TY - JOUR
T1 - In situ 3D printing of implantable energy storage devices
AU - Krishnadoss, Vaishali
AU - Kanjilal, Baishali
AU - Hesketh, Alexander
AU - Miller, Caleb
AU - Mugweru, Amos
AU - Akbard, Mohsen
AU - Khademhosseini, Ali
AU - Leijten, Jeroen
AU - Noshadi, Iman
PY - 2021/4/1
Y1 - 2021/4/1
N2 - The increasing demand for wearable bioelectronic devices has driven tremendous research effort on the fabrication of bioelectronics in microscale. To ensure the functionality and reliability, wearable bioelectronics need to be integrated with independent and internal energy storage systems to avoid frequent charging process from external sources. The supercapacitors has been considered as an electric energy source due to benefits such as a long cycle life, a high power density and fast charge–discharge rate. Miniaturization, biocompatibility, and biodegradability are the primary keys to achieving the requisites for implantable supercapacitors. Rapid, in situ 3D printing of implantable bioelectronic devices can address these needs. However, in situ 3D printing of bioelectronics using currently available materials has remained challenging due to their suboptimal physicochemical properties. Here, we present a novel material platform based on bio ionic liquid (BIL) functionalized biopolymers which can form a hydrogel electrolyte when exposed to visible light. Fine-structure, interdigitated, biocompatible, and implantable soft micro-supercapacitors (MSC) were created by 3D in situ bioprinting of these polymer electrolytes in combination with rheologically optimized graphene hydrogel-laponite (GH-L) blend as electrode material. The hydrogel electrolyte had a specific capacitance of ~ 200F/g, while the MSC had a specific capacitance of ~ 16 μF/g at a current density of 1 A/g, volumetric capacitance of ~ 44 μF/cm3, cyclic stability up to 10,000 cycles, energy densities nearly as high as implantable batteries, and a power density level of implantable supercapacitors. This novel material platform enables in situ 3D printing of flexible bioelectronics structures with integrated life-long power source.
AB - The increasing demand for wearable bioelectronic devices has driven tremendous research effort on the fabrication of bioelectronics in microscale. To ensure the functionality and reliability, wearable bioelectronics need to be integrated with independent and internal energy storage systems to avoid frequent charging process from external sources. The supercapacitors has been considered as an electric energy source due to benefits such as a long cycle life, a high power density and fast charge–discharge rate. Miniaturization, biocompatibility, and biodegradability are the primary keys to achieving the requisites for implantable supercapacitors. Rapid, in situ 3D printing of implantable bioelectronic devices can address these needs. However, in situ 3D printing of bioelectronics using currently available materials has remained challenging due to their suboptimal physicochemical properties. Here, we present a novel material platform based on bio ionic liquid (BIL) functionalized biopolymers which can form a hydrogel electrolyte when exposed to visible light. Fine-structure, interdigitated, biocompatible, and implantable soft micro-supercapacitors (MSC) were created by 3D in situ bioprinting of these polymer electrolytes in combination with rheologically optimized graphene hydrogel-laponite (GH-L) blend as electrode material. The hydrogel electrolyte had a specific capacitance of ~ 200F/g, while the MSC had a specific capacitance of ~ 16 μF/g at a current density of 1 A/g, volumetric capacitance of ~ 44 μF/cm3, cyclic stability up to 10,000 cycles, energy densities nearly as high as implantable batteries, and a power density level of implantable supercapacitors. This novel material platform enables in situ 3D printing of flexible bioelectronics structures with integrated life-long power source.
KW - 2022 OA procedure
KW - Biocompatible
KW - Energy Storage Devices
KW - Hydrogels
KW - In Situ 3D printing
KW - Bio Ionic Liquid
UR - http://www.scopus.com/inward/record.url?scp=85098710026&partnerID=8YFLogxK
U2 - 10.1016/j.cej.2020.128213
DO - 10.1016/j.cej.2020.128213
M3 - Article
AN - SCOPUS:85098710026
SN - 1385-8947
VL - 409
JO - Chemical Engineering Journal
JF - Chemical Engineering Journal
M1 - 128213
ER -