高効率な水素・化学品製造のための新型電極触媒を開発(Scientists Develop Novel Electrocatalyst for Efficient Hydrogen and Chemicals Production)

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2025-04-28 中国科学院(CAS)

高効率な水素・化学品製造のための新型電極触媒を開発(Scientists Develop Novel Electrocatalyst for Efficient Hydrogen and Chemicals Production)

Synthesis of high-entropy nanostructured PtCuCoNiMn electrocatalysts (Image by NIMTE)

中国科学院寧波材料技術与工学研究所の陳亮教授らの研究チームは、高効率な水素と高付加価値化学品(グリセリン誘導体)の同時生産を可能にする高エントロピー電極触媒(PtCuCoNiMnナノ構造体)を開発した。グリセリンのカスケード電気酸化反応を利用することで、従来の酸素発生反応に比べエネルギー消費を大幅に削減。新触媒は高電流密度(200 mA/cm²)で75.2%の選択率を達成し、210時間以上の安定稼働を示した。今回の成果は、カーボンニュートラル社会実現に向けた水素生産技術の進展に大きく寄与する可能性がある。

<関連情報>

ナノスケールの高エントロピー表面工学により、高電流密度でグリセリンへの選択的グリセリン電解酸化が促進される Nanoscale high-entropy surface engineering promotes selective glycerol electro-oxidation to glycerate at high current density

Shuibo Wang,Yichao Lin,Yanle Li,Ziqi Tian,Yu Wang,Zhiyi Lu,Baoxin Ni,Kun Jiang,Hongbo Yu,Shiwei Wang,Hongfeng Yin & Liang Chen
Nature Nanotechnology  Published:17 March 2025
DOI:https://doi.org/10.1038/s41565-025-01881-9

Abstract

Selective production of valuable glycerol chemicals, such as glycerate (which serves as an important chemical intermediate), poses a significant challenge due to the facile cleavage of C–C bonds and the presence of multiple reaction pathways. This challenge is more severe in the electro-oxidation of glycerol, which requires the development of desirable electrocatalysts. To facilitate the glycerol electro-oxidation reaction to glycerate, here we present an approach utilizing a high-entropy PtCuCoNiMn nanosurface. It exhibits exceptional activity (~200 mA cm−2 at 0.75 V versus a reversible hydrogen electrode) and selectivity (75.2%). In situ vibrational measurements and theoretical calculations reveal that the exceptional glycerol electro-oxidation selectivity and activity can be attributed to the unique characteristics of the high-entropy surface, which effectively modifies the electronic structure of the exposed Pt sites. The catalyst is successfully applied in an electrolyser for long-term glycerol electro-oxidation reaction, demonstrating excellent performance (~200 mA cm−2 at 1.2Vcell) over 210 h. The present study highlights that tailoring the catalytic sites at the catalyst–electrolyte interface by constructing a high-entropy surface is an effective strategy for electrochemical catalysis.

0505化学装置及び設備
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