Polyaniline-Supported Bacterial Biofilms as Active Matrices for Platinum Nanoparticles: Enhancement of Electroreduction of Carbon Dioxide

2016 ◽  
Vol 69 (4) ◽  
pp. 411 ◽  
Author(s):  
Ewelina Seta ◽  
Weronika A. Lotowska ◽  
Iwona A. Rutkowska ◽  
Anna Wadas ◽  
Adrianna Raczkowska ◽  
...  

A hybrid matrix composed of a porous polyaniline underlayer, a robust bacterial biofilm and a multiwalled carbon nanotube overlayer has been demonstrated to function as highly active support for dispersed Pt catalytic nanoparticles during the electroreduction of carbon dioxide in neutral medium (phosphate buffer at pH 6.1). In contrast with bare Pt nanoparticles (deposited at a glassy carbon substrate), application of the hybrid system produces sizeable CO2-reduction currents in comparison to those originating from hydrogen evolution. The result is consistent with an enhancement in the reduction of carbon dioxide. However, the biofilm-based matrix tends to inhibit the catalytic properties of platinum towards proton discharge (competitive reaction) or even oxygen reduction. The hydrated structure permits easy unimpeded flow of aqueous electrolyte at the electrocatalytic interface. Although application of the polyaniline underlayer can be interpreted in terms of stabilization and improvement of the biofilm adherence, the use of carbon nanotubes facilitates electron transfer to Pt catalytic sites. It is apparent from the voltammetric stripping-type analytical experiments that, although formation of some methanol and methanoic acid cannot be excluded, carbon monoxide seems to be the main CO2-reduction product.

2020 ◽  
Vol 13 (2) ◽  
pp. 519-526 ◽  
Author(s):  
Hyeon Shin Lee ◽  
Seohyeon Jee ◽  
Raekyung Kim ◽  
Hoang-Tran Bui ◽  
Bupmo Kim ◽  
...  

A photocatalyst heterogenized in discrete cages of metal–organic polyhedra provides highly active and robust conversion of carbon dioxide.


2020 ◽  
Author(s):  
Jennifer A. Rudd ◽  
Ewa Kazimierska ◽  
Louise B. Hamdy ◽  
Odin Bain ◽  
Sunyhik Ahn ◽  
...  

The utilization of carbon dioxide is a major incentive for the growing field of carbon capture. Carbon dioxide could be an abundant building block to generate higher value products. Herein, we describe the use of porous copper electrodes to catalyze the reduction of carbon dioxide into higher value products such as ethylene, ethanol and, notably, propanol. For <i>n</i>-propanol production, faradaic efficiencies reach 4.93% at -0.83 V <i>vs</i> RHE, with a geometric partial current density of -1.85 mA/cm<sup>2</sup>. We have documented the performance of the catalyst in both pristine and urea-modified foams pre- and post-electrolysis. Before electrolysis, the copper electrode consisted of a mixture of cuboctahedra and dendrites. After 35-minute electrolysis, the cuboctahedra and dendrites have undergone structural rearrangement. Changes in the interaction of urea with the catalyst surface have also been observed. These transformations were characterized <i>ex-situ</i> using scanning electron microscopy, X-ray diffraction, and X-ray photoelectron spectroscopy. We found that alterations in the morphology, crystallinity, and surface composition of the catalyst led to the deactivation of the copper foams.


2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Tao Gan ◽  
Jingxiu Yang ◽  
David Morris ◽  
Xuefeng Chu ◽  
Peng Zhang ◽  
...  

AbstractActivation of O2 is a critical step in heterogeneous catalytic oxidation. Here, the concept of increased electron donors induced by nitrogen vacancy is adopted to propose an efficient strategy to develop highly active and stable catalysts for molecular O2 activation. Carbon nitride with nitrogen vacancies is prepared to serve as a support as well as electron sink to construct a synergistic catalyst with Pt nanoparticles. Extensive characterizations combined with the first-principles calculations reveal that nitrogen vacancies with excess electrons could effectively stabilize metallic Pt nanoparticles by strong p-d coupling. The Pt atoms and the dangling carbon atoms surround the vacancy can synergistically donate electrons to the antibonding orbital of the adsorbed O2. This synergistic catalyst shows great enhancement of catalytic performance and durability in toluene oxidation. The introduction of electron-rich non-oxide substrate is an innovative strategy to develop active Pt-based oxidation catalysts, which could be conceivably extended to a variety of metal-based catalysts for catalytic oxidation.


Author(s):  
Qian-Wang Chen ◽  
Minxue Huang ◽  
Shipeng Gong ◽  
Changlai Wang ◽  
Yang Yang ◽  
...  
Keyword(s):  

Nanoscale ◽  
2021 ◽  
Author(s):  
Wei Shao ◽  
Xiaodong Zhang

Carbon dioxide (CO2) from the excessive consumption of fossil fuels has exhibited a huge threat to the planet’s ecosystem. Electrocatalytic CO2 reduction into value-added chemicals have been regarded as a...


Author(s):  
Yinyi Ma ◽  
Zemin Zhang ◽  
Xiao Jiang ◽  
Rongke Sun ◽  
Mingzheng Xie ◽  
...  

Photocatalytic reduction of carbon dioxide into chemical fuels has great practical significance in solving energy crisis and environmental pollution, but remains a big challenge owing to its low light absorption...


Author(s):  
Dui Ma ◽  
Ting Jin ◽  
Keyu Xie ◽  
Haitao Huang

Converting CO2 into value-added fuels or chemical feedstocks through electrochemical reduction is one of the several promising avenues to reduce atmospheric carbon dioxide levels and alleviate global warming. This approach...


2014 ◽  
Vol 53 (49) ◽  
pp. 19077-19086 ◽  
Author(s):  
Hua-Ping Ren ◽  
Yong-Hong Song ◽  
Qing-Qing Hao ◽  
Zhong-Wen Liu ◽  
Wei Wang ◽  
...  

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