No abstract

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.

Aerosols can act as cloud condensation nuclei and/or ice-nucleating particles (INPs), influencing cloud properties. In particular, INPs show a variety of different and complex mechanisms when interacting with water during the freezing process. To gain a fundamental understanding of the heterogeneous freezing mechanisms, studies with proxies for atmospheric INPs must be performed. Graphene and its derivatives offer suitable model systems for soot particles, which are ubiquitous aerosols in the atmosphere. In this work, we present an investigation of the ice nucleation activity (INA) of different types of graphene and graphene oxides. Immersion droplet freezing experiments as well as additional analytical analyses, such as X-ray photoelectron spectroscopy, Raman spectroscopy, and transmission electron microscopy, were performed. We show within a group of samples that a highly ordered graphene lattice (Raman G band intensity >50%) can support ice nucleation more effectively than a lowly ordered graphene lattice (Raman G band intensity <20%). Ammonia-functionalized graphene revealed the highest INA of all samples. Atmospheric ammonia is known to play a primary role in the formation of secondary particulate matter, forming ammonium-containing aerosols. The influence of functionalization on interactions between the particle interface and water molecules, as well as on hydrophobicity and agglomeration processes, is discussed.

We report a simple coumarin-triarylphosphine conjugate that undergoes fluorescence enhancement upon reaction with hydroperoxides and demonstrate its use to follow autoxidations of 7-dehydrocholesterol (at 37 °C) and hexadecane (at 160 °C) and their inhibition by antioxidants.

We demonstrate a new hybrid morphology that facilitates charge transport and charge separation at the interface between the nanocarbon and the semiconductor and so greatly improves their performance in environmental and sustainable energy applications.

In this work we synthesized well-ordered, TaO films with a 3D-interconnected gyroid mesopore architecture with large pore sizes beyond 30 nm and extended crystalline domains through self-assembly of tailor-made triblock-terpolymers. This has effectively eliminated diffusion limitations inherent to previously reported mesoporous photocatalysts and resulted in superior hydrogen evolution with apparent quantum yields of up to 4.6% in the absence of any cocatalyst. We further show that the injection barrier at the solid-liquid interface constitutes a key criterion for photocatalytic performance and can be modified by the choice of the carbon template. This work highlights pore and surface engineering as a promising tool towards high-performance mesoporous catalysts and electrodes for various energy-related applications.

Long-term photovoltaic (PV) module reliability is highly determined by the durability of the polymeric components (backsheet and encapsulation materials). This paper presents the result of experiments on encapsulant degradation influenced by the backsheet permeation properties. Towards this goal, one type of ethylene/vinyl acetate copolymer (EVA) was aged in glass/EVA/backsheet laminates in accelerated aging tests (up to 4000 h for Damp-Heat (DH) and up to 480 kWh/m2 for UV and UV-DH combined). The samples contained three backsheets with different permeation properties to examine their impact on EVA degradation. Thermal and chemical characterization shows that the EVA degradation is stronger with the glass–EVA–polyamide (PA)-based backsheet than with the polyethylene terephthalate (PET)-based backsheets. The higher oxygen transmission rate (OTR) of the PA-based backsheet may increase photo-oxidation and aggravating the degradation of EVA in the laminates. Furthermore, FTIR results were used to demonstrate the effect of damp heat exposure on the EVA interfaces, showing an accelerated degradation at the glass–EVA interface. The comparison of accelerated aging stress factors reveals that EVA suffers the strongest chemical and optical degradation when high UV, high temperature and high relative humidity are combined simultaneously.

The hybridisation of metal oxides and nanocarbons has created a promising new class of functional materials for environmental and sustainable energy applications. The performance of such hybrids can be further improved by rationally designing interfaces and morphologies. Atomic layer deposition (ALD) is among the most powerful techniques for the controlled deposition of inorganic compounds, due to its ability to form conformal coatings on porous substrates at low temperatures with high surface sensitivity and atomic control of film thickness. The hydrophobic nature of the nanocarbon surface has so far limited the applicability of ALD on CNTs. Herein we investigate the role of structural defects in CNTs, both intrinsic and induced by acid treatment, on coverage, uniformity and crystallinity of ZnO coatings. Furthermore, we demonstrate the potential of small aromatic molecules, including benzyl alcohol (BA), naphthalene carboxylic acid (NA) and pyrene carboxylic acid (PCA), as active nucleation sites and linking agents. Importantly, only PCA exhibits sufficiently strong interactions with the pristine CNT surface to withstand desorption under reaction conditions. Thus, PCA enables a versatile and non-destructive alternative route for the deposition of highly uniform metal oxide coatings onto pristine CNTs via ALD over a wide temperature range and without the typical surface corrosion induced by covalent functionalisation. Importantly, preliminary tests demonstrated that the improved morphology obtained with PCA has indeed considerably increased the hybrid's photocatalytic activity towards hydrogen evolution via sacrificial water splitting. The concept demonstrated in this work is transferable to a wide range of other inorganic compounds including metal oxides, metal (oxy)nitrides and metal chalcogenides on a variety of nanocarbons.