithium-rich layered transition metal oxide positive electrodes offer access to anion redox at high potentials, thereby promising high energy densities for lithium-ion batteries. However, anion redox is also associated with several unfavorable electrochemical properties, such as open-circuit voltage hysteresis. Here we reveal that in Li1.17–x Ni0.21Co0.08Mn0.54O2, these properties arise from a strong coupling between anion redox and cation migration. We combine various X-ray spectroscopic, microscopic, and structural probes to show that partially reversible transition metal migration decreases the potential of the bulk oxygen redox couple by > 1 V, leading to a reordering in the anionic and cationic redox potentials during cycling. First principles calculations show that this is due to the drastic change in the local oxygen coordination environments associated with the transition metal migration. We propose that this mechanism is involved in stabilizing the oxygen redox couple, which we observe spectroscopically to persist for 500 charge/discharge cycles.

30 April 2019 in Nature Communications
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Journal Article
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AMAiden Alexander Martin
Aiden Alexander Martin
NCNicholas P. Calta
Nicholas P. Calta
SKSaad A. Khairallah
Saad A. Khairallah
JWJenny Wang
Jenny Wang
PDPhillip J. Depond
Phillip J. Depond
MMManyalibo J. Matthews
Manyalibo J. Matthews
Laser powder bed fusion additive manufacturing is an emerging 3D printing technique for the fabrication of advanced metal components. Widespread adoption of it and similar additive technologies is hampered by poor understanding of laser-metal interactions under such extreme thermal regimes. Here, we elucidate the mechanism of pore formation and liquid-solid interface dynamics during typical laser powder bed fusion conditions using in situ X-ray imaging and multi-physics simulations. Pores are revealed to form during changes in laser scan velocity due to the rapid formation then collapse of deep keyhole depressions in the surface which traps inert shielding gas in the solidifying metal. We develop a universal mitigation strategy which eliminates this pore formation process and improves the geometric quality of melt tracks. Our results provide insight into the physics of laser-metal interaction and demonstrate the potential for science-based approaches to improve confidence in components produced by laser powder bed fusion.

30 August 2017 in ACS Energy Letters
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Journal Article
Closed access
TLTomas Leijtens
Tomas Leijtens
RPRohit Prasanna
Rohit Prasanna
AGAryeh Gold-Parker
Aryeh Gold-Parker
MTMichael F. Toney
Michael F. Toney
MMMichael D. McGehee
Michael D. McGehee

30 March 2012 in Journal of the American Chemical Society
Verified
Journal Article
Closed access
JNJohanna Nelson
Johanna Nelson
SMSumohan Misra
Sumohan Misra
YYYuan Yang
Yuan Yang
AJAriel Jackson
Ariel Jackson
YLYijin Liu
Yijin Liu
MTMichael F. Toney
Michael F. Toney