Ion-Electron Coupling Enables Ionic Thermoelectric Material with New Operation Mode and High Energy Density.

Ionic thermoelectrics (i-TE) possesses great potential in powering distributed electronics because it can generate thermopower up to tens of millivolts per Kelvin. However, as ions cannot enter external circuit, the utilization of i-TE is currently based on capacitive charge/discharge, which results in discontinuous working mode and low energy density. Here, we introduce an ion-electron thermoelectric synergistic (IETS) effect by utilizing an ion-electron conductor.

Real-time observation of the buildup of polaron in α-FAPbI.

The formation of polaron, i.e., the strong coupling process between the carrier and lattice, is considered to play a crucial role in benefiting the photoelectric performance of hybrid organic-inorganic halide perovskites.

Oxidation of Spiro-OMeTAD in High-Efficiency Perovskite Solar Cells.

2,2',7,7'-Tetrakis(N,N-di--methoxyphenylamine)-9,9'-spirobifluorene (spiro-OMeTAD), as an organic small molecule material, is the most commonly employed hole transport material (HTM) in perovskite solar cells (PSCs) because of its excellent properties that result in high photovoltaic performances. However, the material still suffers from low conductivity, leading to the necessary use of dopants and oxidative processes to overcome this issue. The spiro-OMeTAD oxidation process is highlighted in this review, and the main parameters involved in the process have been studied.

Role of Ions in Hydrogels with an Ionic Seebeck Coefficient of 52.9 mV K.

Ionic thermoelectric (i-TE) material with mobile ions as charge carriers has the potential to generate large thermal voltages at low operating temperatures. This study highlights the role of ions in i-TE hydrogels employing a poly(vinyl alcohol) (PVA) polymer matrix and a number of ion providers, e.g.

Volatile Solid Additive-Assisted Sequential Deposition Enables 18.42% Efficiency in Organic Solar Cells.

Morphology optimization of active layer plays a critical role in improving the performance of organic solar cells (OSCs). In this work, a volatile solid additive-assisted sequential deposition (SD) strategy is reported to regulate the molecular order and phase separation in solid state. The OSC adopts polymer donor D18-Cl and acceptor N3 as active layer, as well as 1,4-diiodobenzene (DIB) as volatile additive.

Simultaneous Interfacial Modification and Crystallization Control by Biguanide Hydrochloride for Stable Perovskite Solar Cells with PCE of 24.4.

Interfacial modification, which serves multiple roles, is vital for the fabrication of efficient and stable perovskite solar cells. Here, a multifunctional interfacial material, biguanide hydrochloride (BGCl), is introduced between tin oxide (SnO ) and perovskite to enhance electron extraction, as well as the crystal growth of the perovskite. The BGCl can chemically link to the SnO through Lewis coordination/electrostatic coupling and help to anchor the PbI .