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Many recent advances in metal halide perovskite solar cell (PSC) performance are attributed to surface treatments which passivate interfacial trap states, minimise charge recombination and boost photovoltages. Surprisingly, these photovoltages exceed the cells' built-in potentials, often with large energetic offsets reported between the perovskite and transport layer semiconductor band edges - contradicting standard photovoltaic design principles. Here we show that this tolerance to energetic offsets results from mixed ionic/electronic conduction in the perovskite layer. Combining drift-diffusion simulations with experiments probing the current-voltage performance of PSCs as a function of ion distribution, we demonstrate that electrostatic redistribution of ionic charge reduces surface recombination currents at steady-state, increasing the photovoltage by tens to hundreds of millivolts. Thus, mobile ions can reduce the sensitivity of photovoltage to energetic misalignments at perovskite/transport layer interfaces, benefitting overall efficiency. Building on these insights, we show how photovoltaic design principles are modified to account for mobile ions.

Photovoltaics (PVs) are a critical technology for curbing growing levels of anthropogenic greenhouse gas emissions, and meeting increases in future demand for low-carbon electricity. In order to fulfil ambitions for net-zero carbon dioxide equivalent (CO2eq) emissions worldwide, the global cumulative capacity of solar PVs must increase by an order of magnitude from 0.9 TWp in 2021 to 8.5 TWp by 2050 according to the International Renewable Energy Agency, which is considered to be a highly conservative estimate. In 2020, the Henry Royce Institute brought together the UK PV community to discuss the critical technological and infrastructure challenges that need to be overcome to address the vast challenges in accelerating PV deployment. Herein, we examine the key developments in the global community, especially the progress made in the field since this earlier roadmap, bringing together experts primarily from the UK across the breadth of the photovoltaics community. The focus is both on the challenges in improving the efficiency, stability and levelized cost of electricity of current technologies for utility-scale PVs, as well as the fundamental questions in novel technologies that can have a significant impact on emerging markets, such as indoor PVs, space PVs, and agrivoltaics. We discuss challenges in advanced metrology and computational tools, as well as the growing synergies between PVs and solar fuels, and offer a perspective on the environmental sustainability of the PV industry. Through this roadmap, we emphasize promising pathways forward in both the short- and long-term, and for communities working on technologies across a range of maturity levels to learn from each other., Comment: 160 pages, 21 figures

Over the last two decades the organic solar cell community has synthesised tens of thousands of novel polymers and small molecules in the search for an optimum light harvesting material. These materials were often crudely evaluated simply by measuring the current voltage curves in the light to obtain power conversion efficiencies (PCEs). Materials with low PCEs were quickly disregarded in the search for higher efficiencies. More complex measurements such as frequency/time domain characterisation that could explain why the material performed as it did were often not performed as they were too time consuming/complex. This limited feedback forced the field to advance using a more or less random walk of material development and has significantly slowed progress. Herein, we present a simple technique based on machine learning that can quickly and accurately extract recombination time constants and charge carrier mobilities as a function of light intensity simply from light/dark JV curves alone. This technique reduces the time to fully analyse a working cell from weeks to seconds and opens up the possibility of not only fully characterising new devices as they are fabricated, but also data mining historical data sets for promising materials the community has over looked., Comment: 10 figures, 30 pages

(Photo)electrocatalysts capture sunlight and use it to drive chemical reactions such as water splitting to produce H2. A major factor limiting photocatalyst development is their large heterogeneity which spatially modulates reactivity and precludes establishing robust structure-function relationships. To make such links requires simultaneously probing of the electrochemical environment at microscopic length scales (nm to um) and broad timescales (ns to s). Here, we address this challenge by developing and applying in-situ steady-state and transient optical microscopies to directly map and correlate local electrochemical activity with hole lifetimes, oxygen vacancy concentration and the photoelectrodes crystal structure. Using this combined approach alongside spatially resolved X-Ray absorption measurements, we study microstructural and point defects in prototypical hematite (Fe2O3) photoanodes. We demonstrate that regions of Fe2O3, adjacent to microstructural cracks have a better photoelectrochemical response and reduced back electron recombination due to an optimal oxide vacancy concentration, with the film thickness and carbon impurities also dramatically influencing activity in a complex manner. Our work highlights the importance of microscopic mapping to understand activity and the impact of defects in even, seemingly, homogeneous solid-state metal oxide photoelectrodes.

A deep understanding of defects is essential for the optimisation of materials for solar energy conversion. This is particularly true for metal oxide photo(electro)catalysts, which typically feature high concentrations of charged point defects that are electronically active. In photovoltaic materials, except for selected dopants, defects are considered detrimental and should be eliminated to minimise charge recombination. However, photocatalysis is a more complex process where defects can play an active role, for example, by stabilising charge separation and mediating rate-limiting catalytic steps. Here, we review the behaviour of electronic defects in metal oxides, paying special attention to the principles underpinning the formation and function of trapped charges in the form of polarons. We focus on how defects alter the electronic structure, statically or transiently upon illumination, and discuss the implications of such changes in light-driven catalytic reactions. Finally, we consider the applicability of lessons learned from oxide defect chemistry to new photocatalysts based on carbon nitrides, polymers and metal halide perovskites., Comment: Review paper. Nat Rev Mater (2022)

High power conversion efficiency (PCE) inverted organic photovoltaics (OPVs) usually use thermally evaporated MoO3 as a hole transporting layer (HTL). Despite the high PCE values reported, stability investigations are still limited and the exact degradation mechanisms of inverted OPVs using thermally evaporated MoO3 HTL remain unclear under different environmental stress factors. In this study, we monitor the accelerated lifetime performance of non-encapsulated inverted OPVs using thiophene-based active layer materials and evaporated MoO3 under the ISOS D-2 protocol (heat conditions 65 {\deg}C). The investigation of degradation mechanisms presented focus on optimized P3HT:PC[70]BM-based inverted OPVs. Specifically, we present a systematic study on the thermal stability of inverted P3HT:PC[70]BM OPVs using solution processed PEDOT:PSS and evaporated MoO3 HTL. Using a series of measurements and reverse engineering methods we report that the P3HT:PC[70]BM/MoO3 interface is the main origin of failure of P3HT:PC[70]BM-based inverted OPVs under intense heat conditions.

The formation of bound electron-hole pairs, also called charge-transfer (CT) states, in organic-based photovoltaic devices is one of the dominant loss mechanisms hindering performance. While CT state dynamics following electron transfer from donor to acceptor have been widely studied, there is not much known about the dynamics of bound CT states produced by hole transfer from the acceptor to the donor. In this letter, we compare the dynamics of CT states formed in the different charge-transfer pathways in a range of model systems. We show that the nature and dynamics of the generated CT states are similar in the case of electron and hole transfer. However the yield of bound and free charges is observed to be strongly dependent on the HOMOD-HOMOA and LUMOD-LUMOA energy differences of the material system. We propose a qualitative model in which the effects of static disorder and sampling of states during the relaxation determine the probability of accessing CT states favourable for charge separation.