Boosting electrocatalytic CO2 reduction to formate via carbon nanofiber encapsulated bismuth nanoparticles with ultrahigh mass activity

نویسندگان

چکیده

Electrochemical CO2 conversion is one of the most promising technologies to achieve carbon neutrality. However, it still suffers from some nonnegligible challenges on low production rate and unsatisfied current densities for potential large-scale applications. Herein, we prepare ultrasmall Bi nanoparticles uniformly encapsulated in nanofibers through electrospinning techniques, which denoted as Bi/CNFs-900. Gratifyingly, this Bi/CNFs-900 catalyst demonstrates excellent performance stability electro-reduction a broad window. Specifically, can produce formate with Faradaic efficiency over 90% high partial density –235.3 mA cm−2 at −1.23 V vs. RHE flow-cell. Furthermore, confinement effect largely restricts severe aggregation bismuth during synthesis well electrolysis procedure, greatly increases accessible active sites decreases actual mass fraction composition. Consequently, not only achieves ultrahigh activity –1.6 A mgBi−1, but also possesses an unprecedented 4403.3 μmol h−1 cm−2. DFT calculations situ Raman spectroscopy further uncover possible reaction mechanism reduction toward formate. These results could provide economical industrial-viable strategy preparation electrocatalysts reduction.

برای دانلود رایگان متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Electrocatalytic O2 reduction at glassy carbon electrodes modified with dendrimer-encapsulated Pt nanoparticles.

Platinum dendrimer-encapsulated nanoparticles (DENs) were prepared within fourth-generation, hydroxyl-terminated, poly(amidoamine) dendrimers and immobilized on glassy carbon electrodes using an electrochemical coupling strategy. X-ray photoelectron spectroscopy, electron microscopy, and electrochemical experiments confirmed that the Pt DENs were about 1.4 nm in diameter and that they remained ...

متن کامل

Electrospun Nb-doped TiO2 nanofiber support for Pt nanoparticles with high electrocatalytic activity and durability

This study explores a facile method to prepare an efficient and durable support for Pt catalyst of polymer electrolyte membrane fuel cell (PEMFC). As a candidate, Nb-doped TiO2 (Nb-TiO2) nanofibers are simply fabricated using an electrospinning technique, followed by a heat treatment. Doping Nb into the TiO2 nanofibers leads to a drastic increase in electrical conductivity with doping level of ...

متن کامل

Electrocatalytic Activity of Organically Functionalized Silver Nanoparticles in Oxygen Reduction

Silver nanoparticles capped by a variety of organic ligands (i.e., 1-hexanethiol, 1-octyne, and 4-trifluoromethylphenyl fragments) were synthesized by a chemical reduction route, with the resulting nanoparticles denoted as AgSC6, AgHC8, and AgPhCF3, respectively. The nanoparticle structures were characterized by using a variety of techniques including NMR, UV-vis, infrared, thermogravimetric an...

متن کامل

Organocatalysts with carbon-centered activity for CO2 reduction with boranes.

We report two organocatalysts for CO2 hydroboration to methylborylethers, which upon hydrolysis can produce methanol. These organocatalysts feature carbon-centered reversible CO2 binding, broad borane scopes, and high catalytic activities.

متن کامل

Versatile functionalization of carbon electrodes with a polypyridine ligand: metallation and electrocatalytic H(+) and CO2 reduction.

A strategy is proposed for immobilization of homogeneous catalysts whereby a glassy carbon electrode is functionalized by electro-grafting of a ligand, terpyridine. The modified electrode can easily be metallated with cobalt and shows activity towards catalytic proton and CO2 reduction. The metal can be removed and the electrode re-metallated at will.

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

ژورنال

عنوان ژورنال: Chinese Journal of Catalysis

سال: 2023

ISSN: ['0253-9837', '1872-2067']

DOI: https://doi.org/10.1016/s1872-2067(22)64177-9