Betavoltaic Enhancement Using Defect-Engineered TiO2 Nanotube Arrays through Electrochemical Reduction in Organic Electrolytes.
Yang MaNa WangJiang ChenChangsong ChenHaisheng SanJige ChenZhengdong ChengPublished in: ACS applied materials & interfaces (2018)
Utilizing high-energy beta particles emitted from radioisotopes for long-lifetime betavoltaic cells is a great challenge due to low energy conversion efficiency. Here, we report a betavoltaic cell fabricated using TiO2 nanotube arrays (TNTAs) electrochemically reduced in ethylene glycol electrolyte (EGECR-TNTAs) for the enhancement of the betavoltaic effect. The electrochemical reduction of TNTAs using high cathodic bias in organic electrolytes is indeed a facile and effective strategy to induce in situ self-doping of oxygen vacancy (OV) and Ti3+ defects. The black EGECR-TNTAs are highly stable with a significantly narrower band gap and higher electrical conductivity as well as UV-vis-NIR light absorption. A 20 mCi of 63Ni betavoltaic cell based on the reduced TNTAs exhibits a maximum ECE of 3.79% with open-circuit voltage of 1.04 V, short-circuit current density of 117.5 nA cm-2, and a maximum power density of 39.2 nW cm-2. The betavoltaic enhancement can be attributed to the enhanced charge carrier transport and separation as well as multiple exciton generation of electron-hole pairs due the generation of OV and Ti3+ interstitial bands below the conductive band of TiO2.
Keyphrases
- ionic liquid
- quantum dots
- single cell
- visible light
- gold nanoparticles
- cell therapy
- solid state
- induced apoptosis
- solar cells
- ion batteries
- molecularly imprinted
- reduced graphene oxide
- photodynamic therapy
- label free
- cell death
- stem cells
- signaling pathway
- metal organic framework
- cell cycle arrest
- liquid chromatography
- fluorescence imaging
- transition metal
- pi k akt
- drug delivery
- electron transfer
- drug release
- cell proliferation