A novel electrochemical flow-cell for operando XAS investigations in X-ray opaque supports
文献情報
Guillaume Alizon, Andrea Zitolo, Andrea Di Cicco, Hélène Magnan, Emiliano Fonda
Improvement of electrochemical technologies is one of the most popular topics in the field of renewable energy. However, this process requires a deep understanding of the electrode–electrolyte interface behavior under operando conditions. X-ray absorption spectroscopy (XAS) is widely employed to characterize electrode materials, providing element-selective oxidation state and local structure. Several existing cells allow studies as close as possible to realistic operating conditions, but most of them rely on the deposition of the electrodes on conductive and X-ray transparent materials, from where the radiation impinges the sample. In this work, we present a new electrochemical flow-cell for operando XAS that can be used with X-ray opaque substrates, since the signal is effectively detected from the electrode surface, as the radiation passes through a thin layer of electrolyte (∼17 μm). The electrolyte can flow over the electrode, reducing bubble formation and avoiding strong reactant concentration gradients. We show that high-quality data can be obtained under operando conditions, thanks to the high efficiency of the cell from the hard X-ray regime down to ∼4 keV. We report as a case study the operando XAS investigation at the Fe and Ni K-edges on Ni-doped γ-Fe2O3 films, epitaxially grown on Pt substrates. The effect of the Ni content on the catalytic performances for the oxygen evolution reaction is discussed.
関連文献
Enzymatic synthesis of pharmacologically relevant chiral sulfoxides by improved CbBVMO variants
Chen Zhao, Feng Liu, Min Zhou, Qiang Geng, Hui-Lei Yu
DOI: 10.1039/D3CC05463B
Isolation of the elusive [Ru(bipy)3]+: a key intermediate in photoredox catalysis
Samuel J. Horsewill, Chengyang Cao, Noah Dabney, Eric S. Yang, Stephen Faulkner, Daniel J. Scott
DOI: 10.1039/D3CC04375D
Phenylalanine-based fibrillar systems
Soumen Kuila, Sukantha Dey, Akash Shrivastava, Jayanta Nanda
DOI: 10.1039/D3CC04138G
Ferrocene: an exotic building block for supramolecular assemblies
Chandrakanta Guchhait, Vembanan Suriyaa, Nihar Sahu, Sovik Dey Sarkar, Bimalendu Adhikari
DOI: 10.1039/D3CC03659F
Development of 3-triazenylaryne and its application to iterative aryne reactions via o-triazenylarylboronic acids
Motoki Ito, Yuta Takishima, Rinto Ishikawa, Mao Kamimura, Hana Watanabe, Takehiro Konishi, Kazuhiro Higuchi, Shigeo Sugiyama
DOI: 10.1039/D3CC04878K
Lead-oriented synthesis of epigenetic relevant scaffolds
Timothé Maujean, Prakash Kannaboina, Adam I. Green, George M. Burslem
DOI: 10.1039/D3CC04317G
Iron-based fluorophosphate Na2FePO4F as a cathode for aqueous zinc-ion batteries
Deepa Singh, Yang Hu, Sher Singh Meena, Rishikesh Vengarathody
DOI: 10.1039/D3CC04940J
Towards high-performance nonlinear optical materials through embedding a D–A system into β-ketoenamine-linked COFs
Mingyan Li, Jiahui Chu, Debo Ding, Tingting Li, Endian Su, Yinglin Song, Yun-Fang Yang, Yuanbin She, Jianhong Jia
DOI: 10.1039/D3CC04845D
Access to isoindole-derived BODIPYs by an aminopalladation cascade
Heinrich F. von Köller, Finn J. Geffers, Pedram Kalvani, Adrian Foraita, Patrick-Eric J. Loß, Burkhard Butschke, Peter G. Jones, Daniel B. Werz
DOI: 10.1039/D3CC04913B
こちらもおすすめ
3-イチチルビフェニルはどのように合成されますか?
3-イチチルビフェニルは、ビフェニルとイチプロピオニトリルを回収率約90%で反応させて合成されます。触媒は通常、亜リチウムホウ素を用います。
8-溴-5-三氟甲基喹啉はどのように合成されますか?
8-溴-5-三氟甲基喹啉は、5-トリフルオロメチル-2-メチル-1,3-ベンゼンジオールをブロモエタノールと反応させて生成します。この反応は塩基性条件下で行われ...
ジメチル4-(4,4,5,5-テトラメチル-1,3,2-ドioxaborolan-2-基)-2,6-ピリジンジカルボイル酸フェニルアミニドの代替品はありますか?
ジメチル4-(4,4,5,5-テトラメチル-1,3,2-ドioxaborolan-2-基)-2,6-ピリジンジカルボイル酸フェニルアミニドの代替品としては、4-...
N-(3,5-ヘキサクロロ-4-ピリドインイル)-8-メチオキシ-5-キノリンカーボン酸の市場動向や研究トレンドはどのようなものでしょうか?
N-(3,5-ヘキサクロロ-4-ピリドインイル)-8-メチオキシ-5-キノリンカーボン酸の市場動向は、主に産業用途での需要により影響を受けます。研究トレンドとし...
イソステアロイルグリセリルは安全ですか?
イソステアロイルグリセリルは一般的に安全性が高いとされていますが、過度な使用や個人差により皮�owsん炎などの反応が起こる可能性があります。使用前に医師に相談す...
1-(二苯甲基)-3,3-二氟-氮杂环丁烷の市場動向や研究トレンドはどうですか?
1-(二苯甲基)-3,3-二氟-氮杂环丁烷の市場動向は、医薬品や合成化学の研究分野で注目を集めています。新興研究は、該当化合物の合成改良と生体内での作用メカニズ...
3-チオフェンスチオールの物理化学的性質は何ですか?
3-チオフェンスチオールのCAS番号は7774-73-4です。結晶性の白色粉末で、分子量は122.17です。この化合物は水に微溶解し、エタノールやジクロロメタン...
2-Methyl-2-propanyl (2S)-2-(aminomethyl)-1-piperidinecarboxylateは安全ですか?
2-Methyl-2-propanyl (2S)-2-(aminomethyl)-1-piperidinecarboxylateは一定の安全性基準を満たしていま...
CAS番号1316822-90-8の化合物は安全ですか?
CAS番号1316822-90-8の化合物は安全性に関しては評価が不足していますが、一般的には生物学的に活性な物質であり、取り扱いには適切な安全防護措置が必要で...
Tert-butyl 2-(2-羟基乙基)哌嗪-1-羧酸はどのように保存すればよいですか?
Tert-butyl 2-(2-羟基乙基)哌嗪-1-羧酸は、冷暗所で保存し、直射日光から遠ざけてください。容器は密閉し、高湿度や高温を避けて保管してください。
掲載誌
Physical Chemistry Chemical Physics

Physical Chemistry Chemical Physics (PCCP) is an international journal co-owned by 19 physical chemistry and physics societies from around the world. This journal publishes original, cutting-edge research in physical chemistry, chemical physics and biophysical chemistry. To be suitable for publication in PCCP, articles must include significant innovation and/or insight into physical chemistry; this is the most important criterion that reviewers and Editors will judge against when evaluating submissions. The journal has a broad scope and welcomes contributions spanning experiment, theory, computation and data science. Topical coverage includes spectroscopy, dynamics, kinetics, statistical mechanics, thermodynamics, electrochemistry, catalysis, surface science, quantum mechanics, quantum computing and machine learning. Interdisciplinary research areas such as polymers and soft matter, materials, nanoscience, energy, surfaces/interfaces, and biophysical chemistry are welcomed if they demonstrate significant innovation and/or insight into physical chemistry. Joined experimental/theoretical studies are particularly appreciated when complementary and based on up-to-date approaches.













![6,7-Dihydro-5H-pyrrolo[1,2-a]imidazole-6-carboxylic acid structure 6,7-Dihydro-5H-pyrrolo[1,2-a]imidazole-6-carboxylic acid structure](https://static.chemtradehub.com/structs/136/1369160-12-2-6524.webp)
![N-{3-[Benzyl(methyl)amino]propyl}-9-chloro-5,6,7,8-tetrahydro-2-acridinecarboxamide structure N-{3-[Benzyl(methyl)amino]propyl}-9-chloro-5,6,7,8-tetrahydro-2-acridinecarboxamide structure](https://static.chemtradehub.com/structs/142/1426944-49-1-1e4c.webp)