排序方式: 共有115条查询结果,搜索用时 187 毫秒
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Lisa Ring Bruno G. Pollet Marian Chatenet Sofyane Abbou Karsten Küpper Mercedes Schmidt Marten Huck Aurelia Gries Martin Steinhart Helmut Schfer 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2019,131(48):17544-17553
The electrodeposition of noble metals using corresponding dissolved metal salts represents an interesting process for the improvement of the electrocatalytic hydrogen evolution reaction (HER) properties of less active substrate materials. The fact that only a small fraction of the dissolved noble metals reaches the substrate represents a serious obstacle to this common procedure. We therefore chose a different path. It was found that the HER activity of Ni42 alloy drastically increased (η=140 mV at j=10 mA cm?2; pH 1) when a platinum counter electrode was used during polarization experiments in acid. This improvement was caused by a platinum transfer from the platinum anode to the steel cathode, a process which occurred simultaneously to the hydrogen evolution. The negligible accumulation of Pt (26 μg) in the electrolyte turns this straight‐forward transfer procedure into a highly cost‐effective, environmentally friendly, and waste reducing approach for the generation of cheap, stable and effective HER electrodes. 相似文献
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Wei‐Hong Lai Li‐Fu Zhang Wei‐Bo Hua Sylvio Indris Zi‐Chao Yan Zhe Hu Binwei Zhang Yani Liu Li Wang Min Liu Rong Liu Yun‐Xiao Wang Jia‐Zhao Wang Zhenpeng Hu Hua‐Kun Liu Shu‐Lei Chou Shi‐Xue Dou 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2019,131(34):11994-11999
Both the hydrogen evolution reaction (HER) and the oxygen evolution reaction (OER) are crucial to water splitting, but require alternative active sites. Now, a general π‐electron‐assisted strategy to anchor single‐atom sites (M=Ir, Pt, Ru, Pd, Fe, Ni) on a heterogeneous support is reported. The M atoms can simultaneously anchor on two distinct domains of the hybrid support, four‐fold N/C atoms (M@NC), and centers of Co octahedra (M@Co), which are expected to serve as bifunctional electrocatalysts towards the HER and the OER. The Ir catalyst exhibits the best water‐splitting performance, showing a low applied potential of 1.603 V to achieve 10 mA cm?2 in 1.0 m KOH solution with cycling over 5 h. DFT calculations indicate that the Ir@Co (Ir) sites can accelerate the OER, while the Ir@NC3 sites are responsible for the enhanced HER, clarifying the unprecedented performance of this bifunctional catalyst towards full water splitting. 相似文献
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Metin Karayilan William P. Brezinski Kayla E. Clary Dennis L. Lichtenberger Richard S. Glass Jeffrey Pyun 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2019,131(23):7617-7630
Reviewed herein is the development of novel polymer‐supported [2Fe‐2S] catalyst systems for electrocatalytic and photocatalytic hydrogen evolution reactions. [FeFe] hydrogenases are the best known naturally occurring metalloenzymes for hydrogen generation, and small‐molecule, [2Fe‐2S]‐containing mimetics of the active site (H‐cluster) of these metalloenzymes have been synthesized for years. These small [2Fe‐2S] complexes have not yet reached the same capacity as that of enzymes for hydrogen production. Recently, modern polymer chemistry has been utilized to construct an outer coordination sphere around the [2Fe‐2S] clusters to provide site isolation, water solubility, and improved catalytic activity. In this review, the various macromolecular motifs and the catalytic properties of these polymer‐supported [2Fe‐2S] materials are surveyed. The most recent catalysts that incorporate a single [2Fe‐2S] complex, termed single‐site [2Fe‐2S] metallopolymers, exhibit superior activity for H2 production. 相似文献