The Origin of Thermal Gradient‐Induced Voltage in Polyelectrolytes

AbstractIonic thermoelectric materials can generate large thermal voltages under temperature gradients while also being low‐cost and environmentally friendly. Many electrolytes with large Seebeck coefficients are reported in recent years, however, the mechanism of the thermal voltage is remained elusive. In this work, three types of polyelectrolytes are studied with different cations and identified a significant contribution to their thermal voltage originating from a concentration gradient. This conclusion is based on studies of the loss and gain of water upon temperature changes, variations in conductivity with water content and temperature, and the voltages induced by changes in water content. The results are analyzed by the “hopping mode” dynamics of charge transport in electrolytes. The hydration of different cations influences the water concentration gradient, which affects the barrier height and ion‐induced potential in the electrodes. This work shows that the hydro‐voltage in ionic thermoelectric devices can be one order of magnitude larger than the contribution from thermodiffusion‐induced potentials, and becomes the main contributor to energy harvesting when implemented into ionic thermoelectric supercapacitors. Together with the rationalized theoretical discussion, this work clarifies the mechanism of thermal voltages in electrolytes and provides a new path for the development of ionic thermoelectric materials.</jats:p

Electrical tuning of radiative cooling at ambient conditions

Passive radiative cooling forms a sustainable means for cooling of objects through thermal radiation. Along with progress on static cooling systems, there is an emerging need for dynamic control to enable thermoregulation. Here, we demonstrate temperature regu-lation of devices at ambient pressure and temperature by electri-cally tuning their radiative cooling power. Our concept exploits the possibility to electrochemically tune the thermal emissivity and thereby cooling power of a conducting polymer, which enabled reversible control of device temperatures of around 0.25 degrees C at ambient conditions in a sky simulator. Besides tuneable radiative cooling by exposure to the sky, the concept could also contribute to reduced needs for indoor climate control by enabling dynamic control of thermal energy flows between indoor objects, such as be-tween people and walls.Funding Agencies|Knut and Alice Wallenberg Foundation; Linkoping University; Wallenberg Wood Science Center; Swedish government; Strategic Research Area in Materials Science on Functional Materials at Linkoping University (faculty grant SFO-Mat-LiU) [2009 00971]; Swedish Armed Forces Research; Swedish Research Council [2020-00287]; Wallenberg Academy [2019.0163]</p

Cellulose-Based Radiative Cooling and Solar Heating Powers Ionic Thermoelectrics

Cellulose opens for sustainable materials suitable for radiative cooling thanks to inherent high thermal emissivity combined with low solar absorptance. When desired, solar absorptance can be introduced by additives such as carbon black. However, such materials still shows high thermal emissivity and therefore performs radiative cooling that counteracts the heating process if exposed to the sky. Here, this is addressed by a cellulose-carbon black composite with low mid-infrared (MIR) emissivity and corresponding suppressed radiative cooling thanks to a transparent IR-reflecting indium tin oxide coating. The resulting solar heater provides opposite optical properties in both the solar and thermal ranges compared to the cooler material in the form of solar-reflecting electrospun cellulose. Owing to these differences, exposing the two materials to the sky generated spontaneous temperature differences, as used to power an ionic thermoelectric device in both daytime and nighttime. The study characterizes these effects in detail using solar and sky simulators and through outdoor measurements. Using the concept to power ionic thermoelectric devices shows thermovoltages of &amp;gt;60 mV and 10 degrees C temperature differences already at moderate solar irradiance of approximate to 400 W m(-2).Funding Agencies|Wallenberg Wood Science Center; Swedish Government Strategic Research Area in Materials Science on Functional Materials at Linkoping University [2009 00971]; Swedish Research Council [2018-04037, 2020-00287]; Knut and Alice Wallenberg Foundation; Linkoeping University</p

Nanosized CoO Loaded on Copper Foam for High-Performance, Binder-Free Lithium-Ion Batteries

The synthesis of nanosized CoO anodes with unique morphologies via a hydrothermal method is investigated. By adjusting the pH values of reaction solutions, nanoflakes (CoO-NFs) and nanoflowers (CoO-FLs) are successfully located on copper foam. Compared with CoO-FLs, CoO-NFs as anodes for lithium ion batteries present ameliorated lithium storage properties, such as good rate capability, excellent cycling stability, and large CoO nanoflakes; CoO nanoflowers; anodes; binder free; lithium ion batteriesreversible capacity. The initial discharge capacity is 1470 mA h g−1, while the reversible capacity is maintained at 1776 m Ah g−1 after 80 cycles at a current density of 100 mA h g−1. The excellent electrochemical performance is ascribed to enough free space and enhanced conductivity, which play crucial roles in facilitating electron transport during repetitive Li+ intercalation and extraction reaction as well as buffering the volume expansion