通过真空诱导合成Ni3 B/Ni以实现超高稳定和高效的甲醇氧化
Zhenjie Liu1, Pingping Chang1, Murong Xi1
1State Key Laboratory of Chemistry and Utilization of Carbon Based Energy Resources, College of Chemistry, Xinjiang University, Address Urumqi, Xinjiang, 830017, P. R. China.
Small (Weinheim an der Bergstrasse, Germany)
|August 29, 2023
概括
一种新的玻化/异构催化剂有效氧化甲醇到酸. 这种催化剂表现出高反应性,近100%的选择性,以及电化学合成的特殊稳定性.
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:
- 高效的催化剂对于电化学合成技术至关重要,例如演化反应 (HER) 和二氧化碳减排反应 (CO2 RR).
- 甲醇 (MeOH) 的电化学氧化是生产有价值化学品的关键过程.
研究的目的:
- 开发一种用于电化学氧化甲醇到酸的新型催化剂.
- 研究合成催化剂的催化性能,选择性和稳定性.
主要方法:
- 使用真空感应策略合成化/ (Ni3B/Ni) 异构催化剂.
- 电化学表征包括超电位,电流密度和法拉第效率测量.
- 现场电化学阻抗光谱和密度函数理论 (DFT) 计算用于机制研究.
主要成果:
- Ni3B/Ni催化剂表现出高反应性,具有较低的超电位 (146.9 mV在10 mA cm-2) 和高电流密度.
- 实现了超高的选择性 (接近100%的法拉第效率) 以甲醇转化为酸.
- 证明了超长时间的稳定性,在100 mA cm-2.0下运行超过50小时.
- 现场研究表明,MeOH氧化抑制了催化剂的失活,确保了稳定性和选择性.
- DFT计算确定了Ni3B/Ni异构上*CH2O形成的有利的潜在确定步骤.
结论:
- 新的Ni3B/Ni异构催化剂为高效和选择性的电化学甲醇氧化提供了一个有希望的解决方案.
- 催化剂的独特结构和反应机制有助于其卓越的性能.
- 这些发现为设计用于甲醇氧化和其他电化学合成应用的先进电催化剂提供了宝贵的见解.
更多相关视频
07:57Author Spotlight: A Rapid, Microwave-Assisted Hydrothermal Synthesis Of Nickel Hydroxide Nanosheets
Published on: August 18, 2023
1.9K
07:47Reverse Microemulsion-mediated Synthesis of Monometallic and Bimetallic Early Transition Metal Carbide and Nitride Nanoparticles
Published on: November 27, 2015
10.9K
相关概念视频
Hydroboration-Oxidation of Alkenes
8.4K
In addition to the oxymercuration–demercuration method, which converts the alkenes to alcohols with Markovnikov orientation, a complementary hydroboration-oxidation method yields the anti-Markovnikov product. The hydroboration reaction, discovered in 1959 by H.C. Brown, involves the addition of a B–H bond of borane to an alkene giving an organoborane intermediate. The oxidation of this intermediate with basic hydrogen peroxide forms an alcohol.
8.4K
Alkynes to Aldehydes and Ketones: Hydroboration-Oxidation
18.3K
Introduction
One of the convenient methods for the preparation of aldehydes and ketones is via hydration of alkynes. Hydroboration-oxidation of alkynes is an indirect hydration reaction in which an alkyne is treated with borane followed by oxidation with alkaline peroxide to form an enol that rapidly converts into an aldehyde or a ketone. Terminal alkynes form aldehydes, whereas internal alkynes give ketones as the final product.
One of the convenient methods for the preparation of aldehydes and ketones is via hydration of alkynes. Hydroboration-oxidation of alkynes is an indirect hydration reaction in which an alkyne is treated with borane followed by oxidation with alkaline peroxide to form an enol that rapidly converts into an aldehyde or a ketone. Terminal alkynes form aldehydes, whereas internal alkynes give ketones as the final product.
18.3K
Catalysis
27.0K
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.
27.0K
Preparation of Alcohols via Addition Reactions
6.3K
Overview
The acid-catalyzed addition of water to the double bond of alkenes is a large-scale industrial method used to synthesize low-molecular-weight alcohols. An acidic atmosphere is required to allow the hydrogen in the water molecule to act as an electrophile and attack the double bond in an alkene. The addition of a proton to the double bond creates a carbocation intermediate. The proton preferentially bonds to the less substituted end of the double bond to create a more stable carbocation...
The acid-catalyzed addition of water to the double bond of alkenes is a large-scale industrial method used to synthesize low-molecular-weight alcohols. An acidic atmosphere is required to allow the hydrogen in the water molecule to act as an electrophile and attack the double bond in an alkene. The addition of a proton to the double bond creates a carbocation intermediate. The proton preferentially bonds to the less substituted end of the double bond to create a more stable carbocation...
6.3K
