Liming Dai,*,†,‡ Yuhua Xue,†,‡ Liangti Qu,* Hyun-Jung Choi, and Jong-Beom Baek* †Center of Advanced Science and Engineering for Carbon (Case4Carbon), Department of Macromolecular Science and Engineering, Case Western Reserve University, 10900 Euclid Avenue, Cleveland, Ohio 44106, United States Key Laboratory of Cluster Science, Ministry of Education of China, Beijing Key Laboratory of Photoelectronic/Electrophotonic Conversion Materials, Department of Chemistry, School of Science, Beijing Institute of Technology, Beijing 100081, People’s Republic of China School of Energy and Chemical Engineering/Center for Dimension-Controllable Covalent Organic Frameworks, Ulsan National Institute of Science and Technology (UNIST), 100 Banyeon, Ulsan, 689-798, South Korea

Metal-free catalysts for oxygen reduction reaction.

This article provides an up-to-date perspective on the use of anion-exchange membranes in fuel cells, electrolysers, redox flow batteries, reverse electrodialysis cells, and bioelectrochemical systems (e.g. microbial fuel cells). The aim is to highlight key concepts, misconceptions, the current state-of-the-art, technological and scientific limitations, and the future challenges (research priorities) related to the use of anion-exchange membranes in these energy technologies. All the references that the authors deemed relevant, and were available on the web by the manuscript submission date (30th April 2014), are included.

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Anion-exchange membranes in electrochemical energy systems

Anion exchange membranes for alkaline fuel cells: A review

Direct alcohol fuel cells (DAFCs) are attracting increasing interest as power sources for portable applications due to some unquestionable advantages over analogous devices fed with hydrogen.1 Alcohols, such as methanol, ethanol, ethylene glycol, and glycerol, exhibit high volumetric energy density, and their storage and transport are much easier as compared to hydrogen. On the other hand, the oxidation kinetics of any alcohol are much slower and still H2-fueled polymer electrolyte fuel cells (PEMFCs) exhibit superior electrical performance as compared to DAFCs with comparable electroactive surface areas.2,3 Increasing research efforts are therefore being carried out to design and develop more efficient anode electrocatalysts for DAFCs.

Palladium-Based Electrocatalysts for Alcohol Oxidation in Half Cells and in Direct Alcohol Fuel Cells

Recent development of polymer electrolyte membranes for fuel cells.

In recent decades, fuel cell technology has been undergoing revolutionary developments, with fundamental progress being the replacement of electrolyte solutions with polymer electrolytes, making the device more compact in size and higher in power density. Nowadays, acidic polymer electrolytes, typically Nafion, are widely used. Despite great success, fuel cells based on acidic polyelectrolyte still depend heavily on noble metal catalysts, predominantly platinum (Pt), thus increasing the cost and hampering the widespread application of fuel cells. Here, we report a type of polymer electrolyte fuel cells (PEFC) employing a hydroxide ion-conductive polymer, quaternary ammonium polysulphone, as alkaline electrolyte and nonprecious metals, chromium-decorated nickel and silver, as the catalyst for the negative and positive electrodes, respectively. In addition to the development of a high-performance alkaline polymer electrolyte particularly suitable for fuel cells, key progress has been achieved in catalyst tailoring: The surface electronic structure of nickel has been tuned to suppress selectively the surface oxidative passivation with retained activity toward hydrogen oxidation. This report of a H2–O2 PEFC completely free from noble metal catalysts in both the positive and negative electrodes represents an important advancement in the research and development of fuel cells.

https://www.pnas.org/content/pnas/105/52/20611.full.pdf

Alkaline polymer electrolyte fuel cells completely free from noble metal catalysts

Although the proton exchange membrane fuel cell (PEMFC) has made great progress in recent decades, its commercialization has been hindered by a number of factors, among which is the total dependence on Pt-based catalysts. Alkaline polymer electrolyte fuel cells (APEFCs) have been increasingly recognized as a solution to overcome the dependence on noble metal catalysts. In principle, APEFCs combine the advantages of and alkaline fuel cell (AFC) and a PEMFC: there is no need for noble metal catalysts and they are free of carbonate precipitates that would break the waterproofing in the AFC cathode. However, the performance of most alkaline polyelectrolytes can still not fulfill the requirement offuel cell operations. In the present work, detailed information about the synthesis and physicochemical properties of the quaternary ammonia polysulfone (QAPS), a high-performance alkaline polymer electrolyte that has been successfully applied in the authors' previous work to demonstrate an APEFC completely free from noble metal catalysts (S. Lu, J. Pan, A. Huang, L. Zhuang, J. Lu, Proc. Natl. Acad. Sci. USA 2008, 105, 20611), is reported. Monitored by NMR analysis, the synthetic process of QAPS is seen to be simple and efficient. The chemical and thermal stability, as well as the mechanical strength of the synthetic QAPS membrane, are outstanding in comparison to commercial anion-exchange membranes. The ionic conductivity of QAPS at room temperature is measured to be on the order of 10 -2 S cm -1 Such good mechanical and conducting performances can be attributed to the superior microstructure of the polyelectrolyte, which features interconnected ionic channels in tens of nanometers diameter, as revealed by HRTEM observations. The electrochemical behavior at the Pt/ QAPS interface reveals the strong alkaline nature of this polyelectrolyte, and the preliminary fuel cell test verifies the feasibility of QAPS for fuel cell applications.

High‐Performance Alkaline Polymer Electrolyte for Fuel Cell Applications

All-solid-state electrochromic devices can be used to create smart windows that regulate the transmittance of solar radiation by applying a voltage. However, the devices suffer from a limited ion diffusion speed, which leads to slow colouration and bleaching processes. Here we report fast-switching electrochromic devices that are based on an all-solid-state tandem structure and use protons as the diffusing species. We use tungsten trioxide (WO3) as the electrochromic material, and poly(3,4-ethylenedioxythiophene):polystyrene sulfonate (PEDOT:PSS) as the solid-state proton source. This structure exhibits a low contrast ratio (that is, the difference between on and off transmittance); however, we add a solid polymeric electrolyte layer on top of PEDOT:PSS, which provides sodium ions to PEDOT:PSS and pumps protons to the WO3 layer through ion exchange. The resulting electrochromic devices exhibit high contrast ratios (more than 90% at 650 nm), fast responses (colouration to 90% in 0.7 s and bleaching to 65% in 0.9 s and 90% in 7.1 s), good colouration efficiency (109 cm2 C−1 at 670 nm) and excellent cycling stability (less than 10% degradation of contrast ratio after 3,000 cycles). We also fabricate large-area (30 × 40 cm2) and flexible devices, illustrating the scaling potential of the approach. Solid-state tandem structures that use protons as the diffusing species can be used to create electrochromic devices that exhibit high contrast ratios, fast responses, good colouration efficiency and excellent cycling stability. 

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All-solid-state proton-based tandem structures for fast-switching electrochromic devices

The invention discloses a preparation method of a polymer anion exchange membrane The method comprises the steps of chloromethylation and quaterisation of the polymer and film forming The preparation method is characterized in that metal zinc or aluminium powder and fluorine organic acid are taken as mixed catalyst to carry out high-effect chloromethylation grafting on the polymer where the main chain has benzene rings and benzene rings are connected with each other by ether bonds; the quaterisation of the chloromethylation polymer is then carried out by a gas-liquid or liquid-liquid reaction; for example, trimethylamine gas enters chloromethylation polymer solution to carry out the quaterisation reaction; the film is then formed by spraying and casting so as to obtain the quaterisation anion exchange membrane The method of the invention is simple and convenient and has high efficiency; the polymer anion exchange membrane has high ion exchanging capacity and high chemical and thermal stability; furthermore, the mechanical performance of the film is outstanding

Aibin Huang

Papers

Alkaline polymer electrolyte fuel cells completely free from noble metal catalysts

High‐Performance Alkaline Polymer Electrolyte for Fuel Cell Applications

All-solid-state proton-based tandem structures for fast-switching electrochromic devices

Method for preparing polymer anion-exchange membrane

Deterioration mechanism of vanadium dioxide smart coatings during natural aging: Uncovering the role of water