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Abstract: Porous boron nitride (BN) displays promising properties for interfacial and bulk processes, e.g. molecular separation and storage, or (photo)catalysis. To maximise porous BN's potential in such applications, tuning and controlling its chemical and structural features is key. Functionalisation of porous BN with metal nanoparticle represents one possible route, albeit a hardly explored one. Metal–organic frameworks (MOFs) have been widely used as precursors to synthesise metal functionalised porous carbon-based materials, yet MOF-derived metal functionalised inorganic porous materials remain unexplored. Here, we hypothesise that MOFs could also serve as a platform to produce metal-functionalised porous BN. We have used a Cu-containing MOF, i.e. Cu/ZIF-8, as a precursor and successfully obtained porous BN functionalised with Cu nanoparticles (i.e. Cu/BN). While we have shown control of the Cu content, we have not yet demonstrated it for the nanoparticle size. The functionalisation has led to improved light harvesting and enhanced electron–hole separation, which have had a direct positive impact on the CO2 photoreduction activity (production formation rate 1.5 times higher than pristine BN and 12.5 times higher than g-C3N4). In addition, we have found that the metal in the MOF precursor impacts porous BN's purity. Unlike Cu/ZIF-8, a Co-containing ZIF-8 precursor led to porous C-BN (i.e. BN with a large amount of C in the structure). Overall, given the diversity of metals in MOFs, one could envision our approach as a method to produce a library of different metal functionalised porous BN samples.

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Abstract: Lithium ion battery technology is the state-of-the-art rechargeable energy storage technology for electric vehicles, stationary energy storage and personal electronics. However, a wide variety of degradation effects still contribute to performance limitations. The metallic copper and aluminium current collectors in a lithium ion battery can be subject to dissolution or other reactions with the electrolytes. Corrosion of these metal foils is significantly detrimental to the overall performance of a lithium ion battery, however the mechanisms of this degradation are poorly understood. This review summarises the key effects contributing to metal current collector degradation in lithium ion batteries as well as introduces relevant corrosion and lithium ion battery principles. By developing the understanding of these complex chemistries, lithium ion battery degradation can be mitigated, enabling safer operation and longer lifetimes.

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Abstract: Despite their ubiquitous usage and increasing societal dependence on Li-ion batteries, there remains a lack of detailed empirical evidence of Li intercalation/deintercalation into graphite even though this process dictates the performance, longevity, and safety of the system. Here, we report direct detection and dissociation of specific crystallographic phases in the lithiated graphite, which form through a stepwise staging process. Using operando measurements, LiC18, LiC12, and LiC6 phases are observed via distinct low-frequency Raman features, which are the result of displacement of the graphite lattice by induced local strain. Density functional theory calculations confirm the nature of the Raman-active vibrational modes, to the layer breathing modes (LBMs) of the lithiated graphite. The new findings indicate graphene-like characteristics in the lithiated graphite under the deep charged condition due to the imposed strain by the inserted Li. Moreover, our approach also provides a simple experimental tool to measure induced strain in the graphite structure under full intercalation conditions.

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Abstract: Thick corrosion scales form within carbon steel oilfield pipelines in sweet (CO2 saturated) environments. The morphology and the extent of the resultant pseudo-protective nature of these scales has been seen to be dependent on multiple factors including solution pH, temperature, flow rate, and partial pressure of CO2 present. Different techniques (SEM, XRD, FIB, etc.) have been used in the past to characterise these corrosion scales. However, limitations in these techniques occur due to the fact that only small regions of the scale can be characterised in a feasible time. Further limitations may result in difficulty to relate local scale features with corrosion morphology on the evolving metal surface (i.e. localised corrosion) as the morphology of the substrate surface can only be characterised once the scale is removed. The aim of this work is to address this issue through the use of high resolution x-ray absorption tomography to characterise the internal morphology of the corrosion scales from ex situ specimens exposed to CO2 environments as a function of pH and temperature. X-65 pipeline steel, high purity 99.99 Fe and low purity 99.0 Fe pins were used in these experiments. Specimens were exposed to CO2saturated solutions using two different methods, notably open circuit potential (OCP) immersion for 7-12 days and electrochemical polarisation for two hours at 200 mV(vs OCP). After the scaling experiments, samples were characterised using XRD and SEM. X-ray tomography was subsequently performed at the University of Manchester X-ray Imaging Facilities to characterise the corrosion morphology. Transmission X-ray microscopy (TXM) was used in absorption mode and phase contrast mode to obtain three dimensional reconstructions of the specimens, where the different features of the scale and the internal corroded substrate were imaged and characterised simultaneously. Results indicate differences in the morphology of the corrosion scale depending on the method that was used to corrode the samples. As a consequence of the supersaturation in Fe2+, polarised samples present a thicker scale than the scales obtained by immersion at OCP conditions. The polarisation process also produces a less uniform corroded substrate than when the sample is immersed for 7 days at open circuit in the corroding environments used. In this work high resolution X-ray tomography has been proven to be a very powerful technique to study the scale morphology as well as the features of localised corrosion occurring under scale in the substrate.

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Abstract: The unexpected high failure rates of CoCrMo hip-implants is associated with the release of a large number of inflammatory wear particles. CoCrMo is nominally a stable material, however, previous chemical speciation studies on CoCrMo wear particles obtained from periprosthetic tissue revealed only trace amounts of Co remaining despite Co being the major component of the alloy. The unexpected high levels of Co dissolution in-vivo raised significant clinical concerns particularly related to the Cr speciation in the dissolution process. At high electrochemical potentials, the alloy’s Cr-rich passive film breaks down (transpassive polarisation) facilitating alloy dissolution. The potential release of the carcinogenic Cr(VI) species in vivo has been a subject of debate. While the large scale Co dissolution observed on in vivo produced particles could indicate a highly oxidising in vivo environment, Cr(VI) species were not previously detected in periprosthetic tissue samples. However, Cr(VI) is likely to be an unstable (transient) species in biological environments and studies on periprosthetic tissue does not provide information on intermediate reaction products nor the exposure history of the wear particles. Here, an in situ spectro-microscopy approach was developed, utilising the high chemical resolution of synchrotron radiation, in order to study CoCrMo reactivity as a function of time and oxidising conditions. The results reveal limited Co dissolution from CoCrMo particles, which increases dramatically at a critical electrochemical potential. Furthermore, in-situ XAS detected only Cr(III) dissolution, even at potentials where Cr(VI) is known to be produced, suggesting that Cr(VI) species are extremely transient in simulated biological environments where the oxidation zone is small.