• Energy Research

This review highlights the importance of controlling the crystallization dynamics for the deposition of high-quality photovoltaic perovskite layers on larger-area coatings.

High-efficiency hole transport layer free perovskite solar cells (HTL-free PSCs) with economical and simplified device structure can greatly facilitate the commercialization of PSCs. However, eliminating the key HTL in PSCs results usually in a severe efficiency loss and poor carrier transfer due to the energy-level mismatching at the indium tin oxide (ITO)/perovskite interface. In this study, we solve this issue by introducing an organic monomolecular layer (ML) to raise the effective work function of ITO with the assistance of an interface dipole created by Sn-N bonds. The energy-level alignment at the ITO/perovskite interface is optimized with a barrier-free contact, which favors efficient charge transfer and suppressed nonradiative carrier recombination. The HTL-free PSCs based on the ML-modified ITO yield an efficiency of 19.4%, much higher than those of HTL-free PSCs on bare ITO (10.26%), comparable to state-of-the-art PSCs with a HTL. This study provides an in-depth understanding of the mechanism of interfacial energy-level alignment and facilitates the design of advanced interfacial materials for simplified and efficient PSC devices.

The critical challenge for the practical applications of VO2-based smart windows is to nucleate and propagate the phase transformation in the ambient condition while maintaining a balance between solar energy regulation and visible light transmittance. Doping proves effective in the modification of the thermochromic performance in VO2 but always causes unfavorable degradation accompanied with the significant reduction of phase transition temperature. Joule heating has been introduced in VO2-based devices to activate the metal-insulator transition (MIT) at ambient temperature. A synergy between these two strategies is necessary to achieve a well-balanced performance of VO2 films at the appropriate temperature. Here, we systematically investigate the thermochromic properties of tungsten (W)-doped VO2 composite films with Joule heating triggered MIT. The phase transition temperature of VO2 is effectively decreased by 21.6 °C per at. % W, and the balanced luminous transmittance (Tlum = 50.8%) and solar energy modulation ability (ΔTsol = 11.4%) are achieved at 0.6 at. % W doping. Importantly, as a synergetic result of W doping and hysteresis behavior of MIT in VO2, the optimal infrared blocking performance can be retained at a reduced cost of energy consumption and at the ambient temperature down to 47 °C. This is comparable to the glass window temperature in the summer in subtropical and tropical regions. This result suggests quite low and even zero energy consumption to maintain the optimal infrared blocking performance of VO2 films. This study provides a practical and advanced setup for operable and efficient smart windows in ambient conditions.