Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Concept Videos

Catalysis02:50

Catalysis

26.5K
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.
26.5K

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Retrospective Analysis of Inpatient Rehabilitation Consultation Referrals and Clinical Profiles in a Tertiary Care Teaching Institute (February 2022 to February 2026).

Cureus·2026
Same author

Tightly Knotted Enzymes Inhibit Protein-Protein Aggregation.

bioRxiv : the preprint server for biology·2026
Same author

Crowder-Induced Conformational Fluctuations Modulate the Phase Separation of the Yeast Sup35NM Domain.

Biomacromolecules·2026
Same author

Siglec-G on B cells restrains the germinal center response by controlling T cell help during positive selection.

bioRxiv : the preprint server for biology·2026
Same author

Hydrogen-Bond Gating of Interfacial Capacitance in Amine-Rich Hybrid Interfaces for Redox-Free Ionic Recognition.

Langmuir : the ACS journal of surfaces and colloids·2026
Same author

Generative Machine Learning of Conformational Ensembles of Intrinsically Disordered Proteins: Progress and Opportunities.

Journal of chemical theory and computation·2026
Same journal

Kat5 deficiency in alveolar type II cells licenses STAT6-driven glycolytic reprogramming and pulmonary fibrosis.

Nature communications·2026
Same journal

Continuous nonthermal slab gap formed by progressive tearing beneath Northeast Asia.

Nature communications·2026
Same journal

Zeolitic isolated protonic acid sites-mediated NH<sub>3</sub> storage for robust NO<sub>x</sub> removal.

Nature communications·2026
Same journal

Coaxially nested component with asymmetric fiber resonant cavity and separation membrane for gaseous and dissolved gases detection.

Nature communications·2026
Same journal

Near-unity charge readout signal in a nonlinear resonator without matching the sensor dissipation.

Nature communications·2026
Same journal

Prokaryotic Schlafen proteins cleave tRNAs during type III CRISPR immunity.

Nature communications·2026
See all related articles

Related Experiment Video

Updated: May 29, 2025

In Situ Monitoring of Diffusion of Guest Molecules in Porous Media Using Electron Paramagnetic Resonance Imaging
06:34

In Situ Monitoring of Diffusion of Guest Molecules in Porous Media Using Electron Paramagnetic Resonance Imaging

Published on: September 2, 2016

6.3K

Diffusion-programmed catalysis in nanoporous material.

Suvendu Panda1, Tanmoy Maity1,2, Susmita Sarkar1

  • 1Tata Institute of Fundamental Research Hyderabad, Gopanpally, Hyderabad, 500046, Telangana, India.

Nature Communications
|February 3, 2025
PubMed
Summary
This summary is machine-generated.

Harnessing reactant diffusion length in porous catalysts significantly enhances reaction rates and selectivity. This novel approach using metal-organic frameworks in microfluidic reactors overcomes limitations of traditional catalysts.

More Related Videos

Synthesis of Metal Nanoparticles Supported on Carbon Nanotube with Doped Co and N Atoms and its Catalytic Applications in Hydrogen Production
08:40

Synthesis of Metal Nanoparticles Supported on Carbon Nanotube with Doped Co and N Atoms and its Catalytic Applications in Hydrogen Production

Published on: December 6, 2021

3.5K
A Continuous-flow Photocatalytic Reactor for the Precisely Controlled Deposition of Metallic Nanoparticles
11:49

A Continuous-flow Photocatalytic Reactor for the Precisely Controlled Deposition of Metallic Nanoparticles

Published on: April 10, 2019

9.7K

Related Experiment Videos

Last Updated: May 29, 2025

In Situ Monitoring of Diffusion of Guest Molecules in Porous Media Using Electron Paramagnetic Resonance Imaging
06:34

In Situ Monitoring of Diffusion of Guest Molecules in Porous Media Using Electron Paramagnetic Resonance Imaging

Published on: September 2, 2016

6.3K
Synthesis of Metal Nanoparticles Supported on Carbon Nanotube with Doped Co and N Atoms and its Catalytic Applications in Hydrogen Production
08:40

Synthesis of Metal Nanoparticles Supported on Carbon Nanotube with Doped Co and N Atoms and its Catalytic Applications in Hydrogen Production

Published on: December 6, 2021

3.5K
A Continuous-flow Photocatalytic Reactor for the Precisely Controlled Deposition of Metallic Nanoparticles
11:49

A Continuous-flow Photocatalytic Reactor for the Precisely Controlled Deposition of Metallic Nanoparticles

Published on: April 10, 2019

9.7K

Area of Science:

  • Heterogeneous Catalysis
  • Materials Science
  • Chemical Engineering

Background:

  • Reactant diffusion is crucial for heterogeneous catalysis, affecting reaction rates and selectivity.
  • Porous catalysts like metal-organic frameworks (MOFs) struggle to control diffusion rates.
  • Current methods often rely on catalyst chemical functionality, limiting performance.

Purpose of the Study:

  • To develop a strategy for controlling reactant diffusion length to improve catalyst performance.
  • To augment reaction kinetics and enhance geometric selectivity in porous catalysts.
  • To overcome limitations of conventional nano/microcrystal catalysts.

Main Methods:

  • Utilized a thin film of a porous metal-organic framework catalyst.
  • Employed a cross-flow microfluidic catalytic reactor.
  • Programmed reactant diffusion within the catalyst film.

Main Results:

  • Achieved over a 1000-fold increase in turnover frequency.
  • Enhanced geometric selectivity by approximately 2-fold compared to bulk catalysts.
  • Demonstrated concurrent amplification of reaction rate and selectivity.

Conclusions:

  • Diffusion-programmed catalysis offers a robust solution for enhancing porous catalyst performance.
  • This strategy overcomes diffusion constraints inherent in bulk nano/microcrystals.
  • Represents an advancement in designing porous catalyst-driven organic reactions.