Despite the impressive photovoltaic performances with power conversion efficiency beyond 22%, perovskite solar cells are poorly stable under operation, failing by far the market requirements. Various technological approaches have been proposed to overcome the instability problem, which, while delivering appreciable incremental improvements, are still far from a market-proof solution. Here we show one-year stable perovskite devices by engineering an ultra-stable 2D/3D (HOOC(CH2)4NH3)2PbI4/CH3NH3PbI3 perovskite junction. The 2D/3D forms an exceptional gradually-organized multi-dimensional interface that yields up to 12.9% efficiency in a carbon-based architecture, and 14.6% in standard mesoporous solar cells. To demonstrate the up-scale potential of our technology, we fabricate 10 × 10 cm2 solar modules by a fully printable industrial-scale process, delivering 11.2% efficiency stable for >10,000 h with zero loss in performances measured under controlled standard conditions. This innovative stable and low-cost architecture will enable the timely commercialization of perovskite solar cells.

Carbon based perovskite solar cells are fabricated for the first time in a room temperature environment by employing inkjet infiltration of perovskite precursor ink. The fabricated perovskite solar cells exhibit impressive performance reproducibility with this automated method and exhibit high stability when exposed to 35 °C for a period of 1046 hours.

We report humidity assisted thermal exposure (HTE) as a post-treatment method for carbon based printed perovskite solar cells (CPSCs).

The long term stability of air processed inkjet infiltrated carbon based perovskite solar cells (CPSCs) is investigated under intense ultra-violet light soaking equivalent to 1.5 Sun UV light illumination.

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One of the key challenges of perovskite photovoltaics (PV) is the long‐term stability. Although efforts are made to improve the lifetime of perovskite PV devices, their degradation under reverse‐bias conditions is barely addressed. Herein, perovskite solar cells with carbon‐based electrodes are presented which demonstrate superior resilience against reverse‐bias‐induced degradation. Although their breakdown voltage is identified to be at approximately −3.6 V, cells do not degrade until the applied reverse‐bias exceeds −9 V. Two main degradation mechanisms are identified: 1) iodine loss due to hole tunneling into perovskite, which takes place even at low reverse‐bias but decomposes the perovskite only after long time durations; and 2) rapid heating at large reverse‐bias leading to formation of PbI2, which starts at shunts and then follows the path of the least resistance for the cell current, which is primarily influenced by the electrode sheet resistances. Finally, perovskite solar modules with carbon‐based electrodes are demonstrated, which are subjected to a “hotspot” test described in the IEC 61215:2016 international standard at an accredited module testing laboratory. Passing this accelerated test for the first time confirms the superior stability of perovskite PV devices with carbon‐based electrodes and highlights their large industrialization potential.

The effect of pyrrole- and pyrrolidine-containing ligands (L) on the properties of heteroleptic [RuL2dcbpy]2+ complexes has been investigated. TiO2 electrodes modified with the new complexes exhibited extended absorption domains and high absorbances. Providing that a cobalt-based mediator was used for regeneration of the RuII state, good incident photon-to-current efficiency (near 80%) values were obtained in the pyrrole series.

Improved charge extraction in carbon-based fully printable hole transport layer-free mesoscopic perovskite solar cells with excellent long-term stability.