TY - JOUR
T1 - Synergistic Voltaglue Adhesive Mechanisms with Alternating Electric Fields
AU - Singh, Manisha
AU - Yin, Cheong See
AU - Page, Samuel J.
AU - Liu, Yuqing
AU - Wicaksono, Gautama
AU - Pujar, Rajashekhar
AU - Choudhary, Shyam Kumar
AU - Kulkarni, Giridhar U.
AU - Chen, Jun
AU - Hanna, John V.
AU - Webster, Richard D.
AU - Steele, Terry W.J.
N1 - Publisher Copyright:
© 2020 American Chemical Society.
PY - 2020/3/24
Y1 - 2020/3/24
N2 - Voltage-activated adhesion is a relatively new discovery that relies on direct currents for initiation of cross-linking. Previous investigations have found that direct currents are linearly correlated to the migration rates of electrocuring, but this is limited by high voltages exceeding 100 V with instances of incomplete curing of voltage-activated adhesives on semiconducting substrates. Practical applications of electrocuring would benefit from lower voltages to mitigate high-voltage risks, especially with regard to potential medical applications. Alternative electrocuring strategies based on alternating current (AC), electrolyte ionic radius, and temperature are evaluated herein. Square-waveform AC electric field is hypothesized to initiate a two-sided curing progression of voltage-activated adhesive (PAMAM-g-diazirine, aka Voltaglue), where initiation occurs at the cathode terminal. Structure-activity relationships of Voltaglue as a function of AC frequency at currents of 1-3 mA are evaluated against direct currents, migration rate, storage modulus, and lap-shear adhesion on ex vivo tissue mimics. Numerous improvements in electrocuring are observed with AC stimulation vs direct current, including a 35% decrease in maximum voltage, 180% improvement in kinetic rates, and 100% increase in lap-shear adhesion at 2 mA. Li+ ion electrolytes and curing at 4 °C shifts curing kinetics by +104% and -22% respectively, with respect to the control ion (Na+ ion at 24 °C), suggesting that electrolyte migration is the rate-limiting step. Li+ ion electrolytes and curing at 50 °C improve storage modulus by 110% and 470%, respectively. Further evaluations of electrocured matrices with 19F NMR, solid-state NMR, and infrared spectroscopy provide insights into the probable cross-linking mechanisms.
AB - Voltage-activated adhesion is a relatively new discovery that relies on direct currents for initiation of cross-linking. Previous investigations have found that direct currents are linearly correlated to the migration rates of electrocuring, but this is limited by high voltages exceeding 100 V with instances of incomplete curing of voltage-activated adhesives on semiconducting substrates. Practical applications of electrocuring would benefit from lower voltages to mitigate high-voltage risks, especially with regard to potential medical applications. Alternative electrocuring strategies based on alternating current (AC), electrolyte ionic radius, and temperature are evaluated herein. Square-waveform AC electric field is hypothesized to initiate a two-sided curing progression of voltage-activated adhesive (PAMAM-g-diazirine, aka Voltaglue), where initiation occurs at the cathode terminal. Structure-activity relationships of Voltaglue as a function of AC frequency at currents of 1-3 mA are evaluated against direct currents, migration rate, storage modulus, and lap-shear adhesion on ex vivo tissue mimics. Numerous improvements in electrocuring are observed with AC stimulation vs direct current, including a 35% decrease in maximum voltage, 180% improvement in kinetic rates, and 100% increase in lap-shear adhesion at 2 mA. Li+ ion electrolytes and curing at 4 °C shifts curing kinetics by +104% and -22% respectively, with respect to the control ion (Na+ ion at 24 °C), suggesting that electrolyte migration is the rate-limiting step. Li+ ion electrolytes and curing at 50 °C improve storage modulus by 110% and 470%, respectively. Further evaluations of electrocured matrices with 19F NMR, solid-state NMR, and infrared spectroscopy provide insights into the probable cross-linking mechanisms.
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U2 - 10.1021/acs.chemmater.9b04962
DO - 10.1021/acs.chemmater.9b04962
M3 - Article
AN - SCOPUS:85082694888
SN - 0897-4756
VL - 32
SP - 2440
EP - 2449
JO - Chemistry of Materials
JF - Chemistry of Materials
IS - 6
ER -