Recent advances in heterojunction and interfacial engineering of perovskite solar cells (PSCs) have enabled great progress in developing highly efficient and stable devices. Nevertheless, the effect of halide choice on the formation mechanism, crystallography, and photoelectric properties of the low-dimensional phase still requires further detailed study. In this work, we present key insights into the significance of halide choice when designing passivation strategies comprising large organic spacer salts, clarifying the effect of anions on the formation of quasi-2D/3D heterojunctions. To demonstrate the importance of halide influences, we employ novel neo-pentylammonium halide salts with different halide anions (neoPAX, X=I, Br, or Cl). We find that regardless of halide selection, iodide-based (neoPA)₂(FA)_(n-1)Pb_nI_(3n+1) phases are formed above the perovskite substrate, while the added halide anions diffuse and passivate the perovskite bulk. In addition, we also find the halide choice has an influence on the degree of dimensionality (n). Comparing the three halides, we find that chloride-based salts exhibit superior crystallographic, enhanced carrier transport, and extraction compared to the iodide and bromide analogs. As a result, we report high power conversion efficiency in quasi-2D/3D PSCs, which are optimal when using chloride salts, reaching up to 23.35%, and improving long-term stability.

Thermoelectrics are a promising solution to the recovery of some of the 60% of the worldwide energy wasted as heat. However, their conversion efficiency is low and the best performing materials are brittle, toxic, and made of expensive ceramics. The challenge in developing better performing materials is in disrupting the electrical vs thermal conductivity correlation, to achieve low thermal conductivity simultaneously with a high electrical conductivity. Carbon nanotubes allow for the decoupling of the electronic density of states from the phonon density of states and this paper shows that flexible, thin films of double-walled carbon nanotube (DWCNT) can form effective n- and p-doped semiconductors that can achieve a combined Seebeck coefficient of 157.6 µV K⁻¹, the highest reported for a single DWCNT device to date. This is achieved through selected surfactant doping, whose role is correlated with the length of the hydrocarbon chain of the hydrophobic tail group of the surfactant’s molecules. CNTs functionalized with Triton X-405 show the highest output power consisting of a single junction of p- and n-type thermoelectric elements, reaching as high as 67 nW for a 45 K temperature gradient. Thus enabling flexible, cheaper, and more efficient thermoelectric generators through the use of functionalized CNTs.

Pb-Sn mixed perovskites are becoming increasingly popular as narrow-bandgap (1.2–1.3 eV) light absorbers in single-junction perovskite solar cells (PSCs) and as bottom cells for all-perovskite tandem solar cells, for high-efficiency, low-cost, lightweight, roll-to-roll printable photovoltaic (PV) applications. From the first report of planar Pb:Sn mixed PSCs in 2014, the power conversion efficiencies (PCE) have increased from 10% to 21% by the end of 2020 with an exponential growth in research conducted in this field. Despite much effort, the performance and stability of Pb-Sn mixed PSCs are still limited, which constrains their long-term use in all-perovskite tandem devices. This review highlights the avenues explored in improving different aspects of Pb-Sn mixed PSCs and provides a comprehensive discussion of the interdependent factors affecting the device performance. This includes compositional engineering of the perovskite crystal, absorber layer fabrication and crystallization methods, bandgap tuning, Sn⁴⁺ reduction, and surface passivation of the absorber layer, as well as the selection of interlayers and electrodes of the final PSC.