Reviews & Analysis

The development of bimetallic catalysts is often hindered by the heavy workload of the classical trial-and-error method. Now, a distinct mechanism demonstrates that breaking down the net thermochemical reaction into the corresponding electrochemical half-reactions offers a facile approach to design bimetallic catalysts by analysing each putative half-reaction.

While skeletal editing stands as a powerful approach for simplifying synthetic procedures and obtaining complex molecules, viable methodologies remain limited. Now, a smart photoredox protocol, involving the insertion of carbon atoms into the indene core, gives access to a wide library of functionalized naphthalenes.

The lack of stability of critical raw material-free electrocatalysts during the oxygen evolution reaction in acidic electrolytes lies beneath the use of Ir-based electrocatalysts in polymeric water electrolysis. Here, a strategy to enhance γ-MnO₂ stability in acid is proposed. Theoretical and spectroscopic approaches reveal that increasing the fraction of O atoms in the appropriate position, namely O_pla, prevents Mn dissolution during water electrolysis.

The coenzyme Q biosynthetic pathway has evaded full characterization for decades, in part due to the inherent insolubility of coenzyme Q and the instability of its membrane-associated biosynthetic enzymes. Now, researchers have resurrected an active ancestral coenzyme Q metabolon in vitro that has unveiled valuable insights into previously uncharacterized aspects of coenzyme Q biosynthesis.

A deeper understanding of reaction mechanisms should lead to improvements in the selectivity of organic electrosynthesis methods. This approach has now been used to explain the role of magnesium diacetate in the Ag-electrocatalysed reductive coupling of sp³ organic chlorides with aldehydes or ketones with increased selectivity for the desired alcohol product.

Chiral BINOL-phosphates have qualified as privileged Brønsted acid organocatalysts, providing solutions to many challenging enantioselective transformations for a wide range of substrates under mild reaction conditions. Here we revisit the story of their origins.

The ab initio atomistic thermodynamics approach, coined by Reuter and Scheffler formally in 2001, remains pivotal for understanding and predicting the stable surfaces of thermal catalysts under technical conditions.

Traditional catalyst synthesis primarily hinges on liquid-phase methods. Nevertheless, a quarter of a century ago, the advent of vapour-phase methods such as atomic layer deposition opened up important alternatives to atomically tailor catalysts and boost their performance.

Electrocatalysis would not be the same without the rotating disk electrode. Its invention in the mid-twentieth century enabled immense developments, which rendered it a classic technique in electrochemistry. The rotating disk electrode will remain a cornerstone of electrocatalysis with further advances that bridge the gap with real systems.

Elucidating the origin of light-induced reaction rate enhancement in plasmonic photocatalysis is very challenging. Now, bimetallic supercrystals are reported to boost photocatalytic hydrogen evolution from formic acid with the sole aid of intensified electric fields.

Iron–nitrogen–carbon (FeNC) catalysts are a viable alternative to platinum, but still lack the necessary performance. Now, pyrolysis under forming gas is found as a path to boosting their site density, activity and durability.

Enantioselective synthesis of chiral cyclobutanes via direct cycloaddition of C–C single bonds with C=C double bonds has remained an unmet challenge. Now, a photoelectrocatalytic system enabling asymmetric dehydrogenative [2+2] cycloaddition of alkyl ketones and alkenes has been developed.

With climate change concerns deepening, CO₂ fixation pathways to produce value-added chemicals are currently of interest. Now, synthetic biology and machine learning help developing such a pathway across modules that have been tested in vivo in Escherichia coli for the production of acetyl coenzyme A.

The search for novel biocatalysts for plastic degradation has recently become a hot topic. Now, multiple catalytic triads of well-known serine esterases were introduced into non-catalytic protein nanopores to enable the hydrolysis of PET nanoparticles.

Suppressing the formation of oxide encapsulation layers on the active metal during pretreatment would lead to increased catalytic activity in supported catalysts, but controlling the strong metal-support interactions is challenging. Now it is shown that cleverly introducing TiO_x patches onto Ru/MnO allows engineering effective oxide–oxide interface channels and avoids oxide overlayer formation, thus improving the performance of CO₂ hydrogenation to produce CO.

Diverse cytochrome P450s (CYPs) in nature can modify terpenoid scaffolds toward products with higher structural complexity and chemical diversity, but their discovery remains challenging. Now, an Escherichia coli -based gene screening platform enables high-throughput bacterial CYP screening, leading to efficient and diverse terpenoid biosynthesis.

A better understanding of the mechanism of electrochemical CO₂ reduction should enable development of electrocatalysts that are more active and selective. Now, through an isotopic labelling strategy, it has been discovered that there are at least two types of active sites on Cu electrocatalysts, one responsible for converting CO₂ to CO and another for further converting CO to useful C₂₊ products.

Selective electrochemical oxidation of ammonia provides an ideal pathway to synthesize hydrazine, but this process is outcompeted by a more favourable overoxidation to N₂. A molecular ruthenium catalyst has now flipped the script, circumventing the thermodynamic challenges to selectively generate hydrazine.

CRISPR-Cas9 is a major gene-editing tool that has attracted tremendous interdisciplinary efforts to ameliorate precise genome manipulation. Now, the pivotal structural features behind concerted double-stranded DNA cleavages by the Cas9 endonuclease have been captured through cryo-electron microscopy, laying the groundwork for improved Cas9 engineering.

The selective oxidation of methane to methanol using O₂ under mild conditions has been a challenge for decades. Now, this transformation is selectively achieved at ambient temperature with productivity as high as 67.4 μmol g_cat⁻¹ h⁻¹ on a reduced phosphomolybdate catalyst, where H₂ is required to keep the catalyst surface in a reduced state.