Uwe Schröder

Bio: Uwe Schröder is an academic researcher from Braunschweig University of Technology. The author has contributed to research in topics: Microbial fuel cell & Anode. The author has an hindex of 57, co-authored 175 publications receiving 16419 citations. Previous affiliations of Uwe Schröder include Humboldt University of Berlin & University of Greifswald.

Microbial Fuel Cells: Methodology and Technology†

Abstract: Microbial fuel cell (MFC) research is a rapidly evolving field that lacks established terminology and methods for the analysis of system performance. This makes it difficult for researchers to compare devices on an equivalent basis. The construction and analysis of MFCs requires knowledge of different scientific and engineering fields, ranging from microbiology and electrochemistry to materials and environmental engineering. Describing MFC systems therefore involves an understanding of these different scientific and engineering principles. In this paper, we provide a review of the different materials and methods used to construct MFCs, techniques used to analyze system performance, and recommendations on what information to include in MFC studies and the most useful ways to present results.

Anodic electron transfer mechanisms in microbial fuel cells and their energy efficiency

Abstract: The performance of a microbial fuel cell (MFC) depends on a complex system of parameters. Apart from technical variables like the anode or fuel cell design, it is mainly the paths and mechanisms of the bioelectrochemical energy conversion that decisively determine the MFC power and energy output. Here, the electron transfer from the microbial cell to the fuel cell anode, as a process that links microbiology and electrochemistry, represents a key factor that defines the theoretical limits of the energy conversion. The determination of the energy efficiency of the electron transfer reactions, based on the biological standard potentials of the involved redox species in combination with the known paths (and stoichiometry) of the underlying microbial metabolism, is an important instrument for this discussion. Against the sometimes confusing classifications of MFCs in literature it is demonstrated that the anodic electron transfer is always based on one and the same background: the exploitation of the necessity of every living cell to dispose the electrons liberated during oxidative substrate degradation.

Water-induced accelerated ion diffusion: voltammetric studies in 1-methyl-3-[2,6-(S)-dimethylocten-2-yl]imidazolium tetrafluoroborate, 1-butyl-3-methylimidazolium tetrafluoroborate and hexafluorophosphate ionic liquids

Abstract: The electrochemical properties of the room temperature ionic liquids 1-butyl-3-methylimidazolium tetrafluoroborate (BMIM+BF4−), 1-butyl-3-methylimidazolium hexafluorophosphate (BMIM+PF6−) and 1-methyl-3-[2,6-(S)-dimethylocten-2-yl]imidazolium tetrafluoroborate (MDIM+BF4−) as solvents have been studied using micro-samples, with a volume of 10 μL, of the ionic liquids under vacuum conditions and under conditions with controlled gas and moisture supplies. The impact of water—absorbed into the ionic liquid in a controlled manner from the gas phase—on the voltammetry of dissolved redox systems and on the accessible potential window of the ionic liquids was investigated. The diffusion coefficients for three representative redox systems, the oxidation of neutral N,N,N′,N′-tetramethyl-p-phenylenediamine (TMPD), the reduction of cationic methyl viologen (MV2+) and reduction of anionic hexacyanoferrate(III), Fe(CN)63−, have been determined as a function of the water content of the ionic liquids. Water is shown to have a much more dramatic acceleration effect on the diffusion of the ionic compounds compared to its effect on neutral species in ionic liquids. A model based on nanoscale structural features of wet ionic liquid materials is proposed. The novel methodology, which employs redox-active compounds dissolved or partitioned in microdroplets of ionic liquid, uses conditions suitable for the study of ionic liquids for applications in electrochemical gas phase reactors and gas sensor systems.

Challenges and Constraints of Using Oxygen Cathodes in Microbial Fuel Cells

Abstract: The performance of oxygen reduction catalysts (platinum, pyrolyzed iron(ll) phthalocyanine (pyr-FePc) and cobalt tetramethoxyphenylporphyrin (pyr-CoTMPP)) is discussed in light of their application in microbial fuel cells. It is demonstrated that the physical and chemical environment in microbial fuel cells severely affects the thermodynamics and the kinetics of the electrocatalytic oxygen reduction. The neutral pH in combination with low buffer capacities and low ionic concentrations strongly affect the cathode performance and limit the fuel cell power output. Thus, the limiting current density in galvanodyanamic polarization experiments decreases from 1.5 mA cm(-2) to 0.6 mA cm(-2) (pH 3.3, E(cathode) = 0 V) when the buffer concentration is decreased from 500 to 50 mM. The cathode limitations are superposed by the increasing internal resistance of the MFC that substantially contributes to the decrease of power output. For example, the maximum power output of a model MFC decreased by 35%, from 2.3 to 1.5 mW, whereas the difference between the electrode potentials (deltaE = E(anode) - E(cathode)) decreased only by 10%. The increase of the catalyst load of pyr-FePc from 0.25 to 2 mg cm(-2) increased the cathodic current density from 0.4 to 0.97 mA cm(-2) (pH 7, 50 mM phosphate buffer). The increase of the load of such inexpensive catalyst thus represents a suitable means to improve the cathode performance in microbial fuel cells. Due to the low concentration of protons in MFCs in comparison to relatively high alkali cation levels (ratio C(Na+,K+)/C(H+) = 5 x E5 in pH 7, 50 mM phosphate buffer) the transfer of alkali ions through the proton exchange membrane plays a major role in the charge-balancing ion flux from the anodic into the cathodic compartment. This leads to the formation of pH gradients between the anode and the cathode compartment.

Phd by thesis

Abstract: Deposits of clastic carbonate-dominated (calciclastic) sedimentary slope systems in the rock record have been identified mostly as linearly-consistent carbonate apron deposits, even though most ancient clastic carbonate slope deposits fit the submarine fan systems better. Calciclastic submarine fans are consequently rarely described and are poorly understood. Subsequently, very little is known especially in mud-dominated calciclastic submarine fan systems. Presented in this study are a sedimentological core and petrographic characterisation of samples from eleven boreholes from the Lower Carboniferous of Bowland Basin (Northwest England) that reveals a >250 m thick calciturbidite complex deposited in a calciclastic submarine fan setting. Seven facies are recognised from core and thin section characterisation and are grouped into three carbonate turbidite sequences. They include: 1) Calciturbidites, comprising mostly of highto low-density, wavy-laminated bioclast-rich facies; 2) low-density densite mudstones which are characterised by planar laminated and unlaminated muddominated facies; and 3) Calcidebrites which are muddy or hyper-concentrated debrisflow deposits occurring as poorly-sorted, chaotic, mud-supported floatstones. These

Microbial Fuel Cells: Methodology and Technology†

Abstract: Microbial fuel cell (MFC) research is a rapidly evolving field that lacks established terminology and methods for the analysis of system performance. This makes it difficult for researchers to compare devices on an equivalent basis. The construction and analysis of MFCs requires knowledge of different scientific and engineering fields, ranging from microbiology and electrochemistry to materials and environmental engineering. Describing MFC systems therefore involves an understanding of these different scientific and engineering principles. In this paper, we provide a review of the different materials and methods used to construct MFCs, techniques used to analyze system performance, and recommendations on what information to include in MFC studies and the most useful ways to present results.

Noble metal-free hydrogen evolution catalysts for water splitting

Abstract: Sustainable hydrogen production is an essential prerequisite of a future hydrogen economy. Water electrolysis driven by renewable resource-derived electricity and direct solar-to-hydrogen conversion based on photochemical and photoelectrochemical water splitting are promising pathways for sustainable hydrogen production. All these techniques require, among many things, highly active noble metal-free hydrogen evolution catalysts to make the water splitting process more energy-efficient and economical. In this review, we highlight the recent research efforts toward the synthesis of noble metal-free electrocatalysts, especially at the nanoscale, and their catalytic properties for the hydrogen evolution reaction (HER). We review several important kinds of heterogeneous non-precious metal electrocatalysts, including metal sulfides, metal selenides, metal carbides, metal nitrides, metal phosphides, and heteroatom-doped nanocarbons. In the discussion, emphasis is given to the synthetic methods of these HER electrocatalysts, the strategies of performance improvement, and the structure/composition-catalytic activity relationship. We also summarize some important examples showing that non-Pt HER electrocatalysts could serve as efficient cocatalysts for promoting direct solar-to-hydrogen conversion in both photochemical and photoelectrochemical water splitting systems, when combined with suitable semiconductor photocatalysts.

Hydroxymethylfurfural, A Versatile Platform Chemical Made from Renewable Resources

Abstract: Renewable Resources Robert-Jan van Putten,†,‡ Jan C. van der Waal,† Ed de Jong,*,† Carolus B. Rasrendra,‡,⊥ Hero J. Heeres,*,‡ and Johannes G. de Vries* †Avantium Chemicals, Zekeringstraat 29, 1014 BV Amsterdam, the Netherlands ‡Department of Chemical Engineering, University of Groningen, Nijenborgh 4, 9747 AG Groningen, the Netherlands Stratingh Institute for Chemistry, University of Groningen, Nijenborgh 4, 9747 AG Groningen, the Netherlands DSM Innovative Synthesis BV, P.O. Box 18, 6160 MD Geleen, the Netherlands Department of Chemical Engineering, Institut Teknologi Bandung, Ganesha 10, Bandung 40132, Indonesia