Promotion of dual-reaction pathway in CO2 reduction over Pt0/SrTiO3–δ: Experimental and theoretical verification

نویسندگان

چکیده

The H2 evolution is generally considered a competing reaction in photocatalytic CO2 reduction (CO2RR) using H2O as the proton source. However, reducing gas generated from splitting can be source CO2RR under enhanced dynamic role of thermal effect. reverse water shift (RWGS) reaction, hydrogenation should occur photothermal environment owing to thermodynamically and kinetically favorable. Herein, nanostructured metal-semiconductor contact consisting Pt nanoparticles (NPs) supported on SrTiO3–δ nanosheets with rich oxygen vacancies (Pt-OVs-STO) was constructed for investigating its feasibility efficiency RWGS Our experimental results substantiate that by effectively contributes over Pt-OVs-STO system. Pt0 NPs not only efficiently facilitate surface charge transfer, but also lower energy barrier O–H bond breaking, releasing, thereby showing an outstanding performance. strong interaction between has been extensively demonstrated series characterizations density functional theory calculations. This work elucidates relation Pt0/SrTiO3–δ structure catalytic provides new perspectives subsequent CO2RR.

برای دانلود باید عضویت طلایی داشته باشید

برای دانلود 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

Electrochemical promotion of catalysis over Pd nanoparticles for CO2 reduction.

Electrochemical promotion of catalysis (EPOC) has been shown to accelerate the rate of many heterogeneous catalytic reactions; however, it has rarely been reported in low-temperature aqueous electrochemical reactions. Herein, we report a significant EPOC effect for the CO2 reduction to generate formate over Pd nanoparticles (NPs) in a 1 M KHCO3 aqueous solution. By applying a negative potential...

متن کامل

role of cultural iran in promotion of multilaieralism in central asia and caucasus

cultural iran is a scope that is more extended than the political territories of iran as a political unit. this concept means that cultural geography(mehdi moghanlo-1383-1) of iran is greater than its political geography which, according to history, has a long history extending west-east from kandahar to the euphrates and north-south from the persian gulf to the caucasus including transoxiana a...

15 صفحه اول

synthesis of 3-aryl-2h-benzo[b]-1,4-oxazines in [omim]bf4 and reduction of organic compounds in methylimidazolium formate

در این پروژه ترکیبات 3-آریل-2h-بنزو[b]-4،1-اکسازین ها از مواد اولیه تجاری مشتقات دو آمینو فنول و ?-هالو کتون های آروماتیک در مایع یونی 1-اکتیل-3-متیل ایمیدازولیوم تترا فلورو بورات([omim]bf4) سنتز شده است. این واکنش توسط باز پتاسیم کربنات محلول از طریق o-آلکیلاسیون و سپس یک واکنش آمیداسیون درون مولکولی خود بخود در مدت زمان کوتاه انجام می شود. ترکیبات 4،1-بنزوکسازین به این روش با بهره خوب تا آلی ...

15 صفحه اول

simulation and experimental studies for prediction mineral scale formation in oil field during mixing of injection and formation water

abstract: mineral scaling in oil and gas production equipment is one of the most important problem that occurs while water injection and it has been recognized to be a major operational problem. the incompatibility between injected and formation waters may result in inorganic scale precipitation in the equipment and reservoir and then reduction of oil production rate and water injection rate. ...

Experimental and theoretical investigation of the reaction

The rate coefficient of the reaction NHsX 3S−d+Hs2Sd→ k1a NsSd+H2sX Sg d is determined in a quasistatic laser-flash photolysis, laser-induced fluorescence system at low pressures s2 mbarø p ø10 mbard. The NHsXd radicals are produced via the quenching of NHsaDd sobtained by photolyzing HN3d with Xe whereas the H atoms are generated in a H2/He microwave discharge. The NHsXd concentration profile ...

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)64175-5