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Purdue technology for downscaling transistors could advance semiconductor design

Purdue technology for downscaling transistors could advance semiconductor design
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Purdue University, Houston Methodist researchers develop novel strategy for tuberculosis vaccine

Purdue University, Houston Methodist researchers develop novel strategy for tuberculosis vaccine
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Purdue fund expands scope to accept applications from startups in all agricultural disciplines

Purdue fund expands scope to accept applications from startups in all agricultural disciplines
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Reimagining hydrogen, imaging, databases and oil

Reimagining hydrogen, imaging, databases and oil
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Mobile health diagnostic for animal breeding may help meet demand for food

Mobile health diagnostic for animal breeding may help meet demand for food
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New mobile health diagnostic for animal breeding may help meet growing demand for food

New mobile health diagnostic for animal breeding may help meet growing demand for food
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Nanotechnology Now - Press Release: A molecule like a nanobattery: Chemical scientists decipher complex electronic structure of a three-nuclear metallorganic compound with the capacity of donating and receiving multiple electrons


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Home > Press > A molecule like a nanobattery: Chemical scientists decipher complex electronic structure of a three-nuclear metallorganic compound with the capacity of donating and receiving multiple electrons
The fingertip of a wireless voltage detection glove illuminates when the wearer's hand approaches a live cable. Purdue University engineers have developed a method to transform existing cloth items into battery-free wearables resistant to laundry.
CREDIT
(Purdue University photo/Rebecca McElhoe)
Abstract:
Marina Sala de Medeiros, Debkalpa Goswami, Daniela Chanci, Carolina Moreno, and Ramses V. Martinez
The commercial development of smart garments is currently hindered by significant challenges, such as dependence on batteries, reduced washability, and difficult incorporation into existing large-scale textile manufacturing technologies. This work describes an industrially-scalable approach to transform conventional fabrics into smart textiles--wirelessly powered by omniphobic silk-based coils (OSCs). OSCs are stretchable and lightweight power-receiving coils that can be easily sewn onto any textile, enabling the safe wireless powering of wearable electronics via magnetic resonance coupling without compromising the comfort of the user. OSCs are composed of microfibers made of a novel silk-nanocarbon composite that benefits from the stretchability of silk fibroin and the high conductivity of multiwall carbon nanotubes and chitin carbon nanoflakes. The surface of the OSC-powered electronic textiles (e-textiles) is rendered omniphobic--both hydrophobic and oleophobic--using a spray-based silanization method, which imbues the e-textile with waterproof and stain repellent properties without compromising its flexibility, stretchability, or breathability. OSCs exhibit excellent stability in high moisture environments and under mechanical deformations, allowing them to undergo 50 standard machine-washing cycles without degradation in performance. Moreover, OSC-powered e-textiles can be fabricated at a low cost using scalable manufacturing processes, paving the way toward the rapid development and commercialization of machine-washable and battery-free smart clothing and reusable wearable electrophysiological devices.

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Forget wearables: Future washable smart clothes powered by Wi-Fi will monitor your health

Purdue University engineers have developed a method to transform existing cloth items into battery-free wearables resistant to laundry. These smart clothes are powered wirelessly through a flexible, silk-based coil sewn on the textile.

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Purdue faculty invited to join Entrepreneurial Learning Academy

The Entrepreneurial Learning Academy is now accepting applications for the 2021-22 cohort. Purdue faculty interested in commercializing their research and exploring entrepreneurship are encouraged to apply. The deadline for applications is June 4.

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