Carbon nitride for solar H2 production coupled to organic chemical transformations

Artificial photosynthesis utilises solar-light for clean fuel H2 production and is emerging as a potential solution for renewable energy generation. Photocatalytic systems that combine a light harvester and catalysts in one-pot reactor are promising strategies towards this direction. Yet, most of the reported systems function by consuming excess amount of expensive sacrificial reagents, preventing commercial development. In this thesis, carbon nitrides (CNx) have been selected as non-toxic, stable and low-cost photocatalysts. CNx are first introduced as efficient light harvesters, to couple alcohol oxidation with proton reduction, in the presence of a Ni-based molecular catalyst. This system operated in a single compartment while the oxidation and reduction products were collected in the solution and gaseous phases, respectively, demonstrating a closed redox system. In the presence of an organic substrate and absence of a proton reduction catalyst, photoexcited CNx was found to accumulate long-lived “trapped-electrons”, which enables decoupling oxidation and reduction reactions temporarily and spatially. This allows solar H2 generation in the dark, following light exposure, replication light and dark cycle of natural photosynthesis in an artificial set-up. The stability of the designed system was found to be limited by the Ni-based molecular catalyst, and the spectroscopic studies revealed electron transfer from CNx to catalyst as the kinetic bottleneck. Graphene based conductive scaffolds were introduced to the CNx-Ni system, to accelerate the rate of electron transfer from CNx to the Ni catalyst. Time-resolved spectroscopic techniques revealed that introducing these conductive binders enabled better electronic communication between CNx and Ni, resulting in significantly enhanced photocatalytic activity. To improve the solar-light utilisation and the photocatalytic performance of bulk CNx, a straightforward ultra-sonication approach was introduced. This pre-treatment was found to break aggregates of bulk CNx, and the resulting activated CNx had significantly improved activity. The activated CNx showed record activities per gram of the material used, for H2 evolution with a molecular Ni catalyst. The use of abundant waste sources instead of organic substrates was investigated in the presence of activated CNx. The system demonstrated to photoreform purified and raw lignocellulose samples into H2 in the presence of various H2 evolution catalysts over a wide range of pH.The financial support from the Austrian Federal Ministry for Digital and Economic Affairs, the National Foundation for Research, Technology and Development and OMV to carry out this work is greatly acknowledged. St Edmund’s College is also acknowledged for financial support and guidance

Photoreforming of Non-Recyclable Plastic Waste over a Carbon Nitride/Nickel Phosphide Catalyst

With over 8 billion tons of plastic produced since 1950, polymers represent one of the most widely used – and most widely discarded – materials. Ambient-temperature photoreforming offers a simple and low-energy means for transforming plastic waste into fuel and bulk chemicals, but has previously only been reported using precious-metal- or Cd-based photocatalysts. Here, an inexpensive and non-toxic carbon nitride/nickel phosphide (CNx|Ni2P) photocatalyst is utilized to successfully reform polyethylene terephthalate (PET) and polylactic acid (PLA) to clean H2 fuel and a variety of organic chemicals under alkaline aqueous conditions. Ni2P synthesized on cyanamide-functionalized carbon nitride is shown to promote efficient charge separation and catalysis, with a photostability of at least five days. The real-world applicability of photoreforming is further verified by generating H2 and organics from a selection of non-recyclable waste – including microplastics (polyester microfibers) and food-contaminated plastic – and up-scaling the system from 2 mL to 120 mL while maintaining its efficiency for plastic conversion.This work was supported by the Christian Doppler Research Association, Austrian Federal Ministry for Digital and Economic Affairs, National Foundation for Research, Technology and Development, OMV Group, and EPSRC (NanoDTC, EP/L015978/1). XPS data collection was performed at the EPSRC National Facility for XPS (HarwellXPS), operated by Cardiff University and UCL, under contract No. PR 16195

Photoreforming of lignocellulose into H2 using nano-engineered carbon nitride under benign conditions

Photoreforming of lignocellulose is a promising approach toward sustainable H2 generation, but this kinetically challenging reaction currently requires UV-absorbing or toxic light absorbers under harsh conditions. Here, we report a cyanamide-functionalized carbon nitride, NCNCNx, which shows enhanced performance upon ultra-sonication. This activated NCNCNx allows for the visible-light driven conversion of purified and raw lignocellulose samples into H2 in the presence of various proton reduction co-catalysts. The reported room-temperature photoreforming process operates under benign aqueous conditions (pH ~2-15) without the need for toxic components.Austrian Federal Ministry for Digital and Economic Affairs, the National Foundation for Research, Technology and Development, OM

Solar Reforming of Biomass with Homogeneous Carbon Dots.

A sunlight-powered process is reported that employs carbon dots (CDs) as light absorbers for the conversion of lignocellulose into sustainable H2 fuel and organics. This photocatalytic system operates in pure and untreated sea water at benign pH (2-8) and ambient temperature and pressure. The CDs can be produced in a scalable synthesis directly from biomass itself and their solubility allows for good interactions with the insoluble biomass substrates. They also display excellent photophysical properties with a high fraction of long-lived charge carriers and the availability of a reductive and an oxidative quenching pathway. The presented CD-based biomass photoconversion system opens new avenues for sustainable, practical, and renewable fuel production through biomass valorization

Dark Photocatalysis: Storage of Solar Energy in Carbon Nitride for Time-Delayed Hydrogen Generation

While natural photosynthesis serves as the model system for efficient charge separation and decoupling of redox reactions, bio-inspired artificial systems typically lack applicability owing to synthetic challenges and structural complexity. We present herein a simple and inexpensive system that, under solar irradiation, forms highly reductive radicals in the presence of an electron donor, with lifetimes exceeding the diurnal cycle. This radical species is formed within a cyanamide- functionalized polymeric network of heptazine units and can give off its trapped electrons in the dark to yield H-2, triggered by a co-catalyst, thus enabling the temporal decoupling of the light and dark reactions of photocatalytic hydrogen production through the radical's longevity. The system introduced here thus demonstrates a new approach for storing sunlight as long-lived radicals, and provides the structural basis for designing photocatalysts with long-lived photo-induced states

Electron Accumulation Induces Efficiency Bottleneck for Hydrogen Production in Carbon Nitride Photocatalysts.

This study addresses the light intensity dependence of charge accumulation in a photocatalyst suspension, and its impact on both charge recombination kinetics and steady-state H2 evolution efficiency. Cyanamide surface functionalized melon-type carbon nitride (NCNCNx) has been selected as an example of emerging carbon nitrides photocatalysts because of its excellent charge storage ability. Transient spectroscopic studies (from ps to s) show that the bimolecular recombination of photogenerated electrons and holes in NCNCNx can be well described by a random walk model. Remarkably, the addition of hole scavengers such as 4-methylbenzyl alcohol can lead to ∼400-fold faster recombination kinetics (lifetime shortening to ∼10 ps). We show that this acceleration is not the direct result of ultrafast hole extraction by the scavenger, but is rather caused by long-lived electron accumulation in NCNCNx after hole extraction. The dispersive pseudo-first order recombination kinetics become controlled by the density of accumulated electrons. H2 production and steady-state spectroscopic measurements indicate that the accelerated recombination caused by electron accumulation limits the H2 generation efficiency. The addition of a reversible electron acceptor and mediator, methyl viologen (MV2+), accelerates the extraction of electrons from the NCNCNx and increases the H2 production efficiency under one sun irradiation by more than 30%. These results demonstrate quantitatively that while long-lived electrons are essential to drive photoinduced H2 generation in many photocatalysts, excessive electron accumulation may result in accelerated recombination losses and lower performance, and thus highlight the importance of efficient electron and hole extraction in enabling efficient water splitting photocatalysts.ERC AdG Intersolar grant (Grant No. 291482), The Christian Doppler Research Association The OMV Grou

Solar-Driven Reduction of Aqueous Protons Coupled to Selective Alcohol Oxidation with a Carbon Nitride-Molecular Ni Catalyst System.

Solar water-splitting represents an important strategy toward production of the storable and renewable fuel hydrogen. The water oxidation half-reaction typically proceeds with poor efficiency and produces the unprofitable and often damaging product, O2. Herein, we demonstrate an alternative approach and couple solar H2 generation with value-added organic substrate oxidation. Solar irradiation of a cyanamide surface-functionalized melon-type carbon nitride ((NCN)CNx) and a molecular nickel(II) bis(diphosphine) H2-evolution catalyst (NiP) enabled the production of H2 with concomitant selective oxidation of benzylic alcohols to aldehydes in high yield under purely aqueous conditions, at room temperature and ambient pressure. This one-pot system maintained its activity over 24 h, generating products in 1:1 stoichiometry, separated in the gas and solution phases. The (NCN)CNx-NiP system showed an activity of 763 μmol (g CNx)(-1) h(-1) toward H2 and aldehyde production, a Ni-based turnover frequency of 76 h(-1), and an external quantum efficiency of 15% (λ = 360 ± 10 nm). This precious metal-free and nontoxic photocatalytic system displays better performance than an analogous system containing platinum instead of NiP. Transient absorption spectroscopy revealed that the photoactivity of (NCN)CNx is due to efficient substrate oxidation of the material, which outweighs possible charge recombination compared to the nonfunctionalized melon-type carbon nitride. Photoexcited (NCN)CNx in the presence of an organic substrate can accumulate ultralong-lived "trapped electrons", which allow for fuel generation in the dark. The artificial photosynthetic system thereby catalyzes a closed redox cycle showing 100% atom economy and generates two value-added products, a solar chemical, and solar fuel.This work was supported by the Christian Doppler Research Association (Austrian Federal Ministry of Science, Research, and Economy and the National Foundation for Research, Technology and Development) and the OMV Group (to E.R.), an Oppenheimer PhD scholarship (to B.C.M.M.), a Marie Curie Postdoctoral Fellowship (GAN 624997 to C.A.C.), a FRQNT Postdoctoral Fellowship (to R.G.), and an ERC Starting Grant (B. V. L., Grant No. 639233).This is the final version of the article. It first appeared from American Chemical Society via http://dx.doi.org/10.1021/jacs.6b0432

Raw data supporting article: Photoreforming of non-recyclable plastic waste over a carbon nitride/nickel phosphide catalyst

This is raw data for the publication “Photoreforming of non-recyclable plastic waste over a carbon nitride/nickel phosphide catalyst.” It includes Origin files of photocatalytic experiments, characterization (UV-Vis, FTIR, Fluorimetry, XRD and XPS), and NMR data, as well as microscopy images (SEM and TEM) and ChemDraw figures. See the Readme.txt files for more information.Christian Doppler Research Association, Austrian Federal Ministry for Digital and Economic Affairs, National Foundation for Research, Technology and Development, OMV Group, and EPSRC (NanoDTC, EP/L015978/1)

Interfacial Engineering of a Carbon Nitride-Graphene Oxide-Molecular Ni Catalyst Hybrid for Enhanced Photocatalytic Activity

Abstract can be found here: https://doi.org/10.1021/acscatal.8b0196

Electron Accumulation Induces Efficiency Bottleneck for Hydrogen Production in Carbon Nitride Photocatalysts.

This study addresses the light intensity dependence of charge accumulation in a photocatalyst suspension, and its impact on both charge recombination kinetics and steady-state H2 evolution efficiency. Cyanamide surface functionalized melon-type carbon nitride (NCNCNx) has been selected as an example of emerging carbon nitrides photocatalysts because of its excellent charge storage ability. Transient spectroscopic studies (from ps to s) show that the bimolecular recombination of photogenerated electrons and holes in NCNCNx can be well described by a random walk model. Remarkably, the addition of hole scavengers such as 4-methylbenzyl alcohol can lead to ∼400-fold faster recombination kinetics (lifetime shortening to ∼10 ps). We show that this acceleration is not the direct result of ultrafast hole extraction by the scavenger, but is rather caused by long-lived electron accumulation in NCNCNx after hole extraction. The dispersive pseudo-first order recombination kinetics become controlled by the density of accumulated electrons. H2 production and steady-state spectroscopic measurements indicate that the accelerated recombination caused by electron accumulation limits the H2 generation efficiency. The addition of a reversible electron acceptor and mediator, methyl viologen (MV2+), accelerates the extraction of electrons from the NCNCNx and increases the H2 production efficiency under one sun irradiation by more than 30%. These results demonstrate quantitatively that while long-lived electrons are essential to drive photoinduced H2 generation in many photocatalysts, excessive electron accumulation may result in accelerated recombination losses and lower performance, and thus highlight the importance of efficient electron and hole extraction in enabling efficient water splitting photocatalysts.ERC AdG Intersolar grant (Grant No. 291482), The Christian Doppler Research Association The OMV Grou