TY - JOUR
T1 - The concept of active site in heterogeneous catalysis
AU - Vogt, Charlotte
AU - Weckhuysen, Bert M.
N1 - Funding Information:
B.M.W. acknowledges financial support from the Netherlands Organization for Scientific Research (NWO) in the frame of a Gravitation programme (the Netherlands Center for Multiscale Catalytic Energy Conversion (MCEC), www. mcec-researchcenter.nl), as well as from the Advanced Research Center (ARC) Chemical Buildings Blocks Consortium (CBBC), a public–private research consortium in the Netherlands (www.arc-cbbc.nl). C.V. acknowledges support from a Niels Stensen Fellowship and a VATAT fellowship.
Funding Information:
B.M.W. acknowledges financial support from the Netherlands Organization for Scientific Research (NWO) in the frame of a Gravitation programme (the Netherlands Center for Multiscale Catalytic Energy Conversion (MCEC), www.mcec-researchcenter.nl), as well as from the Advanced Research Center (ARC) Chemical Buildings Blocks Consortium (CBBC), a public?private research consortium in the Netherlands (www.arc-cbbc.nl). C.V. acknowledges support from a Niels Stensen Fellowship and a VATAT fellowship.
Publisher Copyright:
© 2022, Springer Nature Limited.
PY - 2022/2
Y1 - 2022/2
N2 - Catalysis is at the core of chemistry and has been essential to make all the goods surrounding us, including fuels, coatings, plastics and other functional materials. In the near future, catalysis will also be an essential tool in making the shift from a fossil-fuel-based to a more renewable and circular society. To make this reality, we have to better understand the fundamental concept of the active site in catalysis. Here, we discuss the physical meaning — and deduce the validity and, therefore, usefulness — of some common approaches in heterogeneous catalysis, such as linking catalyst activity to a ‘turnover frequency’ and explaining catalytic performance in terms of ‘structure sensitivity’ or ‘structure insensitivity’. Catalytic concepts from the fields of enzymatic and homogeneous catalysis are compared, ultimately realizing that the struggle that one encounters in defining the active site in most solid catalysts is likely the one we must overcome to reach our end goal: tailoring the precise functioning of the active sites with respect to many different parameters to satisfy our ever-growing needs. This article ends with an outlook of what may become feasible within the not-too-distant future with modern experimental and theoretical tools at hand. [Figure not available: see fulltext.].
AB - Catalysis is at the core of chemistry and has been essential to make all the goods surrounding us, including fuels, coatings, plastics and other functional materials. In the near future, catalysis will also be an essential tool in making the shift from a fossil-fuel-based to a more renewable and circular society. To make this reality, we have to better understand the fundamental concept of the active site in catalysis. Here, we discuss the physical meaning — and deduce the validity and, therefore, usefulness — of some common approaches in heterogeneous catalysis, such as linking catalyst activity to a ‘turnover frequency’ and explaining catalytic performance in terms of ‘structure sensitivity’ or ‘structure insensitivity’. Catalytic concepts from the fields of enzymatic and homogeneous catalysis are compared, ultimately realizing that the struggle that one encounters in defining the active site in most solid catalysts is likely the one we must overcome to reach our end goal: tailoring the precise functioning of the active sites with respect to many different parameters to satisfy our ever-growing needs. This article ends with an outlook of what may become feasible within the not-too-distant future with modern experimental and theoretical tools at hand. [Figure not available: see fulltext.].
UR - http://www.scopus.com/inward/record.url?scp=85122394471&partnerID=8YFLogxK
U2 - 10.1038/s41570-021-00340-y
DO - 10.1038/s41570-021-00340-y
M3 - Review article
AN - SCOPUS:85122394471
SN - 2397-3358
VL - 6
SP - 89
EP - 111
JO - Nature Reviews Chemistry
JF - Nature Reviews Chemistry
IS - 2
ER -