通过热氧化诱导的RuO2通过PtRu/C催化剂上的阻断外提高PEMFC阳极中的CO耐受性
Lina Chen1, Pengyang Zhang1, Yan-Qi Jin1
1College of Chemistry and Chemical Engineering, State Key Laboratory of Physical Chemistry of Solid Surfaces, and Tan Kah Kee Innovation Laboratory, Xiamen University, Xiamen 361005, China.
Nano letters
|August 19, 2024
概括
在PtRu/C催化剂上的一种新型Ru氧化物层通过阻断CO吸附,显著提高了质子交换膜燃料电池 (PEMFC) 的性能. 这一突破提高了实际燃料电池应用的二氧化碳耐受性和耐久性.
科学领域:
- 电化学 电化学 电化学
- 材料科学 材料科学 材料科学
- 催化剂是一种催化剂.
背景情况:
- 基于 (Pt) 的阳极催化剂的一氧化碳 (CO) 中毒严重降低了质子交换膜燃料电池 (PEMFC) 的性能.
- 与实验室三电极设置相比,现有的耐CO催化剂在实际的PEMFC系统中通常表现出有限的有效性.
研究的目的:
- 开发一种简单有效的策略,在商业PtRu/C催化剂上创建一个阻CO的层.
- 为了提高极催化剂的CO耐受性和耐用性,用于实际的PEMFC应用.
主要方法:
- 采用简单的热氧化策略,在商业PtRu/C上创建一层氧化物 (RuO2) 阻断层.
- 这涉及一阶段的分离和氧化过程,形成一个薄 (0.7 nm) 的RuO2层.
- 用旋转盘电极测试和在各种CO度下在功能性PEMFC中评估了催化剂性能.
主要成果:
- PtRu@RuO2/C催化剂显著提高了CO耐受性,在旋转盘电极测试中持久1%的CO (比PtRu/C提高了约10倍).
- 在PEMFC中,催化剂保持了高氧化反应 (HOR) 活性和CO耐受性,在100ppm的CO时显示微不足道的性能损失.
- 在经过4小时的稳定性测试后,催化剂保持了85%的HOR活性,这表明了极好的耐用性.
结论:
- 氧化阻断层有效地抑制了CO吸附,从而提高了催化剂对CO中毒的耐受性.
- 这种方法提供了一种实际的方法来提高PEMFC阳极催化剂的性能和耐用性.
- 该机制涉及减缓CO吸附动力学,而不是传统的双功能CO氧化途径.
相关概念视频
Catalysis
26.8K
The presence of a catalyst affects the rate of a chemical reaction. A catalyst is a substance that can increase the reaction rate without being consumed during the process. A basic comprehension of a catalysts’ role during chemical reactions can be understood from the concept of reaction mechanisms and energy diagrams.
26.8K
Oxidation of Alkenes: Syn Dihydroxylation with Potassium Permanganate
11.2K
Alkenes can be dihydroxylated using potassium permanganate. The method encompasses the reaction of an alkene with a cold, dilute solution of potassium permanganate under basic conditions to form a cis-diol along with a brown precipitate of manganese dioxide.
11.2K
Oxidation of Alkenes: Syn Dihydroxylation with Osmium Tetraoxide
10.0K
Alkenes are converted to 1,2-diols or glycols through a process called dihydroxylation. It involves the addition of two hydroxyl groups across the double bond with two different stereochemical approaches, namely anti and syn. Dihydroxylation using osmium tetroxide progresses with syn stereochemistry.
10.0K
Radical Oxidation of Allylic and Benzylic Alcohols
1.9K
Activated manganese(IV) oxide can selectively oxidize allylic and benzylic alcohols via a radical intermediate mechanism. Primary allylic alcohols are oxidized to aldehydes, while secondary allylic alcohols yield ketones. The redox reaction of potassium permanganate with an Mn(II) salt such as manganese sulfate (under either alkaline or acidic conditions), followed by thorough drying, yields the oxidizing agent: activated MnO2. While MnO2 is insoluble in the solvents used for the reaction, the...
1.9K


