Low Temperature Deposition of Highly Cyclable Porous Prussian Blue Cathode for Lithium-Ion Microbattery.

Small dimension Li-ion microbatteries are of great interest for embedded microsystems and on-chip electronics. However, the deposition of fully crystallized cathode thin film generally requires high temperature synthesis or annealing, incompatible with microfabrication processes of integrated Si devices. In this work, a low temperature deposition process of a porous Prussian blue-based cathode on Si wafers is reported. The active material is electrodeposited under aqueous conditions using a pulsed deposition protocol on a porous dendritic metallic current collector that ensures good electronic conductivity of the composite. The high voltage cathodes exhibit a huge areal capacity of ≈650 µAh cm-2 and are able to withstand more than 2000 cycles at 0.25 mA cm-2 rate. The application of these electrode composites with porous Sn based alloying anodes is also demonstrated for the first time in full cell configuration, with high areal energy of 3.1 J cm-2 and more than 95% reversible capacity. This outstanding performance can be attributed to uniform deposition of Prussian blue materials on conductive matrix, which maintains electronic conductivity while simultaneously providing mechanical integrity to the electrode. This finding opens new horizons in the monolithic integration of energy storage components compatible with the semiconductor industry for self-powered microsystems.

High Areal Capacity Porous Sn-Au Alloys with Long Cycle Life for Li-ion Microbatteries.

Long-term stability is one of the most desired functionalities of energy storage microdevices for wearable electronics, wireless sensor networks and the upcoming Internet of Things. Although Li-ion microbatteries have become the dominant energy-storage technology for on-chip electronics, the extension of lifetime of these components remains a fundamental hurdle to overcome. Here, we develop an ultra-stable porous anode based on SnAu alloys able to withstand a high specific capacity exceeding 100 µAh cm-2 at 3 C rate for more than 6000 cycles of charge/discharge. Also, this new anode material exhibits low potential (0.2 V versus lithium) and one of the highest specific capacity ever reported at low C-rates (7.3 mAh cm-2 at 0.1 C). We show that the outstanding cyclability is the result of a combination of many factors, including limited volume expansion, as supported by density functional theory calculations. This finding opens new opportunities in design of long-lasting integrated energy storage for self-powered microsystems.

Cellphone Monitoring of Multi-Qubit Emission Enhancements from Pd-Carbon Plasmonic Nanocavities in Tunable Coupling Regimes with Attomolar Sensitivity.

We demonstrate for the first time the tuning of qubit emission based on cavity engineering on plasmonic silver thin films. This tunable transition from weak to strong coupling regime in plasmon-coupled fluorescence platform was achieved with the use of palladium nanocomposites. In addition to our recently established correlation between Purcell factor and surface plasmon-coupled emission enhancements, we now show that the qubit-cavity environment experiences the Purcell effect, Casimir force, internal fano resonance, and Rabi splitting. Finite-difference time-domain simulations and time correlated single photon counting studies helped probe the molecular structure of the radiating dipole, rhodamine-6G, in palladium-based nanocavities. The sensitivity of the qubit-cavity mode helped attain a DNA detection limit of 1 aM (attomolar) and multianalyte sensing at picomolar concentration with the use of a smartphone camera and CIE color space. We believe that this low-cost technology will lay the groundwork for mobile phone-based next-gen plasmonic sensing devices.