United Kingdom

In this report Quantifying Greenhouse Gas Emissions the Committee on Climate Change assesses how the UK’s greenhouse gas emissions are quantified where uncertainties lie and the implications for setting carbon budgets and measuring progress against climate change targets. The report finds that:

• The methodology for constructing the UK’s greenhouse gas inventory is rigorous but the process for identifying improvements could be strengthened.
• There is high confidence over large parts of the inventory. A small number of sectors contribute most to uncertainty and research efforts should be directed at improving these estimates.
• UK greenhouse gas emissions for 2014 were within ±3% of the estimated level with 95% confidence which is a low level of uncertainty by international standards.
• Methodology revisions in recent years have tended to increase estimated emissions but these changes have been within uncertainty margins.
• Statistical uncertainty in the current greenhouse gas inventory is low but could rise in future.
• Uncertainty also arises from sources of emissions not currently included in the inventory and from potential changes to IPCC guidelines.
• Independent external validation of greenhouse gas emissions is important and new monitoring techniques should be encouraged.
• Government should continue to monitor consumption-based greenhouse gas estimates and support continued research to improve methodology and reduce uncertainty in these estimates.

This is our sixth statutory report to Parliament on progress towards meeting carbon budgets. In it we consider the latest data on emissions and their drivers. This year the report also includes a full assessment of how the first carbon budget (2008-2012) was met drawing out policy lessons and setting out what is required for the future to stay on track for the legislated carbon budgets and the 2050 target. The report includes assessment at the level of the economy the non-traded and traded sectors the key emitting sectors and the devolved administrations. Whilst the first carbon budget has been met and progress made on development and implementation of some policies the main conclusion is that strengthening of policies will be needed to meet future budgets.

This is the Committee’s 2020 report to Parliament assessing progress in reducing UK emissions over the past year. This year the report includes new advice to the UK Government on securing a green and resilient recovery following the COVID-19 pandemic. The Committee’s new analysis expands on its May 2020 advice to the UK Prime Minister in which it set out the principles for building a resilient recovery. In its new report the Committee has assessed a wide set of measures and gathered the latest evidence on the role of climate policies in the economic recovery. Its report highlights five clear investment priorities in the months ahead:

• Low-carbon retrofits and buildings that are fit for the future
• Tree planting peatland restoration and green infrastructure
• Energy networks must be strengthened
• Infrastructure to make it easy for people to walk cycle and work remotely
• Moving towards a circular economy.

There are also opportunities to support the transition and the recovery by investing in the UK’s workforce and in lower-carbon behaviours and innovation:

• Reskilling and retraining programmes
• Leading a move towards positive behaviours
• Targeted science and innovation funding

Energy–structure–function (ESF) maps can aid the targeted discovery of porous molecular crystals by predicting the stable crystalline arrangements along with their functions of interest. Here we compute ESF maps for a series of rigid molecules that comprise either a triptycene or a spiro-biphenyl core functionalized with six different hydrogen-bonding moieties. We show that the positioning of the hydrogen-bonding sites as well as their number has a profound influence on the shape of the resulting ESF maps revealing promising structure–function spaces for future experiments. We also demonstrate a simple and general approach to representing and inspecting the high-dimensional data of an ESF map enabling an efficient navigation of the ESF data to identify ‘landmark’ structures that are energetically favourable or functionally interesting. This is a step toward the automated analysis of ESF maps an important goal for closed-loop autonomous searches for molecular crystals with useful functions.

Thermally sprayed aluminium (TSA) coatings provide protection to offshore steel structures without the use of external cathodic protection (CP) systems. These coatings provide sacrificial protection in the same way as a galvanic anode and thus hydrogen embrittlement (HE) becomes a major concern with the use of high strength steels. The effect of TSA on the HE of steel seems to remain largely unknown. Further the location of hydrogen in TSA-coated steel has not been explored. To address the above knowledge gap API 5L X80 and AISI 4137 steel coupons with and without TSA were prepared and the amount of hydrogen present in these steels when cathodically polarised to −1.1 V (Ag/AgCl) for 30 days in synthetic seawater was determined. One set of TSA-coated specimens was left at open circuit potential (OCP). The study indicates that the amount of hydrogen present in TSA-coated steel is ~100 times more than the amount found in uncoated steel and that the hydrogen seems to be largely localised in the TSA layer.

This research introduces a ‘Hydrogen Interconnector System’ (HIS) as a novel method 7 for transporting electrical energy over long distances. The system takes electricity from 8 stranded renewable energy assets converts it to hydrogen in an electrolyser plant transports 9 hydrogen to the demand centre via pipeline where it is reconverted to electricity in either a 10 gas turbine or fuel cell plant. This paper evaluates the competitiveness of the technology with 11 High Voltage Direct Current (HVDC) systems calculating the following techno-economic 12 indicators; Levelised Cost Of Electricity (LCOE) and Levelised Cost Of Storage (LCOS). The 13 results suggest that the LCOE of the HIS is competitive with HVDC for construction in 2050 14 with distance beyond 350km in case of all scenarios for a 1GW system. The LCOS is lower 15 than an HVDC system using large scale hydrogen storage in 6 out of 12 scenarios analysed 16 including for construction from 2025. The HIS was also applied to three case studies with 17 the results showing that the system outperforms HVDC from LCOS perspectives in all cases 18 and has 15-20% lower investment costs in 2 studies analysed.

Ni-based catalysts are attractive alternatives to noble metal electrocatalysts for the hydrogen evolution reaction (HER). Herein we present a dispersion-corrected density functional theory (DFT-D3) insight into HER activity on the (111) (110) (001) and (100) surfaces of metallic nickel nitride (Ni₃N). A combination of water and hydrogen adsorption was used to model the electrode interactions within the water splitting cell. Surface energies were used to characterise the stabilities of the Ni3N surfaces along with adsorption energies to determine preferable sites for adsorbate interactions. The surface stability order was found to be (111) < (100) < (001) < (110) with calculated surface energies of 2.10 2.27 2.37 and 2.38 Jm⁻² respectively. Water adsorption was found to be exothermic at all surfaces and most favourable on the (111) surface with E_ads = −0.79 eV followed closely by the (100) (110) and (001) surfaces at −0.66 −0.65 and −0.56 eV respectively. The water splitting reaction was investigated at each surface to determine the rate determining Volmer step and the activation energies (Ea) for alkaline HER which has thus far not been studied in detail for Ni₃N. The E_a values for water splitting on the Ni₃N surfaces were predicted in the order (001) < (111) < (110) < (100) which were 0.17 0.73 1.11 and 1.60 eV respectively overall showing the (001) surface to be most active for the Volmer step of water dissociation. Active hydrogen adsorption sites are also presented for acidic HER evaluated through the ΔG_H descriptor. The (110) surface was shown to have an extremely active Ni–N bridging site with ΔG_H = −0.05 eV.

Iron oxide has been widely used as an oxygen carrier material (OCM) for hydrogen production by chemical looping due to its favourable thermodynamic properties. In spite of this iron oxide loses much of its activity after redox cycling mainly due to sintering and agglomeration. Perovskites such as La_0.7Sr_0.3FeO_3-d (LSF731) have been suggested as potential candidate OCMs for hydrogen production due to their excellent oxygen transport properties and stability under cycling. However hydrogen production per cycle for a similar carrier weight is lower than with iron oxide. This work proposes the use of composite OCMs made of iron oxide clusters embedded in an LSF731 matrix. The perovskite matrix facilitates oxygen transport to the iron oxide clusters while preventing agglomeration. Two preparation methods mechanical mixing and a modified Pechini method were used to obtain composite materials with different iron oxide weight fractions 11 and 30 wt.%. The reactivity of these OCMs was studied in a thermogravimetric analyser. Hydrogen production and carrier stability were investigated in a microreactor over 25 redox cycles while periodically feeding carbon monoxide and water in order to produce carbon dioxide and hydrogen in separate streams. Hydrogen production was stable over 25 cycles for LSF731 and the composite OCM with 30 wt.% iron oxide produced by the modified Pechini method but iron oxide particles alone underwent a decrease in the hydrogen production with cycling. The hydrogen production during the 25th cycle was eight times higher for the composite material than for iron oxide alone and four times higher than for LSF731. The hydrogen production was therefore also higher than that expected from a simple combination of the iron oxide and LSF731 alone indicating a synergetic effect whereby the LSF731 may have a higher effective oxygen capacity when in the form of the composite material.

The paper presents an experimental investigation of hydrogen-diesel fuel co-combustion carried out on a naturally aspirated direct injection diesel engine. The engine was supplied with a range of hydrogen-diesel fuel mixture proportions to study the effect of hydrogen addition (aspirated with the intake air) on combustion and exhaust emissions. The tests were performed at fixed diesel injection periods with hydrogen added to vary the engine load between 0 and 6 bar IMEP. In addition a novel inecylinder gas sampling technique was employed to measure species concentrations in the engine cylinder at two inecylinder locations and at various instants during the combustion process. The results showed a decrease in the particulates CO and THC emissions and a slight increase in CO2 emissions with the addition of hydrogen with fixed diesel fuel injection periods. NOx emissions increased steeply with hydrogen addition but only when the combined diesel and hydrogen co-combustion temperatures exceeded the threshold temperature for NOx formation. The inecylinder gas sampling results showed higher NOx levels between adjacent spray cones in comparison to sampling within an individual spray cone.

As Europe is gradually moving towards a hydrogen based society it has been acknowledged that adding certain amount of hydrogen as a clean energy carrier to the existing natural gas pipeline will help reduce the CO2 emissions which contribute to the greenhouse effect. On the other hand hydrogen has been demonstrated to be able to change the behaviour of the pipeline steel such as lower toughness and faster crack growth due to hydrogen embrittlement. Therefore it is necessary that the risks associated with the failure of the pipeline carrying mixtures of natural gas and hydrogen be assessed.<br/>The study reported in this paper is part of European NATURALHY project whose aim is to investigate the possibility of using the existing natural gas transmission pipelines to convey natural gas/hydrogen mixtures. According to the EGIG database the most common cause of failure for the existing natural gas pipelines is third party damage which mainly refers to a gouge a dent/gouge combination of known geometry. Among third party damage failures 90% are the result of immediate failure i.e. leakage or rupture of the pipeline and only 10% of them are the result of delayed failure. While its not expected that hydrogen will impact the immediate failure it could increase the vulnerability of the pipe to delayed failure through the initiation or activation of crack like defects.<br/>This paper will present a methodology to predict the probability of increased failures and describe a software tool that has been developed to perform the calculations.