Enhanced electrocatalytic reduction of CO2 with ternary Ni-Fe4S4 and Co-Fe4S4-based biomimetic chalcogels.
نویسندگان
چکیده
Enzymes that catalytically transform small molecules such as CO, formate, or protons are naturally composed of transition metal cluster units bound into a larger superstructure. Artificial biomimetic catalysts are often modeled after the active sites but are typically molecular in nature. We present here a series of fully integrated porous materials containing Fe(4)S(4) clusters, dubbed "biomimetic chalcogels". We examine the effect of third metal cations on the electrochemical and electrocatalytic properties of the chalcogels. We find that ternary biomimetic chalcogels containing Ni or Co show increased effectiveness in transformations of carbon dioxide and can be thought of as solid-state analogues of NiFe or NiFeS reaction centers in enzymes.
منابع مشابه
Nitrogenase-mimic iron-containing chalcogels for photochemical reduction of dinitrogen to ammonia.
A nitrogenase-inspired biomimetic chalcogel system comprising double-cubane [Mo2Fe6S8(SPh)3] and single-cubane (Fe4S4) biomimetic clusters demonstrates photocatalytic N2 fixation and conversion to NH3 in ambient temperature and pressure conditions. Replacing the Fe4S4 clusters in this system with other inert ions such as Sb(3+), Sn(4+), Zn(2+) also gave chalcogels that were photocatalytically a...
متن کاملSpectroelectrochemical characterization of the metal centers in carbon monoxide dehydrogenase (CODH) and nickel-deficient CODH from Rhodospirillum rubrum.
Carbon-monoxide dehydrogenase (CODH) from Rhodospirillum rubrum contains two metal centers: a Ni-X-[Fe4S4]2+/1+ cluster (C-center) that serves as the COoxidation site and a standard [Fe4S4]2+/1+ cluster (B-center) that mediates electron flow from the C-center to external electron acceptors. Four states of the C-center were previously identified in electron paramagnetic resonance (EPR) and Mössb...
متن کاملFlavodoxin hydroquinone reduces Azotobacter vinelandii Fe protein to the all-ferrous redox state with a S = 0 spin state.
Azotobacter vinelandii flavodoxin hydroquinone (FldHQ) is a physiological reductant to nitrogenase supporting catalysis that is twice as energy efficient (ATP/2e- = 2) as dithionite (ATP/2e- = 4). This catalytic efficiency results from reduction of Fe protein from A. vinelandii (Av2) to the all-ferrous oxidation state ([Fe4S4]0), in contrast to dithionite, which only reduces Av2 to the [Fe4S4]1...
متن کاملInitial synthesis and structure of an all-ferrous analogue of the fully reduced [Fe4S4] cluster of the nitrogenase iron protein
The synthetic cubane-type iron–sulfur clusters [Fe4S4(SR)4] form a four-member electron transfer series (z 3 , 2 , 1 , and 0), all members of which except that with z 0 have been isolated and characterized. They serve as accurate analogues of protein-bound [Fe4S4(SCys)4] redox centers, which, in terms of core oxidation states, exhibit the redox couples [Fe4S4] /2 and [Fe4S4] /1 . Clusters with ...
متن کاملStructural and spectroscopic models of the A-cluster of acetyl coenzyme a synthase/carbon monoxide dehydrogenase: Nature’s Monsanto acetic acid catalyst
Acetyl coenzyme A synthase/carbon monoxide dehydrogenase (ACS/CODH) is a bifunctional enzyme present in a number of anaerobic bacteria. The enzyme catalyzes two separate reactions namely, the reduction of atmospheric CO2 to CO (CODH activity at the C-cluster) and the synthesis of acetyl coenzyme A (ACS activity at the A-cluster) from CO, CH3 from a corrinoid iron-sulfur protein, and the thiol c...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید
ثبت ناماگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید
ورودعنوان ژورنال:
- Journal of the American Chemical Society
دوره 133 40 شماره
صفحات -
تاریخ انتشار 2011