Photosynthesis is a sustainable process that converts light energy into chemical energy. substantial research efforts are directed towards the application of the photosynthetic reaction centres, photosystems I and II, as active components for the light-induced generation of electrical power or fuel products. nonetheless, no integrated photo-bioelectrochemical device that produces electrical power, upon irradiation of an aqueous solution that includes two inter-connected electrodes is known. Here we report the assembly of photobiofuel cells that generate electricity upon irradiation of biomaterial-functionalized electrodes in aqueous solutions. The cells are composed of electrically contacted photosystem II-functionalized photoanodes and an electrically wired bilirubin oxidase/carbon nanotubes-modified cathode. Illumination of the photoanodes yields the oxidation of water to o 2 and the transfer of electrons through the external circuit to the cathode, where o 2 is re-reduced to water.

A novel method to assemble acrylamide/acrydite DNA copolymer hydrogels on surfaces, specifically gold-coated surfaces, is introduced. The method involves the synthesis of two different copolymer chains consisting of hairpin A, HA, modified acrylamide copolymer and hairpin B, HB, acrylamide copolymer. In the presence of a nucleic acid promoter monolayer associated with the surface, the hybridization chain reaction between the two hairpin-modified polymer chains is initiated, giving rise to the cross-opening of hairpins HA and HB and the formation of a cross-linked hydrogel on the surface. By the cofunctionalization of the HA- and HB-modified polymer chains with G-rich DNA tethers that include the G-quadruplex subunits, hydrogels of switchable stiffness are generated. In the presence of K(+)-ions, the hydrogel associated with the surface is cooperatively cross-linked by duplex units of HA and HB, and K(+)-ion-stabilized G-quadruplex units, giving rise to a stiff hydrogel. The 18-crown-6-ether-stimulated elimination of the K(+)-ions dissociates the bridging G-quadruplex units, resulting in a hydrogel of reduced stiffness. The duplex/G-quadruplex cooperatively stabilized hydrogel associated with the surface reveals switchable electrocatalytic properties. The incorporation of hemin into the G-quadruplex units electrocatalyzes the reduction of H2O2. The 18-crown-6-ether stimulated dissociation of the hemin/G-quadruplex bridging units leads to a catalytically inactive hydrogel.

The lack of compact integration, including fusing of skin-interfaced direct, rapid independent data visualization along with light, safe stretchable batteries, hinders progress towards the creation of fully autonomous comprehensive wearable monitoring platforms. Here we present a highly integrated epidermal sensing platform combining electrochemical sensors with stretchable battery and ultra-low power digital display that instantaneously visualizes the results via 10 individually addressable electrochromic pixels. The all-around stretchable patch can operate independently as a standalone device to directly display the concentration of various electrolytes or metabolites, freeing it from any wired or wireless connection to other equipment. Fabricated via high-throughput printing of customized elastomeric inks, the integrated system presents robust mechanical performance, enduring over 1500 stretching cycles without affecting its sensing and display capabilities. The fast-responding display exhibits stability over 10,000 ON/OFF cycles, and upon coupling with the high-performance stretchable battery, can serve 14,000 sensing sessions in a week-long usage. Merging ultra-low power consumption, independent operation, rapid data display and superior mechanical performance, this fully autonomous multifunctional self-sustainable wearable sensing platform is of high practicality and convenience for diverse practical applications in professional sports, personalized wellness management, and beyond. MainSoft electronics have gathered considerable attention over the past decade as attractive alternatives to their rigid bulky counterparts, for applications in on-body sensing and human-machine interfacing. [1][2][3][4] In particular, many integrated epidermal sensing systems have been developed as "labs-on-the-skin", capable of recording a myriad of mechanical, electrical, physiological, and electrochemical signals, towards applications in healthcare, wellness and tness. [5][6][7][8] The current development of wearable sensors has evolved from the study of physical and chemical sensors alone towards the integration of sensors with energy management, signal acquisition, and data interfacing electronics. 9-14 Due to the lack of high-performance wearable batteries, most wearable electronics currently operate with commercial lithium polymer pouches or coin cells, which are rigid, unsafe, and bottlenecks the product design.Avoiding such battery-related design limitations, conformal epidermal sensors were often designed with wired connections or short-range power delivery schemes, which in turn compromise the system autonomy and limit the user's mobility. 9,11,15−18 Furthermore, such integrated sensors rely on wireless data transmissions, which calls for the need for external devices (e.g., computers, mobile smartphones, customized receivers) for users to obtain the sensing results. 9,11,19−21 Such lack of direct access to sensing results has led to the inconvenience and impracticality of many existing wearable sensors in their rea...

The porous high surface area and conducting properties of mesoporous carbon nanoparticles, CNPs (<500 nm diameter of NPs, pore dimensions ∼6.3 nm), are implemented to design electrically contacted enzyme electrodes for biosensing and biofuel cell applications. The relay units ferrocene methanol, Fc-MeOH, methylene blue, MB(+), and 2,2'-azinobis(3-ethylbenzothiazoline-6-sulfonic acid), ABTS(2-), are loaded in the pores of the mesoporous CNPs, and the pores are capped with glucose oxidase, GOx, horseradish peroxidase, HRP, or bilirubin oxidase, BOD, respectively. The resulting relay/enzyme-functionalized CNPs are immobilized on glassy carbon electrodes, and the relays encapsulated in the pores are sufficiently free to electrically contact the different enzymes with the bulk electrode supports. The Fc-MeOH/GOx CNP-functionalized electrode is implemented for the bioelectrocatalyzed sensing of glucose, and the MB(+)/HRP-modified CNPs are applied for the electrochemical sensing of H2O2. The ABTS(2-)/BOD-modified CNPs provide an effective electrically contacted material for the bioelectrocatalyzed reduction of O2 (kcat = 94 electrons·s(-1)). Integration of the Fc-MeOH/GOx CNP electrode and of the electrically wired ABTS(2-)/BOD CNP electrode as anode and cathode, respectively, yields a biofuel cell revealing a power output of ∼95 μW·cm(-2).

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This work demonstrates the first example of sweat-based wearable and stretchable biosupercapacitors (BSCs), capable of generating high-power pulses from human activity. The all-printed, dual-functional, conformal BSC platform can harvest and store energy from sweat lactate. By integrating energy harvesting and storage functionalities on the same footprint of a single epidermal device, the new wearable energy system can deliver highpower pulses and be rapidly self-charged by bioenergy conversion of sweat lactate generated from human activity while simplifying the design and fabrication. The mechanical robustness and conformability of the device are realized through island-bridge patterns and strain-enduring inks. The enhanced capacitance of the BSC is realized by the synergistic effect of carbon nanotube ink with electrodeposited polypyrrole on the anode and of porous cauliflowerlike platinum on the cathode. In the presence of lactate, the BSC shows high power in pulsed output and stable cycling performance. Furthermore, the wearable device can store energy and deliver high-power pulses long after the perspiration stopped. The self-charging hybrid wearable device obtained high power of 1.7 mW cm −2 in vitro, and 343 µW cm −2 on the body during exercise, suggesting considerable potential as a power source for the next generation of wearable electronics.

Information related to the diverse and dynamic metabolite composition of the small intestine is crucial for the diagnosis and treatment of various diseases. However, our current understanding of the physiochemical dynamics of metabolic processes within the small intestine is limited due to the lack of in situ access to the intestinal environment. Here, we report a demonstration of a battery-free ingestible biosensing system for monitoring metabolites in the small intestine. As a proof of concept, we monitor the intestinal glucose dynamics on a porcine model. Battery-free operation is achieved through a self-powered glucose biofuel cell/biosensor integrated into a circuit that performs energy harvesting, biosensing, and wireless telemetry via a power-to-frequency conversion scheme using magnetic human body communication. Such long-term biochemical analysis could potentially provide critical information regarding the complex and dynamic small intestine metabolic profiles.

Inspired by traditional energy-autonomous microgrids, this perspective summarizes the key design and energy-budgeting considerations and outlook of integrated wearable systems.