Joshua DeOtte

Mr. Joshua DeOtte

Lawrence Livermore National Laboratory
orcid

Research Focus & Metrics

Academic Career Length

16Years (2011-Present)

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

Representative Publications

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20 June 2014 in Science
Verified
Journal Article
Open access
PDF file
XZXiaoyu Zheng
Xiaoyu Zheng
HLHowon Lee
Howon Lee
TWTodd H. Weisgraber
Todd H. Weisgraber
MSMaxim Shusteff
Maxim Shusteff
JDJoshua DeOtte
Joshua DeOtte
CSChristopher M. Spadaccini
Christopher M. Spadaccini
Microlattices make marvelous materials: Framework or lattice structures can be remarkably strong despite their very low density. Using a very precise technique known as projection microstereolithography, Zheng et al. fabricated octet microlattices from polymers, metals, and ceramics. The design of the lattices meant that the individual struts making up the materials did not bend under pressure. The materials were therefore exceptionally stiff, strong, and lightweight. Science , this issue p. 1373

1 December 2012 in Review of Scientific Instruments
Verified
Journal Article
Closed access
PDF file
XZXiaoyu Zheng
Xiaoyu Zheng
JDJoshua DeOtte
Joshua DeOtte
MAMatthew P. Alonso
Matthew P. Alonso
GFGeorge R. Farquar
George R. Farquar
TWTodd H. Weisgraber
Todd H. Weisgraber
CSChristopher M. Spadaccini
Christopher M. Spadaccini
The rapid manufacture of complex three-dimensional micro-scale components has eluded researchers for decades. Several additive manufacturing options have been limited by either speed or the ability to fabricate true three-dimensional structures. Projection micro-stereolithography (PμSL) is a low cost, high throughput additive fabrication technique capable of generating three-dimensional microstructures in a bottom-up, layer by layer fashion. The PμSL system is reliable and capable of manufacturing a variety of highly complex, three-dimensional structures from micro- to meso-scales with micro-scale architecture and submicron precision. Our PμSL system utilizes a reconfigurable digital mask and a 395 nm light-emitting diode (LED) array to polymerize a liquid monomer in a layer-by-layer manufacturing process. This paper discusses the critical process parameters that influence polymerization depth and structure quality. Experimental characterization and performance of the LED-based PμSL system for fabricating highly complex three-dimensional structures for a large range of applications is presented.

30 June 2021 in Nature
Verified
Journal Article
Closed access
PDF file
NDNikola A. Dudukovic
Nikola A. Dudukovic
EFErika J. Fong
Erika J. Fong
HGHawi B. Gemeda
Hawi B. Gemeda
JDJoshua DeOtte
Joshua DeOtte
MCMaira R. Cerón
Maira R. Cerón
EDEric B. Duoss
Eric B. Duoss

15 June 2016 in Nature Communications
Verified
Journal Article
Open access
CBCraig D. Blanchette
Craig D. Blanchette
JKJennifer M. Knipe
Jennifer M. Knipe
JSJoshuah K. Stolaroff
Joshuah K. Stolaroff
JDJoshua DeOtte
Joshua DeOtte
JOJames S. Oakdale
James S. Oakdale
SBSarah E. Baker
Sarah E. Baker
An industrial process for the selective activation of methane under mild conditions would be highly valuable for controlling emissions to the environment and for utilizing vast new sources of natural gas. The only selective catalysts for methane activation and conversion to methanol under mild conditions are methane monooxygenases (MMOs) found in methanotrophic bacteria; however, these enzymes are not amenable to standard enzyme immobilization approaches. Using particulate methane monooxygenase (pMMO), we create a biocatalytic polymer material that converts methane to methanol. We demonstrate embedding the material within a silicone lattice to create mechanically robust, gas-permeable membranes, and direct printing of micron-scale structures with controlled geometry. Remarkably, the enzymes retain up to 100% activity in the polymer construct. The printed enzyme-embedded polymer motif is highly flexible for future development and should be useful in a wide range of applications, especially those involving gas–liquid reactions.

15 February 2021 in Energy & Environmental Science
Verified
Journal Article
Closed access
PDF file
DCDaniel Corral
Daniel Corral
JFJeremy T. Feaster
Jeremy T. Feaster
SSSadaf Sobhani
Sadaf Sobhani
JDJoshua DeOtte
Joshua DeOtte
DLDong Un Lee
Dong Un Lee
EDEric B. Duoss
Eric B. Duoss
Changing the reactor design paradigm for improved CO2electrolyzers through advanced manufacturing.

27 July 2011 in The Analyst
Verified
Journal Article
Closed access
PDF file
EWE. K. Wheeler
E. K. Wheeler
CHC. A. Hara
C. A. Hara
JFJ. Frank
J. Frank
JDJoshua DeOtte
Joshua DeOtte
SHS. B. Hall
S. B. Hall
NBN. R. Beer
N. R. Beer
Nucleic acid amplification is enormously useful to the biotechnology and clinical diagnostic communities; however, to date point-of-use PCR has been hindered by thermal cycling architectures and protocols that do not allow for near-instantaneous results. In this work we demonstrate PCR amplification of synthetic SARS respiratory pathogenic targets and bacterial genomic DNA in less than three minutes in a hardware configuration utilizing convenient sample loading and disposal. Instead of sample miniaturization techniques, near-instantaneous heating and cooling of 5 μL reaction volumes is enabled by convective heat transfer of a thermal fluid through porous media combined with an integrated electrical heater. This method of rapid heat transfer has enabled 30 cycles of PCR amplification to be completed in as little as two minutes and eighteen seconds. Surprisingly, multiple enzymes have been shown to work at these breakthrough speeds on our system. A tool for measuring enzyme kinetics now exists and can allow polymerase optimization through directed evolution studies. Pairing this instrument technology with modified polymerases should result in a new paradigm for high-throughput, ultra-fast PCR and will hopefully improve our ability to quickly respond to the next viral pandemic.