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Unveiling the pH-dependent structure-activity relationship of Co-based cataly...

B2FIND2026-04-11 收录

电催化析氧反应

催化剂结构-活性关系

数据链接：

https://b2find.eudat.eu/dataset/9fab23cc-2fd7-5073-aabe-c113945d7c97 数据链接链接失效反馈

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资源简介：

Co-based catalysts are promising candidates to replace the Ir/Ru-based oxides for the oxygen evolution reaction (OER) in an acidic environment. However, both the reaction...

应用场景：

电催化析氧反应

双金属催化剂

Oxygen evolution reaction (OER) is key for electrochemical water splitting. Catalysts minimized in single-atom level (SACs) anchored on two-dimensional substances are highly active for various electro

NIAID Data Ecosystem70

Source_data

电催化析氧反应

难熔高熵合金

Electrocatalytic oxygen evolution reaction (OER) is key to several energy technologies but suffers from low activity. Leveraging the lattice oxygen activation mechanism (LOM) is a strategy for boostin

DataCite Commons2025-03-17 更新50

Air-Stable Pd(R-allyl)LCl (L= Q-Phos, P( t -Bu) 3 , etc.) Systems for C–C/N Couplings: Insight into the Structure–Activity Relationship and Catalyst Activation Pathway

过渡金属催化交叉偶联

催化剂结构-活性关系

A series of Pd(R-allyl)LCl complexes [R = H, 1-Me, 1-Ph, 1-gem-Me2, 2-Me; L = Q-Phos, P(t-Bu)3, P(t-Bu)2(p-NMe2C6H4), P(t-Bu)2Np] have been synthesized and evaluated in the Buchwald–Hartwig aminations

NIAID Data Ecosystem30

Acidic Oxygen Evolution Reaction Activity–Stability Relationships in Ru-Based Pyrochlores

电催化析氧反应

催化剂稳定性

Ru-based oxygen evolution reaction (OER) catalysts show significant promise for efficient water electrolysis, but rapid degradation poses a major challenge for commercial applications. In this work, w

NIAID Data Ecosystem60

Insights into the Structure–Activity Relationships in Metal–Organic Framework-Supported Nickel Catalysts for Ethylene Hydrogenation

催化剂结构-活性关系

烯烃催化氢化

Solid supports play an indispensable role in heterogeneous catalysis, as they can directly affect the catalytic activity and selectivity of supported catalysts. However, the specific roles of such sup

NIAID Data Ecosystem40

Unveiling the pH-dependent structure-activity relationship of Co-based cataly...

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